Section 52

EurekaMag PDF full texts Chapter 51,190


Strachan, S.J. 1949: A note on the use of pertussis vaccine in day nurseries. Glasgow Medical Journal 30(6): 228-229
Sokhey, S.S.; Wagle, P.M. 1946: A note on the use of sulphonamides in the treatment of plague in the field. Indian Medical Gazette 81(9): 343-346
Allen, R.M. 1948: A note on the use of the Bellevue-Wechsler scale mental deterioration index with brain injured patients. Journal of Clinical Psychology 4(1): 88
Gordon, D. 1947: A note on the use of the Lysholm skull table. British Journal of Radiology 20(234): 238
Harris, D.B. 1947: A note on the use of the Woodworth-Mathews questionnaire to predict the emotional adjustment of delinquent boys in a correctional school. Journal of Consulting Psychology 11(3): 151
Meissner, W.W. 2008: A note on the use of the concept of the soul in psychoanalytic discourse. Psychoanalytic Quarterly 77(1): 327-340
Pereira, T.V.; Mingroni-Netto, R.C. 2011: A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. Bmc Research Notes 4: 172
Kühnast, C.; Neuhäuser, M. 2008: A note on the use of the non-parametric Wilcoxon-Mann-Whitney test in the analysis of medical studies. German Medical Science: Gms E-Journal 6: Doc02
Sun, W.; Shults, J.; Leonard, M. 2009: A note on the use of unbiased estimating equations to estimate correlation in analysis of longitudinal trials. Biometrical Journal. Biometrische Zeitschrift 51(1): 5-18
Pascal, G.R.; Zeaman, J.B. 1949: A note on the validity of Wechsler-Bellevue scatter. American Journal of Psychiatry 105(11): 840-842
Yuan, Y.; Zhu, H.; Ibrahim, J.G.; Lin, W.; Peterson, B.S. 2008: A note on the validity of statistical bootstrapping for estimating the uncertainty of tensor parameters in diffusion tensor images. IEEE Transactions on Medical Imaging 27(10): 1506-1514
Gray, S.W. 1947: A note on the values of southern college women, white and Negro. Journal of social psychology 25: 239-241
Sloane, A.B.; Latven, A.R.; Munch, J.C. 1948: A note on the variability of potency of commercial viburnum preparations. Journal of the American Pharmaceutical Association. American Pharmaceutical Association 37(3): 132
Rogers, T.M.; Henderson, D.A.; Cragg, L.H. 1947: A note on the variation with temperature of the intrinsic viscosity of GR-S in benzene. Canadian Journal of Research 25(4): 351-356
Díaz, C.; Olsen, R.A. 2009: A note on the vibrational efficacy in molecule-surface reactions. Journal of Chemical Physics 130(9): 094706
DeMEILLON, B.; Gear, J. 1947: A note on three noxious arthropods occurring on the Witwatersrand. South African Medical Journal 21(11): 407-411
Brumfeld, V.; Charuvi, D.; Nevo, R.; Chuartzman, S.; Tsabari, O.; Ohad, I.; Shimoni, E.; Reich, Z. 2008: A note on three-dimensional models of higher-plant thylakoid networks. Plant cell 20(10): 2546-9; author reply 2549-51
Wicht, J.F.; Rabkin, R. 1947: A note on tick-bite fever. South African Medical Journal 21(1): 30
Coates, J.M.; Page, L. 2009: A note on trader Sharpe Ratios. Plos one 4(11): E8036
Yoshioki, S. 2010: A note on transformation between clathrate hydrate structures I and II. Journal of Molecular Graphics and Modelling 29(2): 290-294
Randhawa, S.Singh.; Chhabra, S.; Randhawa, C.Singh.; Zahid, U.; Dhaliwal, P.Singh. 2014: A note on treatment of hyperthermia in crossbred cattle. Asian Pacific Journal of Tropical Biomedicine 4(Suppl. 1): S272-S274
Dmitrienko, A.; Tamhane, A.C.; Liu, L.; Wiens, B.L. 2008: A note on tree gatekeeping procedures in clinical trials. Statistics in Medicine 27(17): 3446-3451
Servino, V. 1951: A note on tropicaloid ulcer (Castellani); its occurrence in Italy. Journal of Tropical Medicine and Hygiene 54(7): 147-148
Thomsen, S.Francis.; Kyvik, K.Ohm.; Backer, V. 2008: A note on twin-singleton differences in asthma. Twin Research and Human Genetics: the Official Journal of the International Society for Twin Studies 11(2): 161-164
Dong, X.; Guo, Y.; Tsong, Y. 2012: A note on two approaches of testing bridging evidence to a new region. Journal of Biopharmaceutical Statistics 22(5): 966-976
Mulhearn, C.R. 1946: A note on two blood parasites of cattle (Spirochaeta theileri and Bartonella bovis) recorded for the first time in Australia. Australian Veterinary Journal 22(4): 118
Chiclana, F.; Herrera-Viedma, E.; Alonso, S. 2009: A note on two methods for estimating missing pairwise preference values. IEEE Transactions on Systems Man and Cybernetics. Part B Cybernetics: a Publication of the IEEE Systems Man and Cybernetics Society 39(6): 1628-1633
Giorgi, E.E.; Bhattacharya, T. 2012: A note on two-sample tests for comparing intra-individual genetic sequence diversity between populations. Biometrics 68(4): 1323-6; author reply 1326
Neuhaus, J.M.; McCulloch, C.E.; Boylan, R. 2011: A note on type II error under random effects misspecification in generalized linear mixed models. Biometrics 67(2): 654-6; Disucssion 656-60
Wang, P.J.; Fu, H.H.; Liu, W.T. 1948: A note on typhus fever in Lanchow. Chinese Medical Journal 66(2): 79-83
Cass, G.V. 1947: A note on use of Schultz and Olson lethal-rate paper for calculation of thermal processes for food products in tin containers. Food Research 12(1): 24-26
Rae, G. 2008: A note on using alpha and stratified alpha to estimate the reliability of a test composed of item parcels. British Journal of Mathematical and Statistical Psychology 61(Pt 2): 515-525
Zhuang, H. 1998: A note on using only position equations for robotic hand/eye calibration. IEEE Transactions on Systems Man and Cybernetics. Part B Cybernetics: a Publication of the IEEE Systems Man and Cybernetics Society 28(3): 426-427
Rae, G. 2007: A note on using stratified alpha to estimate the composite reliability of a test composed of interrelated nonhomogeneous items. Psychological Methods 12(2): 177-184
Allignol, A.; Schumacher, M.; Beyersmann, J. 2010: A note on variance estimation of the Aalen-Johansen estimator of the cumulative incidence function in competing risks, with a view towards left-truncated data. Biometrical Journal. Biometrische Zeitschrift 52(1): 126-137
Zhao, J-hua.; Yu, P.L.H. 2009: A note on variational Bayesian factor analysis. Neural Networks: the Official Journal of the International Neural Network Society 22(7): 988-997
Bilodeau, I.M. 1969: A note on verbal reinforcement combinations. Journal of Motor Behavior 1(1): 61-64
Fourcin, A. 2010: A note on voice timing and the evolution of connected speech. Logopedics Phoniatrics Vocology 35(2): 74-80
Bleile, K.M. 1989: A note on vowel patterns in two normally developing children. Clinical Linguistics and Phonetics 3(2): 203-212
Gregory, N.G.; Alam, M.R.; Rahman, M.M.; Jabbar, M.A.; Uddin, M.S. 2011: A note on water quality associated with slaughter premises in Bangladesh. Meat Science 88(4): 791-793
Franz, S.; Parisi, G.; Ricci-Tersenghi, F.; Rizzo, T.; Urbani, P. 2013: A note on weakly discontinuous dynamical transitions. Journal of Chemical Physics 138(6): 064504
Magis, D. 2015: A note on weighted likelihood and Jeffreys modal estimation of proficiency levels in polytomous item response models. Psychometrika 80(1): 200-204
Hoehn, A.A. 1946: A note on writing prescription labels. Journal of the American Pharmaceutical Association. American Pharmaceutical Association 7: 73
Al-Hakim, L. 2011: A note on "Improving cardiac surgical care: a work systems approach". Applied Ergonomics 42(6): 941
Oshikoya, K.A.; Senbanjo, I.O. 2009: A note on "Malaria at parturition in Nigeria: current status and delivery outcome". Infectious Diseases in Obstetrics and Gynecology 2009: 426201
Wang, Y. 1997: A note on "Solving the find-path problem by good representation of free space". IEEE Transactions on Systems Man and Cybernetics. Part B Cybernetics: a Publication of the IEEE Systems Man and Cybernetics Society 27(4): 723-724
Dalla-Zuanna, G.; Rosina, A. 2010: A note on: the joint effect of maternal malnutrition and cold weather on neonatal mortality in nineteenth-century Venice: an assessment of the hypothermia hypothesis, Population Studies 63(3): 233-251 by Renzo Derosas. Population Studies 64(2): 193-195
Senn, S. 2014: A note regarding 'random effects'. Statistics in Medicine 33(16): 2876-2877
Senn, S.; Jude-Eze, E.Nijedeka. 2014: A note regarding Lee's checks for minimum numbers of subjects where relative risks have been calculated. Statistics in Medicine 33(23): 4135-4138
Senn, S. 2014: A note regarding meta-analysis of sequential trials with stopping for efficacy. Pharmaceutical Statistics 13(6): 371-375
Einsporn, R.L.; Jia, Z. 2014: A note regarding problems with interaction and varying block sizes in a comparison of endotracheal tubes. Computational and Mathematical Methods in Medicine 2014: 956917
Rohde, A.R. 1948: A note regarding the use of the sentence completions test in military installations since the beginning of World War II. Journal of Consulting Psychology 12(3): 190-193
Krumholz, H.M. 2012: A note to my younger colleagues...be brave. Circulation. Cardiovascular Quality and Outcomes 5(3): 245-246
Waisser, K.; Petrlíková, E.; Perina, M.; Klimesová, V.; Kunes, Jí.; Palát, K.; Kaustová, J.; Dahse, H-Martin.; Möllmann, U. 2010: A note to the biological activity of benzoxazine derivatives containing the thioxo group. European Journal of Medicinal Chemistry 45(7): 2719-2725
Zusman, M. 2012: A note to the musculoskeletal physiotherapist. Journal of Back and Musculoskeletal Rehabilitation 25(2): 103-107
Coulthard, C.E. 1939: A note upon the maintenance of cultures of Bacterium typhosum for testing by the Rideal-Walker method. Journal of Hygiene 39(3): 268-270
Sivak, M.; Schoettle, B. 2012: A note: the changing gender demographics of U.S. drivers. Traffic Injury Prevention 13(6): 575-576
Boyd, G. 2010: A noteworthy effort. Radiology Management 32(6): 48-49
Khoury, C.; Bianchi, R.; Massa, A.Andrea.; Severini, F.; Di Luca, M.; Toma, L. 2011: A noteworthy record of Ornithodoros (Alectorobius) coniceps (Ixodida: Argasidae) from Central Italy. Experimental and Applied Acarology 54(2): 205-209
Mauron, A. 2011: A noteworthy special case. Revue Medicale Suisse 7(297): 1226-1227
C 1887: A noteworthy specimen of Devonian lepidodendron. Science 9(225): 516
Huang, X.; Lu, L-ling.; Deng, X-ling.; Huang, Q.; Liang, J-hua.; Zhang, Y-hui.; Yang, X-fen. 2012: A notice from epidemiological investigation of Shiga-toxin-producing Escherichia coli O104:H4 outbreak in Germany, 2011. Zhonghua Liu Xing Bing Xue Za Zhi 33(1): 111-114
Wang, C.; Cheng, X.; Sui, Y.; Luo, X.; Jiang, G.; Wang, Y.; Huang, Z.; She, Z.; Deng, Y. 2013: A noticeable phenomenon: thiol terminal PEG enhances the immunogenicity of PEGylated emulsions injected intravenously or subcutaneously into rats. European Journal of Pharmaceutics and Biopharmaceutics: Official Journal of Arbeitsgemeinschaft für Pharmazeutische Verfahrenstechnik E.V 85(3 Pt A): 744-751
Walker, A.N.; Dickerman, E.H. 2001: A notorious woman: possession, witchcraft and sexuality in seventeenth-century Provence. Historical Reflections. Reflexions Historiques 27(1): 1-26
Tripathi, S.; Chand, P.; Singh, R.D.; Siddharth, R.; Singh, B.P. 2011: A noval approach of altered cast technique in bilateral partial maxillectomy patient with severely restricted mouth opening. Isrn Dentistry 2011: 607175
Slim, H.; Huang, D.; Rashid, H. 2010: A noval approach using angioplasty for recanalization of a chronically occluded bypass vein graft for limb salvage. Vascular and Endovascular Surgery 44(5): 377-380
Mills, A.; Skinner, G.A. 2011: A novel 'fizziness' indicator. Analyst 136(5): 894-896
Lin, J-wen.; Annoura, T.; Sajid, M.; Chevalley-Maurel, Séverine.; Ramesar, J.; Klop, O.; Franke-Fayard, B.M.D.; Janse, C.J.; Khan, S.M. 2011: A novel 'gene insertion/marker out' (GIMO) method for transgene expression and gene complementation in rodent malaria parasites. Plos one 6(12): E29289
Singh, S.; Saikia, J.P.; Buragohain, A.K. 2013: A novel 'green' synthesis of colloidal silver nanoparticles (SNP) using Dillenia indica fruit extract. Colloids and Surfaces. B Biointerfaces 102: 83-85
Sarode, S.C.; Sarode, G.S. 2012: A novel 'microscopic method' of shrinkage calculation in the pursuance of shrinkage based histopathological guidelines for interpretation of surgical margins. Oral Oncology 48(6): E15-E16
Wang, F.; Yan, X.; Song, L.; Wang, P.; Lu, D.; Feng, J.; Yang, D.; Yan, X. 2013: A novel 'pipeline' system for downstream preparation of therapeutic monoclonal antibodies. Biotechnology Letters 35(9): 1411-1418
Matsubara, S.; Kuwata, T.; Baba, Y.; Usui, R.; Suzuki, H.; Takahashi, H.; Ohkuchi, A.; Suzuki, M. 2014: A novel 'uterine sandwich' for haemorrhage at caesarean section for placenta praevia. Australian and New Zealand Journal of Obstetrics and Gynaecology 54(3): 283-286
Camici, P.G.; Rimoldi, O.E. 2009: A novel (18)F-labeled tracer for the quantification of myocardial blood flow and infarct size with positron-emission tomography: another way to avoid the need of an on-site cyclotron. CIRCULATION. Cardiovascular Imaging 2(2): 75-76
Santos, H.M.; Glez-Peña, D.; Reboiro-Jato, M.; Fdez-Riverola, F.; Diniz, M.ár.S.; Lodeiro, C.; Capelo-Martínez, J.é-L. 2010: A novel (18)O inverse labeling-based workflow for accurate bottom-up mass spectrometry quantification of proteins separated by gel electrophoresis. Electrophoresis 31(20): 3407-3419
Bonetto, F.; Srinivas, M.; Heerschap, A.; Mailliard, R.; Ahrens, E.T.; Figdor, C.G.; de Vries, I.J.M. 2011: A novel (19)F agent for detection and quantification of human dendritic cells using magnetic resonance imaging. International Journal of Cancer 129(2): 365-373
Sun, L.; Xing, H.; Xu, J.; Liang, Z.; Yu, J.; Xu, R. 2013: A novel (3,3,6)-connected luminescent metal-organic framework for sensing of nitroaromatic explosives. Dalton Transactions 42(15): 5508-5513
Zhang, P.; Li, B.; Zhao, Y.; Meng, X.; Zhang, T. 2011: A novel (3,36)-connected and self-interpenetrated metal-organic framework with high thermal stability and gas-sorption capabilities. Chemical Communications 47(27): 7722-7724
Zhou, Y.; Zhao, W.N.; Han, L. 2009: A novel (3,4,10)-connected three-dimensional hydrogen-bonded supramolecular network containing a cyclic water hexamer. Acta Crystallographica. Section C Crystal Structure Communications 65(Part 6): O287-O289
Lu, Q.; Wang, D.; Wang, S. 2010: A novel (4,6)-connected double-layered Ba(II) coordination polymer based on the flexible tricarboxylate ligand 2,2',2''-[1,3,5-triazine-2,4,6-triyltris(sulfanediyl)]triacetic acid. Acta Crystallographica. Section C Crystal Structure Communications 66(Part 11): M351-M354
Kühle, B.; Müller, C.; Ross, T.L. 2013: A novel (68)Ga-labeled pteroic acid-based pet tracer for tumor imaging via the folate receptor. Recent Results in Cancer Research. Fortschritte der Krebsforschung. Progres Dans les Recherches sur le Cancer 194: 257-267
Wuillemin, M.A.; Stuber, W.T.; Fox, T.; Reber, M.J.; Brühwiler, D.; Alberto, R.; Braband, H. 2014: A novel (99m)Tc labelling strategy for the development of silica based particles for medical applications. Dalton Transactions 43(11): 4260-4263
Yang, E.J.; Song, G.-Y.; Lee, J.-S.; Yun, C.-Y.; Kim, I.S. 2009: A novel (S)-(+)-decursin derivative, (S)-(+)-3-(3,4-dihydroxy-phenyl)-acrylic acid 2,2-dimethyl-8-oxo-3,4-dihydro-2H,8H-pyrano[3,2-g]chromen-3-yl-ester, inhibits ovalbumin-induced lung inflammation in a mouse model of asthma. Biological and Pharmaceutical Bulletin 32(3): 444-449
Qiu, J.; Wei, Y.; Ma, Y.; Wen, R.; Wen, Y.; Liu, W. 2014: A novel (S)-6-hydroxynicotine oxidase gene from Shinella sp. strain HZN7. Applied and Environmental Microbiology 80(18): 5552-5560
Rose, C.; Rossignol, J.; Lambilliotte, A.; Depret, S.; Le Metayer, N.; Pissard, S. 2009: A novel (epsilongammadeltabeta)(o)-thalassemia deletion associated with an alpha globin gene triplication leading to a severe transfusion dependent fetal thalassemic syndrome. Haematologica 94(4): 593-594
Atack, E.; Fairtlough, H.; Smith, K.; Balasubramanian, M. 2014: A novel (paternally inherited) duplication 13q31.3q32.3 in a 12-year-old patient with facial dysmorphism and developmental delay. Molecular Syndromology 5(5): 245-250
Otsuka, Y. 2009: A novel 0.010-inch guidewire for crossing jailed sidebranches. Catheterization and Cardiovascular Interventions: Official Journal of the Society for Cardiac Angiography and Interventions 73(3): 346-349
Cook-Bolden, F. 2011: A novel 0.65 millisecond pulsed 1064 nm laser to treat skin of color without skin cooling or anesthetics. Journal of Drugs in Dermatology: Jdd 10(12 Suppl): S10-S11
Fang, S-Tao.; Liu, J-Kai.; Li, B. 2010: A novel 1,10-seco withanolide from Physalis peruviana. Journal of Asian Natural Products Research 12(7): 618-622
Li, D.-D.; Tian, J.-L.; Gu, W.; Liu, X.; Yan, S.-P. 2010: A novel 1,2,4-triazole-based copper(II) complex: synthesis, characterization, magnetic property and nuclease activity. Journal of Inorganic Biochemistry 104(2): 171-179
Gong, W.; Hu, E.; Dou, H.; Song, Y.; Yang, L.; Ji, J.; Li, E.; Tan, R.; Hou, Y. 2014: A novel 1,2-benzenediamine derivative FC-99 suppresses TLR3 expression and ameliorates disease symptoms in a mouse model of sepsis. British Journal of Pharmacology 171(21): 4866-4878
Barna, B.P.; Malur, A.; Dalrymple, H.; Karnekar, R.; Culver, D.A.; Abraham, S.; Singh, R.J.; Brescia, D.; Kavuru, M.S.; Thomassen, M.Jane. 2009: A novel 1,25-dihydroxyvitamin D-activin A pathway in human alveolar macrophages is dysfunctional in patients with pulmonary alveolar proteinosis (PAP). Autoimmunity 42(1): 56-62
Yin, L-Lin.; Li, M-Hui.; Wang, X.; Zhang, W-Yu. 2009: A novel 1,5-diarylpyrazole derivative exerts its anti-inflammatory effect by inhibition of cyclooxygenase-2 activity as a prodrug. Biological and Pharmaceutical Bulletin 32(6): 1032-1036
Berry, V.; Francis, P.J.; Prescott, Q.; Waseem, N.H.; Moore, A.T.; Bhattacharya, S.S. 2011: A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract. Molecular Vision 17: 1249-1253
Kong, X.-D.; Liu, N.; Shi, H.-R.; Yang, Y.-X. 2014: A novel 1-bp deletion mutation of the EDA gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia. Journal of Dermatology 41(7): 659-661
Okpekon, T.; Millot, M.; Champy, P.; Gleye, C.; Yolou, S.; Bories, C.; Loiseau, P.; Laurens, A.; Hocquemiller, R. 2009: A novel 1-indanone isolated from Uvaria afzelii roots. Natural Product Research 23(10): 909-915
Reddy, S.; Dolzhanskaya, N.; Krogh, J.; Velinov, M. 2009: A novel 1.4 Mb de novo microdeletion of chromosome 1q21.3 in a child with microcephaly, dysmorphic features and mental retardation. European Journal of Medical Genetics 52(6): 443-445
Steines, D.A.; Eom, K.-B.; Manuccia, T.; Zderic, V. 2008: A novel 100 watt high intensity focused ultrasound driving system. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference 2008: 2530-2533
Morales-Ríos, E.; de la Rosa-Morales, F.; Mendoza-Hernández, G.; Rodríguez-Zavala, Jé.S.; Celis, H.; Zarco-Zavala, M.; García-Trejo, Jé.J. 2010: A novel 11-kDa inhibitory subunit in the F1FO ATP synthase of Paracoccus denitrificans and related alpha-proteobacteria. Faseb Journal: Official Publication of the Federation of American Societies for Experimental Biology 24(2): 599-608
Sandhya, D.G.; Ahmed, F.; Khadke, K.; Murthy, S.S.; Rajappa, S.J. 2012: A novel 11;18 translocation in a case of acute myeloid leukemia with maturation. Indian Journal of Human Genetics 18(3): 369-372
Park, J.S.; Bae, S.J.; Choi, S.-W.; Son, Y.H.; Park, S.B.; Rhee, S.D.; Kim, H.Y.; Jung, W.H.; Kang, S.K.; Ahn, J.H.; Kim, S.H.; Kim, K.Y. 2014: A novel 11β-HSD1 inhibitor improves diabesity and osteoblast differentiation. Journal of Molecular Endocrinology 52(2): 191-202
Anil, T.M.; Dandu, A.; Harsha, K.; Singh, J.; Shree, N.; Kumar, V.S.; Lakshmi, M.N.; Sunil, V.; Harish, C.; Balamurali, G.V.; Naveen Kumar, B.S.; Gopala, A.S.; Pratibha, S.; Sadasivuni, M.; Anup, M.O.; Moolemath, Y.; Venkataranganna, M.V.; Jagannath, M.R.; Somesh, B.P. 2014: A novel 11β-hydroxysteroid dehydrogenase type1 inhibitor CNX-010-49 improves hyperglycemia, lipid profile and reduces body weight in diet induced obese C57B6/J mice with a potential to provide cardio protective benefits. Bmc Pharmacology and Toxicology 15: 43
Sakabe, J.-I.; Susa, S.; Daimon, M.; Lan, M.-Y.; Kato, T. 2008: A novel 12-base pair deletion mutation in exon 15 of the porphobilinogen deaminase gene in a Taiwanese patient with acute intermittent porphyria. Blood Cells Molecules and Diseases 41(2): 202
Farrar, J.T.; Messina, J.; Xie, F.; Portenoy, R.K. 2010: A novel 12-week study, with three randomized, double-blind placebo-controlled periods to evaluate fentanyl buccal tablets for the relief of breakthrough pain in opioid-tolerant patients with noncancer-related chronic pain. Pain Medicine 11(9): 1313-1327
Rivolta, C.M.; Gil, M.Susana.Mallea.; Ballarino, C.; Ridruejo, M.Carolina.; Miguel, C.M.; Gimenez, S.B.; Bernacchi, S.S.; Targovnik, Héctor.M. 2004: A novel 1297-1304delGCCTGCCA mutation in the exon 10 of the thyroid hormone receptor β gene causes resistance to thyroid hormone. Molecular diagnosis: a journal devoted to the understanding of human disease through the clinical application of molecular biology 8(3): 163-169
Laurell, T.; Vandermeer, J.E.; Wenger, A.M.; Grigelioniene, G.; Nordenskjöld, A.; Arner, M.; Ekblom, A.G.; Bejerano, G.; Ahituv, N.; Nordgren, A. 2012: A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb. Human Mutation 33(7): 1063-1066
Laborde, J.C.; Kipshidze, N.; Ruiz, C.E. 2010: A novel 14F endograft for abdominal aortic aneurysm: first in man. Catheterization and Cardiovascular Interventions: Official Journal of the Society for Cardiac Angiography and Interventions 76(7): 1059-1064
Behar, D.M.; Blue-Smith, J.; Soria-Hernanz, D.F.; Tzur, S.; Hadid, Y.; Bormans, C.; Moen, A.; Tyler-Smith, C.; Quintana-Murci, L.; Wells, R.S.; Schurr, T.G.; Santos, F.R.; Quintana-Murci, L.; Bertranpetit, J.; Comas, D.; Tyler-Smith, C.; Balanovska, E.; Behar, D.M.; Mitchell, R.J.; Jin, L.; Soodyall, H.; Pitchappan, R.; Cooper, A.; Royyuru, A.K.; Rosset, S.; Parida, L.; Blue-Smith, J.; Hernanz, D.S.; Wells, R.S. 2008: A novel 154-bp deletion in the human mitochondrial DNA control region in healthy individuals. Human Mutation 29(12): 1387-1391
Li, H.; Choy, K.W.; Lei, Y.-P.; Wang, W.; Wang, H.-Y.; Chen, Y. 2011: A novel 15bp micro-duplication in SF-1 gene showing diverse phenotypic spectrum in a Chinese family. Journal of Maternal-Fetal and Neonatal Medicine: the Official Journal of the European Association of Perinatal Medicine the Federation of Asia and Oceania Perinatal Societies the International Society of Perinatal Obstetricians 24(1): 132-136
Huys, R.; Braeken, D.; Wouters, J.; Loo, J.; Severi, S.; Vleugels, F.; Bartic, C.; Borghs, G.; Eberle, W. 2010: A novel 16k micro-nail CMOS-chip for in-vitro single-cell recording, stimulation and impedance measurements. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference 2010: 2726-2729
Brusse, E.; Majoor-Krakauer, D.; de Graaf, B.M.; Visser, G.H.; Swagemakers, S.; Boon, A.J.W.; Oostra, B.A.; Bertoli-Avella, A.M. 2009: A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?. Neurogenetics 10(4): 289-297
Das, T.; Chakraborty, S.; Sarma, H.D.; Banerjee, S.; Venakatesh, M. 2010: A novel 177Lu-labeled porphyrin for possible use in targeted tumor therapy. Nuclear Medicine and Biology 37(5): 655-663
He, H.; Liu, X.; Gu, Y.; Liu, Y. 2010: A novel 18-bp deletion mutation of the AMPD1 gene affects carcass traits in Qinchuan cattle. Molecular Biology Reports 37(8): 3945-3949
Wu, Y.; Hou, G-Ge.; Ma, J-Ping.; Dong, Y-Bin. 2010: A novel 18-membered metallocycle in {2,5-bis[3-(1H-1,3-imidazol-1-ylmethyl)phenyl]-1,3,4-oxadiazole}dichloridocobalt(II). Acta Crystallographica. Section C Crystal Structure Communications 66(Pt 6): M163-M165
Huang, X.-Z.; Cheng, C.-M.; Dai, Y.; Fu, G.-M.; Guo, J.-M.; Yin, Y.; Liang, H. 2010: A novel 18-norclerodane diterpenoid from the roots of Tinospora sagittata var. yunnanensis. Molecules 15(11): 8360-8365
Cheng, Y.; Ono, M.; Kimura, H.; Kagawa, S.; Nishii, R.; Saji, H. 2010: A novel 18F-labeled pyridyl benzofuran derivative for imaging of β-amyloid plaques in Alzheimer's brains. Bioorganic and Medicinal Chemistry Letters 20(20): 6141-6144
Yrjönen, A.; Pischik, E.; Mehtälä, S.; Kauppinen, R. 2008: A novel 19-bp deletion of exon 15 in the HMBS gene causing acute intermittent porphyria associating with rhabdomyolysis during an acute attack. Clinical Genetics 74(4): 396-398
Cheng, Y.; Liang, P.; Geng, H.; Wang, Z.; Li, L.; Cheng, S.H.; Ying, J.; Su, X.; Ng, K.M.; Ng, M.H.L.; Mok, T.S.K.; Chan, A.T.C.; Tao, Q. 2012: A novel 19q13 nucleolar zinc finger protein suppresses tumor cell growth through inhibiting ribosome biogenesis and inducing apoptosis but is frequently silenced in multiple carcinomas. Molecular Cancer Research: Mcr 10(7): 925-936
Bauer, E.M.; Bellitto, C.; Imperatori, P.; Righini, G.; Colapietro, M.; Portalone, G.; Gómez-García, C.J. 2010: A novel 1D-AF hybrid organic-inorganic chromium(II) methyl phosphonate dihydrate: synthesis, X-ray crystal and molecular structure, and magnetic properties. Inorganic Chemistry 49(16): 7472-7477
Koehler, U.; Holinski-Feder, E.; Ertl-Wagner, B.; Kunz, J.; von Moers, A.; von Voss, H.; Schell-Apacik, C. 2010: A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum. European Journal of Pediatrics 169(4): 463-468
Del Turco, S.; Sartini, S.; Sentieri, C.; Saponaro, C.; Navarra, T.; Dario, B.; Da Settimo, F.; La Motta, C.; Basta, G. 2014: A novel 2,3-diphenyl-4H-pyrido[1,2-a]pyrimidin-4-one derivative inhibits endothelial cell dysfunction and smooth muscle cell proliferation/activation. European Journal of Medicinal Chemistry 72: 102-109
Xiao, Z.; Huo, F.; Huang, Y.; Zhu, X.; Lu, J.R. 2012: A novel 2,3-xylenol-utilizing Pseudomonas isolate capable of degrading multiple phenolic compounds. Bioresource Technology 104: 59-64
Tan, Y.; Yu, J.; Cui, Y.; Yang, Y.; Wang, Z.; Hao, X.; Qian, G. 2011: A novel 2,6-dicarbonylpyridine-based fluorescent chemosensor for Co2+ with high selectivity and sensitivity. Analyst 136(24): 5283-5286
Jana, A.; Sukul, P.K.; Mandal, S.K.; Konar, S.; Ray, S.; Das, K.; Golen, J.A.; Rheingold, A.L.; Mondal, S.; Mondal, T.K.; Khuda-Bukhsh, A.R.; Kar, S.K. 2014: A novel 2,6-diformyl-4-methylphenol based chemosensor for Zn(II) ions by ratiometric displacement of Cd(II) ions and its application for cell imaging on human melanoma cancer cells. Analyst 139(2): 495-504
Altenburg, J.D.; Harvey, K.A.; McCray, S.; Xu, Z.; Siddiqui, R.A. 2011: A novel 2,6-diisopropylphenyl-docosahexaenoamide conjugate induces apoptosis in T cell acute lymphoblastic leukemia cell lines. Biochemical and Biophysical Research Communications 411(2): 427-432
Song, C.; Fei, Q.; Shan, H.; Feng, G.; Cui, M.; Liu, Y.; Huan, Y. 2013: A novel 2-(2-Formyl-4-methyl-phenoxy)-N-phenyl-acetamide-based fluorescence turn-on chemosensor for selenium determination with high selectivity and sensitivity. Spectrochimica Acta. Part a Molecular and Biomolecular Spectroscopy 116: 497-500
Chen, L.; Guo, J.-Y.; Xu, X.; Ju, W.-W.; Zhang, D.; Zhu, D.-R.; Xu, Y. 2013: A novel 2-D coordination polymer constructed from high-nuclearity waist drum-like pure Ho48 clusters. Chemical Communications 49(84): 9728-9730
Lyu, S.J.; Tian, Y.D.; Wang, S.H.; Han, R.L.; Mei, X.X.; Kang, X.T. 2014: A novel 2-bp indel within Krüppel-like factor 15 gene (KLF15) and its associations with chicken growth and carcass traits. British Poultry Science 55(4): 427-434
Mallipeddi, R.; Stark, J.; Xie, X-Jin.; Matthews, M.; Taylor, R.Stan. 2008: A novel 2-hour method for rapid preparation of permanent paraffin sections when treating melanoma in situ with mohs micrographic surgery. Dermatologic Surgery: Official Publication for American Society for Dermatologic Surgery 34(11): 1520-1526
Simčič, M.; Pureber, K.; Kristan, K.; Urleb, U.š; Kocjan, D.; Grdadolnik, S.G.č 2014: A novel 2-oxoindolinylidene inhibitor of bacterial MurD ligase: Enzyme kinetics, protein-inhibitor binding by NMR and a molecular dynamics study. European Journal of Medicinal Chemistry 83: 92-101
Bläuer, M.; Sand, J.; Nordback, I.; Laukkarinen, J. 2014: A novel 2-step culture model for long-term in vitro maintenance of human pancreatic acinar cells. Pancreas 43(5): 762-767
Blyth, M.; Beal, S.; Huang, S.; Crolla, J.; Foulds, N. 2008: A novel 2.43 Mb deletion of 7q11.22-q11.23. American Journal of Medical Genetics. Part a 146a (24): 3206-3210
Pebworth, M.-P.; Cismas, S.A.; Asuri, P. 2014: A novel 2.5D culture platform to investigate the role of stiffness gradients on adhesion-independent cell migration. Plos one 9(10): E110453
Kumar, A.; Mamidi, P.; Das, I.; Nayak, T.K.; Kumar, S.; Chhatai, J.; Chattopadhyay, S.; Suryawanshi, A.R.; Chattopadhyay, S. 2014: A novel 2006 Indian outbreak strain of Chikungunya virus exhibits different pattern of infection as compared to prototype strain. Plos one 9(1): E85714
Li, M.; Xu, T.-Y.; Yang, L.-J.; Zhu, X.-H. 2008: A novel 22-bp deletion mutation in a Chinese family with X-linked hypohidrotic ectodermal dysplasia. Archives of Dermatological Research 300(7): 389-391
Edison, E.S.; Venkatesan, R.S.; Govindanattar, S.D.; George, B.; Shaji, R.V. 2012: A novel 26 bp deletion [HBB: c.20_45del26bp] in exon 1 of the β-globin gene causing β-thalassemia major. Hemoglobin 36(1): 98-102
Zhu, Y.; Duan, Z.; Mo, G.; Shen, C.; Lv, L.; Chen, W.; Lai, R. 2014: A novel 26RFa peptide containing both analgesic and anti-inflammatory functions from Chinese tree shrew. Biochimie 102: 112-116
Lan, X.Y.; Zhao, H.Y.; Li, Z.J.; Li, A.M.; Lei, C.Z.; Chen, H.; Pan, C.Y. 2012: A novel 28-bp insertion-deletion polymorphism within goat PRNP gene and its association with production traits in Chinese native breeds. Genome 55(7): 547-552
Altenstein, G.; Nill, S.; Heller, J.; Heid, O.; Oelfke, U. 2012: A novel 2D binary collimator for IMRT dose delivery: dosimetric characterization using Monte Carlo simulations. Physics in Medicine and Biology 57(19): N345-N364
Wang, X.; Liu, X.; Tian, A.; Ying, J.; Lin, H.; Liu, G.; Gao, Q. 2012: A novel 2D → 3D {Co6PW9}-based framework extended by semi-rigid bis(triazole) ligand. Dalton Transactions 41(32): 9587-9589
Ambort, D.; Stalder, D.; Lottaz, D.; Huguenin, M.; Oneda, B.; Heller, M.; Sterchi, E.E. 2008: A novel 2D-based approach to the discovery of candidate substrates for the metalloendopeptidase meprin. Febs Journal 275(18): 4490-4509
Bernard Cher, T.H.; Chan, H.S.; Klein, G.F.; Jabkowski, J.ör.; Schadenböck-Kranzl, G.; Zach, O.; Roca, X.; Law, S.K.A. 2011: A novel 3' splice-site mutation and a novel gross deletion in leukocyte adhesion deficiency (LAD)-1. Biochemical and Biophysical Research Communications 404(4): 1099-1104
Rocha, M.R.e.; de Souza, J.J.; Barcellos, L.T.; Sant'Anna, C.M.R.; Braz-Filho, R.; Vieira, I.J.é C. 2014: A novel 3,9-(1,2,3-trioxocine)-type steroid of Rauia nodosa (Rutaceae). Molecules 19(9): 14637-14648
Han, J.-H.; Yang, S.; Lee, B.-U. 2011: A novel 3-D color histogram equalization method with uniform 1-D gray scale histogram. IEEE Transactions on Image Processing: a Publication of the IEEE Signal Processing Society 20(2): 506-512
Kristensen, E.; Parsons, T.E.; Hallgrímsson, B.; Boyd, S.K. 2008: A novel 3-D image-based morphological method for phenotypic analysis. IEEE Transactions on Bio-Medical Engineering 55(12): 2826-2831
Pathi, S.P.; Kowalczewski, C.; Tadipatri, R.; Fischbach, C. 2010: A novel 3-D mineralized tumor model to study breast cancer bone metastasis. Plos one 5(1): E8849
Zhang, X.; Xie, Y.; Koh, C.G.; James Lee, L. 2009: A novel 3-D model for cell culture and tissue engineering. Biomedical Microdevices 11(4): 795-799
Yang, X.; Coleman, D.P.; Pugh, N.D.; Nokes, L.D.M. 2011: A novel 3-D power Doppler ultrasound approach to the quantification of achilles tendon neovascularity. Ultrasound in Medicine and Biology 37(7): 1046-1055
Gong, Y.-D.; Dong, M.-S.; Lee, S.-B.; Kim, N.; Bae, M.-S.; Kang, N.-S. 2011: A novel 3-arylethynyl-substituted pyrido[2,3,-b]pyrazine derivatives and pharmacophore model as Wnt2/β-catenin pathway inhibitors in non-small-cell lung cancer cell lines. Bioorganic and Medicinal Chemistry 19(18): 5639-5647
Galassi, A.R.; Tomasello, S.D.; Capodanno, D.; Seminara, D.; Canonico, L.; Occhipinti, M.; Tamburino, C. 2010: A novel 3-d reconstruction system for the assessment of bifurcation lesions treated by the mini-crush technique. Journal of Interventional Cardiology 23(1): 46-53
Adachi, O.; Ano, Y.; Toyama, H.; Matsushita, K. 2008: A novel 3-dehydroquinate dehydratase catalyzing extracellular formation of 3-dehydroshikimate by oxidative fermentation of Gluconobacter oxydans IFO 3244. Bioscience Biotechnology and Biochemistry 72(6): 1475-1482
Sempere, L.F.; Gunn, J.R.; Korc, M. 2011: A novel 3-dimensional culture system uncovers growth stimulatory actions by TGFβ in pancreatic cancer cells. Cancer Biology and Therapy 12(3): 198-207
Komai, Y.; Sakai, Y.; Gotohda, N.; Kobayashi, T.; Kawakami, S.; Saito, N. 2014: A novel 3-dimensional image analysis system for case-specific kidney anatomy and surgical simulation to facilitate clampless partial nephrectomy. Urology 83(2): 500-506
Walker, M.; Campbell, B.R.; Azer, K.; Tong, C.; Fang, K.; Cook, J.J.; Forrest, M.J.; Kempadoo, K.; Wright, S.D.; Saltzman, J.S.; MacIntyre, E.; Hargreaves, R. 2009: A novel 3-dimensional micro-ultrasound approach to automated measurement of carotid arterial plaque volume as a biomarker for experimental atherosclerosis. Atherosclerosis 204(1): 55-65
Eyre, D.R.; Weis, M.; Hudson, D.M.; Wu, J.-J.; Kim, L. 2011: A novel 3-hydroxyproline (3Hyp)-rich motif marks the triple-helical C terminus of tendon type i collagen. Journal of Biological Chemistry 286(10): 7732-7736
Wollam, J.; Magner, D.B.; Magomedova, L.; Rass, E.; Shen, Y.; Rottiers, V.; Habermann, B.; Cummins, C.L.; Antebi, A. 2012: A novel 3-hydroxysteroid dehydrogenase that regulates reproductive development and longevity. Plos Biology 10(4): E1001305
Webb, K.J.; Zurita-Lopez, C.I.; Al-Hadid, Q.; Laganowsky, A.; Young, B.D.; Lipson, R.S.; Souda, P.; Faull, K.F.; Whitelegge, J.P.; Clarke, S.G. 2010: A novel 3-methylhistidine modification of yeast ribosomal protein Rpl3 is dependent upon the YIL110W methyltransferase. Journal of Biological Chemistry 285(48): 37598-37606
Zhou, C.; Song, S.; Zhang, J. 2009: A novel 3017-bp deletion mutation in the FERMT1 (KIND1) gene in a Chinese family with Kindler syndrome. British Journal of Dermatology 160(5): 1119-1122
Zhang, S.; Han, R.L.; Gao, Z.Y.; Zhu, S.K.; Tian, Y.D.; Sun, G.R.; Kang, X.T. 2014: A novel 31-bp indel in the paired box 7 (PAX7) gene is associated with chicken performance traits. British Poultry Science 55(1): 31-36
Hamid, M.; Karimipoor, M.; Chaleshtori, M.Hashemzadeh.; Akbari, M.Taghi. 2009: A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients. Journal of Genetics 88(3): 359-362
Liu, H.-M.; Tsai, L.-P.; Chien, Y.-H.; Wu, J.-F.; Weng, W.-C.; Peng, S.-F.; Wu, E.-T.; Huang, P.-H.; Lee, W.-T.; Tsai, I.-J.; Hwu, W.-L.; Lee, N.-C. 2012: A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a child. Pediatrics and Neonatology 53(4): 264-268
Wang, X.; Liu, G.; Zhang, J.; Chen, Y.; Lin, H.; Zheng, W. 2009: A novel 3D Cd(II) metal-organic framework with an unprecedented (5,6)-connected topology based on isophthalate and 2-(3-pyridyl)imidazo[4,5-f]1,10-phenanthroline. Dalton Transactions 36: 7347-7349
Kau, C.H.; Pan, P.; Gallerano, R.L.; English, J.D. 2009: A novel 3D classification system for canine impactions--the KPG index. International Journal of Medical Robotics + Computer Assisted Surgery: Mrcas 5(3): 291-296
Zhang, L.; Liu, B.; Xin, X.; Liu, D. 2013: A novel 3D constellation-masked method for physical security in hierarchical OFDMA system. Optics Express 21(13): 15627-15633
Rodríguez-Diéguez, A.; Kivekäs, R.; Sakiyama, H.; Debdoubi, A.; Colacio, E. 2007: A novel 3D cyano-bridged mixed-valence CoII/CoIIi canted antiferromagnet constructed from defective cubanes. Synthesis, X-ray structure and magnetic properties. Dalton Transactions 21: 2145-2149
Polackwich, R.J.; Koch, D.; Arevalo, R.; Miermont, A.M.; Jee, K.J.; Lazar, J.; Urbach, J.; Mueller, S.C.; McAllister, R.G. 2013: A novel 3D fibril force assay implicates src in tumor cell force generation in collagen networks. Plos one 8(3): E58138
Abe, Y.; Sato, S.; Kato, K.; Hyakumachi, T.; Yanagibashi, Y.; Ito, M.; Abumi, K. 2013: A novel 3D guidance system using augmented reality for percutaneous vertebroplasty: technical note. Journal of Neurosurgery. Spine 19(4): 492-501
Krause, S.; Maffini, M.V.; Soto, A.M.; Sonnenschein, C. 2008: A novel 3D in vitro culture model to study stromal-epithelial interactions in the mammary gland. Tissue Engineering. Part C Methods 14(3): 261-271
Fei, B.-L.; Li, W.; Wang, J.-H.; Liu, Q.-B.; Long, J.-Y.; Li, Y.-G.; Shao, K.-Z.; Su, Z.-M.; Sun, W.-Y. 2014: A novel 3D inorganic heteropoly blue as visible light responsive photocatalyst. Dalton Transactions 43(26): 10005-10012
El-Baz, A.; Gimel'farb, G.; Falk, R.; Abou El-Ghar, M.; Kumar, V.; Heredia, D. 2009: A novel 3D joint Markov-Gibbs model for extracting blood vessels from PC-MRA images. Medical Image Computing and Computer-Assisted Intervention: Miccai . International Conference on Medical Image Computing and Computer-Assisted Intervention 12(Part 2): 943-950
Jahnke, H.-G.; Steel, D.; Fleischer, S.; Seidel, D.; Kurz, R.; Vinz, S.; Dahlenborg, K.; Sartipy, P.; Robitzki, A.A. 2013: A novel 3D label-free monitoring system of hES-derived cardiomyocyte clusters: a step forward to in vitro cardiotoxicity testing. Plos one 8(7): E68971
Wong, M.D.; Dorr, A.E.; Walls, J.R.; Lerch, J.P.; Henkelman, R.M. 2012: A novel 3D mouse embryo atlas based on micro-CT. Development 139(17): 3248-3256
Bennink, H.E.; van Assen, H.C.; Streekstra, G.J.; ter Wee, R.; Spaan, J.A.E.; ter Haar Romeny, B.M. 2007: A novel 3D multi-scale lineness filter for vessel detection. Medical Image Computing and Computer-Assisted Intervention: Miccai . International Conference on Medical Image Computing and Computer-Assisted Intervention 10(Part 2): 436-443
Liao, D.; Zhao, J.; Gregersen, H. 2012: A novel 3D shape context method based strain analysis on a rat stomach model. Journal of Biomechanics 45(9): 1566-1573
Duan, P.; Raz, O.; Smalbrugge, B.E.; Duis, J.; Dorren, H.J.S. 2012: A novel 3D stacking method for Opto-electronic dies on CMOS ICs. Optics Express 20(26): B386-B392
Brown, P.M.; Hamilton, N.M.; Denison, A.R. 2012: A novel 3D stereoscopic anatomy tutorial. Clinical Teacher 9(1): 50-53
Tanaka, R.; Kikuchi, T.; Nakasuji, S.; Ue, Y.; Shuto, D.; Igarashi, K.; Okada, R.; Yamada, T. 2013: A novel 3α-p-Nitrobenzoylmultiflora-7:9(11)-diene-29-benzoate and two new triterpenoids from the seeds of zucchini (Cucurbita pepo L). Molecules 18(7): 7448-7459
Asgharinezhad, A.Akbar.; Ebrahimzadeh, H.; Rezvani, M.; Shekari, N.; Loni, M. 2014: A novel 4-(2-pyridylazo) resorcinol functionalised magnetic nanosorbent for selective extraction of Cu(II) and Pb(II) ions from food and water samples. Food Additives and Contaminants. Part A Chemistry Analysis Control Exposure and Risk Assessment 31(7): 1196-1204
Wei, S.; Sun, Y.; Guo, P.; Hu, X.; Fan, J. 2012: A novel 4-(tetrahydro-2-furanmethoxy)-N-octadecyl-1,8-naphthalimide based blue emitiing probe: solvent effect on the photophysical properties and protein detection. Bioorganicheskaia Khimiia 38(5): 535-544
Tariq, M.; Wasif, N.; Ayub, M.; Ahmad, W. 2007: A novel 4-bp insertion mutation in EDA1 gene in a Pakistani family with X-linked hypohidrotic ectodermal dysplasia. European Journal of Dermatology: Ejd 17(3): 209-212
Lee, S.H.; Goto, T.; Oe, T. 2008: A novel 4-oxo-2(E)-nonenal-derived modification to angiotensin II: oxidative decarboxylation of N-terminal aspartic acid. Chemical Research in Toxicology 21(12): 2237-2244
Cyr, A.B.; Nimmakayalu, M.; Longmuir, S.Q.; Patil, S.R.; Keppler-Noreuil, K.M.; Shchelochkov, O.A. 2011: A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features. American Journal of Medical Genetics. Part a 155a (9): 2224-2228
Shimada, T.; Ohkubo, K.; Abe, K.; Watanabe, I.; Makita, N. 2012: A novel 5' splice site mutation of SCN5A associated with Brugada syndrome resulting in multiple cryptic transcripts. International Journal of Cardiology 158(3): 441-443
Wang, Z.; Liu, Y.; Liu, J.; Niu, Q.; Wen, J.; Wen, S.; Wu, Z. 2013: A novel 5'-uncoding region -1248 A>G variation of mitofusin-2 gene is associated with hypertension in Chinese. Yonsei Medical Journal 54(3): 603-608
Pandey, D.K.; Mahesh, R.; Kumar, A.A.; Rao, V.S.; Arjun, M.; Rajkumar, R. 2010: A novel 5-HT(2A) receptor antagonist exhibits antidepressant-like effects in a battery of rodent behavioural assays: approaching early-onset antidepressants. Pharmacology Biochemistry and Behavior 94(3): 363-373
Hughes, T.V.; Xu, G.; Wetter, S.K.; Connolly, P.J.; Emanuel, S.L.; Karnachi, P.; Pollack, S.R.; Pandey, N.; Adams, M.; Moreno-Mazza, S.; Middleton, S.A.; Greenberger, L.M. 2008: A novel 5-[1,3,4-oxadiazol-2-yl]-N-aryl-4,6-pyrimidine diamine having dual EGFR/HER2 kinase activity: design, synthesis, and biological activity. Bioorganic and Medicinal Chemistry Letters 18(17): 4896-4899
Akoury, E.; El Zir, E.; Mansour, A.; Mégarbané, A.é; Majewski, J.; Slim, R. 2011: A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome. Ophthalmic Genetics 32(4): 245-249
Li, M.; Dai, X.; Cheng, R.; Yang, L.; Yao, Z.; Liu, J. 2014: A novel 5-bp deletion mutation in AAGAB gene in a Chinese family with punctate palmoplantar keratoderma. Acta Dermato-Venereologica 94(3): 339-340
Peng, R.-H.; Tian, Y.-S.; Xiong, A.-S.; Zhao, W.; Fu, X.-Y.; Han, H.-J.; Chen, C.; Jin, X.-F.; Yao, Q.-H. 2012: A novel 5-enolpyruvylshikimate-3-phosphate synthase from Rahnella aquatilis with significantly reduced glyphosate sensitivity. Plos one 7(8): E39579
Cao, G.; Liu, Y.; Zhang, S.; Yang, X.; Chen, R.; Zhang, Y.; Lu, W.; Liu, Y.; Wang, J.; Lin, M.; Wang, G. 2012: A novel 5-enolpyruvylshikimate-3-phosphate synthase shows high glyphosate tolerance in Escherichia coli and tobacco plants. Plos one 7(6): E38718
Musiyenko, A.; Correa, L.; Stock, N.; Hutchinson, J.H.; Lorrain, D.S.; Bain, G.; Evans, J.F.; Barik, S. 2009: A novel 5-lipoxygenase-activating protein inhibitor, AM679, reduces inflammation in the respiratory syncytial virus-infected mouse eye. Clinical and Vaccine Immunology: Cvi 16(11): 1654-1659
Liu, M.-X.; Wei, T.-B.; Lin, Q.; Zhang, Y.-M. 2011: A novel 5-mercapto triazole Schiff base as a selective chromogenic chemosensor for Cu2+. Spectrochimica Acta. Part a Molecular and Biomolecular Spectroscopy 79(5): 1837-1842
Patil, A.V. 2010: A novel 5-part Percutaneous Access Needle with Glidewire technique (5-PANG) for percutaneous nephrolithotomy: our initial experience. Urology 75(5): 1206-1208
Rooks, H.; Clark, B.; Best, S.; Rushton, P.; Oakley, M.; Thein, O.S.; Cuthbert, A.C.; Britland, A.; Ruf, A.; Thein, S.L. 2012: A novel 506kb deletion causing εγδβ thalassemia. Blood Cells Molecules and Diseases 49(3-4): 121-127
Wang, Z.; Luo, G.; Ji, Y. 2013: A novel 519_525dup mutation of KLF1 gene identified in a Chinese blood donor with Lu(a-b-) phenotype. Transfusion 53(7): 1619-1620
Cao, Q.; Peng, Y.; Ge, J.; Zhang, Y.; Zhu, J.; Zhao, L. 2014: A novel 5p15.33-14.1 deletion and 4q34.24-35.2 duplication in a patient with mental retardation, dysmorphic features and severe speech delay. Journal of Genetics 93(1): 159-162
Parveen, M.; Azaz, S.; Ali, A.; Basudan, O.A.; Pereira Silva, P.S.; Vivas, C.Y. 2014: A novel 6-hydroxy-8,11,11-trimethyl-bicyclo[7.2.0]undec-4-ene-4-carboxylic acid: a potent antioxidant agent from Iphiona scabra. Journal of Asian Natural Products Research 16(4): 406-411
Fereshtehnejad, S-Mohammad.; Shafieesabet, M.; Rahmani, A.; Farhadi, F.; Hadizadeh, H.; Shahidi, G.Ali.; Delbari, A.; Lökk, J. 2014: A novel 6-item screening questionnaire for Parkinsonism: validation and comparison between different instruments. Neuroepidemiology 43(3-4): 178-193
Hanff, L.M.; Mathot, R.A.A.; Smeets, O.; Postma, D.J.; Ramnarain, S.; Vermes, A.; Pieters, R.; Zwaan, C.M. 2014: A novel 6-mercaptopurine oral liquid formulation for pediatric acute lymphoblastic leukemia patients - results of a randomized clinical trial. International Journal of Clinical Pharmacology and Therapeutics 52(8): 653-662
Ozgen, H.M.; Staal, W.G.; Barber, J.C.; de Jonge, M.V.; Eleveld, M.J.; Beemer, F.A.; Hochstenbach, R.; Poot, M. 2009: A novel 6.14 Mb duplication of chromosome 8p21 in a patient with autism and self mutilation. Journal of Autism and Developmental Disorders 39(2): 322-329
Rodrigues, C.E.; Velloso, E.R.P.; Pereira, R.M.R.; Bonfá, E.ís.; Teixeira, F.áv.K.; Bueno, C.; Dorlhiac-Laccer, P.E.; Kondo, A.éa.T.; Viana, V.S.T.; Carvalho, J.él.F. 2011: A novel 60 kDa reactivity in cyclic neutropenia: high titer cytoplasmic ANCA immunostaining pattern and negative anti-proteinase-3 antibody. Joint Bone Spine 78(3): 319-320
Tang, S.; Ou, J.; Sun, D.; Zhang, Y.; Xu, G.; Zhang, Y. 2011: A novel 62-bp indel mutation in the promoter region of transforming growth factor-beta 2 (TGFB2) gene is associated with body weight in chickens. Animal Genetics 42(1): 108-112
Lico, D.T.P.; Rosa, J.C.; DeGiorgis, J.A.; de Vasconcelos, E.J.R.; Casaletti, L.; Tauhata, S.B.F.; Baqui, M.M.A.; Fukuda, M.; Moreira, J.E.; Larson, R.E. 2010: A novel 65 kDa RNA-binding protein in squid presynaptic terminals. Neuroscience 166(1): 73-83
Saini, S.; Robinson, P.N.; Singh, J.R.; Vanita, V. 2012: A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family. Experimental Eye Research 104: 82-88
Xu, J.-j.; Dai, X.-m.; Liu, H.-l.; Guo, W.-j.; Gao, J.; Wang, C.-h.; Li, W.-b.; Yao, Q.-z. 2011: A novel 7-azaisoindigo derivative-induced cancer cell apoptosis and mitochondrial dysfunction mediated by oxidative stress. Journal of Applied Toxicology: Jat 31(2): 164-172
Liu, L.; Kritsanida, M.; Magiatis, P.; Gaboriaud, N.; Wang, Y.; Wu, J.; Buettner, R.; Yang, F.; Nam, S.; Skaltsounis, L.; Jove, R. 2012: A novel 7-bromoindirubin with potent anticancer activity suppresses survival of human melanoma cells associated with inhibition of STAT3 and Akt signaling. Cancer Biology and Therapy 13(13): 1255-1261
Lins, E.C.; Oliveira, C.F.; Guimarães, O.C.C.; Costa, C.A.d.S.; Kurachi, C.; Bagnato, V.S. 2013: A novel 785-nm laser diode-based system for standardization of cell culture irradiation. Photomedicine and Laser Surgery 31(10): 466-473
Bordoni, V.; Casetti, R.; Capuano, G.; De Stefani, B.; Piselli, P.; Gioia, C.; Agrati, C.; Martini, F. 2012: A novel 8-color flow cytometry panel to study activation, maturation and senescence of CD4 and CD8 T lymphocytes in HIV-infected individuals at different stages of disease. International Journal of Immunopathology and Pharmacology 25(2): 415-424
Yoshimi, R.; Ihata, A.; Kunishita, Y.; Kishimoto, D.; Kamiyama, R.; Minegishi, K.; Hama, M.; Kirino, Y.; Asami, Y.; Ohno, S.; Ueda, A.; Takeno, M.; Ishigatsubo, Y. 2015: A novel 8-joint ultrasound score is useful in daily practice for rheumatoid arthritis. Modern Rheumatology 25(3): 379-385
Gulati, V.; Fan, S.; Hays, C.L.; Samuelson, T.W.; Ahmed, I.I.K.; Toris, C.B. 2013: A novel 8-mm Schlemm's canal scaffold reduces outflow resistance in a human anterior segment perfusion model. Investigative Ophthalmology and Visual Science 54(3): 1698-1704
Nath, S.; Banerjee, R.; Sen, U. 2014: A novel 8-nm protein cage formed by Vibrio cholerae acylphosphatase. Journal of Molecular Biology 426(1): 36-38
Lin, L-Chwen.; Tsai, T-Hu.; Su, S-Chieh. 2011: A novel 8.O.6'-neolignan from Taxillus theifer. Natural Product Research 25(14): 1319-1323
Banka, S.; Fitzgibbon, G.J.; Gaunt, L.; Rankin, W.J.; Clayton-Smith, J. 2011: A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion. American Journal of Medical Genetics. Part a 155a(6): 1453-1457
Wang, S.; Kong, L.; Yang, H.; He, Z.; Jiang, Z.; Li, D.; Zeng, S.; Niu, M.; Song, Y.; Dou, J. 2011: A novel 9-MC-3 and 15-MC-6 onset stacked metallacrown single-molecule magnet: synthesis and crystal structure. Inorganic Chemistry 50(7): 2705-2707
Dubey, S.; Idicula-Thomas, S.; Anwaruddin, M.; Saravanan, C.; Varma, R.R.; Maitra, A. 2009: A novel 9-bp insertion detected in steroid 21-hydroxylase gene (CYP21A2): prediction of its structural and functional implications by computational methods. Journal of Biomedical Science 16: 3
Kaiser, N.K.; Quinn, J.P.; Blakney, G.T.; Hendrickson, C.L.; Marshall, A.G. 2011: A novel 9.4 tesla FTICR mass spectrometer with improved sensitivity, mass resolution, and mass range. Journal of the American Society for Mass Spectrometry 22(8): 1343-1351
Zhao, Q.; Yan, P.; Wang, R.F.; Zhang, C.L.; Li, L.; Yin, L. 2013: A novel 99mTc-labeled molecular probe for tumor angiogenesis imaging in hepatoma xenografts model: a pilot study. Plos one 8(4): E61043
Salgado, J.; Santisteban, M.; Gutiérrez, C.; Gil, C.; Robles, M.; Viedma, A.; Patiño-García, A. 2013: A novel BRCA1 mutation in a patient with breast and ovarian cancer: A case report. Oncology Letters 6(3): 725-727
Kurt, B.; Naini, A.B.; Copeland, W.C.; Lu, J.; Dimauro, S.; Hirano, M. 2012: A novel POLG gene mutation in a patient with SANDO. Journal of Experimental and Integrative Medicine 2(2)
Guo, J.; Zhou, G.; Zhang, W.; Song, Y.; Bian, Z. 2013: A novel POLH mutation causes XP-V disease and XP-V tumor proneness may involve imbalance of numerous DNA polymerases. Oncology Letters 6(6): 1583-1590
Tian, L.; Yao, Z.-Q.; Deng, Y.-F.; Hong, L.; Song, N. 2013: A novel a allele with the 595C >T mutation identified in a Chinese individual with the Am phenotype. Transfusion Medicine 23(2): 134-135
Felderbauer, P.; Schnekenburger, J.; Lebert, R.; Bulut, K.; Parry, M.; Meister, T.; Schick, V.; Schmitz, F.; Domschke, W.; Schmidt, W.E. 2008: A novel A121T mutation in human cationic trypsinogen associated with hereditary pancreatitis: functional data indicating a loss-of-function mutation influencing the R122 trypsin cleavage site. Journal of Medical Genetics 45(8): 507-512
Oliveira, T.íc.M.F.d.S.; de Vasconcelos, E.J.é R.; Nakaghi, A.éa.C.H.; Defina, T.ân.P.A.; Jusi, M.ár.M.G.; Baldani, C.D.; Cruz, A.K.; Machado, R.Z. 2011: A novel A2 allele found in Leishmania (Leishmania) infantum chagasi. Revista Brasileira de Parasitologia Veterinaria 20(1): 42-48
Hirsch, B.; Grünbaum, M.; Wagner, F.; Bi, Y.; Lucka, L.; Du, M.-Q.; Stein, H.; Dürkop, H. 2012: A novel A20 (TNFAIP3) antibody (Ber-A20) can be used to detect unmutated A20 by immunohistology. Histopathology 60(6b): E19-E27
Cafferata, E.G.; Macció, D.R.; Lopez, M.V.; Viale, D.L.; Carbone, C.; Mazzolini, G.; Podhajcer, O.L. 2009: A novel A33 promoter-based conditionally replicative adenovirus suppresses tumor growth and eradicates hepatic metastases in human colon cancer models. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 15(9): 3037-3049
Biswas, B.; Chan, P.K.; Gresshoff, P.M. 2009: A novel ABA insensitive mutant of Lotus japonicus with a wilty phenotype displays unaltered nodulation regulation. Molecular Plant 2(3): 487-499
Popovic, M.; Zaja, R.; Loncar, J.; Smital, T. 2010: A novel ABC transporter: the first insight into zebrafish (Danio rerio) ABCH1. Marine Environmental Research 69 Suppl: S11-S13
Hooper, A.J.; Robertson, K.; Ng, L.; Kattampallil, J.S.; Latchem, D.; Willsher, P.C.; Thom, J.; Baker, R.I.; Burnett, J.R. 2009: A novel ABCA1 nonsense mutation, R1270X, in Tangier disease associated with an unrecognised bleeding tendency. Clinica Chimica Acta; International Journal of Clinical Chemistry 409(1-2): 136-139
Saber, S.; Vazifehmand, R.; Bagherizadeh, I.; Kasiri, M. 2013: A novel ABCB11 mutation in an Iranian girl with progressive familial intrahepatic cholestasis. Indian Journal of Human Genetics 19(3): 366-368
Babenko, A.P. 2008: A novel ABCC8 (SUR1)-dependent mechanism of metabolism-excitation uncoupling. Journal of Biological Chemistry 283(14): 8778-8782
Klee, P.; Bellanné-Chantelot, C.; Depret, G.; Llano, J.P.; Paget, C.; Nicolino, M. 2012: A novel ABCC8 mutation illustrates the variability of the diabetes phenotypes associated with a single mutation. Diabetes and Metabolism 38(2): 179-182
Cai, Y.-n.; Jiang, M.-y.; Liang, C.-l.; Peng, M.-z.; Cheng, J.; Sheng, H.-y.; Fan, L.-p.; Chen, X.-q.; Liu, L. 2015: A novel ABCD1 gene mutation in a Chinese patient with X-linked adrenoleukodystrophy. Journal of Pediatric Endocrinology and Metabolism: Jpem 28(5-6): 725-729
Liu, Y.-T.; Lin, K.-H.; Soong, B.-W.; Liao, K.-K.; Lin, K.-P. 2007: A novel ABCD1 gene mutation in a Chinese-Taiwanese patient with adrenomyeloneuropathy. Pediatric Neurology 36(5): 348-350
Tian, L.; Yao, Z.-Q.; Fan, W.-C.; Li, H.; Song, N. 2012: A novel ABO allele caused by an in-frame triplet deletion in ABO gene. Vox Sanguinis 103(4): 362-363
Yun, J.W.; Jo, K.I.; Woo, H.I.; Lee, S.-Y.; Ki, C.-S.; Kim, J.-W.; Song, J.; Lee, D.H.; Lee, Y.-W.; Park, H.-D. 2015: A novel ACAD8 mutation in asymptomatic patients with isobutyryl-CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum. Clinical Genetics 87(2): 196-198
Zhao, Y.; Li, B.; Dong, S.; Liu, Z.; Zhao, X.; Wang, J.; Zeng, M. 2009: A novel ACE inhibitory peptide isolated from Acaudina molpadioidea hydrolysate. Peptides 30(6): 1028-1033
Haga, S.; Tsuchiya, H.; Hirai, T.; Hamano, T.; Mimori, A.; Ishizaka, Y. 2015: A novel ACE2 activator reduces monocrotaline-induced pulmonary hypertension by suppressing the JAK/STAT and TGF-β cascades with restored caveolin-1 expression. Experimental Lung Research 41(1): 21-31
DePriest, J.; Fee-Mulhearn, A.L.; Teleron, A. 2013: A novel ACLS team leader checklist implemented to improve resuscitation efforts. Resuscitation 84(9): E115
Ravenscroft, G.; Wilmshurst, J.M.; Pillay, K.; Sivadorai, P.; Wallefeld, W.; Nowak, K.J.; Laing, N.G. 2011: A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type i fibre predominance. Neuromuscular Disorders: Nmd 21(1): 31-36
Gregson, C.L.; Hollingworth, P.; Williams, M.; Petrie, K.A.; Bullock, A.N.; Brown, M.A.; Tobias, J.H.; Triffitt, J.T. 2011: A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date. Bone 48(3): 654-658
Christensen, A.E.; Fiskerstrand, T.; Knappskog, P.M.; Boman, H.; Rødahl, E. 2010: A novel ADAMTSL4 mutation in autosomal recessive ectopia lentis et pupillae. Investigative Ophthalmology and Visual Science 51(12): 6369-6373
Bueno, A.C.; Sun, K.; Martins, C.S.; Elias Junior, J.; Miranda, W.; Tao, C.; Foss-Freitas, M.C.; Barbieri, M.A.; Bettiol, H.ís.; de Castro, M.; Scherer, P.E.; Antonini, S.R. 2014: A novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome. Journal of Clinical Endocrinology and Metabolism 99(4): E683-E693
Ashihara, E.; Nakamura, S.; Inaba, T.; Taki, T.; Hayashi, Y.; Shimazaki, C. 2007: A novel AF10-CALM fusion transcript in gamma/delta-T cell type lymphoblastic lymphoma. American Journal of Hematology 82(9): 859-860
Max, E.; Häfner, W.; Bartels, F.W.; Sugiharto, A.; Wood, C.; Fery, A. 2010: A novel AFM based method for force measurements between individual hair strands. Ultramicroscopy 110(4): 320-324
Ebrahimi, A.P.; Toloui Ashlaghi, A.; Mahdavy Rad, M. 2013: A novel AIDS/HIV intelligent medical consulting system based on expert systems. Journal of Education and Health Promotion 2: 54
Li, X.; Welch, E.B.; Arlinghaus, L.R.; Chakravarthy, A.B.; Xu, L.; Farley, J.; Loveless, M.E.; Mayer, I.A.; Kelley, M.C.; Meszoely, I.M.; Means-Powell, J.A.; Abramson, V.G.; Grau, A.M.; Gore, J.C.; Yankeelov, T.E. 2011: A novel AIF tracking method and comparison of DCE-MRi parameters using individual and population-based AIFs in human breast cancer. Physics in Medicine and Biology 56(17): 5753-5769
Shi, H.; Hong, A.; Kong, X.; Koya, R.C.; Song, C.; Moriceau, G.; Hugo, W.; Yu, C.C.; Ng, C.; Chodon, T.; Scolyer, R.A.; Kefford, R.F.; Ribas, A.; Long, G.V.; Lo, R.S. 2014: A novel AKT1 mutant amplifies an adaptive melanoma response to BRAF inhibition. Cancer Discovery 4(1): 69-79
Kwok, J.S.-S.; Yuen, C.L.; Law, L.K.; Tang, N.L.-S.; Cherk, S.W.-W.; Yuen, Y.P. 2012: A novel ALDH5A1 mutation in a patient with succinic semialdehyde dehydrogenase deficiency. Pathology 44(3): 280-282
Püttmann, L.; Stehr, H.; Garshasbi, M.; Hu, H.; Kahrizi, K.; Lipkowitz, B.; Jamali, P.; Tzschach, A.; Najmabadi, H.; Ropers, H.-H.; Musante, L.; Kuss, A.W. 2013: A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family. American Journal of Medical Genetics. Part a 161a (8): 1915-1922
Owusu-Brackett, N.; Johnson, R.; Schindel, D.T.; Koduru, P.; Cope-Yokoyama, S. 2013: A novel ALK rearrangement in an inflammatory myofibroblastic tumor in a neonate. Cancer Genetics 206(9-10): 353-356
Brotherton, T.; Polak, M.; Kelly, C.; Birve, A.; Andersen, P.; Marklund, S.L.; Glass, J.D. 2011: A novel ALS SOD1 C6S mutation with implications for aggregation related toxicity and genetic counseling. Amyotrophic Lateral Sclerosis: Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 12(3): 215-219
Mintchev, N.; Zamba-Papanicolaou, E.; Kleopa, K.A.; Christodoulou, K. 2009: A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis family. Neurology 72(1): 28-32
Van der Zwan, Y.G.; Brüggenwirth, H.T.; Drop, S.L.S.; Wolffenbuttel, K.P.; Madern, G.C.; Looijenga, L.H.J.; Visser, J.A. 2012: A novel AMH missense mutation in a patient with persistent Müllerian duct syndrome. Sexual Development: Genetics Molecular Biology Evolution Endocrinology Embryology and Pathology of Sex Determination and Differentiation 6(6): 279-283
Wang, J.; Ma, H.; Zhang, X.; He, L.; Wu, J.; Gao, X.; Ren, J.; Li, J. 2009: A novel AMPK activator from Chinese herb medicine and ischemia phosphorylate the cardiac transcription factor FOXO3. International Journal of Physiology Pathophysiology and Pharmacology 1(2): 116-126
Valtorta, S.; Nicolini, G.; Tripodi, F.; Meregalli, C.; Cavaletti, G.; Avezza, F.; Crippa, L.; Bertoli, G.; Sanvito, F.; Fusi, P.; Pagliarin, R.; Orsini, F.; Moresco, R.M.; Coccetti, P. 2014: A novel AMPK activator reduces glucose uptake and inhibits tumor progression in a mouse xenograft model of colorectal cancer. Investigational new Drugs 32(6): 1123-1133
Lian, Z.; Li, Y.; Gao, J.; Qu, K.; Li, J.; Hao, L.; Wu, S.; Zhu, H. 2011: A novel AMPK activator, WS070117, improves lipid metabolism discords in hamsters and HepG2 cells. Lipids in Health and Disease 10: 67
Pantazis, D.; Simpson, G.V.; Weber, D.L.; Dale, C.L.; Nichols, T.E.; Leahy, R.M. 2009: A novel ANCOVA design for analysis of MEG data with application to a visual attention study. Neuroimage 44(1): 164-174
Liu, J-Jing.; Lin, X-Jia.; Yang, X-Jing.; Zhou, L.; He, S.; Zhuang, S-Mei.; Yang, J. 2014: A novel AP-1/miR-101 regulatory feedback loop and its implication in the migration and invasion of hepatoma cells. Nucleic Acids Research 42(19): 12041-12051
Aya, K.; Hobo, T.; Sato-Izawa, K.; Ueguchi-Tanaka, M.; Kitano, H.; Matsuoka, M. 2014: A Novel Ap2-Type Transcription Factor, small Organ Size1, Controls Organ Size Downstream of an Auxin Signaling Pathway. Plant and Cell Physiology 55(5): 897-912
Papa, A.; Chaligiannis, I.; Kontana, N.; Sourba, T.; Tsioka, K.; Tsatsaris, A.; Sotiraki, S. 2014: A novel AP92-like Crimean-Congo hemorrhagic fever virus strain, Greece. Ticks and Tick-Borne Diseases 5(5): 590-593
Fritch Lilla, S.A.; Yi, J.S.; Hall, B.A.C.; Moertel, C.L. 2014: A novel APC gene mutation associated with a severe phenotype in a patient with Turcot syndrome. Journal of Pediatric Hematology/Oncology 36(3): E177-E179
Loot, A.E.; Fleming, I. 2013: A novel APJ signaling cascade that regulates cardiovascular development. Circulation Research 113(1): 4-6
Okubo, M.; Ishihara, M.; Iwasaki, T.; Ebara, T.; Aoyama, Y.; Murase, T.; Hattori, H. 2009: A novel APOA5 splicing mutation IVS2+1g>a in a Japanese chylomicronemia patient. Atherosclerosis 207(1): 24-25
Kersten, H.; Derpmann, V.; Barnes, I.; Brockmann, K.J.; O'Brien, R.; Benter, T. 2011: A novel APPI-MS setup for in situ degradation product studies of atmospherically relevant compounds: capillary atmospheric pressure photo ionization (cAPPI). Journal of the American Society for Mass Spectrometry 22(11): 2070-2081
Wang, G.; Scott, W.K.; Whitehead, P.; Court, B.L.; Kovach, J.L.; Schwartz, S.G.; Agarwal, A.; Dubovy, S.; Haines, J.L.; Pericak-Vance, M.A. 2012: A novel ARMS2 splice variant is identified in human retina. Experimental Eye Research 94(1): 187-191
Absoud, M.; Parr, J.R.; Halliday, D.; Pretorius, P.; Zaiwalla, Z.; Jayawant, S. 2010: A novel ARX phenotype: rapid neurodegeneration with Ohtahara syndrome and a dyskinetic movement disorder. Developmental Medicine and Child Neurology 52(3): 305-307
Dean, P.J.; Siwiec, T.; Waterworth, W.M.; Schlögelhofer, P.; Armstrong, S.J.; West, C.E. 2009: A novel ATM-dependent X-ray-inducible gene is essential for both plant meiosis and gametogenesis. Plant Journal: for Cell and Molecular Biology 58(5): 791-802
Cao, L.; Kawai, H.; Sasatani, M.; Iizuka, D.; Masuda, Y.; Inaba, T.; Suzuki, K.; Ootsuyama, A.; Umata, T.; Kamiya, K.; Suzuki, F. 2014: A novel ATM/TP53/p21-mediated checkpoint only activated by chronic γ-irradiation. Plos one 9(8): E104279
Prosecka, J.; Orlov, A.V.; Fantin, Y.S.; Zinchenko, V.V.; Babykin, M.M.; Tichy, M. 2009: A novel ATP-binding cassette transporter is responsible for resistance to viologen herbicides in the cyanobacterium Synechocystis sp. PCC 6803. Febs Journal 276(15): 4001-4011
Auger, C.; Appanna, V.D. 2015: A novel ATP-generating machinery to counter nitrosative stress is mediated by substrate-level phosphorylation. Biochimica et Biophysica Acta 1850(1): 43-50
Rosewich, H.; Baethmann, M.; Ohlenbusch, A.; Gärtner, J.; Brockmann, K. 2014: A novel ATP1A3 mutation with unique clinical presentation. Journal of the Neurological Sciences 341(1-2): 133-135
Moriuchi, R.; Akiyama, M.; Onozuka, T.; Shimizu, H. 2008: A novel ATP2A2 missense mutation p.Asp254Gly in Darier disease restricted to the extremities. Journal of the American Academy of Dermatology 58(5 Suppl 1: S116-S118
Shibata, A.; Sugiura, K.; Kimura, U.; Takamori, K.; Akiyama, M. 2013: A novel ATP2C1 early truncation mutation suggests haploinsufficiency as a pathogenic mechanism in a patient with Hailey-Hailey disease. Acta Dermato-Venereologica 93(6): 719-720
Park, H.-D.; Moon, H.-K.; Lee, J.; Lee, M.; Lee, S.-Y.; Kim, J.-W.; Ki, C.-S. 2009: A novel ATP7A gross deletion mutation in a Korean patient with Menkes disease. Annals of Clinical and Laboratory Science 39(2): 188-191
Chen, L.; Li, X.; Zheng, Z.; Lu, X.; Lin, M.; Pan, C.; Liu, J. 2014: A novel ATP7B gene mutation in a liver failure patient with normal ceruloplasmin and low serum alkaline phosphatase. Gene 538(1): 204-206
Tansel, T.; Paçal, F.; Ustek, D. 2014: A novel ATP8 gene mutation in an infant with tetralogy of Fallot. Cardiology in the Young 24(3): 531-533
Ekgasit, S.; Pattayakorn, N.; Tongsakul, D.; Thammacharoen, C.; Kongyou, T. 2007: A novel ATR FT-IR microspectroscopy technique for surface contamination analysis without interference of the substrate. Analytical Sciences: the International Journal of the Japan Society for Analytical Chemistry 23(7): 863-868
Blackford, A.N.; Schwab, R.A.; Niedzwiedz, W. 2010: A novel ATRibute of FANCM. Cell Cycle 9(8): 1453-1455
Huang, L.; Li, W.; Tang, W.; Lu, G. 2011: A novel AVPR2 missense mutation in a Chinese boy with severe inherited nephrogenic diabetes insipidus. Journal of Pediatric Endocrinology and Metabolism: Jpem 24(9-10): 807-809
Portelius, E.; Dean, R.A.; Gustavsson, M.K.; Andreasson, U.; Zetterberg, H.; Siemers, E.; Blennow, K. 2010: A novel Abeta isoform pattern in CSF reflects gamma-secretase inhibition in Alzheimer disease. Alzheimer's Research and Therapy 2(2): 7
Li, X.; Mao, Q.; Wang, D.; Xia, H. 2012: A novel Ad5/11 chimeric oncolytic adenovirus for improved glioma therapy. International Journal of Oncology 41(6): 2159-2165
Wang, Y.; Miao, Z.; Ren, G.; Xu, Y.; Cheng, Z. 2014: A novel Affibody bioconjugate for dual-modality imaging of ovarian cancer. Chemical Communications 50(85): 12832-12835
Tang, J.; Liu, Y.; Li, H.; Tan, Z.; Li, D. 2013: A novel Ag3AsO4 visible-light-responsive photocatalyst: facile synthesis and exceptional photocatalytic performance. Chemical Communications 49(48): 5498-5500
Nawa, M.; Kanekura, K.; Hashimoto, Y.; Aiso, S.; Matsuoka, M. 2008: A novel Akt/PKB-interacting protein promotes cell adhesion and inhibits familial amyotrophic lateral sclerosis-linked mutant SOD1-induced neuronal death via inhibition of PP2A-mediated dephosphorylation of Akt/PKB. Cellular signalling 20(3): 493-505
Tokuda, S.; Mahaffey, C.L.; Monks, B.; Faulkner, C.R.; Birnbaum, M.J.; Danzer, S.C.; Frankel, W.N. 2011: A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice. Human Molecular Genetics 20(5): 988-999
Lou, X.; Hou, Y.; Liang, D.; Peng, L.; Chen, H.; Ma, S.; Zhang, L. 2015: A novel Alu-based real-time PCR method for the quantitative detection of plasma circulating cell-free DNA: sensitivity and specificity for the diagnosis of myocardial infarction. International Journal of Molecular Medicine 35(1): 72-80
Singh, H.R.; Yang, Z.; Siddiqui, S.; Peña, L.S.; Westerfield, B.H.; Fan, Y.; Towbin, J.A.; Vatta, M. 2009: A novel Alu-mediated Xq28 microdeletion ablates TAZ and partially deletes DNL1L in a patient with Barth syndrome. American Journal of Medical Genetics. Part a 149a (5): 1082-1085
Seabra, C.M.; Quental, S.; Neto, A.P.; Carvalho, F.; Gonçalves, J.ão.; Oliveira, J.ão.P.; Fernandes, S.; Sousa, M.ár.; Barros, A.; Amorim, A.ón.; Lopes, A.M. 2014: A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia. Reproductive Biomedicine Online 29(3): 388-391
Shinomura, M.; Kishi, K.; Tomita, A.; Kawasumi, M.; Kanezashi, H.; Kuroda, Y.; Tsunekawa, N.; Ozawa, A.; Aiyama, Y.; Yoneda, A.; Suzuki, H.; Saito, M.; Picard, J.-Y.; Kohno, K.; Kurohmaru, M.; Kanai-Azuma, M.; Kanai, Y. 2014: A novel Amh-Treck transgenic mouse line allows toxin-dependent loss of supporting cells in gonads. Reproduction 148(6): H1-H9
Conforti, F.L.; Sprovieri, T.; Mazzei, R.; Ungaro, C.; La Bella, V.; Tessitore, A.; Patitucci, A.; Magariello, A.; Gabriele, A.L.; Tedeschi, G.; Simone, I.L.; Majorana, G.; Valentino, P.; Condino, F.; Bono, F.; Monsurrò, M.R.; Muglia, M.; Quattrone, A. 2008: A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy. Neuromuscular Disorders: Nmd 18(1): 68-70
Kurosawa, Y. 2010: A novel Antibody based approach to Cancer Treatment. Journal of Stem Cells and Regenerative Medicine 6(3): 166
Anthanont, P.; Polisecki, E.; Asztalos, B.F.; Diffenderfer, M.R.; Barrett, P.H.R.; Millar, J.S.; Billheimer, J.; Cuchel, M.; Rader, D.J.; Schaefer, E.J. 2014: A novel ApoA-i truncation (ApoA-IMytilene) associated with decreased ApoA-i production. Atherosclerosis 235(2): 470-476
Petutschnig, E.K.; Stolze, M.; Lipka, U.; Kopischke, M.; Horlacher, J.; Valerius, O.; Rozhon, W.; Gust, A.A.; Kemmerling, B.; Poppenberger, B.; Braus, G.H.; Nürnberger, T.; Lipka, V. 2014: A Novel Arabidopsis Chitin Elicitor Receptor Kinase 1 (Cerk1) Mutant with Enhanced Pathogen-Induced cell Death and Altered Receptor Processing. New Phytologist 204(4): 955-967
Wang, Y.; Bouwmeester, K.; van de Mortel, J.E.; Shan, W.; Govers, F. 2013: A novel Arabidopsis-oomycete pathosystem: differential interactions with Phytophthora capsici reveal a role for camalexin, indole glucosinolates and salicylic acid in defence. Plant Cell and Environment 36(6): 1192-1203
Sharma, V.; Singh, R.; Thangaraj, K.; Jyothy, A. 2011: A novel Arg615Ser mutation of androgen receptor DNA-binding domain in three 46,XY sisters with complete androgen insensitivity syndrome and bilateral inguinal hernia. Fertility and Sterility 95(2): 804.E19
Yli-Mattila, T.; Gagkaeva, T.; Ward, T.J.; Aoki, T.; Kistler, H.Corby.; O'Donnell, K. 2009: A novel Asian clade within the Fusarium graminearum species complex includes a newly discovered cereal head blight pathogen from the Russian Far East. Mycologia 101(6): 841-852
Robert-Ebadi, H.; Le Querrec, A.ès.; de Moerloose, P.; Gandon-Laloum, S.; Borel Derlon, A.; Neerman-Arbez, M. 2008: A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis. Blood Coagulation and Fibrinolysis: An International Journal in Haemostasis and Thrombosis 19(7): 697-699
Koseki, T.; Mihara, K.; Murayama, T.; Shiono, Y. 2010: A novel Aspergillus oryzae esterase that hydrolyzes 4-hydroxybenzoic acid esters. Febs Letters 584(18): 4032-4036
Zheng, S.; Pan, T.; Fan, L.; Qiu, Q.-S. 2013: A novel AtKEA gene family, homolog of bacterial K+/H+ antiporters, plays potential roles in K+ homeostasis and osmotic adjustment in Arabidopsis. Plos one 8(11): E81463
Pan, N.; Jahan, I.; Kersigo, J.; Duncan, J.S.; Kopecky, B.; Fritzsch, B. 2012: A novel Atoh1 "self-terminating" mouse model reveals the necessity of proper Atoh1 level and duration for hair cell differentiation and viability. Plos one 7(1): E30358
Yagi, E.; Akita, T.; Kawahara, T. 2011: A novel au SINE sequence found in a gymnosperm. Genes and Genetic Systems 86(1): 19-25
Li, D.; Li, J.; Jia, X.; Xia, Y.; Zhang, X.; Wang, E. 2013: A novel Au-Ag-Pt three-electrode microchip sensing platform for chromium(VI) determination. Analytica Chimica Acta 804: 98-103
Wang, W.; Gao, Y.; Jia, X.; Xi, K. 2013: A novel Au-Pt@PPy(polypyrrole) coral-like structure: facile synthesis, high SERS effect, and good electro catalytic activity. Journal of Colloid and Interface Science 396: 23-28
Choi, J.Ha.; Kim, H.Soo.; Choi, J-Woo.; Hong, J.Wook.; Kim, Y-Kee.; Oh, B-Keun. 2013: A novel Au-nanoparticle biosensor for the rapid and simple detection of PSA using a sequence-specific peptide cleavage reaction. Biosensors and Bioelectronics 49: 415-419
Chowdhury, A.; Chowdhury, S.; Tsai, M.Y. 2012: A novel Aurora kinase a inhibitor MK-8745 predicts TPX2 as a therapeutic biomarker in non-Hodgkin lymphoma cell lines. Leukemia and Lymphoma 53(3): 462-471
Görgün, G.ül.ü; Calabrese, E.; Hideshima, T.; Ecsedy, J.; Perrone, G.; Mani, M.; Ikeda, H.; Bianchi, G.; Hu, Y.; Cirstea, D.; Santo, L.; Tai, Y.-T.; Nahar, S.; Zheng, M.; Bandi, M.; Carrasco, R.D.; Raje, N.; Munshi, N.; Richardson, P.; Anderson, K.C. 2010: A novel Aurora-A kinase inhibitor MLN8237 induces cytotoxicity and cell-cycle arrest in multiple myeloma. Blood 115(25): 5202-5213
Ahn, H.J.; Glickman, J.F.; Poon, K.L.; Zamolodchikov, D.; Jno-Charles, O.C.; Norris, E.H.; Strickland, S. 2014: A novel Aβ-fibrinogen interaction inhibitor rescues altered thrombosis and cognitive decline in Alzheimer's disease mice. Journal of Experimental Medicine 211(6): 1049-1062
Chen, Q.; Xiao, J.; Lu, L.; Du, L.; Huang, C.; Li, M.; Li, P.; Yao, G. 2015: A novel B allele with c.502C>G mutation identified in a Chinese individual. Transfusion 55(6 Part 2): 1582-1583
Buffa, S.; Pellicanò, M.; Bulati, M.; Martorana, A.; Goldeck, D.; Caruso, C.; Pawelec, G.; Colonna-Romano, G. 2013: A novel B cell population revealed by a CD38/CD24 gating strategy: CD38(-)CD24 (-) B cells in centenarian offspring and elderly people. Age 35(5): 2009-2024
Hjelm, F.; Karlsson, M.C.I.; Heyman, B. 2008: A novel B cell-mediated transport of IgE-immune complexes to the follicle of the spleen. Journal of Immunology 180(10): 6604-6610
Thuresson, B.; Hosseini-Maaf, B.; Hult, A.K.; Hustinx, H.; Alan Chester, M.; Olsson, M.L. 2012: A novel B(weak) hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels. Vox Sanguinis 102(1): 55-64
Yang, H.; Chen, H.; Liu, Z.; Ma, H.; Qin, L.; Jin, R.; Zheng, R.; Feng, Y.; Cui, Z.; Wang, J.; Liu, J.; Hu, Z. 2013: A novel B-cell epitope identified within Mycobacterium tuberculosis CFP10/ESAT-6 protein. Plos one 8(1): E52848
Yu, D.; Han, Z.; Xu, J.; Shao, Y.; Li, H.; Kong, X.; Liu, S. 2010: A novel B-cell epitope of avian infectious bronchitis virus N protein. Viral Immunology 23(2): 189-199
Chen, X.; Dai, B.; Liu, Z.; Gao, J.; Ji, Z.; Guo, J.; Chen, G.; Deng, Z.; Shao, Z. 2014: A novel B/C inter-genotype recombinant of hepatitis B virus identified in north-west China. Journal of General Virology 95(Part 1): 153-155
Kapsogeorgou, E.K.; Moutsopoulos, H.M.; Manoussakis, M.N. 2008: A novel B7-2 (CD86) splice variant with a putative negative regulatory role. Journal of Immunology 180(6): 3815-3823
Han, R.; Shen, S.; Yue, G.; Ding, H. 2014: A novel BA complex network model on color template matching. Thescientificworldjournal 2014: 918453
Yu-Taeger, L.; Petrasch-Parwez, E.; Osmand, A.P.; Redensek, A.; Metzger, S.; Clemens, L.E.; Park, L.; Howland, D.; Calaminus, C.; Gu, X.; Pichler, B.; Yang, X.W.; Riess, O.; Nguyen, H.P. 2012: A novel BACHD transgenic rat exhibits characteristic neuropathological features of Huntington disease. Journal of Neuroscience: the Official Journal of the Society for Neuroscience 32(44): 15426-15438
Kämper, N.; Kessler, J.ör.; Temme, S.; Wegscheid, C.; Winkler, J.; Koch, N. 2012: A novel BAT3 sequence generated by alternative RNA splicing of exon 11B displays cell type-specific expression and impacts on subcellular localization. Plos one 7(4): E35972
Zhang, Y.; Zhao, Q.; Jin, J.; Wang, X.; Cichocki, A. 2012: A novel BCi based on ERP components sensitive to configural processing of human faces. Journal of Neural Engineering 9(2): 026018
Cirulli, F.; Reif, A.; Herterich, S.; Lesch, K.P.; Berry, A.; Francia, N.; Aloe, L.; Barr, C.S.; Suomi, S.J.; Alleva, E. 2011: A novel BDNF polymorphism affects plasma protein levels in interaction with early adversity in rhesus macaques. Psychoneuroendocrinology 36(3): 372-379
Jahagirdar, R.; Zhang, H.; Azhar, S.; Tobin, J.; Attwell, S.; Yu, R.; Wu, J.; McLure, K.G.; Hansen, H.C.; Wagner, G.S.; Young, P.R.; Srivastava, R.A.K.; Wong, N.C.W.; Johansson, J. 2014: A novel BET bromodomain inhibitor, RVX-208, shows reduction of atherosclerosis in hyperlipidemic ApoE deficient mice. Atherosclerosis 236(1): 91-100
Amin, A.N.; El-Khouly, M.E.; Subbaiyan, N.K.; Zandler, M.E.; Fukuzumi, S.; D'Souza, F. 2012: A novel BF2-chelated azadipyrromethene-fullerene dyad: synthesis, electrochemistry and photodynamics. Chemical Communications 48(2): 206-208
Zhang, Z.; Song, T.; Zhang, T.; Gao, J.; Wu, G.; An, L.; Du, G. 2011: A novel BH3 mimetic S1 potently induces Bax/Bak-dependent apoptosis by targeting both Bcl-2 and Mcl-1. International Journal of Cancer 128(7): 1724-1735
Liu, Y.; Xie, M.; Song, T.; Sheng, H.; Yu, X.; Zhang, Z. 2015: A novel BH3 mimetic efficiently induces apoptosis in melanoma cells through direct binding to anti-apoptotic Bcl-2 family proteins, including phosphorylated Mcl-1. Pigment Cell and Melanoma Research 28(2): 161-170
Pellegrino, R.; Kavakli, I.H.; Goel, N.; Cardinale, C.J.; Dinges, D.F.; Kuna, S.T.; Maislin, G.; Van Dongen, H.P.A.; Tufik, S.; Hogenesch, J.B.; Hakonarson, H.; Pack, A.I. 2014: A novel BHLHE41 variant is associated with short sleep and resistance to sleep deprivation in humans. Sleep 37(8): 1327-1336
Soh, S.; Ong, S.T. 2013: A novel BIM deletion polymorphism: implications and lessons for cancer targeted therapies. Japanese Journal of Clinical Hematology 54(10): 1714-1719
Lakhal, B.; Laissue, P.; Braham, R.; Elghezal, H.; Saâd, A.; Fellous, M.; Veitia, R.A. 2009: A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure. Clinical Endocrinology 71(5): 752-753
Möller, T.; Leren, T.P.; Eiklid, K.L.; Holmstrøm, H.; Fredriksen, P.M.; Thaulow, E. 2010: A novel BMPR2 gene mutation associated with exercise-induced pulmonary hypertension in septal defects. Scandinavian Cardiovascular Journal: Scj 44(6): 331-336
Johri, S.; Dunnington, G.H.; Vnencak-Jones, C.L. 2010: A novel BMPR2 mutation associated with pulmonary arterial hypertension in an octogenarian. Lung 188(4): 349-352
Zalaudek, I.; Ciarrocchi, A.; Piana, S.; Argenziano, G.; Torricelli, F.; Sancisi, V.; Gandolfi, G.; Longo, C.; Moscarella, E.; Banzi, C.; Nicoli, D. 2015: A novel BRAF mutation in association with primary amelanotic melanoma with oral metastases. Journal of the European Academy of Dermatology and Venereology: JEADV 29(2): 387-390
Salgado, J.; Gil, C.; Robles, M.; García-Foncillas, J.ús. 2009: A novel BRCA1 mutation in a Spanish patient with ovarian cancer. Breast Cancer Research and Treatment 113(1): 71-73
Salgado, J.; Aramendía, J.é M.; Gutierrez, C.; Gil, C.; Robles, M.; García-Foncillas, J.ús. 2010: A novel BRCA2 mutation that segregates with breast and prostate cancer in a Spanish family. Breast Cancer Research and Treatment 121(1): 219-220
Iglesias, P.; Costoya, J.A. 2009: A novel BRET-based genetically encoded biosensor for functional imaging of hypoxia. Biosensors and Bioelectronics 24(10): 3126-3130
Wu, F.; Zhao, J.; Chen, L.; Liu, X.; Su, P.; Han, Y.; Feng, B.; Li, Q. 2012: A novel BTK-like protein involved in immune response in Lethenteron japonicum. Immunology Letters 146(1-2): 57-63
Yuan, S.; Shi, C.; Lv, Y.; Wang, T.; Wang, H.; Han, W. 2009: A novel Bacillus Calmette-Guérin-based breast cancer vaccine that coexpresses multiple tandem repeats of MUC1 and CD80 breaks the immune tolerance and inhibits MUC1-positive breast cancer growth. Cancer BioTherapy and Radiopharmaceuticals 24(5): 607-613
Buzanello, E.B.; Rezende, R.P.; Sousa, F.M.O.; Marques, E.d.L.S.; Loguercio, L.L. 2014: A novel Bacillus pumilus-related strain from tropical landfarm soil is capable of rapid dibenzothiophene degradation and biodesulfurization. Bmc Microbiology 14: 257
Reddy, S.V.; Thirumala, M.; Mahmood, S.K. 2009: A novel Bacillus sp. accumulating poly (3-hydroxybutyrate-co-3-hydroxyvalerate) from a single carbon substrate. Journal of Industrial Microbiology and Biotechnology 36(6): 837-843
Ammons, D.R.; Reyna, A.; Granados, J.C.; Ventura-Suárez, A.; Rojas-Avelizapa, L.I.; Short, J.D.; Rampersad, J.N. 2013: A novel Bacillus thuringiensis Cry-like protein from a rare filamentous strain promotes crystal localization within the exosporium. Applied and Environmental Microbiology 79(18): 5774-5776
Habib, N.; Kaplan, T.; Margalit, H.; Friedman, N. 2008: A novel Bayesian DNA motif comparison method for clustering and retrieval. Plos Computational Biology 4(2): E1000010
Vehtari, A.; Mäkinen, V-Petteri.; Soininen, P.; Ingman, P.; Mäkelä, S.M.; Savolainen, M.J.; Hannuksela, M.L.; Kaski, K.; Ala-Korpela, M. 2007: A novel Bayesian approach to quantify clinical variables and to determine their spectroscopic counterparts in 1H NMR metabonomic data. Bmc Bioinformatics 8(Suppl): S8
Xing, H.; Liao, W.; Mo, Y.; Zhang, M.Q. 2012: A novel Bayesian change-point algorithm for genome-wide analysis of diverse ChIPseq data types. Journal of Visualized Experiments: Jove 70: E4273
Suk, H.-I.; Lee, S.-W. 2013: A novel Bayesian framework for discriminative feature extraction in Brain-Computer Interfaces. IEEE Transactions on Pattern Analysis and Machine Intelligence 35(2): 286-299
Matsen, F.A.; Small, C.T.; Soliven, K.; Engel, G.A.; Feeroz, M.M.; Wang, X.; Craig, K.L.; Hasan, M.K.; Emerman, M.; Linial, M.L.; Jones-Engel, L. 2014: A novel Bayesian method for detection of APOBEC3-mediated hypermutation and its application to zoonotic transmission of simian foamy viruses. Plos Computational Biology 10(2): E1003493
Uyeda, J.C.; Harmon, L.J. 2014: A novel Bayesian method for inferring and interpreting the dynamics of adaptive landscapes from phylogenetic comparative data. Systematic Biology 63(6): 902-918
Pan, H.; Huang, P.; Wang, Z.; Wang, L.; Li, C.; Xia, J. 2013: A novel Bayesian seamless phase I/Ii design. Plos one 8(9): E73060
Majumdar, A.; Bhattacharya, S.; Basu, A.; Ghosh, S. 2013: A novel Bayesian semiparametric algorithm for inferring population structure and adjusting for case-control association tests. Biometrics 69(1): 164-173
Lin, J.; Zheng, Z.; Li, Y.; Yu, W.; Zhong, W.; Tian, S.; Zhao, F.; Ren, X.; Xiao, J.; Wang, N.; Liu, S.; Wang, L.; Sheng, F.; Chen, Y.; Jin, C.; Li, S.; Xia, B. 2009: A novel Bcl-XL inhibitor Z36 that induces autophagic cell death in Hela cells. Autophagy 5(3): 314-320
Tsai, B.Pinjou.; Jimenez, J.; Lim, S.; Fitzgerald, K.D.; Zhang, M.; Chuah, C.T.H.; Axelrod, H.; Wilson, L.; Ong, S.Tiong.; Semler, B.L.; Waterman, M.L. 2014: A novel Bcr-Abl-mTOR-eIF4A axis regulates IRES-mediated translation of LEF-1. Open Biology 4(11): 140180
Cao, S.; Guo, C.; Lv, Y.; Guo, Y.; Liu, Q. 2009: A novel BiOCl film with flowerlike hierarchical structures and its optical properties. Nanotechnology 20(27): 275702
Tang, W.; He, Y.; Zhou, S.; Ma, Y.; Liu, G. 2009: A novel Bifidobacterium infantis-mediated TK/GCV suicide gene therapy system exhibits antitumor activity in a rat model of bladder cancer. Journal of Experimental and Clinical Cancer Research: Cr 28: 155
Ponassi, R.; Biasotti, B.; Tomati, V.; Bruno, S.; Poggi, A.; Malacarne, D.; Cimoli, G.; Salis, A.; Pozzi, S.; Miglino, M.; Damonte, G.; Cozzini, P.; Spyrakis, F.; Spyraki, F.; Campanini, B.; Bagnasco, L.; Castagnino, N.; Tortolina, L.; Mumot, A.; Frassoni, F.; Daga, A.; Cilli, M.; Piccardi, F.; Monfardini, I.; Perugini, M.; Zoppoli, G.; D'Arrigo, C.; Pesenti, R.; Parodi, S. 2008: A novel Bim-BH3-derived Bcl-XL inhibitor: biochemical characterization, in vitro, in vivo and ex-vivo anti-leukemic activity. Cell Cycle 7(20): 3211-3224
Grant-Downton, R.T.; Terhem, R.B.; Kapralov, M.V.; Mehdi, S.; Rodriguez-Enriquez, M.J.; Gurr, S.J.; van Kan, J.A.L.; Dewey, F.M. 2014: A novel Botrytis species is associated with a newly emergent foliar disease in cultivated Hemerocallis. Plos one 9(6): E89272
Schlabritz-Loutsevitch, N.E.; Whatmore, A.M.; Quance, C.R.; Koylass, M.S.; Cummins, L.Bill.; Dick, E.J.; Snider, C.L.; Cappelli, D.; Ebersole, J.L.; Nathanielsz, P.W.; Hubbard, G.B. 2009: A novel Brucella isolate in association with two cases of stillbirth in non-human primates - first report. Journal of Medical Primatology 38(1): 70-73
Xiang, P.; Wu, K.-C.; Zhu, Y.; Xiang, L.; Li, C.; Chen, D.-L.; Chen, F.; Xu, G.; Wang, A.; Li, M.; Jin, Z.-B. 2014: A novel Bruch's membrane-mimetic electrospun substrate scaffold for human retinal pigment epithelium cells. Biomaterials 35(37): 9777-9788
Chear, C.T.; Gill, H.K.; Ramly, N.H.; Dhaliwal, J.S.; Bujang, N.; Ripen, A.M.; Mohamad, S.B. 2013: A novel Bruton's tyrosine kinase gene (BTK) invariant splice site mutation in a Malaysian family with X-linked agammaglobulinemia. Asian Pacific Journal of Allergy and Immunology 31(4): 320-324
Zheng, B.; Zhang, Y.; Jin, Y.; Yu, H. 2014: A novel Bruton's tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia. Bmc Pediatrics 14: 265
Verhoff, M.; Seitz, S.; Northoff, H.; Jauch, J.; Schaible, A.M.; Werz, O. 2012: A novel C(28)-hydroxylated lupeolic acid suppresses the biosynthesis of eicosanoids through inhibition of cytosolic phospholipase A(2). Biochemical Pharmacology 84(5): 681-691
Trmcic, M.V.; Matovic, R.V.; Tovilovic, G.I.; Ristic, B.Z.; Trajkovic, V.S.; Ferjancic, Z.B.; Saicic, R.N. 2012: A novel C,D-spirolactone analogue of paclitaxel: autophagy instead of apoptosis as a previously unknown mechanism of cytotoxic action for taxoids. Organic and Biomolecular Chemistry 10(25): 4933-4942
Palacio, C.; Connon, S.J. 2012: A novel C-5' substituted cinchona alkaloid-derived catalyst promotes additions of alkyl thiols to nitroolefins with excellent enantioselectivity. Chemical Communications 48(23): 2849-2851
Okamoto, M.; Fuchigami, M.; Suzuki, T.; Watanabe, N. 2012: A novel C-C chemokine receptor 2 antagonist prevents progression of albuminuria and atherosclerosis in mouse models. Biological and Pharmaceutical Bulletin 35(11): 2069-2074
Zhang, L.-H. 2010: A novel C-di-GMP effector linking intracellular virulence regulon to quorum sensing and hypoxia sensing. Virulence 1(5): 391-394
Chen, G.; Wei, S-Hu.; Huang, J.; Sun, J. 2009: A novel C-glycosylflavone from the leaves of Diospyros kaki. Journal of Asian Natural Products Research 11(6): 503-507
Prabhakar, A.; Mukherji, S. 2010: A novel C-shaped, gold nanoparticle coated, embedded polymer waveguide for localized surface plasmon resonance based detection. Lab on a Chip 10(24): 3422-3425
Samadi, A.K.; Zhang, X.; Mukerji, R.; Donnelly, A.C.; Blagg, B.S.; Cohen, M.S. 2011: A novel C-terminal HSP90 inhibitor KU135 induces apoptosis and cell cycle arrest in melanoma cells. Cancer Letters 312(2): 158-167
Singh, M.; Shah, V.; Tatu, U. 2014: A novel C-terminal homologue of Aha1 co-chaperone binds to heat shock protein 90 and stimulates its ATPase activity in Entamoeba histolytica. Journal of Molecular Biology 426(8): 1786-1798
Iwata, T.; Yamada, S.; Ito, J.; Inoshita, N.; Mizusawa, N.; Ono, S.; Yoshimoto, K. 2014: A novel C-terminal nonsense mutation, Q315X, of the aryl hydrocarbon receptor-interacting protein gene in a Japanese familial isolated pituitary adenoma family. Endocrine Pathology 25(3): 273-281
Ramu, T.; Prasad, M.Esther.; Connors, E.; Mishra, A.; Thomassin, J-Lee.; Leblanc, J.; Rainey, J.K.; Thomas, N.A. 2013: A novel C-terminal region within the multicargo type III secretion chaperone CesT contributes to effector secretion. Journal of Bacteriology 195(4): 740-756
Zhang, H.; Wang, H.; Wang, L.; Song, X.; Zhao, J.; Qiu, L.; Li, L.; Cong, M.; Song, L. 2009: A novel C-type lectin (Cflec-3) from Chlamys farreri with three carbohydrate-recognition domains. Fish and Shellfish Immunology 26(5): 707-715
Wang, X.-W.; Zhang, X.-W.; Xu, W.-T.; Zhao, X.-F.; Wang, J.-X. 2009: A novel C-type lectin (FcLec4) facilitates the clearance of Vibrio anguillarum in vivo in Chinese white shrimp. Developmental and Comparative Immunology 33(9): 1039-1047
Guo, X.-N.; Jin, X.-K.; Li, S.; Yu, A.-Q.; Wu, M.-H.; Tan, S.-J.; Zhu, Y.-T.; Li, W.-W.; Zhang, P.; Wang, Q. 2013: A novel C-type lectin from Eriocheir sinensis functions as a pattern recognition receptor with antibacterial activity. Fish and Shellfish Immunology 35(5): 1554-1565
Kong, P.; Wang, L.; Zhang, H.; Song, X.; Zhou, Z.; Yang, J.; Qiu, L.; Wang, L.; Song, L. 2011: A novel C-type lectin from bay scallop Argopecten irradians (AiCTL-7) agglutinating fungi with mannose specificity. Fish and Shellfish Immunology 30(3): 836-844
Zhao, Z.-Y.; Yin, Z.-X.; Xu, X.-P.; Weng, S.-P.; Rao, X.-Y.; Dai, Z.-X.; Luo, Y.-W.; Yang, G.; Li, Z.-S.; Guan, H.-J.; Li, S.-D.; Chan, S.-M.; Yu, X.-Q.; He, J.-G. 2009: A novel C-type lectin from the shrimp Litopenaeus vannamei possesses anti-white spot syndrome virus activity. Journal of Virology 83(1): 347-356
Zhang, X.-W.; Xu, W.-T.; Wang, X.-W.; Mu, Y.; Zhao, X.-F.; Yu, X.-Q.; Wang, J.-X. 2009: A novel C-type lectin with two CRD domains from Chinese shrimp Fenneropenaeus chinensis functions as a pattern recognition protein. Molecular Immunology 46(8-9): 1626-1637
Wang, Q.; Wang, C.; Mu, C.; Wu, H.; Zhang, L.; Zhao, J. 2013: A novel C-type lysozyme from Mytilus galloprovincialis: insight into innate immunity and molecular evolution of invertebrate C-type lysozymes. Plos one 8(6): E67469
Spence, T.; Perotti, C.; Sin-Chan, P.; Picard, D.; Wu, W.; Singh, A.; Anderson, C.; Blough, M.D.; Cairncross, J.G.; Lafay-Cousin, L.; Strother, D.; Hawkins, C.; Narendran, A.; Huang, A.; Chan, J.A. 2014: A novel C19MC amplified cell line links Lin28/let-7 to mTOR signaling in embryonal tumor with multilayered rosettes. Neuro-Oncology 16(1): 62-71
Yu, Y.; Huang, H.; Wang, Y.; Yu, Y.; Yuan, S.; Huang, S.; Pan, M.; Feng, K.; Xu, A. 2008: A novel C1q family member of amphioxus was revealed to have a partial function of vertebrate C1q molecule. Journal of Immunology 181(10): 7024-7032
Nakamura, O.; Wada, Y.; Namai, F.; Saito, E.; Araki, K.; Yamamoto, A.; Tsutsui, S. 2009: A novel C1q family member with fucose-binding activity from surfperch, Neoditrema ransonnetii (Perciformes, Embiotocidae). Fish and Shellfish Immunology 27(6): 714-720
Liu, H.-H.; Xiang, L.-X.; Shao, J.-Z. 2014: A novel C1q-domain-containing (C1qDC) protein from Mytilus coruscus with the transcriptional analysis against marine pathogens and heavy metals. Developmental and Comparative Immunology 44(1): 70-75
Wang, K.-W.; Ju, X.-Y.; Zhang, L.; Wang, W.; Shen, L.-Q. 2012: A novel C27-steroidal glycoside sulfate from Liriope graminifolia. Yao Xue Xue Bao 47(5): 619-623
Schoberle, T.J.; Nguyen-Coleman, C.K.; Herold, J.; Yang, A.; Weirauch, M.; Hughes, T.R.; McMurray, J.S.; May, G.S. 2014: A novel C2H2 transcription factor that regulates gliA expression interdependently with GliZ in Aspergillus fumigatus. Plos Genetics 10(5): E1004336
Steindl, K.; Alazami, A.M.; Bhatia, K.P.; Wuerfel, J.T.; Petersen, D.; Cartolari, R.; Neri, G.; Klein, C.; Mongiardo, B.; Alkuraya, F.S.; Schneider, S.A. 2010: A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome. Clinical Genetics 78(6): 594-597
Wu, J.; Lei, G.; Mei, M.; Tang, Y.; Li, H. 2010: A novel C53/LZAP-interacting protein regulates stability of C53/LZAP and DDRGK domain-containing Protein 1 (DDRGK1) and modulates NF-kappaB signaling. Journal of Biological Chemistry 285(20): 15126-15136
Cavaco, C.K.; Patras, K.A.; Zlamal, J.E.; Thoman, M.L.; Morgan, E.L.; Sanderson, S.D.; Doran, K.S. 2013: A novel C5a-derived immunobiotic peptide reduces Streptococcus agalactiae colonization through targeted bacterial killing. Antimicrobial Agents and ChemoTherapy 57(11): 5492-5499
Molloy, A.; Kimmich, O.; Martindale, J.; Moore, H.; Hutchinson, M.; O'Riordan, S. 2013: A novel CACNA1A mutation associated with adult-onset, paroxysmal head tremor. Movement Disorders: Official Journal of the Movement Disorder Society 28(6): 842-843
Stawarczyk, B.; Eichberger, M.; Hoffmann, R.; Noack, F.; Schweiger, J.; Edelhoff, D.; Beuer, F. 2014: A novel CAD/CAM base metal compared to conventional CoCrMo alloys: an in-vitro study of the long-term metal-ceramic bond strength. Oral Health and Dental Management 13(2): 446-452
Huang, D.; Lim, S.; Chua, R.Y.R.; Shi, H.; Ng, M.L.; Wong, S.H. 2010: A novel CARD containing splice-isoform of CIITA regulates nitric oxide synthesis in dendritic cells. Protein and Cell 1(3): 291-306
Diaz-Thomas, A.; Cannon, J.; Iyer, P.; Al-Maawali, A.; Fazalullah, M.; Diamond, F.; Mueller, O.T.; Root, A.W.; Alyaarubi, S. 2014: A novel CASR mutation associated with neonatal severe hyperparathyroidism transmitted as an autosomal recessive disorder. Journal of Pediatric Endocrinology and Metabolism: Jpem 27(9-10): 851-856
Contartese, A.; Valoti, M.; Corelli, F.; Pasquini, S.; Mugnaini, C.; Pessina, F.; Aldinucci, C.; Sgaragli, G.; Frosini, M. 2012: A novel CB2 agonist, COR167, potently protects rat brain cortical slices against OGD and reperfusion injury. Pharmacological Research 66(6): 555-563
Larson, M.Jo.; Amodeo, M.; Storti, S.A.; Steketee, G.; Blitzman, G.; Smith, L. 2009: A novel CBT Web course for the substance abuse workforce: community counselors' perceptions. Substance Abuse 30(1): 26-39
Nakagami, Y.; Kawashima, K.; Etori, M.; Yonekubo, K.; Suzuki, C.; Jojima, T.; Kuribayashi, T.; Nara, F.; Yamashita, M. 2010: A novel CC chemokine receptor 4 antagonist RS-1269 inhibits ovalbumin-induced ear swelling and lipopolysaccharide-induced endotoxic shock in mice. Basic and Clinical Pharmacology and Toxicology 107(4): 793-797
Komai, M.; Tanaka, H.; Nagao, K.; Ishizaki, M.; Kajiwara, D.; Miura, T.; Ohashi, H.; Haba, T.; Kawakami, K.; Sawa, E.; Yoshie, O.; Inagaki, N.; Nagai, H. 2010: A novel CC-chemokine receptor 3 antagonist, Ki19003, inhibits airway eosinophilia and subepithelial/peribronchial fibrosis induced by repeated antigen challenge in mice. Journal of Pharmacological Sciences 112(2): 203-213
Gutman, J.A.; Hoffner, B. 2012: A novel CCAAT/enhancer binding protein α germline variant in a case of acute myeloid leukemia. Leukemia and Lymphoma 53(5): 1006-1007
Zhao, Y.; Xie, L.; Li, P.; Song, J.; Qu, T.; Fan, W.; Chen, H.; Chen, D.; Lu, D.; Zhou, L.; Mao, Y. 2011: A novel CCM1 gene mutation causes cerebral cavernous malformation in a Chinese family. Journal of Clinical Neuroscience: Official Journal of the Neurosurgical Society of Australasia 18(1): 61-65
Lanfranconi, S.; Ronchi, D.; Ahmed, N.; Civelli, V.; Basilico, P.; Bresolin, N.; Comi, G.P.; Corti, S. 2014: A novel CCM1 mutation associated with multiple cerebral and vertebral cavernous malformations. Bmc Neurology 14: 158
Riddick, N.E.; Hermann, E.A.; Loftin, L.M.; Elliott, S.T.; Wey, W.C.; Cervasi, B.; Taaffe, J.; Engram, J.C.; Li, B.; Else, J.G.; Li, Y.; Hahn, B.H.; Derdeyn, C.A.; Sodora, D.L.; Apetrei, C.; Paiardini, M.; Silvestri, G.; Collman, R.G. 2010: A novel CCR5 mutation common in sooty mangabeys reveals SIVsmm infection of CCR5-null natural hosts and efficient alternative coreceptor use in vivo. Plos Pathogens 6(8): E1001064
Dahl, M.E.; Berson, A.; Lora, J.; Fuentes, M. 2008: A novel CCR5-specific pharmacodynamic assay in whole blood using phosphoflow cytometry highlights different ligand-dependent responses but similar properties of antagonists in CD8+ and CD4+ T lymphocytes. Journal of pharmacology and experimental therapeutics 327(3): 926-933
Zeng, S.; Wang, S.; Wang, L.; Yang, L.; Chen, Z.; Liang, Z. 2012: A novel CD105 determination system based on an ultrasensitive bioelectrochemical strategy with Pt nanoparticles. Sensors 12(10): 13471-13479
Hochweller, K.; Striegler, J.ör.; Hämmerling, G.ün.J.; Garbi, N. 2008: A novel CD11c.DTR transgenic mouse for depletion of dendritic cells reveals their requirement for homeostatic proliferation of natural killer cells. European Journal of Immunology 38(10): 2776-2783
Kellner, C.; Bruenke, J.; Stieglmaier, J.; Schwemmlein, M.; Schwenkert, M.; Singer, H.; Mentz, K.; Peipp, M.; Lang, P.; Oduncu, F.; Stockmeyer, B.; Fey, G.H. 2008: A novel CD19-directed recombinant bispecific antibody derivative with enhanced immune effector functions for human leukemic cells. Journal of ImmunoTherapy 31(9): 871-884
Wang, X.; Santin, A.D.; Bellone, S.; Gupta, S.; Nakagawa, M. 2009: A novel CD4 T-cell epitope described from one of the cervical cancer patients vaccinated with HPV 16 or 18 E7-pulsed dendritic cells. Cancer Immunology Immunotherapy: Cii 58(2): 301-308
Mohammadzadeh, I.; Shahbaznejad, L.; Wang, N.; Farhadi, E.; Aghamohammadi, A.; Hammarström, L.; Rezaei, N. 2013: A novel CD40 ligand mutation in a patient with pneumonia, neutropenia, and hyperimmunoglobulin M phenotype. Journal of Investigational Allergology and Clinical Immunology 23(1): 50-51
Ugarte-Berzal, E.ía.; Bailón, E.; Amigo-Jiménez, I.; Albar, J.P.; García-Marco, J.é A.; García-Pardo, A. 2014: A novel CD44-binding peptide from the pro-matrix metalloproteinase-9 hemopexin domain impairs adhesion and migration of chronic lymphocytic leukemia (CLL) cells. Journal of Biological Chemistry 289(22): 15340-15349
Sandström, K.; Haylock, A.K.; Spiegelberg, D.; Qvarnström, F.; Wester, K.; Nestor, M. 2012: A novel CD44v6 targeting antibody fragment with improved tumor-to-blood ratio. International Journal of Oncology 40(5): 1525-1532
Rossio, R.; Lotta, L.A.; Pontiggia, S.; Borsa, N.ò G.; Garagiola, I.; Ardissino, G.; Mikovic, D.; Cugno, M.; Peyvandi, F. 2015: A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity. Haematologica 100(3): E87-E89
Zekavat, G.; Mozaffari, R.; Arias, V.J.; Rostami, S.Y.; Badkerhanian, A.; Tenner, A.J.; Nichols, K.E.; Naji, A.; Noorchashm, H. 2010: A novel CD93 polymorphism in non-obese diabetic (NOD) and NZB/W F1 mice is linked to a CD4+ iNKT cell deficient state. Immunogenetics 62(6): 397-407
Chiofalo, M.G.; Sparaneo, A.; Chetta, M.; Franco, R.; Baorda, F.; Cinque, L.; Granatiero, M.; D'Agruma, L.; Pezzullo, L.; Scillitani, A.; Guarnieri, V. 2014: A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome. Cellular Oncology 37(4): 281-288
Yin, T.; Lallena, M.J.; Kreklau, E.L.; Fales, K.R.; Carballares, S.; Torrres, R.; Wishart, G.N.; Ajamie, R.T.; Cronier, D.M.; Iversen, P.W.; Meier, T.I.; Foreman, R.T.; Zeckner, D.; Sissons, S.E.; Halstead, B.W.; Lin, A.B.; Donoho, G.P.; Qian, Y.; Li, S.; Wu, S.; Aggarwal, A.; Ye, X.S.; Starling, J.J.; Gaynor, R.B.; de Dios, A.; Du, J. 2014: A novel CDK9 inhibitor shows potent antitumor efficacy in preclinical hematologic tumor models. Molecular Cancer Therapeutics 13(6): 1442-1456
Sartori, S.; Di Rosa, G.; Polli, R.; Bettella, E.; Tricomi, G.; Tortorella, G.; Murgia, A. 2009: A novel CDKL5 mutation in a 47,XXY boy with the early-onset seizure variant of Rett syndrome. American Journal of Medical Genetics. Part a 149a (2): 232-236
Lendner, M.; Böttcher, D.; Delling, C.; Ojo, K.K.; Van Voorhis, W.C.; Daugschies, A. 2015: A novel CDPK1 inhibitor--a potential treatment for cryptosporidiosis in calves?. Parasitology Research 114(1): 335-336
Witek, M.E.; Snook, A.E.; Lin, J.E.; Blomain, E.S.; Xiang, B.; Magee, M.S.; Magee, M.; Waldman, S.A. 2014: A novel CDX2 isoform regulates alternative splicing. Plos one 9(8): E104293
Besbas, N.; Gulhan, B.; Gucer, S.; Korkmaz, E.; Ozaltin, F. 2014: A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl. Journal of Nephrology 27(4): 457-460
Andreeva, A.; Tidow, H. 2008: A novel CHHC Zn-finger domain found in spliceosomal proteins and tRNA modifying enzymes. Bioinformatics 24(20): 2277-2280
Sher, G.; Naeem, M. 2014: A novel CHSY1 gene mutation underlies Temtamy preaxial brachydactyly syndrome in a Pakistani family. European Journal of Medical Genetics 57(1): 21-24
Sugita, S.; Arai, Y.; Tonooka, A.; Hama, N.; Totoki, Y.; Fujii, T.; Aoyama, T.; Asanuma, H.; Tsukahara, T.; Kaya, M.; Shibata, T.; Hasegawa, T. 2014: A novel CIC-FOXO4 gene fusion in undifferentiated small round cell sarcoma: a genetically distinct variant of Ewing-like sarcoma. American Journal of Surgical Pathology 38(11): 1571-1576
Mozzillo, E.; Delvecchio, M.; Carella, M.; Grandone, E.; Palumbo, P.; Salina, A.; Aloi, C.; Buono, P.; Izzo, A.; D'Annunzio, G.; Vecchione, G.; Orrico, A.; Genesio, R.; Simonelli, F.; Franzese, A. 2014: A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2. Bmc Medical Genetics 15: 88
Kumar, K.R.; Ng, K.; Vandebona, H.; Davis, M.R.; Sue, C.M. 2010: A novel CLCN1 mutation (G1652A) causing a mild phenotype of thomsen disease. Muscle and Nerve 41(3): 412-415
Ji, L.-N.; Chen, C.-Y.; Wang, J.-J.; Cao, L. 2014: A novel CLCN5 mutation in a Chinese boy with Dent's disease. World Journal of Pediatrics: Wjp 10(3): 275-277
Bogdanović, R.; Draaken, M.; Toromanović, A.; Dordević, M.; Stajić, N.; Ludwig, M. 2010: A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency. Pediatric Nephrology 25(11): 2363-2368
Valina, M.R.; Larsen, C.P.; Kanosky, S.; Suchy, S.F.; Nield, L.S.; Onder, A.M. 2013: A novel CLCN5 mutation in a boy with asymptomatic proteinuria and focal global glomerulosclerosis. Clinical Nephrology 80(5): 377-384
Besbas, N.; Draaken, M.; Ludwig, M.; Deren, O.; Orhan, D.; Bilginer, Y.; Ozaltin, F. 2009: A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis. European Journal of Pediatrics 168(12): 1449-1454
Deeb, A.; Abood, S.A.; Simon, J.; Dastoor, H.; Pearce, S.H.; Sayer, J.A. 2013: A novel CLDN16 mutation in a large family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis. Bmc Research Notes 6: 527
Wang, Y.-L.; Zeng, Z.-Y.; Song, X.-W.; Hao, Z.-F.; Shi, Y.-W.; Tang, B.; Chen, S.-Q.; Gao, M.-M.; Di, W.; Long, Y.-S.; Yi, Y.-H.; Liao, W.-P. 2011: A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis. Neurogenetics 12(1): 93-95
Vantaggiato, C.; Redaelli, F.; Falcone, S.; Perrotta, C.; Tonelli, A.; Bondioni, S.; Morbin, M.; Riva, D.; Saletti, V.; Bonaglia, M.C.; Giorda, R.; Bresolin, N.; Clementi, E.; Bassi, M.T. 2009: A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function. Human Mutation 30(7): 1104-1116
Mohapatra, P.K.; Kandwal, P.; Iqbal, M.; Huskens, J.; Murali, M.S.; Verboom, W. 2013: A novel CMPO-functionalized task specific ionic liquid: synthesis, extraction and spectroscopic investigations of actinide and lanthanide complexes. Dalton Transactions 42(13): 4343-4347
Liu, X.; Ling, Y.; Huang, L.; Gao, W. 2013: A novel CO sensor based on the point contact between Pd decorated TiO2 nanotubes array. Journal of Nanoscience and Nanotechnology 13(2): 869-872
Liang, F.; Luo, H.; Partovi, K.; Ravkina, O.; Cao, Z.; Liu, Y.; Caro, J.ür. 2014: A novel CO2-stable dual phase membrane with high oxygen permeability. Chemical Communications 50(19): 2451-2454
Muchemwa, F.C.; Jinnin, M.; Wakasugi, S.; Sakamoto, M.; Inoue, Y.; Ishihara, T.; Ihn, H. 2010: A novel COL1A1 exon 14/PDGFB fusion gene in dermatofibrosarcoma protuberans. European Journal of Dermatology: Ejd 20(3): 390-391
Barbirato, C.; Almeida, M.G.; Milanez, M.; Sipolatti, V.; Rebouças, M.R.G.O.; Akel, A.N.; Nunes, V.R.R.; Perrone, A.M.S.; Zatz, M.; Louro, I.D.; Paula, F. 2009: A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta. Genetics and Molecular Research: Gmr 8(1): 173-178
Xia, X.-Y.; Li, N.; Cao, X.; Wu, Q.-Y.; Li, T.-F.; Zhang, C.; Li, W.-W.; Cui, Y.-X.; Li, X.-J.; Xue, C.-Y. 2014: A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese family. Bmc Medical Genetics 15: 97
Uzak, A.S.; Tokgoz, B.; Dundar, M.; Tekin, M. 2013: A novel COL4A3 mutation causes autosomal-recessive Alport syndrome in a large Turkish family. Genetic Testing and Molecular Biomarkers 17(3): 260-264
Xiu, X.; Yuan, J.; Deng, X.; Xiao, J.; Xu, H.; Zeng, Z.; Guan, L.; Xu, F.; Deng, S. 2014: A novel COL4A5 mutation identified in a Chinese Han family using exome sequencing. Biomed Research International 2014: 186048
Tang, Z.; Dai, Y.; Wan, Z.; Zhan, T.; Tan, J.; Ren, X.; Liu, J.; Wang, Q.; Liu, M. 2008: A novel COL4A5 splicing mutation causing Alport syndrome in a Chinese family. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 25(6): 649-652
Liu, Y-Hui.; Shang, X.; Li, Z-Tao.; Wu, Y-Min.; Li, L-Fen.; Xu, X-Min. 2013: A novel COL7A1 gene mutation causing pretibial epidermolysis bullosa: report of a Chinese family with intra-familial phenotypical diversity. Gene 524(2): 377-380
Galehdari, H.; Mohammadian, G.; Azmoon, S.; Salehi, B.; Pedram, M. 2010: A novel COL7A1 gene mutation in an Iranian individual suffering dystrophic epidermolysis bullosa. Journal of Molecular Diagnostics: Jmd 12(3): 377-379
Park, J.; Chae, H.; Kim, M.; Kim, Y.; Park, I.Y.; Shin, J.C.; Park, Y.M. 2013: A novel COL7A1 mutation in a Korean patient with Hallopeau-Siemens recessive dystrophic epidermolysis bullosa. Genetics and Molecular Research: Gmr 12(1): 678-682
Pang, B.; Durso, M.B.; Hamilton, R.L.; Nikiforova, M.N. 2013: A novel COLD-PCR/FMCA assay enhances the detection of low-abundance IDH1 mutations in gliomas. Diagnostic Molecular Pathology: the American Journal of Surgical Pathology Part B 22(1): 28-34
Gupta, A.; Chattopadhyay, I.; Mukherjee, S.; Sengupta, M.; Das, S.K.; Ray, K. 2010: A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient. Behavioral and Brain Functions: Bbf 6: 33
Elliott, A.M.; Bocangel, P.; Reed, M.H.; Greenberg, C.R. 2010: A novel COMP mutation in an Inuit patient with pseudoachondroplasia and severe short stature. Genetics and Molecular Research: Gmr 9(3): 1785-1790
Mohy El-Din, M.M.; Senbel, A.M.; Bistawroos, A.A.; El-Mallah, A.; Nour El-Din, N.A.; Bekhit, A.A.; Abd El Razik, H.A. 2011: A novel COX-2 inhibitor pyrazole derivative proven effective as an anti-inflammatory and analgesic drug. Basic and Clinical Pharmacology and Toxicology 108(4): 263-273
Liggett, J.L.; Min, K.-W.; Smolensky, D.; Baek, S.J. 2014: A novel COX-independent mechanism of sulindac sulfide involves cleavage of epithelial cell adhesion molecule protein. Experimental Cell Research 326(1): 1-9
Hoang, R.V.; Tanna, D.; Jayet Bray, L.C.; Dascalu, S.M.; Harris, F.C. 2013: A novel CPU/GPU simulation environment for large-scale biologically realistic neural modeling. Frontiers in Neuroinformatics 7: 19
Zhang, B.; Liu, Y.; Zhang, P.; Wei, Y.; Yin, X.; Zheng, J. 2011: A novel CRAd in combination with cisplatin enhanced the antitumor efficacy in ovarian cancer. International Journal of Gynecological Cancer: Official Journal of the International Gynecological Cancer Society 21(9): 1540-1546
Qiao, Q.; Teng, X.; Wang, N.; Lu, R.; Guo, L.; Zhang, X.; Du, Y.; Wang, W.; Chen, S.; Wu, Q.; He, G.; Wang, Y.; Hu, W. 2014: A novel CRIg-targeted complement inhibitor protects cells from complement damage. Faseb Journal: Official Publication of the Federation of American Societies for Experimental Biology 28(11): 4986-4999
Sacconi, S.; Féasson, L.éo.; Antoine, J.C.; Pécheux, C.; Bernard, R.; Cobo, A.M.; Casarin, A.; Salviati, L.; Desnuelle, C.; Urtizberea, A. 2012: A novel CRYAB mutation resulting in multisystemic disease. Neuromuscular Disorders: Nmd 22(1): 66-72
Faletra, F.; d'Adamo, A.P.; Pensiero, S.; Athanasakis, E.; Catalano, D.; Bruno, I.; Gasparini, P. 2013: A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian family. Ophthalmic Genetics 34(1-2): 115-117
Wang, B.; Yu, C.; Xi, Y.-B.; Cai, H.-C.; Wang, J.; Zhou, S.; Zhou, S.; Wu, Y.; Yan, Y.-B.; Ma, X.; Xie, L. 2011: A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family. Human Mutation 32(1): E1939-E1947
Low, D.A.; White, B.M.; Lee, P.P.; Thomas, D.H.; Gaudio, S.; Jani, S.S.; Wu, X.; Lamb, J.M. 2013: A novel CT acquisition and analysis technique for breathing motion modeling. Physics in Medicine and Biology 58(11): L31-L36
An, M.; Xie, Y. 2013: A novel CT imaging system with adjacent double X-ray sources. Computational and Mathematical Methods in Medicine 2013: 391212
Strumwasser, A.; Chu, E.; Yeung, L.; Miraflor, E.; Sadjadi, J.; Victorino, G.P. 2011: A novel CT volume index score correlates with outcomes in polytrauma patients with pulmonary contusion. Journal of Surgical Research 170(2): 280-285
Parris, D.; Fischbein, N.; Mackey, S.; Carroll, I. 2010: A novel CT-guided transpsoas approach to diagnostic genitofemoral nerve block and ablation. Pain Medicine 11(5): 785-789
Jahromi, A.H.; Nguyen, L.; Fu, Y.; Miller, K.A.; Baranger, A.M.; Zimmerman, S.C. 2013: A novel CUG(exp)·MBNL1 inhibitor with therapeutic potential for myotonic dystrophy type 1. Acs Chemical Biology 8(5): 1037-1043
Muenchmeier, N.; Boecker, S.; Bankel, L.; Hinz, L.; Rieth, N.; Lapa, C.; Mendler, A.N.; Noessner, E.; Mocikat, R.; Nelson, P.J. 2013: A novel CXCL10-based GPI-anchored fusion protein as adjuvant in NK-based tumor therapy. Plos one 8(8): E72749
Bedke, J.; Nelson, P.J.; Kiss, E.; Muenchmeier, N.; Rek, A.; Behnes, C.-L.; Gretz, N.; Kungl, A.J.; Gröne, H.-J. 2010: A novel CXCL8 protein-based antagonist in acute experimental renal allograft damage. Molecular Immunology 47(5): 1047-1057
Balan, M.; Pal, S. 2014: A novel CXCR3-B chemokine receptor-induced growth-inhibitory signal in cancer cells is mediated through the regulation of Bach-1 protein and Nrf2 protein nuclear translocation. Journal of Biological Chemistry 289(6): 3126-3137
Tan, Y.; Li, Y.; Xiao, J.; Shao, H.; Ding, C.; Arteel, G.E.; Webster, K.A.; Yan, J.; Yu, H.; Cai, L.; Li, X. 2009: A novel CXCR4 antagonist derived from human SDF-1beta enhances angiogenesis in ischaemic mice. Cardiovascular Research 82(3): 513-521
Fricker, S.P. 2008: A novel CXCR4 antagonist for hematopoietic stem cell mobilization. Expert Opinion on Investigational Drugs 17(11): 1749-1760
Yang, Y.; Zhang, Q.; Gao, M.; Yang, X.; Huang, Z.; An, J. 2014: A novel CXCR4-selective high-affinity fluorescent probe and its application in competitive binding assays. Biochemistry 53(30): 4881-4883
Naidoo, R.; Jordaan, N.; Chan, K.W.; Le Roux, D.M.; Pienaar, S.; Nuttall, J.; Lau, Y.L.; Eley, B.S. 2011: A novel CYBB mutation with the first genetically confirmed case of chronic granulomatous disease in South Africa. South African Medical Journal 101(10): 768-769
Guardoli, D.; Argenziano, G.; Ponti, G.; Nasti, S.; Zalaudek, I.; Moscarella, E.; Lallas, A.; Piana, S.; Specchio, F.; Martinuzzi, C.; Raucci, M.; Pellacani, G.; Longo, C. 2015: A novel CYLD germline mutation in Brooke-Spiegler syndrome. Journal of the European Academy of Dermatology and Venereology: Jeadv 29(3): 457-462
Løvås, K.; McFarlane, I.; Nguyen, H.-H.; Curran, S.; Schwabe, J.; Halsall, D.; Bernhardt, R.; Wallace, A.M.; Chatterjee, V.K.K. 2009: A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency. Journal of Clinical Endocrinology and Metabolism 94(3): 914-919
Alzuhairy, S.; Abu-Amero, K.K.; Al-Shahwan, S.; Edward, D.P. 2015: A novel CYP1B1 mutation with congenital glaucoma and total aniridia. Ophthalmic Genetics 36(1): 89-91
Uehara, S.; Murayama, N.; Yamazaki, H.; Uno, Y. 2010: A novel CYP2A26 identified in cynomolgus monkey liver metabolizes coumarin. Xenobiotica; the Fate of Foreign Compounds in Biological Systems 40(9): 621-629
Pereira, S.L.; Kummerle, A.E.; Fraga, C.A.M.; Barreiro, E.J.; Rocha, N.d.N.; Ferraz, E.B.; do Nascimento, J.é H.M.; Sudo, R.T.; Zapata-Sudo, G. 2013: A novel Ca2+ channel antagonist reverses cardiac hypertrophy and pulmonary arteriolar remodeling in experimental pulmonary hypertension. European Journal of Pharmacology 702(1-3): 316-322
Ito, S.; Kume, H.; Naruse, K.; Kondo, M.; Takeda, N.; Iwata, S.; Hasegawa, Y.; Sokabe, M. 2008: A novel Ca2+ influx pathway activated by mechanical stretch in human airway smooth muscle cells. American Journal of Respiratory Cell and Molecular Biology 38(4): 407-413
Khan, S.; Verma, G.; Sharma, S. 2010: A novel Ca2+-activated protease from germinating Vigna radiata seeds and its role in storage protein mobilization. Journal of Plant Physiology 167(11): 855-861
Mander, P.; Simkhada, J.R.; Cho, S.S.; Park, S.J.; Choi, H.S.; Lee, H.C.; Sohng, J.K.; Yoo, J.C. 2009: A novel Ca2+-dependent phospholipase D from Streptomyces tendae, possessing only hydrolytic activity. Archives of Pharmacal Research 32(10): 1461-1467
Jung, H.J.; Kim, J.H.; Shim, J.S.; Kwon, H.J. 2010: A novel Ca2+/calmodulin antagonist HBC inhibits angiogenesis and down-regulates hypoxia-inducible factor. Journal of Biological Chemistry 285(33): 25867-25874
Hoover, C.M.; Edwards, S.L.; Yu, S.-c.; Kittelmann, M.; Richmond, J.E.; Eimer, S.; Yorks, R.M.; Miller, K.G. 2014: A novel CaM kinase Ii pathway controls the location of neuropeptide release from Caenorhabditis elegans motor neurons. Genetics 196(3): 745-765
Tonyushkina, K.N.; O'Connor, S.; Dunbar, N.S. 2012: A novel CaSR mutation presenting as a severe case of neonatal familial hypocalciuric hypercalcemia. International Journal of Pediatric Endocrinology 2012(1): 13
Bravo-Martínez, J.; Arenas, I.; Vivas, O.; Rebolledo-Antúnez, S.; Vázquez-García, M.; Larrazolo, A.; García, D.E. 2012: A novel CaV2.2 channel inhibition by piracetam in peripheral and central neurons. Experimental Biology and Medicine 237(10): 1209-1218
Sleigh, J.N.; Buckingham, S.D.; Esmaeili, B.; Viswanathan, M.; Cuppen, E.; Westlund, B.M.; Sattelle, D.B. 2011: A novel Caenorhabditis elegans allele, smn-1(cb131), mimicking a mild form of spinal muscular atrophy, provides a convenient drug screening platform highlighting new and pre-approved compounds. Human molecular genetics 20(2): 245-260
Morris, G.A.J.; Ikumapayi, U.N.; Antonio, M.; Howie, S.R.C.; Adegbola, R.A. 2008: A novel Campylobacter jejuni sequence type from a culture-negative patient in the Gambia. Plos one 3(3): E1773
Reeves, G.; Monroy-Barbosa, A.; Bosland, P.W. 2013: A novel Capsicum gene inhibits host-specific disease resistance to Phytophthora capsici. Phytopathology 103(5): 472-478
Singh, M.K.; Dadke, D.; Nicolas, E.; Serebriiskii, I.G.; Apostolou, S.; Canutescu, A.; Egleston, B.L.; Golemis, E.A. 2008: A novel Cas family member, HEPL, regulates FAK and cell spreading. Molecular Biology of the Cell 19(4): 1627-1636
Sun, X.-y.; Takagishi, Y.; Okabe, E.; Chishima, Y.ûk.; Kanou, Y.; Murase, S.; Mizumura, K.; Inaba, M.; Komatsu, Y.; Hayashi, Y.; Peles, E.; Oda, S.-i.; Murata, Y. 2009: A novel Caspr mutation causes the shambling mouse phenotype by disrupting axoglial interactions of myelinated nerves. Journal of Neuropathology and Experimental Neurology 68(11): 1207-1218
Kawai, F.; Oda, M.; Tamashiro, T.; Waku, T.; Tanaka, N.; Yamamoto, M.; Mizushima, H.; Miyakawa, T.; Tanokura, M. 2014: A novel Ca²⁺-activated, thermostabilized polyesterase capable of hydrolyzing polyethylene terephthalate from Saccharomonospora viridis AHK190. Applied Microbiology and Biotechnology 98(24): 10053-10064
Wang, X.; Tao, G.; Meng, Y. 2009: A novel CdSe/CdS quantum dot-based competitive fluoroimmunoassay for the detection of clenbuterol residue in pig urine using magnetic core/shell Fe3O4/Au nanoparticles as a solid carrier. Analytical Sciences: the International Journal of the Japan Society for Analytical Chemistry 25(12): 1409-1413
Walsby, E.; Pratt, G.; Shao, H.; Abbas, A.Y.; Fischer, P.M.; Bradshaw, T.D.; Brennan, P.; Fegan, C.; Wang, S.; Pepper, C. 2014: A novel Cdk9 inhibitor preferentially targets tumor cells and synergizes with fludarabine. Oncotarget 5(2): 375-385
Riesterer, O.; Matsumoto, F.; Wang, L.; Pickett, J.; Molkentine, D.; Giri, U.; Milas, L.; Raju, U. 2011: A novel Chk inhibitor, XL-844, increases human cancer cell radiosensitivity through promotion of mitotic catastrophe. Investigational new Drugs 29(3): 514-522
Okada, N.; Yabuta, N.; Suzuki, H.; Aylon, Y.; Oren, M.; Nojima, H. 2011: A novel Chk1/2-Lats2-14-3-3 signaling pathway regulates P-body formation in response to UV damage. Journal of Cell Science 124(Part 1): 57-67
Christerson, L.; Blomqvist, M.; Grannas, K.; Thollesson, M.; Laroucau, K.; Waldenström, J.; Eliasson, I.; Olsen, B.ör.; Herrmann, B.ör. 2010: A novel Chlamydiaceae-like bacterium found in faecal specimens from sea birds from the Bering Sea. Environmental Microbiology Reports 2(4): 605-610
Itabashi, T.; Sugitachi, A.; Kimura, Y.; Ikeda, M.; Kumagai, M.; Matsuo, T.; Fujii, H.; Nishizuka, S.; Otsuka, K.; Koeda, K.; Sasaki, A.; Wakabayashi, G. 2011: A novel Cisplatin delivery system for malignant ascites-bearing mice-a basic experimentation. Gan to Kagaku Ryoho. Cancer and ChemoTherapy 38(12): 2081-2083
Ogawa, S.; Ooki, S.; Morohashi, M.; Yamagata, K.; Higashi, T. 2013: A novel Cookson-type reagent for enhancing sensitivity and specificity in assessment of infant vitamin D status using liquid chromatography/tandem mass spectrometry. Rapid Communications in Mass Spectrometry: Rcm 27(21): 2453-2460
Abhyankar, M.M.; Urekar, C.; Reddi, P.P. 2007: A novel CpG-free vertebrate insulator silences the testis-specific SP-10 gene in somatic tissues: role for TDP-43 in insulator function. Journal of Biological Chemistry 282(50): 36143-36154
Dutia, B.M.; Reid, S.J.; Drummond, D.D.; Ligertwood, Y.; Bennet, I.; Rietberg, W.; Silvia, O.; Jarvis, M.A.; Nash, A.A. 2009: A novel Cre recombinase imaging system for tracking lymphotropic virus infection in vivo. Plos one 4(8): E6492
Naimov, S.; Nedyalkova, R.; Staykov, N.; Weemen-Hendriks, M.; Minkov, I.; de Maagd, R.A. 2014: A novel Cry9Aa with increased toxicity for Spodoptera exigua (Hübner). Journal of Invertebrate Pathology 115: 99-101
Fang, J.; Wan, S.; Qin, J.; Zhang, C.; Quan, W.; Yuan, H.; Dong, H. 2013: A novel Cs-(129)Xe atomic spin gyroscope with closed-loop Faraday modulation. Review of Scientific Instruments 84(8): 083108
Qu, S.; Qin, C.; Islam, A.; Wu, Y.; Zhu, W.; Hua, J.; Tian, H.; Han, L. 2012: A novel D-A-π-A organic sensitizer containing a diketopyrrolopyrrole unit with a branched alkyl chain for highly efficient and stable dye-sensitized solar cells. Chemical Communications 48(55): 6972-6974
De Barros, A.é L.ís.B.; Cardoso, V.N.; Mota, L.d.G.ça.; Leite, E.A.; de Oliveira, M.ôn.C.; Alves, R.J.é 2010: A novel D-glucose derivative radiolabeled with technetium-99m: synthesis, biodistribution studies and scintigraphic images in an experimental model of Ehrlich tumor. Bioorganic and Medicinal Chemistry Letters 20(8): 2478-2480
Roy, A.; Bera, S.; Patra, S.; Ray, S.; Ray, M. 2009: A novel D-glyceraldehyde-3-phosphate binding protein, a truncated albumin, with D-glyceraldehyde-3-phosphate dehydrogenase inhibitory property. Iubmb Life 61(10): 995-1000
Gao, F.; Yang, Z-Kun.; Chen, Q-Hong.; Chen, X-Guang.; Wang, F-Peng. 2012: A novel D-ring modified taxoid: synthesis and biological evaluation of a γ-lactone analogue of docetaxel. Organic and Biomolecular Chemistry 10(2): 361-366
Gallimore, W.A.; Cabral, C.; Kelly, M.; Scheuer, P.J. 2008: A novel D-ring unsaturated A-nor sterol from the Indonesian sponge, Axinella carteri Dendy. Natural Product Research 22(15): 1339-1343
Enayat, S.; Ravanbod, S.; Rassoulzadegan, M.; Jazebi, M.; Tarighat, S.; Ala, F.; Emsley, J.; Othman, M. 2012: A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand disease. Thrombosis and Haemostasis 108(5): 946-954
Ekiz Kanik, F.; Ag, D.; Seleci, M.; Barlas, F.B.; Kesik, M.; Hizalan, G.; Akpinar, H.; Timur, S.; Toppare, L. 2014: A novel DAD type and folic acid conjugated fluorescent monomer as a targeting probe for imaging of folate receptor overexpressed cells. Biotechnology Progress 30(4): 952-959
Poli, A.; Ramazzotti, G.; Matteucci, A.; Manzoli, L.; Lonetti, A.; Suh, P.-G.; McCubrey, J.A.; Cocco, L. 2014: A novel DAG-dependent mechanism links PKCɑ and Cyclin B1 regulating cell cycle progression. Oncotarget 5(22): 11526-11540
Durmaz, E.; Turkkahraman, D.; Berdeli, A.; Atan, M.; Karaguzel, G.; Akcurin, S.; Bircan, I. 2013: A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree. Journal of Pediatric Endocrinology and Metabolism: Jpem 26(5-6): 551-555
Ozer, E.A.; Kaya, A.; Yildirimer, M.; Guler, O.; Can, S.; Aydinlioglu, H. 2009: A novel DAX1 gene mutation in a Turkish infant with X-linked adrenal hypoplasia congenita. European Journal of Pediatrics 168(3): 367-369
Battistin, C.; Menezes Filho, H.C.d.; Domenice, S.; Nishi, M.Y.; Della Manna, T.; Kuperman, H.; Steinmetz, L.; Dichtchekenian, V.ê; Setian, N.; Damiani, D. 2012: A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia e Metabologia 56(8): 496-500
Watanabe, M.; Ishimaru, N.; Ashrin, M.N.; Arakaki, R.; Yamada, A.; Ichikawa, T.; Hayashi, Y. 2011: A novel DC therapy with manipulation of MKK6 gene on nickel allergy in mice. Plos one 6(4): E19017
Djarmati-Westenberger, A.; Brüggemann, N.; Espay, A.J.; Bhatia, K.P.; Klein, C. 2011: A novel DCC mutation and genetic heterogeneity in congenital mirror movements. Neurology 77(16): 1580
Araki, E.; Tsuboi, Y.; Daechsel, J.; Milnerwood, A.; Vilarino-Guell, C.; Fujii, N.; Mishima, T.; Oka, T.; Hara, H.; Fukae, J.; Farrer, M.J. 2014: A novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy. Movement Disorders: Official Journal of the Movement Disorder Society 29(9): 1201-1204
E, X.; Savidis, G.; Chin, C.R.; Wang, S.; Lu, S.; Brass, A.L.; Kowalik, T.F. 2014: A novel DDB2-ATM feedback loop regulates human cytomegalovirus replication. Journal of Virology 88(4): 2279-2290
Murase, Y.; Asai, T.; Katanasaka, Y.; Sugiyama, T.; Shimizu, K.; Maeda, N.; Oku, N. 2010: A novel DDS strategy, "dual-targeting", and its application for antineovascular therapy. Cancer Letters 287(2): 165-171
Fang, D.-A.; Wang, Q.; Wang, J.; He, L.; Liu, L.-H.; Wang, Y. 2011: A novel DDX5 gene in the freshwater crayfish Cherax quadricarinatus is highly expressed during ontogenesis and spermatogenesis. Genetics and Molecular Research: Gmr 10(4): 3963-3975
Prakash, K.; Tuteja, R. 2010: A novel DEAD box helicase Has1p from Plasmodium falciparum: N-terminal is essential for activity. Parasitology International 59(2): 271-277
Zhao, Y.; Wang, D.; Zong, L.; Zhao, F.; Guan, L.; Zhang, P.; Shi, W.; Lan, L.; Wang, H.; Li, Q.; Han, B.; Yang, L.; Jin, X.; Wang, J.; Wang, J.; Wang, Q. 2014: A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family. Plos one 9(5): E97064
Cheng, J.; Han, D.Y.; Dai, P.; Sun, H.J.; Tao, R.; Sun, Q.; Yan, D.; Qin, W.; Wang, H.Y.; Ouyang, X.M.; Yang, S.Z.; Cao, J.Y.; Feng, G.Y.; Du, L.L.; Zhang, Y.Z.; Zhai, S.Q.; Yang, W.Y.; Liu, X.Z.; He, L.; Yuan, H.J. 2007: A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family. Clinical Genetics 72(5): 471-477
Wilch, E.; Azaiez, H.; Fisher, R.A.; Elfenbein, J.; Murgia, A.; Birkenhäger, R.; Bolz, H.; Da Silva-Costa, S.M.; Del Castillo, I.; Haaf, T.; Hoefsloot, L.; Kremer, H.; Kubisch, C.; Le Marechal, C.; Pandya, A.; Sartorato, E.L.; Schneider, E.; Van Camp, G.; Wuyts, W.; Smith, R.J.H.; Friderici, K.H. 2010: A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression. Clinical Genetics 78(3): 267-274
Audo, I.; Bujakowska, K.; Mohand-Saïd, S.; Tronche, S.; Lancelot, M.-E.; Antonio, A.; Germain, A.; Lonjou, C.; Carpentier, W.; Sahel, J.é-A.; Bhattacharya, S.; Zeitz, C. 2011: A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family. Molecular Vision 17: 1598-1606
Ko, J.S.; Choi, B.S.; Seo, J.K.; Shin, J.Y.; Chae, J.H.; Kang, G.H.; Lee, R.; Ki, C.-S.; Kim, J.-W. 2010: A novel DHCR7 mutation in a Smith-Lemli-Opitz syndrome infant presenting with neonatal cholestasis. Journal of Korean Medical Science 25(1): 159-162
Fuccio, A.; Iorio, M.; Amato, F.; Elce, A.; Ingino, R.; Filocamo, M.; Castaldo, G.; Salvatore, F.; Tomaiuolo, R. 2011: A novel DHPLC-based procedure for the analysis of COL1A1 and COL1A2 mutations in osteogenesis imperfecta. Journal of Molecular Diagnostics: Jmd 13(6): 648-656
Rossing, M.; Gerdes, A-Marie.; Juul, A.; Rechnitzer, C.; Rudnicki, M.; Nielsen, F.C.; Vo Hansen, T. 2014: A novel DICER1 mutation identified in a female with ovarian Sertoli-Leydig cell tumor and multinodular goiter: a case report. Journal of Medical Case Reports 8: 112
Lu, X.; Guanga, G.P.; Wan, C.; Rose, R.B. 2012: A novel DNA binding mechanism for maf basic region-leucine zipper factors inferred from a MafA-DNA complex structure and binding specificities. Biochemistry 51(48): 9706-9717
Johnsen, L.; Weigel, C.; von Kries, J.; Møller, M.; Skarstad, K. 2010: A novel DNA gyrase inhibitor rescues Escherichia coli dna Acos mutant cells from lethal hyperinitiation. Journal of Antimicrobial ChemoTherapy 65(5): 924-930
Sharma, S.; Panjamurthy, K.; Choudhary, B.; Srivastava, M.; Shahabuddin, M.; Giri, R.; Advirao, G.M.; Raghavan, S.C. 2013: A novel DNA intercalator, 8-methoxy pyrimido[4',5':4,5]thieno (2,3-b)quinoline-4(3H)-one induces apoptosis in cancer cells, inhibits the tumor progression and enhances lifespan in mice with tumor. Molecular Carcinogenesis 52(6): 413-425
Shahabuddin, M.S.; Nambiar, M.; Choudhary, B.; Advirao, G.M.; Raghavan, S.C. 2010: A novel DNA intercalator, butylamino-pyrimido[4',5':4,5]selenolo(2,3-b)quinoline, induces cell cycle arrest and apoptosis in leukemic cells. Investigational new Drugs 28(1): 35-48
Hushiarian, R.; Yusof, N.Azah.; Abdullah, A.Halim.; Ahmad, S.Ainliah.Alang.; Dutse, S.Wada. 2014: A novel DNA nanosensor based on CdSe/ZnS quantum dots and synthesized Fe3O4 magnetic nanoparticles. Molecules 19(4): 4355-4368
Roseti, L.; Bassi, A.; Fornasari, P.M.; Serra, M.; Canella, F.; Maso, A.; Dallari, D.; Bini, C.; Pelotti, S. 2013: A novel DNA profiling application for the monitoring of cross-contamination in autologous chondrocyte implantation. European Review for Medical and Pharmacological Sciences 17(6): 820-833
Forsythe, E.; Wild, R.; Sellick, G.; Houlston, R.S.; Lehmann, A.R.; Wakeling, E. 2009: A novel DNA repair disorder with thrombocytopenia, nephrosis and features overlapping Cockayne syndrome. American Journal of Medical Genetics. Part a 149a (10): 2075-2079
Wang, A-Bang.; Cheng, C-Wei.; Lin, I-Chun.; Lu, F-Yau.; Tsai, H-Jen.; Lin, C-Chun.; Yang, C-Hui.; Pan, P-Ting.; Kuan, C-Chi.; Chen, Y-Chih.; Lin, Y-Wei.; Chang, C-Ning.; Wu, Y-Hung.; Kurniawan, T.; Lin, C-Wann.; Wo, A.M.; Chen, L-Chi. 2011: A novel DNA selection and direct extraction process and its application in DNA recombination. Electrophoresis 32(3-4): 423-430
Borhani Haghighi, A.; Houlden, H.; Lankarani, K.B.; Taghavi, A.; Masnadi, K.; Ashraf, A.R.; Safari, A. 2006: A novel DNA sequence variation in the first genetically confirmed allgrove syndrome in iran. Journal of Clinical Neuromuscular Disease 7(3): 123-127
Wu, N.; Wu, X.-W.; Agama, K.; Pommier, Y.; Du, J.; Li, D.; Gu, L.-Q.; Huang, Z.-S.; An, L.-K. 2010: A novel DNA topoisomerase i inhibitor with different mechanism from camptothecin induces G2/M phase cell cycle arrest to K562 cells. Biochemistry 49(47): 10131-10136
Qu, P.; Ma, J.-H.; Zhang, X.-M.; Huang, X.-J.; Yang, X.-W.; Yan-Fang, S. 2010: A novel DNA vaccine constructed by heat shock protein 70 and melanoma antigen-encoding gene 3 against tumorigenesis. Indian Journal of Experimental Biology 48(5): 436-443
Gao, H.; Li, K.; Yu, S.; Xiong, S. 2009: A novel DNA vaccine containing multiple TB-specific epitopes cast in a natural structure elicits enhanced Th1 immunity compared with BCG. Microbiology and Immunology 53(10): 541-549
Gao, H.; Yue, Y.; Hu, L.; Xu, W.; Xiong, S. 2009: A novel DNA vaccine containing multiple TB-specific epitopes casted in a natural structure (ECANS) confers protective immunity against pulmonary mycobacterial challenge. Vaccine 27(39): 5313-5319
Dutton, J.L.; Li, B.; Woo, W.-P.; Marshak, J.O.; Xu, Y.; Huang, M.-l.; Dong, L.; Frazer, I.H.; Koelle, D.M. 2013: A novel DNA vaccine technology conveying protection against a lethal herpes simplex viral challenge in mice. Plos one 8(10): E76407
Xu, X.; Pozzo-Miller, L. 2013: A novel DNA-binding feature of MeCP2 contributes to Rett syndrome. Frontiers in Cellular Neuroscience 7: 64
Ender, M.; Berger-Bächi, B.; McCallum, N. 2009: A novel DNA-binding protein modulating methicillin resistance in Staphylococcus aureus. Bmc Microbiology 9: 15
Cai, S.; Cai, L.; Zhao, D.; Liu, G.; Han, J.; Zhou, J.; Xiang, H. 2015: A novel DNA-binding protein, PhaR, plays a central role in the regulation of polyhydroxyalkanoate accumulation and granule formation in the haloarchaeon Haloferax mediterranei. Applied and Environmental Microbiology 81(1): 373-385
Shen, Q.; Tang, S.; Li, W.; Nie, Z.; Liu, Z.; Huang, Y.; Yao, S. 2012: A novel DNA-templated click chemistry strategy for fluorescent detection of copper(II) ions. Chemical Communications 48(2): 281-283
Zhang, K.-q.; Yang, F.; Ye, J.; Jiang, M.; Liu, Y.; Jin, F.-s.; Wu, Y.-z. 2012: A novel DNA/peptide combined vaccine induces PSCA-specific cytotoxic T-lymphocyte responses and suppresses tumor growth in experimental prostate cancer. Urology 79(6): 1410.E7
Lassen, K.S.; Schultz, H.; Heegaard, N.H.H.; He, M. 2012: A novel DNAseq program for enhanced analysis of Illumina GAII data: a case study on antibody complementarity-determining regions. New Biotechnology 29(3): 271-278
Gopalakrishnan, S.; Van Emburgh, B.O.; Shan, J.; Su, Z.; Fields, C.R.; Vieweg, J.; Hamazaki, T.; Schwartz, P.H.; Terada, N.; Robertson, K.D. 2009: A novel DNMT3B splice variant expressed in tumor and pluripotent cells modulates genomic DNA methylation patterns and displays altered DNA binding. Molecular Cancer Research: Mcr 7(10): 1622-1634
Norman, P. 2011: A novel DP2 receptor antagonist (AM-461): a patent evaluation of WO2011085033. Expert Opinion on Therapeutic Patents 21(12): 1931-1936
Lynch, A.M.; Pathak, N.; Pathak, V.; O'Harte, F.P.M.; Flatt, P.R.; Irwin, N.; Gault, V.A. 2014: A novel DPP IV-resistant C-terminally extended glucagon analogue exhibits weight-lowering and diabetes-protective effects in high-fat-fed mice mediated through glucagon and GLP-1 receptor activation. Diabetologia 57(9): 1927-1936
Gao, Z.; Tang, Y.; Chen, J.; Bai, R.; Zhang, Q.; Hou, Y.; Lu, Y.; Bai, G. 2009: A novel DPP-IV-resistant analog of glucagon-like peptide-1 (GLP-1): KGLP-1 alone or in combination with long-acting PLGA microspheres. Peptides 30(10): 1874-1881
Maffie, J.; Blenkinsop, T.; Rudy, B. 2009: A novel DPP6 isoform (DPP6-E) can account for differences between neuronal and reconstituted A-type K(+) channels. Neuroscience Letters 449(3): 189-194
Wang, G.; Ma, M.; Zhang, Z.; Xiang, Y.; Harrington, P.de.B. 2013: A novel DPSO-SVM system for variable interval selection of endometrial tissue sections by near infrared spectroscopy. Talanta 112: 136-142
Marvaldi, L.; Hausott, B.; Auer, M.; Leban, J.; Klimaschewski, L. 2014: A novel DRAK inhibitor, SC82510, promotes axon branching of adult sensory neurons in vitro. Neurochemical Research 39(2): 403-407
Voisey, J.; Swagell, C.D.; Hughes, I.P.; Lawford, B.R.; Young, R.M.; Morris, C.P. 2012: A novel DRD2 single-nucleotide polymorphism associated with schizophrenia predicts age of onset: HapMap tag-single-nucleotide polymorphism analysis. Genetic Testing and Molecular Biomarkers 16(2): 77-81
Bai, H.; Agula, H.; Wu, Q.; Zhou, W.; Sun, Y.; Qi, Y.; Latu, S.; Chen, Y.; Mutu, J.; Qiu, C. 2010: A novel DSPP mutation causes dentinogenesis imperfecta type Ii in a large Mongolian family. Bmc Medical Genetics 11: 23
Buffa, R.; Běťák, J.ří; Kettou, S.; Hermannová, M.; Pospíšilová, L.; Velebný, V.ír. 2011: A novel DTPA cross-linking of hyaluronic acid and metal complexation thereof. Carbohydrate Research 346(13): 1909-1915
Sievänen, H.; Weynand, L.S.; Wacker, W.K.; Simonelli, C.; Burke, P.K.; Ragi, S.; Del Rio, L. 2008: A novel DXA-based hip failure index captures hip fragility independent of BMD. Journal of clinical densitometry: the official journal of the International Society for Clinical Densitometry 11(3): 367-372
Ashford, A.L.; Oxley, D.; Kettle, J.; Hudson, K.; Guichard, S.; Cook, S.J.; Lochhead, P.A. 2014: A novel DYRK1B inhibitor AZ191 demonstrates that DYRK1B acts independently of GSK3β to phosphorylate cyclin D1 at Thr(286), not Thr(288). Biochemical Journal 457(1): 43-56
Smith, S.T.; Sherrington, C.; Studenski, S.; Schoene, D.; Lord, S.R. 2011: A novel Dance Dance Revolution (DDR) system for in-home training of stepping ability: basic parameters of system use by older adults. British Journal of Sports Medicine 45(5): 441-445
Yoshida, N.; Ye, L.; Baba, D.; Katayama, A. 2009: A novel Dehalobacter species is involved in extensive 4,5,6,7-tetrachlorophthalide dechlorination. Applied and Environmental Microbiology 75(8): 2400-2405
Elron-Gross, I.; Glucksam, Y.; Biton, I.E.; Margalit, R. 2009: A novel Diclofenac-carrier for local treatment of osteoarthritis applying live-animal MRi. Journal of Controlled Release: Official Journal of the Controlled Release Society 135(1): 65-70
Zhang, E.-F.; Qiu, G.-F. 2010: A novel Dmrt gene is specifically expressed in the testis of Chinese mitten crab, Eriocheir sinensis. Development Genes and Evolution 220(5-6): 151-159
Fukuda, Y.; Soeki, T.; Sata, M. 2013: A novel Doppler echocardiographic index integrating left and right ventricular function is superior to conventional indices for predicting adverse outcome of acute myocardial infarction. journal of medical investigation: JMI 60(1-2): 97-105
Wu, T.-J.; Shiao, J.S.-C.; Lu, J.-Y. 2011: A novel Doppler spectral index for differentiating benign from malignant lung tumors. Journal of Clinical Ultrasound: Jcu 39(5): 256-262
Ibsen, S.; Zahavy, E.; Wrasdilo, W.; Berns, M.; Chan, M.; Esener, S. 2010: A novel Doxorubicin prodrug with controllable photolysis activation for cancer chemotherapy. Pharmaceutical Research 27(9): 1848-1860
Puseenam, A.; Yoshioka, Y.; Nagai, R.; Hashimoto, R.; Suyari, O.; Itoh, M.; Enomoto, A.; Takahashi, M.; Yamaguchi, M. 2009: A novel Drosophila Girdin-like protein is involved in Akt pathway control of cell size. Experimental Cell Research 315(19): 3370-3380
Celotto, A.M.; Liu, Z.; Vandemark, A.P.; Palladino, M.J. 2012: A novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and disease. Brain and Behavior 2(4): 424-434
Tortoriello, G.; Accardo, M.C.; Scialò, F.; Angrisani, A.; Turano, M.; Furia, M. 2009: A novel Drosophila antisense scaRNA with a predicted guide function. Gene 436(1-2): 56-65
Fang, Y.; Soares, L.; Teng, X.; Geary, M.; Bonini, N.M. 2012: A novel Drosophila model of nerve injury reveals an essential role of Nmnat in maintaining axonal integrity. Current Biology: Cb 22(7): 590-595
Labkovsky, E.; Rosenfeld, J.P. 2014: A novel Dual Probe Complex Trial Protocol for detection of concealed information. Psychophysiology 51(11): 1122-1130
Elstak, E.D.; te Loo, M.; Tesselaar, K.; van Kerkhof, P.; Loeffen, J.; Grivas, D.; Hennekam, E.; Boelens, J.J.; Hoogerbrugge, P.M.; van der Sluijs, P.; van Gijn, M.E.; van de Corput, L. 2012: A novel Dutch mutation in UNC13D reveals an essential role of the C2B domain in munc13-4 function. Pediatric Blood and Cancer 58(4): 598-605
Fiorentino, G.; Ronca, R.; Bartolucci, S. 2009: A novel E. coli biosensor for detecting aromatic aldehydes based on a responsive inducible archaeal promoter fused to the green fluorescent protein. Applied Microbiology and Biotechnology 82(1): 67-77
Liu, C.-C.; Liu, J.-H.; Wu, S.-C.; Yen, C.-C.; Chen, W.-S.; Tsai, Y.-C. 2010: A novel E1B-55kD-deleted oncolytic adenovirus carrying mutant KRAS-regulated hdm2 transgene exerts specific antitumor efficacy on colorectal cancer cells. Molecular Cancer Therapeutics 9(2): 450-460
Su, L.-H.; Pan, Y.-J.; Huang, Y.-C.; Cho, C.-C.; Chen, C.-W.; Huang, S.-W.; Chuang, S.-F.; Sun, C.-H. 2011: A novel E2F-like protein involved in transcriptional activation of cyst wall protein genes in Giardia lamblia. Journal of Biological Chemistry 286(39): 34101-34120
Hazar-Rethinam, M.; de Long, L.M.; Gannon, O.M.; Topkas, E.; Boros, S.; Vargas, A.C.; Dzienis, M.; Mukhopadhyay, P.; Simpson, F.; Endo-Munoz, L.; Saunders, N.A. 2015: A novel E2F/sphingosine kinase 1 axis regulates anthracycline response in squamous cell carcinoma. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 21(2): 417-427
Barboza-Cerda, M.ía.C.; Wong, L.-J.; Martínez-de-Villarreal, L.E.; Zhang, V.W.; Déctor, M.A. 2014: A novel EBP c.224T>A mutation supports the existence of a male-specific disorder independent of CDPX2. American Journal of Medical Genetics. Part a 164a (7): 1642-1647
Zhang, L.; Xin, X.; Liu, B.; Yu, J.; Zhang, Q. 2010: A novel ECDM-OFDM-PON architecture for next-generation optical access network. Optics Express 18(17): 18347-18353
Csernath, G.; Szilagyi, L.; Fordos, G.; Szilagyi, S.M. 2008: A novel ECG telemetry and monitoring system based on Z-Wave communication. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference 2008: 2361-2364
Hetland, M.; Haugaa, K.H.; Sarvari, S.I.; Erikssen, G.; Kongsgaard, E.; Edvardsen, T. 2014: A novel ECG-index for prediction of ventricular arrhythmias in patients after myocardial infarction. Annals of Noninvasive Electrocardiology: the Official Journal of the International Society for Holter and Noninvasive Electrocardiology Inc 19(4): 330-337
Kintarak, J.; Liewluck, T.; Sangruchi, T.; Hirano, M.; Kulkantrakorn, K.; Muengtaweepongsa, S. 2007: A novel ECGF1 mutation in a Thai patient with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). Clinical Neurology and Neurosurgery 109(7): 613-616
Biscotti, M.; Singh, G.; Downey, P.; Bacchetta, M. 2014: A novel ECMO circuit using a SYNERGY circulite pump in a swine model. Asaio Journal 60(5): 519-523
Ranney, M.L.; Rennert-May, E.; Spitzer, R.; Chitai, M.A.; Mamlin, S.E.; Mabeya, H. 2011: A novel ED-based sexual assault centre in western Kenya: description of patients and analysis of treatment patterns. Emergency Medicine Journal: Emj 28(11): 927-931
Cañueto, J.; Zafra-Cobo, M.I.; Ciria, S.; Unamuno, P.; González-Sarmiento, R. 2012: A novel EDA gene mutation in a Spanish family with X-linked hypohidrotic ectodermal dysplasia. Actas Dermo-Sifiliograficas 102(9): 722-725
Lanatà, A.; Valenza, G.; Scilingo, E.P. 2012: A novel EDA glove based on textile-integrated electrodes for affective computing. Medical and Biological Engineering and Computing 50(11): 1163-1172
Ohisa, N.; Ogawa, H.; Murayama, N.; Yoshida, K. 2011: A novel EEG index for evaluating the sleep quality in patients with obstructive sleep apnea-hypopnea syndrome. Tohoku Journal of Experimental Medicine 223(4): 285-289
Shin, Y.K.; Lee, D.R.; Hwang, H.J.; You, S.J.H.; Im, C.H. 2012: A novel EEG-based brain mapping to determine cortical activation patterns in normal children and children with cerebral palsy during motor imagery tasks. Neurorehabilitation 31(4): 349-355
Sato, H.; Washizawa, Y. 2014: A novel EEG-based spelling system using N100 and P300. Studies in Health Technology and Informatics 205: 428-432
Hogue, J.; Shankar, S.; Perry, H.; Patel, R.; Vargervik, K.; Slavotinek, A. 2010: A novel EFNB1 mutation (c.712delG) in a family with craniofrontonasal syndrome and diaphragmatic hernia. American Journal of Medical Genetics. Part a 152a (10): 2574-2577
Gotoh, K.; Kariya, R.; Matsuda, K.; Hattori, S.; Vaeteewoottacharn, K.; Okada, S. 2014: A novel EGFP-expressing nude mice with complete loss of lymphocytes and NK cells to study tumor-host interactions. Bioscience Trends 8(4): 202-205
Zhou, M.; Wang, H.; Zhou, K.; Luo, X.; Pan, X.; Shi, B.; Jiang, H.; Zhang, J.; Li, K.; Wang, H.-M.; Gao, H.; Lu, S.; Yao, M.; Mao, Y.; Wang, H.-Y.; Yang, S.; Gu, J.; Li, C.; Li, Z. 2013: A novel EGFR isoform confers increased invasiveness to cancer cells. Cancer Research 73(23): 7056-7067
Sasaki, H.; Okuda, K.; Takada, M.; Kawahara, M.; Kitahara, N.; Matsumura, A.; Iuchi, K.; Kawaguchi, T.; Kubo, A.; Endo, K.; Kawano, O.; Yukiue, H.; Yano, M.; Fujii, Y. 2008: A novel EGFR mutation D1012H and polymorphism at exon 25 in Japanese lung cancer. Journal of Cancer Research and Clinical Oncology 134(12): 1371-1376
Brandão, E.P.; Pantarotto, M.G.; Cruz, M. 2012: A novel EGFR mutation in exon 18 with high sensitivity to EGFR TKi treatment with reduced dose. Journal of Thoracic Oncology: Official Publication of the International Association for the Study of Lung Cancer 7(11): E32
Van der Wekken, A.J.; Stigt, J.A.; A't Hart, N. 2012: A novel EGFR mutation in exon 19 showed stable disease after TKi treatment. Journal of Thoracic Oncology: Official Publication of the International Association for the Study of Lung Cancer 7(8): E8
González Manzano, R.; Martínez Navarro, E.; Eugenieva, E.; Fernández Morejón, F.J.; Farré, J.; Brugarolas, A. 2008: A novel EGFR nonsense mutation in a non-small-cell lung cancer (NSCLC) patient who did not derive any clinical benefit with combination chemotherapy and erlotinib. Clinical and Translational Oncology: Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 10(7): 442-444
Yin, Z.; Liu, N.; Ma, M.; Wang, L.; Hao, Y.; Zhang, X. 2012: A novel EGFR-targeted gene delivery system based on complexes self-assembled by EGF, DNA, and activated PAMAM dendrimers. International Journal of Nanomedicine 7: 4625-4635
Sang, Y.; Liu, M.; Yang, W.; Yan, J.; Chengzhu; Ni, G. 2011: A novel EIF2AK3 mutation leading to Wolcott-Rallison syndrome in a Chinese child. Journal of Pediatric Endocrinology and Metabolism: Jpem 24(3-4): 181-184
Allred, C.C.; Krennmayr, T.; Koutsari, C.; Zhou, L.; Ali, A.H.; Jensen, M.D. 2011: A novel ELISA for measuring CD36 protein in human adipose tissue. Journal of Lipid Research 52(2): 408-415
Messingham, K.A.N.; Noe, M.H.; Chapman, M.A.; Giudice, G.J.; Fairley, J.A. 2009: A novel ELISA reveals high frequencies of BP180-specific IgE production in bullous pemphigoid. Journal of Immunological Methods 346(1-2): 18-25
Nojima, J.; Motoki, Y.; Aoki, N.; Tsuneoka, H.; Ichihara, K. 2014: A novel ELISA system for simultaneous detection of six subclasses of anti-phospholipid antibodies for prediction of thrombotic complications among SLE patients. Thrombosis Research 133(6): 1135-1140
Dogruman-Al, F.; Turk, S.; Adiyaman-Korkmaz, G.; Hananel, A.; Levi, L.; Kopelowitz, J.; Babai, O.; Gross, S.; Greenberg, Z.; Herschkovitz, Y.; Mumcuoglu, I. 2015: A novel ELISA test for laboratory diagnosis of Blastocystis spp. in human stool specimens. Parasitology Research 114(2): 495-500
Sel, S.; Schlaf, G.; Schurat, O.; Altermann, W.W. 2012: A novel ELISA-based crossmatch procedure to detect donor-specific anti-HLA antibodies responsible for corneal allograft rejections. Journal of Immunological Methods 381(1-2): 23-31
Zhao, X.; Town, J.R.; Yang, A.; Zhang, X.; Paur, N.; Sawicki, G.; Gordon, J.R. 2010: A novel ELR-CXC chemokine antagonist reduces intestinal ischemia reperfusion-induced mortality, and local and remote organ injury. Journal of Surgical Research 162(2): 264-273
Penzel, R.; Schirmacher, P.; Warth, A. 2012: A novel EML4-ALK variant: exon 6 of EML4 fused to exon 19 of ALK. Journal of Thoracic Oncology: Official Publication of the International Association for the Study of Lung Cancer 7(7): 1198-1199
Suzuki, A.; Nakashima, D.; Miyawaki, Y.; Fujita, J.; Maki, A.; Fujimori, Y.; Takagi, A.; Murate, T.; Teranishi, M.; Matsushita, T.; Saito, H.; Kojima, T. 2012: A novel ENG mutation causing impaired co-translational processing of endoglin associated with hereditary hemorrhagic telangiectasia. Thrombosis Research 129(5): E200-E208
Hughes, M.R.; Anderson, N.; Maltby, S.; Wong, J.; Berberovic, Z.; Birkenmeier, C.S.; Haddon, D.J.; Garcha, K.; Flenniken, A.; Osborne, L.R.; Adamson, S.L.; Rossant, J.; Peters, L.L.; Minden, M.D.; Paulson, R.F.; Wang, C.; Barber, D.L.; McNagny, K.M.; Stanford, W.L. 2011: A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis. Experimental Hematology 39(3): 305
Lee, B.; Bokryeon, L.; Kano, K.; Young, J.; John, S.W.M.; Nishina, P.M.; Naggert, J.K.; Naito, K. 2009: A novel ENU-induced mutation, peewee, causes dwarfism in the mouse. Mammalian Genome: Official Journal of the International Mammalian Genome Society 20(7): 404-413
Greth, A.; Lampkin, S.; Mayura-Guru, P.; Rodda, F.; Drysdale, K.; Roberts-Thomson, M.; McMorran, B.J.; Foote, S.J.; Burgio, G.ét. 2012: A novel ENU-mutation in ankyrin-1 disrupts malaria parasite maturation in red blood cells of mice. Plos one 7(6): E38999
Ma, J.; Zhang, Y.; Cichocki, A.; Matsuno, F. 2015: A novel EOG/EEG hybrid human-machine interface adopting eye movements and ERPs: application to robot control. IEEE Transactions on Bio-Medical Engineering 62(3): 876-889
Fu, X.; Deng, J.; Yang, H.; Masuda, T.; Goto, F.; Yoshihara, T.; Zhao, G. 2010: A novel EP-involved pathway for iron release from soya bean seed ferritin. Biochemical Journal 427(2): 313-321
Scully, M.S.; Ort, T.A.; James, I.E.; Bugelski, P.J.; Makropoulos, D.A.; Deutsch, H.A.; Pieterman, E.J.; van den Hoek, A.M.; Havekes, L.M.; Dubell, W.H.; Wertheimer, J.D.; Picha, K.M. 2011: A novel EPO receptor agonist improves glucose tolerance via glucose uptake in skeletal muscle in a mouse model of diabetes. Experimental Diabetes Research 2011: 910159
Yamamoto, Y.-h.; Kimura, T.; Momohara, S.; Takeuchi, M.; Tani, T.; Kimata, Y.; Kadokura, H.; Kohno, K. 2010: A novel ER J-protein DNAJB12 accelerates ER-associated degradation of membrane proteins including CFTR. Cell Structure and Function 35(2): 107-116
Urra, H.; Hetz, C. 2014: A novel ER stress-independent function of the UPR in angiogenesis. Molecular Cell 54(4): 542-544
Li, Y.; Zhao, Y.; Hu, J.; Xiao, J.; Qu, L.; Wang, Z.; Ma, D.; Chen, Y. 2013: A novel ER-localized transmembrane protein, EMC6, interacts with RAB5A and regulates cell autophagy. Autophagy 9(2): 150-163
Swartz, J.M.; Akinci, A.; Andrew, S.F.; Siğirci, A.; Hirschhorn, J.N.; Rosenfeld, R.G.; Dauber, A.; Hwa, V. 2014: A novel ERCC6 splicing variant associated with a mild Cockayne syndrome phenotype. Hormone Research in Paediatrics 82(5): 344-352
Huang, X.; Huang, J.; Zhang, L.; Zhu, Y.; Li, Y. 2014: A novel ERα-mediated reporter gene assay for screening estrogenic/antiestrogenic chemicals based on LLC-MK2 cells. Toxicology Mechanisms and Methods 24(9): 627-632
Jiang, X.; Pan, H.; Nabhan, J.F.; Krishnan, R.; Koziol-White, C.; Panettieri, R.A.; Lu, Q. 2012: A novel EST-derived RNAi screen reveals a critical role for farnesyl diphosphate synthase in β2-adrenergic receptor internalization and down-regulation. Faseb Journal: Official Publication of the Federation of American Societies for Experimental Biology 26(5): 1995-2007
Kennedy, G.M.; Hooley, G.C.; Champion, M.M.; Mba Medie, F.; Champion, P.A.D. 2014: A novel ESX-1 locus reveals that surface-associated ESX-1 substrates mediate virulence in Mycobacterium marinum. Journal of Bacteriology 196(10): 1877-1888
Debelenko, L.V.; McGregor, L.M.; Shivakumar, B.R.; Dorfman, H.D.; Raimondi, S.C. 2011: A novel EWSR1-CREB3L1 fusion transcript in a case of small cell osteosarcoma. Genes Chromosomes and Cancer 50(12): 1054-1062
Li, Y.; Wang, J.; Li, H.; Wang, J.; Wang, X.; Fu, Q. 2010: A novel EXT1 gene mutation causing hereditary multiple exostoses in a Chinese pedigree. Pathology 42(1): 91-93
Paal, M.; Heel, T.; Schneider, R.; Auer, B. 2009: A novel Ecotin-Ubiquitin-Tag (ECUT) for efficient, soluble peptide production in the periplasm of Escherichia coli. Microbial Cell Factories 8: 7
Aguiar, D.M.; Ziliani, T.F.; Zhang, X.; Melo, A.L.T.; Braga, I.A.; Witter, R.; Freitas, L.C.; Rondelli, A.é L.H.; Luis, M.A.; Sorte, E.C.B.; Jaune, F.W.; Santarém, V.A.; Horta, M.C.; Pescador, C.A.; Colodel, E.M.; Soares, H.S.; Pacheco, R.C.; Onuma, S.S.M.; Labruna, M.B.; McBride, J.W. 2014: A novel Ehrlichia genotype strain distinguished by the TRP36 gene naturally infects cattle in Brazil and causes clinical manifestations associated with ehrlichiosis. Ticks and Tick-Borne Diseases 5(5): 537-544
He, C.; Nora, G.P.; Schneider, E.L.; Kerr, I.D.; Hansell, E.; Hirata, K.; Gonzalez, D.; Sajid, M.; Boyd, S.E.; Hruz, P.; Cobo, E.R.; Le, C.; Liu, W.-T.; Eckmann, L.; Dorrestein, P.C.; Houpt, E.R.; Brinen, L.S.; Craik, C.S.; Roush, W.R.; McKerrow, J.; Reed, S.L. 2010: A novel Entamoeba histolytica cysteine proteinase, EhCP4, is key for invasive amebiasis and a therapeutic target. Journal of Biological Chemistry 285(24): 18516-18527
Löser, B.; Nalaskowski, M.M.; Fanick, W.; Lin, H.; Tannich, E.; Mayr, G.W. 2012: A novel Entamoeba histolytica inositol phosphate kinase catalyzes the formation of 5PP-Ins(1,2,3,4,6)P(5). Molecular and Biochemical Parasitology 181(1): 49-52
Hong, K.; Lou, L.; Gupta, S.; Ribeiro-Neto, F.; Altschuler, D.L. 2008: A novel Epac-Rap-PP2A signaling module controls cAMP-dependent Akt regulation. Journal of Biological Chemistry 283(34): 23129-23138
Troise, F.; Monti, M.; Merlino, A.; Cozzolino, F.; Fedele, C.; Russo Krauss, I.; Sica, F.; Pucci, P.; D'Alessio, G.; De Lorenzo, C. 2011: A novel ErbB2 epitope targeted by human antitumor immunoagents. Febs Journal 278(7): 1156-1166
Desmolaize, B.; Rose, S.; Warrass, R.; Douthwaite, S. 2011: A novel Erm monomethyltransferase in antibiotic-resistant isolates of Mannheimia haemolytica and Pasteurella multocida. Molecular Microbiology 80(1): 184-194
Xiong, Y.; Wang, P.; Lan, R.; Ye, C.; Wang, H.; Ren, J.; Jing, H.; Wang, Y.; Zhou, Z.; Bai, X.; Cui, Z.; Luo, X.; Zhao, A.; Wang, Y.; Zhang, S.; Sun, H.; Wang, L.; Xu, J. 2012: A novel Escherichia coli O157:H7 clone causing a major hemolytic uremic syndrome outbreak in China. Plos one 7(4): E36144
Song, J.-A.; Lee, D.-S.; Park, J.-S.; Han, K.-Y.; Lee, J. 2011: A novel Escherichia coli solubility enhancer protein for fusion expression of aggregation-prone heterologous proteins. Enzyme and Microbial Technology 49(2): 124-130
Ward, T.L.; Prtenjaca, A.; Hill, K.A. 2010: A novel Escherichia coli-derived mutation detected with the Big Blue cIi mutant selectable assay. Environmental and Molecular Mutagenesis 51(4): 344-348
Chen, R.; Guo, W.; Yin, Y.; Gong, Z.-H. 2014: A novel F-box protein CaF-box is involved in responses to plant hormones and abiotic stress in pepper (Capsicum annuum L.). International Journal of Molecular Sciences 15(2): 2413-2430
Bader, M.; Arama, E.; Steller, H. 2010: A novel F-box protein is required for caspase activation during cellular remodeling in Drosophila. Development 137(10): 1679-1688
Kim, Y.Y.; Jung, K.W.; Jeung, J.U.; Shin, J.S. 2012: A novel F-box protein represses endothecial secondary wall thickening for anther dehiscence in Arabidopsis thaliana. Journal of Plant Physiology 169(2): 212-216
Kim, J.; Kim, Y.; Shin, S.; Lyu, C.J.; Choi, J.R.; Lee, K.-A. 2013: A novel F11 mutation in a Korean pediatric patient with recurrent epistaxis. Blood Coagulation and Fibrinolysis: An International Journal in Haemostasis and Thrombosis 24(4): 433-435
Nielsen, L.N.; Wiinberg, B.; Häger, M.; Holmberg, H.L.; Hansen, J.J.; Roepstorff, K.; Tranholm, M. 2014: A novel F8 -/- rat as a translational model of human hemophilia A. Journal of Thrombosis and Haemostasis: Jth 12(8): 1274-1282
Yang, G.; Chu, M.; Zhai, X.; Zhao, J. 2012: A novel FBN1 mutation in a Chinese family with isolated ectopia lentis. Molecular Vision 18: 945-950
Rasmussen, M.; Pedersen, S.Fjord.; Sunde, L.; Andersen, N.Holmmark.; Ostergaard, J.R.; Lildballe, D.L. 2014: A novel FBN1 variant in a large Marfan family with high penetrance of aortic dissection or rupture. Danish Medical Journal 61(11): A4949
Peng, D.; Yu, F. 2009: A novel FEA simulation model for RFID SAW tag. IEEE Transactions on Ultrasonics Ferroelectrics and Frequency Control 56(8): 1753-1760
Piazza, S.; Torricelli, D.; Brunetti, F.; del-Ama, A.J.; Gil-Agudo, A.; Pons, J.L. 2012: A novel FES control paradigm based on muscle synergies for postural rehabilitation therapy with hybrid exoskeletons. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference 2012: 1868-1871
Fan, L.; Xie, H.; Chen, L.; Ye, H.; Ying, S.; Wang, C.; Wu, X.; Li, W.; Wu, J.; Liang, G.; Li, X. 2014: A novel FGF2 antagonist peptide P8 with potent antiproliferation activity. Tumour Biology: the Journal of the International Society for Oncodevelopmental Biology and Medicine 35(10): 10571-10579
Jin, M.; Yu, Y.; Qi, H.; Xie, Y.; Su, N.; Wang, X.; Tan, Q.; Luo, F.; Zhu, Y.; Wang, Q.; Du, X.; Xian, C.J.; Liu, P.; Huang, H.; Shen, Y.; Deng, C.-X.; Chen, D.; Chen, L. 2012: A novel FGFR3-binding peptide inhibits FGFR3 signaling and reverses the lethal phenotype of mice mimicking human thanatophoric dysplasia. Human Molecular Genetics 21(26): 5443-5455
Salemi, S.; Yousefi, S.; Simon, D.; Schmid, I.; Moretti, L.; Scapozza, L.; Simon, H.-U. 2009: A novel FIP1L1-PDGFRA mutant destabilizing the inactive conformation of the kinase domain in chronic eosinophilic leukemia/hypereosinophilic syndrome. Allergy 64(6): 913-918
Norville, I.H.; Breitbach, K.; Eske-Pogodda, K.; Harmer, N.J.; Sarkar-Tyson, M.; Titball, R.W.; Steinmetz, I. 2011: A novel FK-506-binding-like protein that lacks peptidyl-prolyl isomerase activity is involved in intracellular infection and in vivo virulence of Burkholderia pseudomallei. Microbiology 157(Part 9): 2629-2638
McKeen, H.D.; McAlpine, K.; Valentine, A.; Quinn, D.J.; McClelland, K.; Byrne, C.; O'Rourke, M.; Young, S.; Scott, C.J.; McCarthy, H.O.; Hirst, D.G.; Robson, T. 2008: A novel FK506-like binding protein interacts with the glucocorticoid receptor and regulates steroid receptor signaling. Endocrinology 149(11): 5724-5734
Kiyoi, H.; Shiotsu, Y.; Ozeki, K.; Yamaji, S.; Kosugi, H.; Umehara, H.; Shimizu, M.; Arai, H.; Ishii, K.; Akinaga, S.; Naoe, T. 2007: A novel FLT3 inhibitor FI-700 selectively suppresses the growth of leukemia cells with FLT3 mutations. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 13(15 Part 1): 4575-4582
DiGiovanni, R.M.; Erickson, R.P.; Ohlson, E.C.; Bernas, M.; Witte, M.H. 2014: A novel FLT4 mutation identified in a patient with Milroy disease. Lymphology 47(1): 44-47
Filipovic-Sadic, S.; Sah, S.; Chen, L.; Krosting, J.; Sekinger, E.; Zhang, W.; Hagerman, P.J.; Stenzel, T.T.; Hadd, A.G.; Latham, G.J.; Tassone, F. 2010: A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome. Clinical Chemistry 56(3): 399-408
Carré, A.; Hamza, R.T.; Kariyawasam, D.; Guillot, L.ïc.; Teissier, R.ël.; Tron, E.; Castanet, M.; Dupuy, C.; El Kholy, M.; Polak, M. 2014: A novel FOXE1 mutation (R73S) in Bamforth-Lazarus syndrome causing increased thyroidal gene expression. Thyroid: Official Journal of the American Thyroid Association 24(4): 649-654
Wang, L.; Wang, Y.; Ragauskas, A.J. 2010: A novel FRET approach for in situ investigation of cellulase-cellulose interaction. Analytical and Bioanalytical Chemistry 398(3): 1257-1262
Schneider, U.V.; Severinsen, J.K.; Géci, I.; Okkels, L.M.; Jøhnk, N.; Mikkelsen, N.D.; Klinge, T.; Pedersen, E.B.; Westh, H.; Lisby, G. 2010: A novel FRET pair for detection of parallel DNA triplexes by the LightCycler. Bmc Biotechnology 10: 4
Bhargava, A.; Punde, R.; Varshney, S.; Pathak, N.; Mishra, P.K. 2011: A novel FRET probe-based approach for identification, quantification, and characterization of occult HCV infections in patients with cryptogenic liver cirrhosis. Indian Journal of Pathology and Microbiology 54(2): 420-421
Mizutani, T.; Kondo, T.; Darmanin, S.; Tsuda, M.; Tanaka, S.; Tobiume, M.; Asaka, M.; Ohba, Y. 2010: A novel FRET-based biosensor for the measurement of BCR-ABL activity and its response to drugs in living cells. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 16(15): 3964-3975
Batey, S.; Vuillaume, I.; Devos, D.; Destée, A.; Curtis, A.J.; Lombes, A.; Curtis, A.; Burn, J.; Chinnery, P.F. 2010: A novel FTL insertion causing neuroferritinopathy. Journal of Medical Genetics 47(1): 71-72
Moutton, S.éb.; Fergelot, P.; Trocello, J.-M.; Plante-Bordeneuve, V.; Houcinat, N.; Wenisch, E.; Larue, V.; Brugières, P.; Clot, F.; Lacombe, D.; Arveiler, B.; Goizet, C. 2014: A novel FTL mutation responsible for neuroferritinopathy with asymmetric clinical features and brain anomalies. Parkinsonism and Related Disorders 20(8): 935-937
Lopez, G.H.; Condon, J.A.; Wilson, B.; Martin, J.R.; Liew, Y.-W.; Flower, R.L.; Hyland, C.A. 2015: A novel FY*A allele with the 265T and 298A SNPs formerly associated exclusively with the FY*B allele and weak Fy(b) antigen expression: implication for genotyping interpretative algorithms. Vox Sanguinis 108(1): 52-57
De Zoysa, M.; Nikapitiya, C.; Moon, D.-O.; Whang, I.; Kim, G.-Y.; Lee, J. 2009: A novel Fas ligand in mollusk abalone: molecular characterization, immune responses and biological activity of the recombinant protein. Fish and Shellfish Immunology 27(3): 423-432
Flinsenberg, T.W.H.; Janssen, W.J.; Herczenik, E.; Boross, P.; Nederend, M.; Jongeneel, L.H.; Scholman, R.C.; Boelens, J.-J.; Maas, C.; van Gijn, M.E.; van Montfrans, J.M.; Leusen, J.H.; Boes, M. 2014: A novel FcγRIIa Q27W gene variant is associated with common variable immune deficiency through defective FcγRIIa downstream signaling. Clinical Immunology 155(1): 108-117
Cruse, G.; Kaur, D.; Leyland, M.; Bradding, P. 2010: A novel FcεRIβ-chain truncation regulates human mast cell proliferation and survival. Faseb Journal: Official Publication of the Federation of American Societies for Experimental Biology 24(10): 4047-4057
Hibi, M.; Kawashima, T.; Kasahara, T.; Sokolov, P.M.; Smirnov, S.V.; Kodera, T.; Sugiyama, M.; Shimizu, S.; Yokozeki, K.; Ogawa, J. 2012: A novel Fe(II)/α-ketoglutarate-dependent dioxygenase from Burkholderia ambifaria has β-hydroxylating activity of N-succinyl l-leucine. Letters in Applied Microbiology 55(6): 414-419
Vervoort, V.S.; Lu, M.; Valencia, F.; Lesperance, J.; Breier, G.; Oshima, R.; Pasquale, E.B. 2008: A novel Flk1-TVA transgenic mouse model for gene delivery to angiogenic vasculature. Transgenic Research 17(3): 403-415
Kaiser, N.K.; Skulason, G.E.; Weisbrod, C.R.; Bruce, J.E. 2009: A novel Fourier transform ion cyclotron resonance mass spectrometer with improved ion trapping and detection capabilities. Journal of the American Society for Mass Spectrometry 20(5): 755-762
Houlden, H.; Hammans, S.; Katifi, H.; Reilly, M.M. 2009: A novel Frabin (FGD4) nonsense mutation p.R275X associated with phenotypic variability in CMT4H. Neurology 72(7): 617-620
Kunhimangalam, R.; Ovallath, S.; Joseph, P.K. 2013: A novel Fuzzy Expert System for the identification of severity of carpal tunnel syndrome. Biomed Research International 2013: 846780
El-Shehabi, F.; Taman, A.; Moali, L.S.; El-Sakkary, N.; Ribeiro, P. 2012: A novel G protein-coupled receptor of Schistosoma mansoni (SmGPR-3) is activated by dopamine and is widely expressed in the nervous system. Plos Neglected Tropical Diseases 6(2): E1523
Basundra, R.; Kumar, A.; Amrane, S.; Verma, A.; Phan, A.T.ân.; Chowdhury, S. 2010: A novel G-quadruplex motif modulates promoter activity of human thymidine kinase 1. Febs Journal 277(20): 4254-4264
Joaquin, M.; Gubern, A.; Posas, F. 2012: A novel G1 checkpoint mediated by the p57 CDK inhibitor and p38 SAPK promotes cell survival upon stress. Cell Cycle 11(18): 3339-3340
Alzahrani, A.S.; Zou, M.; Baitei, E.Y.; Alshaikh, O.M.; Al-Rijjal, R.A.; Meyer, B.F.; Shi, Y. 2010: A novel G102E mutation of CYP27B1 in a large family with vitamin D-dependent rickets type 1. Journal of Clinical Endocrinology and Metabolism 95(9): 4176-4183
Susa, S.; Daimon, M.; Kato, T.; Maeda, N. 2013: A novel G168X mutation and a recurrent 730-731delCT mutation of the porphobilinogen deaminase gene in Japanese patients with acute intermittent porphyria. Blood Cells Molecules and Diseases 51(2): 130-131
Zifa, E.; Theotokis, P.; Kaminari, A.; Maridaki, H.; Leze, H.; Petsiava, E.; Mamuris, Z.; Stathopoulos, C. 2008: A novel G3337A mitochondrial ND1 mutation related to cardiomyopathy co-segregates with tRNALeu(CUN) A12308G and tRNAThr C15946T mutations. Mitochondrion 8(3): 229-236
Chen, X.; Yue, L.; Li, C.; Li, C. 2010: A novel G473A mutation in the glucose-6-phosphate dehydrogenase gene. Pediatric Blood and Cancer 55(2): 383-385
Aytekin, C.; Germeshausen, M.; Tuygun, N.; Dogu, F.; Ikinciogullari, A. 2013: A novel G6PC3 gene mutation in a patient with severe congenital neutropenia. Journal of Pediatric Hematology/Oncology 35(2): E81-E83
Arikoglu, T.; Kuyucu, N.; Germeshausen, M.; Kuyucu, S. 2015: A novel G6PC3 gene mutation in severe congenital neutropenia: pancytopenia and variable bone marrow phenotype can also be part of this syndrome. European Journal of Haematology 94(1): 79-82
Aróstegui, J.I.; de Toledo, J.é S.án.; Pascal, M.; García, C.; Yagüe, J.; Díaz de Heredia, C. 2009: A novel G6PC3 homozygous 1-bp deletion as a cause of severe congenital neutropenia. Blood 114(8): 1718-1719
McDade, J.; Abramova, T.; Mortier, N.; Howard, T.; Ware, R.E. 2008: A novel G6PD mutation leading to chronic hemolytic anemia. Pediatric Blood and Cancer 51(6): 816-819
Sieghart, W.; Ramerstorfer, J.; Sarto-Jackson, I.; Varagic, Z.; Ernst, M. 2012: A novel GABA(A) receptor pharmacology: drugs interacting with the α(+) β(-) interface. British Journal of Pharmacology 166(2): 476-485
Liang, C.-L.; Marks, G.A. 2009: A novel GABAergic afferent input to the pontine reticular formation: the mesopontine GABAergic column. Brain Research 1297: 32-40
Johnston, A.J.; Kang, J.-Q.; Shen, W.; Pickrell, W.O.; Cushion, T.D.; Davies, J.S.; Baer, K.; Mullins, J.G.L.; Hammond, C.L.; Chung, S.-K.; Thomas, R.H.; White, C.; Smith, P.E.M.; Macdonald, R.L.; Rees, M.I. 2014: A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes. Neurobiology of Disease 64: 131-141
Feng, Z.; Li, W.; Xue, X.; Geng, X.; Wu, Y.; Huang, J.; Wu, Z. 2011: A novel GAP460 biopolymer for use as a carrier in drug-delivery applications. Journal of Biomaterials Science. Polymer Edition 22(15): 2023-2040
Singleton, B.K.; Roxby, D.J.; Stirling, J.W.; Spring, F.A.; Wilson, C.; Poole, J.; Anstee, D.J. 2013: A novel GATA1 mutation (Stop414Arg) in a family with the rare X-linked blood group Lu(a-b-) phenotype and mild macrothrombocytic thrombocytopenia. British Journal of Haematology 161(1): 139-142
Nanba, K.; Usui, T.; Nakamura, M.; Toyota, Y.; Hirota, K.; Tamanaha, T.; Kawashima, S.-T.; Nakao, K.; Yuno, A.; Tagami, T.; Naruse, M.; Shimatsu, A. 2013: A novel GATA3 nonsense mutation in a newly diagnosed adult patient of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome. Endocrine Practice: Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 19(1): E17-E20
Zhao, L.; Xu, J.-H.; Xu, W.-J.; Yu, H.; Wang, Q.; Zheng, H.-Z.; Jiang, W.-F.; Jiang, J.-F.; Yang, Y.-Q. 2014: A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy. International Journal of Molecular Medicine 33(3): 654-660
Yang, Y.-q.; Tang, Y.-q.; Liu, X.-y.; Lin, X.-p.; Chen, Y.-h. 2010: A novel GATA4 mutation leading to congenital ventricular septal defect. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 27(5): 512-516
Wang, J.; Fang, M.; Liu, X.-Y.; Xin, Y.-F.; Liu, Z.-M.; Chen, X.-Z.; Wang, X.-Z.; Fang, W.-Y.; Liu, X.; Yang, Y.-Q. 2011: A novel GATA4 mutation responsible for congenital ventricular septal defects. International Journal of Molecular Medicine 28(4): 557-564
Wang, X.-H.; Huang, C.-X.; Wang, Q.; Li, R.-G.; Xu, Y.-J.; Liu, X.; Fang, W.-Y.; Yang, Y.-Q. 2013: A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation. International Journal of Molecular Medicine 31(1): 43-50
Zheng, G.-F.; Wei, D.; Zhao, H.; Zhou, N.; Yang, Y.-Q.; Liu, X.-Y. 2012: A novel GATA6 mutation associated with congenital ventricular septal defect. International Journal of Molecular Medicine 29(6): 1065-1071
Eifes, S.; Chudasama, K.K.; Molnes, J.; Wagner, K.; Hoang, T.; Schierloh, U.; Rocour-Brumioul, D.; Johansson, S.; Njølstad, P.ål.R.; de Beaufort, C. 2013: A novel GATA6 mutation in a child with congenital heart malformation and neonatal diabetes. Clinical Case Reports 1(2): 86-90
Catli, G.; Abaci, A.; Flanagan, S.E.; De Franco, E.; Ellard, S.; Hattersley, A.; Guleryuz, H.; Bober, E. 2013: A novel GATA6 mutation leading to congenital heart defects and permanent neonatal diabetes: a case report. Diabetes and Metabolism 39(4): 370-374
Votsi, C.; Zamba-Papanicolaou, E.; Middleton, L.T.; Pantzaris, M.; Christodoulou, K. 2014: A novel GBA2 gene missense mutation in spastic ataxia. Annals of Human Genetics 78(1): 13-22
Wu, L.; Shen, X.-M.; Liu, D.Q. 2008: A novel GC-MS method for rapid determination of headspace oxygen in vials of pharmaceutical formulations. Journal of Pharmaceutical and Biomedical Analysis 48(1): 8-12
Jiang, L.; Wheaton, D.; Bereta, G.; Zhang, K.; Palczewski, K.; Birch, D.G.; Baehr, W. 2008: A novel GCAP1(N104K) mutation in EF-hand 3 (EF3) linked to autosomal dominant cone dystrophy. Vision Research 48(23-24): 2425-2432
Chung, K.W.; Kim, S.M.; Sunwoo, I.N.; Cho, S.Y.; Hwang, S.J.; Kim, J.; Kang, S.H.; Park, K.-D.; Choi, K.-G.; Choi, I.S.; Choi, B.-O. 2008: A novel GDAP1 Q218E mutation in autosomal dominant Charcot-Marie-Tooth disease. Journal of Human Genetics 53(4): 360-364
Adler, L.N.; Gomez, T.A.; Clarke, S.G.; Linster, C.L. 2011: A novel GDP-D-glucose phosphorylase involved in quality control of the nucleoside diphosphate sugar pool in Caenorhabditis elegans and mammals. Journal of Biological Chemistry 286(24): 21511-21523
Zhang, J.; Gratchev, A.; Riabov, V.; Mamidi, S.; Schmuttermaier, C.; Krusell, L.; Kremmer, E.; Workman, G.; Sage, E.H.; Jalkanen, S.; Goerdt, S.; Kzhyshkowska, J. 2009: A novel GGA-binding site is required for intracellular sorting mediated by stabilin-1. Molecular and Cellular Biology 29(22): 6097-6105
Petkovic, V.; Eblé, A.ée.; Pandey, A.V.; Betta, M.; Mella, P.; Flück, C.E.; Buzi, F.; Mullis, P.E. 2011: A novel GH-1 gene mutation (GH-P59L) causes partial GH deficiency type Ii combined with bioinactive GH syndrome. Growth Hormone and Igf Research: Official Journal of the Growth Hormone Research Society and the International Igf Research Society 21(3): 160-166
Gucev, Z.; Tasic, V.; Saranac, L.; Stobbe, H.; Kratzsch, J.ür.; Klammt, J.ür.; Pfäffle, R. 2012: A novel GH1 mutation in a family with isolated growth hormone deficiency type Ii. Hormone Research in Paediatrics 77(3): 200-204
Shinozaki, A.; Kawakami, T.; Hosokawa, S.; Sakamoto, T. 2014: A novel GH43 α-l-arabinofuranosidase of Penicillium chrysogenum that preferentially degrades single-substituted arabinosyl side chains in arabinan. Enzyme and Microbial Technology 58-59: 80-86
Feigerlova, E.; Swinyard, M.; Derr, M.A.; Farnsworth, J.; Andrew, S.F.; Rosenfeld, R.G.; Hwa, V. 2013: A novel GHR intronic variant, c.266+83G>T , activates a cryptic 5' splice site causing severe GHR deficiency and classical GH insensitivity syndrome. Hormone Research in Paediatrics 80(6): 397-405
Harada, N.; Yamada, Y.; Tsukiyama, K.; Yamada, C.; Nakamura, Y.; Mukai, E.; Hamasaki, A.; Liu, X.; Toyoda, K.; Seino, Y.; Inagaki, N. 2008: A novel GIP receptor splice variant influences GIP sensitivity of pancreatic beta-cells in obese mice. American Journal of Physiology. Endocrinology and Metabolism 294(1): E61-E68
Jamsheer, A.; Wisniewska, M.; Szpak, A.; Bugaj, G.; Krawczynski, M.R.; Budny, B.; Wawrocka, A.; Latos-Bieleńska, A. 2009: A novel GJA1 missense mutation in a Polish child with oculodentodigital dysplasia. Journal of Applied Genetics 50(3): 297-299
Furuta, N.; Ikeda, M.; Hirayanagi, K.; Fujita, Y.; Amanuma, M.; Okamoto, K. 2012: A novel GJA1 mutation in oculodentodigital dysplasia with progressive spastic paraplegia and sensory deficits. Internal Medicine 51(1): 93-98
Yao, K.; Wang, W.; Zhu, Y.; Jin, C.; Shentu, X.; Jiang, J.; Zhang, Y.; Ni, S. 2011: A novel GJA3 mutation associated with congenital nuclear pulverulent and posterior polar cataract in a Chinese family. Human Mutation 32(12): 1367-1370
Wang, K.; Wang, B.; Wang, J.; Zhou, S.; Yun, B.; Suo, P.; Cheng, J.; Ma, X.; Zhu, S. 2009: A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family. Molecular Vision 15: 2813-2820
Sakaguchi, H.; Yamashita, S.; Miura, A.; Hirahara, T.; Kimura, E.; Maeda, Y.; Terasaki, T.; Hirano, T.; Uchino, M. 2011: A novel GJB1 frameshift mutation produces a transient CNS symptom of X-linked Charcot-Marie-Tooth disease. Journal of Neurology 258(2): 284-290
Luigetti, M.; Fabrizi, G.M.; Ranieri, F.; Taioli, F.; Conte, A.; Del Grande, A.; Sabatelli, M. 2011: A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signs. Muscle and Nerve 44(4): 613-615
Wang, Z.-X.; Lu, W.-S.; Li, H.; Lin, D.; Zhou, F.-S.; Sun, L.-D.; Yang, S.; Zhang, X.-J. 2011: A novel GJB3 (Cx31) missense mutation in a Chinese patient with erythrokeratodermia variabilis. Journal of the European Academy of Dermatology and Venereology: Jeadv 25(1): 113-115
Baris, H.N.; Zlotogorski, A.; Peretz-Amit, G.; Doviner, V.; Shohat, M.; Reznik-Wolf, H.; Pras, E. 2008: A novel GJB6 missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis. British Journal of Dermatology 159(6): 1373-1376
Pisani, A.; Visciano, B.; Russo, R.; Mozzillo, G.R.; Porto, C.; De Maggio, I.; Russo, R.; Pontarelli, G.; Villani, G.R.D.; Cianciaruso, B.; Di Natale, P. 2012: A novel GLA mutation in a Fabry family with glucose-6-phosphate dehydrogenase deficiency. Journal of Nephrology 25(4): 582-585
Volodarsky, M.; Langer, Y.; Birk, O.S. 2014: A novel GLI3 mutation affecting the zinc finger domain leads to preaxial-postaxial polydactyly-syndactyly complex. Bmc Medical Genetics 15: 110
Li, C.; Huan, Y.; Shen, N.; Ji, L.; Sun, S.; Liu, S.; Liu, Q.; Gao, L.; Tan, F.; Wang, Y.; Shen, Z. 2010: A novel GLP-1 analog, BPI3006, with potent DPP IV resistance and good glucoregulatory effect. Biochemical and Biophysical Research Communications 400(4): 563-568
Gregory, M.L.; Guzauskas, G.F.; Edgar, T.S.; Clarkson, K.B.; Srivastava, A.K.; Holden, K.R. 2008: A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. Journal of Child Neurology 23(12): 1433-1438
Forsyth, R.J.; Gika, A.D.; Ginjaar, I.; Tijssen, M.A.J. 2007: A novel GLRA1 mutation in a recessive hyperekplexia pedigree. Movement Disorders: Official Journal of the Movement Disorder Society 22(11): 1643-1645
Reis, M.T.A.; Cattani, A.; Mendonca, B.B.; Corrêa, P.H.S.; Martin, R.M. 2010: A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levels. Arquivos Brasileiros de Endocrinologia e Metabologia 54(8): 728-731
Klagge, A.; Jessnitzer, B.; Pfaeffle, R.; Stumvoll, M.; Fuhrer, D. 2010: A novel GNAS1 mutation in a German family with Albright's hereditary osteodystrophy. Experimental and Clinical Endocrinology and Diabetes: Official Journal German Society of Endocrinology and German Diabetes Association 118(9): 586-590
Trusolino, L.; Rabino, M.; Prat, M.; Cremona, O.; Savoia, P.; Marchisio, P.C. 1993: A novel GPI-anchored glycoprotein shows properties of a coohterminus truncated cadherin involved in cell-cell contacts of cultured human epithelial cells. Cytotechnology 11(Suppl 1): S97-S99
Peng, Y.; Meng, Y.; Wang, Z.; Qin, M.; Li, X.; Dian, Y.; Huang, S. 2009: A novel GPR143 duplication mutation in a Chinese family with X-linked congenital nystagmus. Molecular Vision 15: 810-814
Hu, J.; Liang, D.; Xue, J.; Liu, J.; Wu, L. 2011: A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmus. Molecular Vision 17: 715-722
Zhang, W.; Yang, F.; Luo, J.; Chen, F.; Gu, J.; Guan, X. 2014: A novel GPR30 rs10235056 A>G polymorphism associated with post-transcriptional regulation in lymphoblastoid cell lines. Biomarkers: Biochemical Indicators of Exposure Response and Susceptibility to Chemicals 19(5): 417-423
Verma, M.K.; Biswas, S.; Chandravanshi, B.; Neelima, K.; Oommen, A.M.; Jagannath, M.R.; Somesh, B.P. 2014: A novel GPR40 agonist, CNX-011-67, suppresses glucagon secretion in pancreatic islets under chronic glucolipotoxic conditions in vitro. Bmc Research Notes 7: 595
Fiol, D.F.; Sanmarti, E.; Lim, A.H.; Kültz, D. 2011: A novel GRAIL E3 ubiquitin ligase promotes environmental salinity tolerance in euryhaline tilapia. Biochimica et Biophysica Acta 1810(4): 439-445
Bit-Ivan, E.N.; Suh, E.; Shim, H-Sub.; Weintraub, S.; Hyman, B.T.; Arnold, S.E.; McCarty-Wood, E.; Van Deerlin, V.M.; Schneider, J.A.; Trojanowski, J.Q.; Frosch, M.P.; Baker, M.C.; Rademakers, R.; Mesulam, M.; Bigio, E.H. 2014: A novel GRN mutation (GRN c.708+6_+9delTGAG) in frontotemporal lobar degeneration with TDP-43-positive inclusions: clinicopathologic report of 6 cases. Journal of Neuropathology and Experimental Neurology 73(5): 467-473
Zeng, C.; Wang, R.; Li, D.; Lin, X.-J.; Wei, Q.-K.; Yuan, Y.; Wang, Q.; Chen, W.; Zhuang, S.-M. 2010: A novel GSK-3 beta-C/EBP alpha-miR-122-insulin-like growth factor 1 receptor regulatory circuitry in human hepatocellular carcinoma. Hepatology 52(5): 1702-1712
Serenó, L.; Coma, M.; Rodríguez, M.; Sánchez-Ferrer, P.; Sánchez, M.B.; Gich, I.; Agulló, J.M.; Pérez, M.; Avila, J.; Guardia-Laguarta, C.; Clarimón, J.; Lleó, A.; Gómez-Isla, T. 2009: A novel GSK-3beta inhibitor reduces Alzheimer's pathology and rescues neuronal loss in vivo. Neurobiology of Disease 35(3): 359-367
Arbajian, E.; Magnusson, L.; Mertens, F.; Domanski, H.A.; Vult von Steyern, F.; Nord, K.H. 2013: A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development. Genes Chromosomes and Cancer 52(3): 330-331
Guo, Y.; Zanetti, G.; Schekman, R. 2013: A novel GTP-binding protein-adaptor protein complex responsible for export of Vangl2 from the trans Golgi network. Elife 2: E00160
Zhao, X.; Ren, Y.; Zhang, X.; Chen, C.; Dong, B.; Li, Y. 2013: A novel GUCY2D mutation in a Chinese family with dominant cone dystrophy. Molecular Vision 19: 1039-1046
Hughes, A.E.; Meng, W.; Lotery, A.J.; Bradley, D.T. 2012: A novel GUCY2D mutation, V933A, causes central areolar choroidal dystrophy. Investigative Ophthalmology and Visual Science 53(8): 4748-4753
Hytönen, M.K.; Arumilli, M.; Lappalainen, A.K.; Kallio, H.; Snellman, M.; Sainio, K.; Lohi, H. 2012: A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VIi. Plos one 7(7): E40281
Bertz, H.; Spyridonidis, A.; Wäsch, R.; Grüllich, C.; Egger, M.; Finke, J.ür. 2009: A novel GVHD-prophylaxis with low-dose alemtuzumab in allogeneic sibling or unrelated donor hematopoetic cell transplantation: the feasibility of deescalation. Biology of Blood and Marrow Transplantation: Journal of the American Society for Blood and Marrow Transplantation 15(12): 1563-1570
Runesson, J.; Saar, I.; Lundström, L.; Järv, J.; Langel, U. 2009: A novel GalR2-specific peptide agonist. Neuropeptides 43(3): 187-192
Conte, R.; Fu, B.; Kamarchik, E.; Bowman, J.M. 2013: A novel Gaussian Binning (1GB) analysis of vibrational state distributions in highly excited H2O from reactive quenching of OH∗ by H2. Journal of Chemical Physics 139(4): 044104
Mathews, J.L.; Smrcka, A.V.; Bidlack, J.M. 2008: A novel Gbetagamma-subunit inhibitor selectively modulates mu-opioid-dependent antinociception and attenuates acute morphine-induced antinociceptive tolerance and dependence. Journal of Neuroscience: the Official Journal of the Society for Neuroscience 28(47): 12183-12189
So, J.Y.; Lee, H.J.; Smolarek, A.K.; Paul, S.; Wang, C.-X.; Maehr, H.; Uskokovic, M.; Zheng, X.; Conney, A.H.; Cai, L.; Liu, F.; Suh, N. 2011: A novel Gemini vitamin D analog represses the expression of a stem cell marker CD44 in breast cancer. Molecular Pharmacology 79(3): 360-367
Todd, L.R.; Gomathinayagam, R.; Sankar, U. 2010: A novel Gfer-Drp1 link in preserving mitochondrial dynamics and function in pluripotent stem cells. Autophagy 6(6): 821-822
Kim, S.; Hall, S.D.; Li, L. 2009: A novel Gibbs maximum a posteriori (GMAP) approach on Bayesian nonlinear mixed-effects population pharmacokinetics (PK) models. Journal of Biopharmaceutical Statistics 19(4): 700-720
Coy, S.; Caamaño, J.H.; Carvajal, J.; Cleary, M.L.; Borycki, A.-G.ël. 2011: A novel Gli3 enhancer controls the Gli3 spatiotemporal expression pattern through a TALE homeodomain protein binding site. Molecular and Cellular Biology 31(7): 1432-1443
Aggarwal, A.; Aggarwal, N.; Nagral, A.; Jankharia, G.; Bhatt, M. 2009: A novel Global Assessment Scale for Wilson's Disease (GAS for WD). Movement Disorders: Official Journal of the Movement Disorder Society 24(4): 509-518
Sun, X.; Yang, S.; Sun, M.; Wang, S.; Ding, X.; Zhu, D.; Ji, W.; Cai, H.; Zhao, C.; Wang, X.; Zhu, Y. 2014: A novel Glycine soja cysteine proteinase inhibitor GsCPI14, interacting with the calcium/calmodulin-binding receptor-like kinase GsCBRLK, regulated plant tolerance to alkali stress. Plant Molecular Biology 85(1-2): 33-48
Wang, X.; Li, Y.; Ji, W.; Bai, X.; Cai, H.; Zhu, D.; Sun, X.-L.; Chen, L.-J.; Zhu, Y.-M. 2011: A novel Glycine soja tonoplast intrinsic protein gene responds to abiotic stress and depresses salt and dehydration tolerance in transgenic Arabidopsis thaliana. Journal of Plant Physiology 168(11): 1241-1248
Wang, X.; Wang, D.; Jing, P.; Wu, Y.; Xia, Y.; Chen, M.; Hong, L. 2013: A novel Golgi retention signal RPWS for tumor suppressor UBIAD1. Plos one 8(8): E72015
Accardo, C.; Himel, V.T.; Lallier, T.E. 2014: A novel GuttaFlow sealer supports cell survival and attachment. Journal of Endodontics 40(2): 231-234
Al-Romaiyan, A.; Liu, B.; Asare-Anane, H.; Maity, C.R.; Chatterjee, S.K.; Koley, N.; Biswas, T.; Chatterji, A.K.; Huang, G.-C.; Amiel, S.A.; Persaud, S.J.; Jones, P.M. 2010: A novel Gymnema sylvestre extract stimulates insulin secretion from human islets in vivo and in vitro. PhytoTherapy Research: Ptr 24(9): 1370-1376
Nakaminami, H.; Sato-Nakaminami, K.; Noguchi, N. 2014: A novel GyrB mutation in meticillin-resistant Staphylococcus aureus (MRSA) confers a high level of resistance to third-generation quinolones. International Journal of Antimicrobial Agents 43(5): 478-479
Wu, Y.-C.; Lai, H.-L.; Chang, W.-C.; Lin, J.-T.; Liu, Y.-J.; Chern, Y. 2013: A novel Gαs-binding protein, Gas-2 like 2, facilitates the signaling of the A2A adenosine receptor. Biochimica et Biophysica Acta 1833(12): 3145-3154
Chen, X.; Chen, Z.; Zhu, J.; Xu, C.; Yan, W.; Yao, C. 2011: A novel H(2)O(2) amperometric biosensor based on gold nanoparticles/self-doped polyaniline nanofibers. Bioelectrochemistry 82(2): 87-94
Dellas, C.; Tschepe, M.; Seeber, V.; Zwiener, I.; Kuhnert, K.; Schäfer, K.; Hasenfuß, G.; Konstantinides, S.; Lankeit, M. 2014: A novel H-FABP assay and a fast prognostic score for risk assessment of normotensive pulmonary embolism. Thrombosis and Haemostasis 111(5): 996-1003
Nishizawa, A.; Toyomaki, Y.; Nakano, A.; Takeuchi, S.; Matsuzaki, Y.; Takeda, H.; Kaneko, T.; Mitsuhashi, Y.; Nakano, H. 2007: A novel H1 domain mutation in the keratin 2 gene in a Japanese family with ichthyosis bullosa of Siemens. British Journal of Dermatology 156(5): 1042-1044
Berteaux, N.; Aptel, N.; Cathala, G.; Genton, Céline.; Coll, J.; Daccache, A.; Spruyt, N.; Hondermarck, H.; Dugimont, T.; Curgy, J-Jacques.; Forné, T.; Adriaenssens, E. 2008: A novel H19 antisense RNA overexpressed in breast cancer contributes to paternal IGF2 expression. Molecular and Cellular Biology 28(22): 6731-6745
Peiris, J.S.M.; Tu, W.-w.; Yen, H.-l. 2009: A novel H1N1 virus causes the first pandemic of the 21st century. European Journal of Immunology 39(11): 2946-2954
Sorasio, L.; Biamino, E.; Garelli, E.; Ferrero, G.B.; Silengo, M.C. 2009: A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting. Clinical and Experimental Dermatology 34(8): E726-E728
Tang, N.; Zheng, J.; Sheng, Q.; Zhang, H.; Liu, R. 2011: A novel H2O2 sensor based on the enzymatically induced deposition of polyaniline at a horseradish peroxide/aligned single-wall carbon nanotubes modified au electrode. Analyst 136(4): 781-786
Wei, Y.; Guo, M. 2009: A novel H2O2-triggered anti-Fenton fluorescent pro-chelator excitable with visible light. Chemical Communications 11: 1413-1415
Faiyaz-Ul-Haque, M.; Al-Jefri, A.; Al-Dayel, F.; Bhuiyan, J.A.K.M.; Abalkhail, H.A.; Al-Nounou, R.; Al-Abdullatif, A.; Pulicat, M.S.; Gaafar, A.; Alaiya, A.A.; Peltekova, I.; Zaidi, S.H.E. 2010: A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations. European Journal of Pediatrics 169(6): 661-666
Borgio, J.F.; AbdulAzeez, S.; Al-Nafie, A.N.; Naserullah, Z.A.; Al-Jarrash, S.; Al-Madan, M.S.; Al-Muhanna, F.; Steinberg, M.H.; Al-Ali, A.K. 2014: A novel HBA2 gene conversion in cis or trans: "α12 allele" in a Saudi population. Blood Cells Molecules and Diseases 53(4): 199-203
Zhi, X.; Deng, M.; Yang, H.; Gao, G.; Wang, K.; Fu, H.; Zhang, Y.; Chen, D.; Cui, D. 2014: A novel HBV genotypes detecting system combined with microfluidic chip, loop-mediated isothermal amplification and GMR sensors. Biosensors and Bioelectronics 54: 372-377
Arankalle, V.A.; Gandhe, S.S.; Borkakoty, B.J.; Walimbe, A.M.; Biswas, D.; Mahanta, J. 2010: A novel HBV recombinant (genotype I) similar to Vietnam/Laos in a primitive tribe in eastern India. Journal of Viral Hepatitis 17(7): 501-510
Zhou, J.; Ding, W.-G.; Makiyama, T.; Miyamoto, A.; Matsumoto, Y.; Kimura, H.; Tarutani, Y.; Zhao, J.; Wu, J.; Zang, W.-J.; Matsuura, H.; Horie, M. 2014: A novel HCN4 mutation, G1097W, is associated with atrioventricular block. Circulation Journal: Official Journal of the Japanese Circulation Society 78(4): 938-942
Chase, R.; Skelton, A.; Xia, E.; Curry, S.; Liu, S.; McMonagle, P.; Huang, H.-C.; Tong, X. 2009: A novel HCV NS3 protease mutation selected by combination treatment of the protease inhibitor boceprevir and NS5B polymerase inhibitors. Antiviral Research 84(2): 178-184
Yamada, T.; Horinaka, M.; Shinnoh, M.; Yoshioka, T.; Miki, T.; Sakai, T. 2013: A novel HDAC inhibitor OBP-801 and a PI3K inhibitor LY294002 synergistically induce apoptosis via the suppression of survivin and XIAP in renal cell carcinoma. International Journal of Oncology 43(4): 1080-1086
Kemp, M.M.; Wang, Q.; Fuller, J.H.; West, N.; Martinez, N.M.; Morse, E.M.; Weïwer, M.; Schreiber, S.L.; Bradner, J.E.; Koehler, A.N. 2011: A novel HDAC inhibitor with a hydroxy-pyrimidine scaffold. Bioorganic and Medicinal Chemistry Letters 21(14): 4164-4169
Wilson, J.R.F.; Bateman, A.C.; Hanson, H.; An, Q.; Evans, G.; Rahman, N.; Jones, J.L.; Eccles, D.M. 2010: A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations. Journal of Medical Genetics 47(11): 771-774
Wang, S.Z.; Cachón-González, M.B.; Stein, P.E.; Lachmann, R.H.; Corry, P.C.; Wraith, J.E.; Cox, T.M. 2008: A novel HEXB mutation and its structural effects in juvenile Sandhoff disease. Molecular Genetics and Metabolism 95(4): 236-238
Pointon, J.J.; Lok, C.Y.; Shearman, J.D.; Suckling, R.J.; Rochette, J.; Merryweather-Clarke, A.T.; Robson, K.J.H. 2009: A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient. Blood Cells Molecules and Diseases 43(2): 194-198
Lai, F.-F.; Liu, X.-Y.; Niu, F.; Lang, L.-W.; Xie, P.; Chen, X.-G. 2014: A novel HIF-1 inhibitor--manassantin a derivative LXY6099 inhibits tumor growth. Yao Xue Xue Bao 49(5): 622-626
Jin, X.; Newman, M.J.; De-Rosa, S.; Cooper, C.; Thomas, E.; Keefer, M.; Fuchs, J.; Blattner, W.; Livingston, B.D.; McKinney, D.M.; Noonan, E.; Decamp, A.; Defawe, O.D.; Wecker, M. 2009: A novel HIV T helper epitope-based vaccine elicits cytokine-secreting HIV-specific CD4+ T cells in a Phase i clinical trial in HIV-uninfected adults. Vaccine 27(50): 7080-7086
Pattacini, L.; Mize, G.J.; Graham, J.B.; Fluharty, T.R.; Graham, T.M.; Lingnau, K.; Wizel, B.; Perdiguero, B.; Esteban, M.; Pantaleo, G.; Shen, M.; Spies, G.A.; McElrath, M.J.; Lund, J.M. 2012: A novel HIV vaccine adjuvanted by IC31 induces robust and persistent humoral and cellular immunity. Plos one 7(7): E42163
Suree, N.; Koizumi, N.; Sahakyan, A.; Shimizu, S.; An, D.Sung. 2012: A novel HIV-1 reporter virus with a membrane-bound Gaussia princeps luciferase. Journal of Virological Methods 183(1): 49-56
Zhou, T.; Han, Y.; Dang, Y.; Wang, X.; Zheng, Y.-H. 2009: A novel HIV-1 restriction factor that is biologically distinct from APOBEC3 cytidine deaminases in a human T cell line CEM.NKR. Retrovirology 6: 31
Zhang, Y.; Fan, M.; Geng, G.; Liu, B.; Huang, Z.; Luo, H.; Zhou, J.; Guo, X.; Cai, W.; Zhang, H. 2014: A novel HIV-1-encoded microRNA enhances its viral replication by targeting the TATA box region. Retrovirology 11: 23
Chentoufi, A.A.; Dasgupta, G.; Christensen, N.D.; Hu, J.; Choudhury, Z.S.; Azeem, A.; Jester, J.V.; Nesburn, A.B.; Wechsler, S.L.; BenMohamed, L. 2010: A novel HLA (HLA-A*0201) transgenic rabbit model for preclinical evaluation of human CD8+ T cell epitope-based vaccines against ocular herpes. Journal of Immunology 184(5): 2561-2571
Schiller, J.J.; Gaba, S.M.; Hasse, T.R.; Fisher, T.L.; Ellis, T.M. 2011: A novel HLA allele derived from a likely DRB1/DRB3 gene conversion event: HLA-DRB3*01:15. Tissue Antigens 78(5): 405-407
Longa, L.A.; Perotti, L.; Piovano, F.; Prucca, M.; Menardi, G.; Peano, G. 2013: A novel HLA allele, HLA-A*02:393, identified in a two generation Italian family. Tissue Antigens 82(3): 203-204
Fabreti-Oliveira, R.A.; Nascimento, E.; Santos, M.A. 2013: A novel HLA allele, HLA-A*80:03, identified in a Brazilian individual. Tissue Antigens 82(5): 349-350
Li, X.; Zou, H.; Gu, B.; Zhu, Y.; Chen, Q. 2014: A novel HLA allele, HLA-B*37:06:02, identified in a Chinese family. Tissue Antigens 84(5): 516-517
Wang, W.; He, J.; Zhang, W.; Zhu, F.-M.; Lv, H.-J. 2013: A novel HLA allele, HLA-B*40:227, was identified by polymerase chain reaction sequence-based typing in a Chinese individual. Tissue Antigens 82(3): 208-209
Zhang, K.-L.; Li, X.-F.; Zhang, X.; Lin, F.-Q.; Li, J.-P. 2014: A novel HLA allele, HLA-B*55:50, was identified by sequence-based typing. Tissue Antigens 84(5): 517-518
Wang, D.; Xu, Y.; Zou, H.; Deng, Z. 2012: A novel HLA-A allele detected by sequence-based typing: A*11:01:18. Tissue Antigens 80(2): 192-193
Song, Y.-H.; Zhang, Y.; Qiao, W.-B.; Liu, Y.; Zhu, C.-F. 2013: A novel HLA-A allele, A*24:191, was identified by sequence-based typing in a Chinese donor. Tissue Antigens 82(6): 423-424
Chen, Y.-F.; Yang, L.; Zhuang, Y.-L.; Nie, X.-M.; Zhu, C.-F. 2013: A novel HLA-A allele, A*31:65, was identified by sequence-based typing in a Chinese potential donor. Tissue Antigens 81(3): 173-175
Arrieta-Bolaños, E.; McWhinnie, A.J.; Madrigal-Sánchez, J.J.; Calvo, L.; Salazar-Sánchez, L.; Madrigal, J.A.; Marsh, S.G.E.; Shaw, B.E. 2014: A novel HLA-A allele, A*74:23, identified in an individual from Costa Rica. Tissue Antigens 84(6): 583-584
Li, W.-X.; Xia, J.-A.; Zhang, D.-Y.; Yao, L.; Lu, H.-Q.; Shen, G.; Bi, H.; Ma, Y.; Yin, J.-P.; Liu, G.-J.; Zhu, Y.-Y.; Zou, J. 2014: A novel HLA-A allele, HLA-A*02:441, identified by sequence-based typing in Chinese individuals. Tissue Antigens 83(4): 290-291
Jindra, P.; Venigová, P.; Houdová, L.; Steinerová, K. 2013: A novel HLA-A null allele (A*02:395N) with stop codon in exon 2 generated by single nucleotide exchange. Tissue Antigens 81(6): 451-452
Zhang, K.Y.; Zhang, Z.X.; Wang, L.J.; Liu, N.; Shan, X.Y. 2013: A novel HLA-A*02 allele, HLA-A*02:129. Tissue Antigens 81(6): 450-451
Zhang, M.; Sukhumalchandra, P.; Enyenihi, A.A.; St John, L.S.; Hunsucker, S.A.; Mittendorf, E.A.; Sergeeva, A.; Ruisaard, K.; Al-Atrache, Z.; Ropp, P.A.; Jakher, H.; Rodriguez-Cruz, T.; Lizee, G.; Clise-Dwyer, K.; Lu, S.; Molldrem, J.J.; Glish, G.L.; Armistead, P.M.; Alatrash, G. 2013: A novel HLA-A*0201 restricted peptide derived from cathepsin G is an effective immunotherapeutic target in acute myeloid leukemia. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 19(1): 247-257
Yu, M.; Hall, J.E.; Hartman, K.; Czech, J.; Jennings, L. 2010: A novel HLA-A*03 allele, HLA-A*03:71. Tissue Antigens 76(4): 331
Feng, Z.-H.; Hu, B.; Chi, X.-Y.; Zhao, L.; Jiao, S.-X. 2012: A novel HLA-A*11 allele, A*11:97, was identified by sequencing-based typing. Tissue Antigens 80(3): 267-268
Jennings, L.; Hall, J.E.; Caparelli, E.; Silva, M.; Yu, M. 2012: A novel HLA-A*30 allele, HLA-A*30:36. Tissue Antigens 79(2): 132-134
Ko, S.-Y.; Oh, H.-B.; Heo, Y.-S.; Jun, J.H.; Kwon, O.-J. 2011: A novel HLA-A*31 allele, A*31:34, identified by sequence-based typing. Tissue Antigens 77(1): 80-81
Lim, J.; Kim, Y.; Han, K.; Kim, H.-J.; Min, W.-S. 2008: A novel HLA-A*3315 allele identified by haplotype-specific extraction and sequence-based typing. Tissue Antigens 72(1): 76-77
Dongmei, W.; Li, W.; Wang, L.; Ni, L.; Zhixin, Z. 2012: A novel HLA-A*66 allele, A*66:07. Tissue Antigens 80(6): 542-543
Tu, S.-H.; Huang, H.-I.; Lin, S.-I.; Liu, H.-Y.; Sher, Y.-P.; Chiang, S.-K.; Chong, P.; Roffler, S.; Tseng, G.-C.; Chen, H.-W.; Liu, S.-J. 2012: A novel HLA-A2-restricted CTL epitope of tumor-associated antigen L6 can inhibit tumor growth in vivo. Journal of ImmunoTherapy 35(3): 235-244
Emmerich, F.; Daskalakis, M.; Niemeyer, C. 2010: A novel HLA-B allele, B*14:10, identified by haplotype-specific sequencing. Tissue Antigens 76(6): 497-498
Aggarwal, R.; Stamm, L.; Zhao, W.; Fernandez-Vina, M.; Senitzer, D.; Berka, N. 2008: A novel HLA-B allele, B*4093, sharing sequences with B*4006 and B*0702 in an Asian Indian donor. Tissue Antigens 72(5): 492-494
Zhang, Y.; Lu, H.-X.; Liu, Y.; Zhu, C.-F. 2009: A novel HLA-B allele, B*4096 was identified by sequence-based typing in a Chinese individual. Tissue Antigens 74(5): 440-442
Lee, K.W. 2010: A novel HLA-B allele, B*40:123, carrying a nucleotide substitution at a conserved codon. Tissue Antigens 76(6): 499-500
Chen, M.J.; Chu, C.C.; Shyr, M.H.; Lin, C.L.; Lin, P.Y.; Yang, K.L. 2010: A novel HLA-B allele, B*5214, detected in a Taiwanese volunteer bone marrow donor using a sequence-based typing method. International Journal of Immunogenetics 37(1): 39-41
Zhuang, Y.-L.; Song, Y.-H.; Zhang, Y.; Nie, X.-M.; Zhu, C.-F. 2010: A novel HLA-B allele, B*5535, was identified by sequence-based typing in a Chinese individual. Tissue Antigens 75(2): 178-179
Ou, G.; Wang, J.; Wang, C.; Ji, X.; Chen, Q. 2014: A novel HLA-B allele, HLA-B*15:325, is identified by sequence-based typing in a HIV infected individual. Tissue Antigens 84(5): 514-515
Miyazono, T.; Shiina, T.; Michino, J.; Yasumura, S.; Sugiyama, T. 2013: A novel HLA-B allele, HLA-B*39:01:16, identified by super high-resolution single-molecule sequence-based typing in a Japanese individual. Tissue Antigens 82(3): 205-206
Wada, A.; Shiina, T.; Michino, J.; Yasumura, S.; Sugiyama, T. 2014: A novel HLA-B allele, HLA-B*44:184, identified by super high-resolution single-molecule sequence-based typing in a Japanese individual. Tissue Antigens 83(3): 198-199
Lee, K.W.; Seo, J.J. 2009: A novel HLA-B allele: HLA-B*5419. Tissue Antigens 74(5): 444-445
Chi, X.-Y.; Feng, Z.-H.; Hu, B.; Zhao, L.; Jiao, S.-X. 2013: A novel HLA-B*13 allele, B*13:68, was identified by sequencing-based typing. Tissue Antigens 82(3): 204-205
Zhu, F.-M.; He, J.-J.; He, J.; Yan, L.-X. 2007: A novel HLA-B*15 allele, B*9524, identified by sequence-based tying in the Chinese population. Tissue Antigens 70(6): 521-522
Lochmann, E.; Frison, S.; Longhi, E.; Moscetti, A.; Vecchiato, C. 2014: A novel HLA-B*18:80 allele identified by SBT typing in an Italian bone marrow volunteer donor. International Journal of Immunogenetics 41(3): 262-263
Nie, X.-M.; Zhang, Y.; Zhuang, Y.-L.; Song, Y.-H.; Zhu, C.-F. 2012: A novel HLA-B*35 allele, B*35:189 with a new motif GGG at codon 35, identified by sequence-based typing in a Chinese potential donor. Tissue Antigens 80(5): 467-469
Martínez-Martínez, L.; González-Santesteban, C.; Agustí-Martí, M.; Pérez-Ranz, E.; de la Calle-Martín, O. 2010: A novel HLA-B*35 variant, HLA-B*35:02:03, identified by sequence-based typing in a bone marrow donor. Tissue Antigens 76(2): 152-153
Jin, S.-Z.; Li, Z.; Zou, H.-Y.; Cheng, X.; Cheng, L.-H.; Wang, D.-M. 2009: A novel HLA-B*37 allele, B*370105, was identified in a Chinese Han individual. Tissue Antigens 74(4): 344-345
Zhu, C.; Zhang, Y.; Nie, X.; He, W.; Fang, Y.; Liu, Y. 2008: A novel HLA-B*40 allele, B*4086, was identified by sequence-based typing in a Chinese donor. Tissue Antigens 72(2): 181-182
Li, J.-P.; Li, X.-F.; Zhang, K.-L.; Zhang, X.; Liu, X.-Z. 2012: A novel HLA-B*40 allele, HLA-B*40:74, detected in a Chinese individual. Tissue Antigens 79(1): 78-80
Street, J.; Johnson, J.; Hammond, L.; Pepperall, J.; Darke, C. 2011: A novel HLA-B*40 sequence--B*40:92. International Journal of Immunogenetics 38(2): 161-166
Redman, H.; Marcus, N.; Marlowe, M.; Endres, R.O. 2009: A novel HLA-B*44 allele, B*4466, discovered in a potential donor for a hematopoietic stem cell transplant. Tissue Antigens 74(4): 347-348
Hammond, L.; Dunn, P.P.J. 2008: A novel HLA-B*44 allele, HLA-B*4459, identified in a renal patient with aberrant B44 serology and characterized by sequence-based typing. Tissue Antigens 72(5): 494-495
Kang, J.-E.; Hwang, S.-H.; Song, E.-J.; Kwon, O.-J.; Kim, H.-H. 2011: A novel HLA-B*48 allele, B*48:01:03, identified by sequence-based typing. Tissue Antigens 78(5): 401-402
Barbuti, S.; Fornaciari, S.; Mariotti, M.L.; Curcio, M.; Scatena, F. 2012: A novel HLA-B*51:01:29 allele identified by sequence-based typing. Tissue Antigens 79(4): 310-311
Cheng, L.-H.; Zhu, W.-G.; Lan, Y.-X.; Zou, H.-Y.; Li, Z.; Jin, S.-Z. 2009: A novel HLA-B*54 allele, B*5417, identified in a Northern Chinese Han individual. Tissue Antigens 74(5): 442-444
Gong, Z.; Zhang, Z.X.; Shan, X.; Li, D.; Li, W. 2013: A novel HLA-B*54 allele, B*54:16. Tissue Antigens 81(1): 57-58
Zhao, R.Y.; Mifsud, N.A.; Xiao, K.; Chan, K.-F.; Oveissi, S.; Jackson, H.M.; Dimopoulos, N.; Guillaume, P.; Knights, A.J.; Lowen, T.; Robson, N.C.; Russell, S.E.; Scotet, E.; Davis, I.D.; Maraskovsky, E.; Cebon, J.; Luescher, I.F.; Chen, W. 2012: A novel HLA-B18 restricted CD8+ T cell epitope is efficiently cross-presented by dendritic cells from soluble tumor antigen. Plos one 7(9): E44707
Tao, S.-D.; Zhang, W.; Wang, W.; He, J.; Zhu, F.-M.; Lv, H.-J. 2014: A novel HLA-C allele, C*08:01:10 was identified in a Chinese leukemia patient. Tissue Antigens 84(4): 419-420
Faé, I.; Rosenmayr, A.; Mayr, W.R.; Fischer, G.F. 2008: A novel HLA-C allele, Cw*0617. Tissue Antigens 72(5): 499-500
Wang, J.; Xia, L.; Luo, M.; Chen, Q. 2013: A novel HLA-C allele, HLA-C*06:45, identified by sequence-based typing in a Chinese individual. Tissue Antigens 82(1): 67-68
Emmerich, F.; Daskalakis, M.; Niemeyer, C.M. 2010: A novel HLA-C allele, HLA-Cw*06:20. Tissue Antigens 76(5): 425
Cauwelier, B.; Nollet, F.; Gadisseur, A.; Schroyens, W.; Berneman, Z. 2014: A novel HLA-C null allele, HLA-C*05:99N. Tissue Antigens 84(4): 420-421
Deng, Z.-H.; Zhou, H.-Y.; Wang, D.-M.; Xu, Y.-P. 2011: A novel HLA-C*01 variant allele, HLA-C*01:38. Tissue Antigens 77(1): 81-83
Zhang, K.Y.; Zhang, Z.X.; Wang, L.J.; Liu, N.; Shan, X.Y. 2013: A novel HLA-C*15 allele, HLA-C*15:02:04. Tissue Antigens 82(1): 70-71
Deng, Z.-H.; Wang, D.-M. 2009: A novel HLA-Cw*01 variant allele, HLA-Cw*0130. Tissue Antigens 74(6): 549-551
Jin, S.-Z.; Zhu, W.-G.; Lan, Y.-X.; Zou, H.-Y.; Cheng, L.-H. 2009: A novel HLA-Cw*0124 allele found in a Chinese Han patient from Southern China. Tissue Antigens 74(6): 547-549
Kim, M.-H.; Oh, H.-B.; Kwon, O.-J. 2007: A novel HLA-Cw*03 allele, Cw*033802, identified by sequence-based typing. Tissue Antigens 70(6): 522-524
Xu, Y.; Deng, Z.; Zeng, J.; Gao, S.; Wang, D. 2009: A novel HLA-Cw*04 allele, Cw*04010103, identified by genomic full length cloning and sequencing. Tissue Antigens 74(5): 453-455
Lim, J.; Kim, Y.; Cho, B.; Chung, N.-G.; Bok, J.-N. 2009: A novel HLA-Cw*0436 allele identified by haplotype-specific extraction and sequence-based typing. Tissue Antigens 73(1): 78-79
Martínez-Martínez, L.; González-Santesteban, C.; Agustí-Martí, M.; Pérez-Ranz, E.; de la Calle-Martín, O. 2009: A novel HLA-Cw*07 variant, HLA-Cw*0760, identified by sequence-based typing in a bone marrow donor. Tissue Antigens 74(2): 172-173
Xu, Y.-P.; Deng, Z.-H.; Wang, D.-M.; Zeng, J.-Q.; Gao, S.-Q. 2009: A novel HLA-Cw*08 allele, Cw*0822, identified by genomic full-length cloning and sequencing. Tissue Antigens 74(6): 555-556
Kanga, U.; McWhinnie, A.J.; Mourya, M.; Shaw, B.E.; Madrigal, J.A.; Mehra, N.K. 2011: A novel HLA-DPB1 allele, DPB1*125:01, identified by sequence-based typing in an Indian individual. Tissue Antigens 77(1): 85-87
Todorova, K.; Schulze, H.; Diederich, G.; Ebell, W.; Salama, A.; Schoenemann, C. 2011: A novel HLA-DQB1*03:02 variant designated DQB1*03:02:05. Tissue Antigens 78(5): 404-405
Oka, S.; Furukawa, H.; Kashiwase, K.; Tsuchiya, N.; Tohma, S. 2013: A novel HLA-DQB1*04 allele, DQB1*04:10, identified in a Japanese individual. Tissue Antigens 82(2): 148-149
Han, Z.-D.; Wang, W.; He, J.; Zhu, F.-M.; Lv, H.-J. 2014: A novel HLA-DQB1*05:15 allele was identified in a Chinese individual. Tissue Antigens 84(2): 246-248
Chu, C.-C.; Lee, H.-L.; Lin, M. 2009: A novel HLA-DRB1 allele, DRB*090202, is identified in a Taiwanese family. Tissue Antigens 74(3): 262-263
Chu, C.-C.; Lee, H.-L.; Lin, M. 2009: A novel HLA-DRB1 allele, DRB*1611, is identified in two Taiwanese individuals. Tissue Antigens 74(2): 175-176
Barbuti, S.; Curcio, M.; Marchetti, L.; Vittorio, O.; Mariotti, M.L.; Scatena, F. 2013: A novel HLA-DRB1 allele, DRB1*01:54, identified by sequence-based typing. Tissue Antigens 82(1): 80-81
Dang, C.-W.; Chu, C.-C.; Liu, T.Y.-C.; Lin, M.; Lee, Y.-J. 2007: A novel HLA-DRB1 allele, DRB1*0832, identified by sequence-based typing method. Tissue Antigens 70(6): 527-529
Liu, J.; Liu, N.; Shan, X.; Li, W.; Zhang, Z. 2010: A novel HLA-DRB1 allele, DRB1*08:36, identified by sequence-based typing. Tissue Antigens 76(5): 426-427
Li, Z.; Zhang, L.-H.; Zou, H.-Y.; Jin, S.-Z. 2009: A novel HLA-DRB1 allele, DRB1*112802, was identified in a Chinese individual. Tissue Antigens 74(4): 350-352
Nie, X.-M.; Fang, Y.-H.; Zhang, Y.; He, W.-D.; Zhu, C.-F. 2009: A novel HLA-DRB1 allele, DRB1*1219, was identified by sequence-based typing in a Chinese leukaemia family. Tissue Antigens 74(4): 352-354
Mrazek, F.; Onderkova, J.; Ambruzova, Z.; Zachova, S.; Petrek, M. 2014: A novel HLA-DRB1 allele, HLA-DRB1*13:116, identified by sequencing-based typing in a member of the Czech National Marrow Donor Registry. International Journal of Immunogenetics 41(2): 149-150
Sun, Y.; Ji, Y.; Xie, J.; Liu, Y.; Du, K. 2011: A novel HLA-DRB1 allele: DRB1*15:02:08. Tissue Antigens 78(2): 157
Ji, Y.; Sun, Y.; Xie, J.H.; Yang, J.H.; Liu, Y.; Du, K.M. 2009: A novel HLA-DRB1*120204 allele found in a Chinese individual. Tissue Antigens 74(5): 462-463
Yan, L.-X.; Zhu, F.-M.; He, Y.-M. 2008: A novel HLA-DRB1*135002 allele was identified in a cord blood donor. Tissue Antigens 72(1): 78-79
Park, H.; Lee, Y.J.; Han, B.Y.; Song, E.Y.; Park, M.H. 2013: A novel HLA-DRB1*14 allele, HLA-DRB1*14:136, identified from a registered marrow donor in Korea. Tissue Antigens 81(4): 239-240
Lee, E.; Ozaki, S.; Ishii, H.; Takimoto, T.; Matsumoto, T. 2011: A novel HLA-DRB4 allele, DRB4*01:08, identified by sequence-based typing. Tissue Antigens 78(2): 158-159
Benedek, G.; Zhu, W.; Libal, N.; Casper, A.; Yu, X.; Meza-Romero, R.; Vandenbark, A.A.; Alkayed, N.J.; Offner, H. 2014: A novel HLA-DRα1-MOG-35-55 construct treats experimental stroke. Metabolic Brain Disease 29(1): 37-45
Veiga-Castelli, L.C.; Castelli, E.C.; Beauchemin, K.; Donadi, E.A.; Roger, M. 2012: A novel HLA-E allele, E*01:03:05, identified in two Brazilian individuals. Tissue Antigens 80(2): 200-201
Taborri, J.; Rossi, S.; Palermo, E.; Patanè, F.; Cappa, P. 2014: A novel HMM distributed classifier for the detection of gait phases by means of a wearable inertial sensor network. Sensors 14(9): 16212-16234
Levkovitz, L.; Yosef, N.; Gershengorn, M.C.; Ruppin, E.; Sharan, R.; Oron, Y. 2010: A novel HMM-based method for detecting enriched transcription factor binding sites reveals RUNX3 as a potential target in pancreatic cancer biology. Plos one 5(12): E14423
Zhu, H.-J.; Wang, J.-S.; Patrick, K.S.; Donovan, J.L.; DeVane, C.L.; Markowitz, J.S. 2007: A novel HPLC fluorescence method for the quantification of methylphenidate in human plasma. Journal of Chromatography. B Analytical Technologies in the Biomedical and Life Sciences 858(1-2): 91-95
Heideloff, C.; Bunch, D.R.; Wang, S. 2010: A novel HPLC method for quantification of 10 antiepileptic drugs or metabolites in serum/plasma using a monolithic column. Therapeutic Drug Monitoring 32(1): 102-106
Giorgi, M.G.; Howland, K.; Martin, C.; Bonner, A.B. 2012: A novel HPLC method for the concurrent analysis and quantitation of seven water-soluble vitamins in biological fluids (plasma and urine): a validation study and application. Thescientificworldjournal 2012: 359721
Evers, D.L.; Fowler, C.B.; Cunningham, R.E.; Mason, J.T.; O'Leary, T.J. 2007: A novel HPLC method reveals that precipitation of 2'-deoxyadenosine 5'-monophosphate with lithium perchlorate/acetone leads to base depurination. Analytical Biochemistry 370(2): 255-257
Olennikov, D.N.; Kashchenko, N.I.; Chirikova, N.K. 2014: A novel HPLC-assisted method for investigation of the Fe2+-chelating activity of flavonoids and plant extracts. Molecules 19(11): 18296-18316
Sarkes, D.; Rameh, L.E. 2010: A novel HPLC-based approach makes possible the spatial characterization of cellular PtdIns5P and other phosphoinositides. Biochemical Journal 428(3): 375-384
Saracino, M.A.; Cannistraci, C.; Bugamelli, F.; Morganti, E.; Neri, I.; Balestri, R.; Patrizi, A.; Raggi, M.A. 2013: A novel HPLC-electrochemical detection approach for the determination of D-penicillamine in skin specimens. Talanta 103: 355-360
Monroy-García, A.; Gómez-Lim, M.A.; Weiss-Steider, B.; la Rosa, G.Paz-de.; Hernández-Montes, J.; Pérez-Saldaña, K.; Tapia-Guerrero, Y.S.; Toledo-Guzmán, M.E.; Santiago-Osorio, E.; Sanchez-Peña, Héctor.I.; Mora-García, Mía.de.Lourdes. 2011: A novel HPV 16 L1-based chimeric virus-like particle containing E6 and E7 seroreactive epitopes permits highly specific detection of antibodies in patients with CIN 1 and HPV-16 infection. Virology Journal 8: 59
Gripp, K.W.; Bifeld, E.; Stabley, D.L.; Hopkins, E.; Meien, S.; Vinette, K.; Sol-Church, K.; Rosenberger, G. 2012: A novel HRAS substitution (c.266C>G; p.S89C) resulting in decreased downstream signaling suggests a new dimension of RAS pathway dysregulation in human development. American Journal of Medical Genetics. Part a 158a (9): 2106-2118
Sajjad, N.; Goebel, I.; Kakar, N.; Cheema, A.M.; Kubisch, C.; Ahmad, J. 2008: A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan. Bmc Medical Genetics 9: 99
Lv, H.; Huang, C.; Zhang, J.; Liu, Z.; Zhang, Z.; Xu, H.; You, Y.; Hu, J.; Li, X.; Wang, W. 2014: A novel HSF4 gene mutation causes autosomal-dominant cataracts in a Chinese family. G3 4(5): 823-828
Lamoureux, F.; Thomas, C.; Yin, M.-J.; Kuruma, H.; Fazli, L.; Gleave, M.E.; Zoubeidi, A. 2011: A novel HSP90 inhibitor delays castrate-resistant prostate cancer without altering serum PSA levels and inhibits osteoclastogenesis. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 17(8): 2301-2313
Samadi, A.; Loo, P.; Mukerji, R.; O'Donnell, G.; Tong, X.; Timmermann, B.N.; Cohen, M.S. 2009: A novel HSP90 modulator with selective activity against thyroid cancers in vitro. Surgery 146(6): 1196-1207
Luigetti, M.; Fabrizi, G.M.; Madia, F.; Ferrarini, M.; Conte, A.; Del Grande, A.; Tasca, G.; Tonali, P.A.; Sabatelli, M. 2010: A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. Journal of the Neurological Sciences 298(1-2): 114-117
Wan, Q-Hong.; Zhang, P.; Ni, X-Wei.; Wu, H-Long.; Chen, Y-Yan.; Kuang, Y-Ye.; Ge, Y-Fa.; Fang, S-Guo. 2011: A novel HURRAH protocol reveals high numbers of monomorphic MHC class II loci and two asymmetric multi-locus haplotypes in the Père David's deer. Plos One 6(1): e14518
Sybirna, K.; Petryk, N.; Zhou, Y.-F.; Sibirny, A.; Bolotin-Fukuhara, M. 2010: A novel Hansenula polymorpha transcriptional factor HpHAP4-B, able to functionally replace the S. cerevisiae HAP4 gene, contains an additional bZip motif. Yeast 27(11): 941-954
Mejia, L.A.; Litterman, N.; Ikeuchi, Y.; de la Torre-Ubieta, L.; Bennett, E.J.; Zhang, C.; Harper, J.W.; Bonni, A. 2013: A novel Hap1-Tsc1 interaction regulates neuronal mTORC1 signaling and morphogenesis in the brain. Journal of Neuroscience: the Official Journal of the Society for Neuroscience 33(46): 18015-18021
Zhou, P.; Li, Y.; Sun, P.; Zhou, J.; Bao, J. 2007: A novel Heck reaction catalyzed by Co hollow nanospheres in ligand-free condition. Chemical Communications 2007(14): 1418-1420
Choi, H.J.; Lee, S.M.; Kim, S.-H.; Kim, D.W.; Choi, Y.W.; Joo, W.H. 2012: A novel Helicosporium isolate and its antimicrobial and cytotoxic pigment. Journal of Microbiology and Biotechnology 22(9): 1214-1217
Griffin, M.J.; Pote, L.M.; Wise, D.J.; Greenway, T.E.; Mauel, M.J.; Camus, A.C. 2008: A novel Henneguya species from channel catfish described by morphological, histological, and molecular characterization. Journal of Aquatic Animal Health 20(3): 127-135
Luscombe, C.A.; Huang, Z.; Murray, M.G.; Miller, M.; Wilkinson, J.; Ewart, G.D. 2010: A novel Hepatitis C virus p7 ion channel inhibitor, BIT225, inhibits bovine viral diarrhea virus in vitro and shows synergism with recombinant interferon-alpha-2b and nucleoside analogues. Antiviral Research 86(2): 144-153
Fantappiè, L.; Oriente, F.; Muzzi, A.; Serruto, D.; Scarlato, V.; Delany, I. 2011: A novel Hfq-dependent sRNA that is under FNR control and is synthesized in oxygen limitation in Neisseria meningitidis. Molecular Microbiology 80(2): 507-523
Shang, G.-Q.; Gao, X.; Chen, M.-X.; Zheng, H.; Xu, J.-G. 2008: A novel Hg2+ selective ratiometric fluorescent chemodosimeter based on an intramolecular FRET mechanism. Journal of Fluorescence 18(6): 1187-1192
Saxena, A.; Bronner, M.E. 2014: A novel HoxB cluster protein expressed in the hindbrain and pharyngeal arches. Genesis 52(10): 858-863
Chan, K.C.; Ting, C.M.; Chan, P.S.; Lo, M.C.; Lo, K.W.; Curry, J.E.; Smyth, T.; Lee, A.W.M.; Ng, W.T.; Tsao, G.S.W.; Wong, R.N.S.; Lung, M.L.; Mak, N.K. 2013: A novel Hsp90 inhibitor AT13387 induces senescence in EBV-positive nasopharyngeal carcinoma cells and suppresses tumor formation. Molecular Cancer 12(1): 128
Escuret, V.; Collins, P.J.; Casalegno, J.-S.éb.; Vachieri, S.G.; Cattle, N.; Ferraris, O.; Sabatier, M.; Frobert, E.; Caro, V.ér.; Skehel, J.J.; Gamblin, S.; Valla, F.éd.ér.; Valette, M.; Ottmann, M.èl.; McCauley, J.W.; Daniels, R.S.; Lina, B. 2014: A novel I221L substitution in neuraminidase confers high-level resistance to oseltamivir in influenza B viruses. Journal of Infectious Diseases 210(8): 1260-1269
Kuang, P.; Liu, T.; Huang, Q.; Ye, Y.; Xiang, B.; Huang, J.; Diwu, L.; Wang, Y.; Meng, W.; Dong, T.; Yang, S.; Lu, X. 2012: A novel I293MP mutation within BCR-ABL kinase domain in a Ph-positive acute lymphoblastic leukemia patient presenting resistant to imatinib but sensitive to nilotinib. Leukemia Research 36(8): E159-E162
Farber, C.R.; Reich, A.; Barnes, A.M.; Becerra, P.; Rauch, F.; Cabral, W.A.; Bae, A.; Quinlan, A.; Glorieux, F.H.; Clemens, T.L.; Marini, J.C. 2014: A novel IFITM5 mutation in severe atypical osteogenesis imperfecta type Vi impairs osteoblast production of pigment epithelium-derived factor. Journal of Bone and Mineral Research: the Official Journal of the American Society for Bone and Mineral Research 29(6): 1402-1411
Chessler, A.-D.C.; Ferreira, L.R.P.; Chang, T.-H.; Fitzgerald, K.A.; Burleigh, B.A. 2008: A novel IFN regulatory factor 3-dependent pathway activated by trypanosomes triggers IFN-beta in macrophages and fibroblasts. Journal of Immunology 181(11): 7917-7924
Hamaya, R.; Ogawa, M.; Kobayashi, N.; Suzuki, J-Ichi.; Itai, A.; Hirata, Y.; Nagai, R.; Isobe, M. 2012: A novel IKK inhibitor prevents progression of restenosis after arterial injury in mice. International Heart Journal 53(2): 133-138
Wakatsuki, S.; Suzuki, J.-i.; Ogawa, M.; Masumura, M.; Muto, S.; Shimizu, T.; Takayama, K.; Itai, A.; Isobe, M. 2008: A novel IKK inhibitor suppresses heart failure and chronic remodeling after myocardial ischemia via MMP alteration. Expert Opinion on Therapeutic Targets 12(12): 1469-1476
Ito, M.; Hamano, T.; Komatsu, T.; Asamitsu, K.; Yamakawa, T.; Okamoto, T. 2014: A novel IKKα inhibitor, noraristeromycin, blocks the chronic inflammation associated with collagen-induced arthritis in mice. Modern Rheumatology 24(5): 775-780
Ray, A.; Basu, S.; Williams, C.B.; Salzman, N.H.; Dittel, B.N. 2012: A novel IL-10-independent regulatory role for B cells in suppressing autoimmunity by maintenance of regulatory T cells via GITR ligand. Journal of Immunology 188(7): 3188-3198
Sieve, A.N.; Meeks, K.D.; Bodhankar, S.; Lee, S.; Kolls, J.K.; Simecka, J.W.; Berg, R.E. 2009: A novel IL-17-dependent mechanism of cross protection: respiratory infection with mycoplasma protects against a secondary listeria infection. European Journal of Immunology 39(2): 426-438
Estévez, O.A.; Ortega, C.; Fernández, S.; Aguado, R.; Rumbao, J.é; Perez-Navero, J.; Santamaría, M. 2014: A novel IL2RG mutation presenting with atypical T(-)B(+)NK+ phenotype: rapid elucidation of NK cell origin. Pediatric Blood and Cancer 61(1): 178-179
Sugiura, K.; Takeichi, T.; Kono, M.; Ogawa, Y.; Shimoyama, Y.; Muro, Y.; Akiyama, M. 2012: A novel IL36RN/IL1F5 homozygous nonsense mutation, p.Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis. British Journal of Dermatology 167(3): 699-701
Callea, M.; Nieminen, P.; Willoughby, C.E.; Clarich, G.; Yavuz, I.; Vinciguerra, A.; Di Stazio, M.; Giglio, S.; Sani, I.; Maglione, M.; Pensiero, S.; Tadini, G.; Bellacchio, E. 2016: A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family. Journal of the European Academy of Dermatology and Venereology: Jeadv 30(2): 341-343
Park, H.J.; Kim, H.J.; Hong, Y.B.; Nam, S.H.; Chung, K.W.; Choi, B.-O. 2014: A novel INF2 mutation in a Korean family with autosomal dominant intermediate Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis. Journal of the Peripheral Nervous System: Jpns 19(2): 175-179
Unoki, M.; Kumamoto, K.; Robles, A.I.; Shen, J.Cheng.; Zheng, Z-Ming.; Harris, C.C. 2008: A novel ING2 isoform, ING2b, synergizes with ING2a to prevent cell cycle arrest and apoptosis. Febs Letters 582(28): 3868-3874
Tang, K.; Wang, J.; Li, W.; Wu, W. 2013: A novel INS and Doppler sensors calibration method for long range underwater vehicle navigation. Sensors 13(11): 14583-14600
Bruni, D.; Sebastia, J.; Dunne, S.; Schröder, M.; Butler, M.P. 2013: A novel IRAK1-IKKε signaling axis limits the activation of TAK1-IKKβ downstream of TLR3. Journal of Immunology 190(6): 2844-2856
Cullik, A.; Pfeifer, Y.; Prager, R.; von Baum, H.; Witte, W. 2010: A novel IS26 structure surrounds blaCTX-M genes in different plasmids from German clinical Escherichia coli isolates. Journal of Medical Microbiology 59(Part 5): 580-587
Oleson, E.B.; Richardson, J.M.; Roberts, D.C.S. 2011: A novel IV cocaine self-administration procedure in rats: differential effects of dopamine, serotonin, and GABA drug pre-treatments on cocaine consumption and maximal price paid. Psychopharmacology 214(2): 567-577
Cohen, E.S.; Dobson, C.L.; Käck, H.; Wang, B.; Sims, D.A.; Lloyd, C.O.; England, E.; Rees, D.G.; Guo, H.; Karagiannis, S.N.; O'Brien, S.; Persdotter, S.; Ekdahl, H.; Butler, R.; Keyes, F.; Oakley, S.; Carlsson, M.; Briend, E.; Wilkinson, T.; Anderson, I.K.; Monk, P.D.; von Wachenfeldt, K.; Eriksson, P.-O.F.; Gould, H.J.; Vaughan, T.J.; May, R.D. 2014: A novel IgE-neutralizing antibody for the treatment of severe uncontrolled asthma. Mabs 6(3): 756-764
Zatovsky, I.V.; Baumer, V.N.; Strutynska, N.Y.; Slobodyanik, N.S.; Shishkin, O.V. 2010: A novel In3O16 fragment in Cs3In3(PO4)4. Acta Crystallographica. Section C Crystal Structure Communications 66(Part 7): I71-I74
Poirel, L.; Carattoli, A.; Bernabeu, S.; Bruderer, T.; Frei, R.; Nordmann, P. 2010: A novel IncQ plasmid type harbouring a class 3 integron from Escherichia coli. Journal of Antimicrobial ChemoTherapy 65(8): 1594-1598
Swallow, V.; Carolan, I.; Smith, T.; Webb, N.J.A.; Knafl, K.; Santacroce, S.; Campbell, M.; Harper-Jones, M.; Hanif, N.; Hall, A. 2016: A novel Interactive Health Communication Application (IHCA) for parents of children with long-term conditions: Development, implementation and feasibility assessment. Informatics for Health and Social Care 41(1): 20-46
Tsugihashi, Y.; Kakudate, N.; Yokoyama, Y.; Yamamoto, Y.; Mishina, H.; Fukumori, N.; Nakamura, F.; Takegami, M.; Ohno, S.; Wakita, T.; Watanabe, K.; Yamaguchi, T.; Fukuhara, S. 2013: A novel Internet-based blended learning programme providing core competency in clinical research. Journal of Evaluation in Clinical Practice 19(2): 250-255
Zhu, S.; Wang, X.; Wang, A.; Cong, Y.; Zhang, T. 2007: A novel Ir-hexaaluminate catalyst for N(2)O as a propellant. Chemical Communications 17: 1695-1697
Keeler, S.P.; Yabsley, M.J.; Adams, H.C.; Hernandez, S.M. 2014: A novel Isospora species (Apicomplexa: Eimeriidae) from warblers (Passeriformes: Parulidae) of Costa Rica. Journal of Parasitology 100(3): 302-304
Marcon, G.; Di Fede, G.; Giaccone, G.; Rossi, G.; Giovagnoli, A.R.; Maccagnano, E.; Tagliavini, F. 2009: A novel Italian presenilin 2 gene mutation with prevalent behavioral phenotype. Journal of Alzheimer's Disease: Jad 16(3): 509-511
Wang, Y.; Yu, Y.; Wang, J.; Tsuei, S.H.-T.; Zaho, L.; Fu, Q. 2010: A novel JAG1 mutation in a patient with Alagille's syndrome. Pathology 42(5): 496-498
Burjanivova, T.; Marcinek, J.; Lasabova, Z.; Minarik, G.; Szepe, P.; Balharek, T.; Vanochova, A.; Polacek, H.; Plank, L. 2009: A novel JAK2 exon 12 mutation identified in the retrospective analysis of paraffin-embedded tissues of polycythemia vera patients. Diagnostic Molecular Pathology: the American Journal of Surgical Pathology Part B 18(2): 108-111
Ohnishi, H.; Hosoi, K.-i.; Yoshino, H.; Sugiura, M.; Matsushima, S.; Watanabe, T.; Bessho, F. 2009: A novel JAK2 splicing mutation in neonatal myeloproliferative disorder accompanying congenital anomalies. British Journal of Haematology 145(5): 676-678
Velotta, J.B.; Deuse, T.; Haddad, M.; Masuda, E.; Park, G.; Carroll, D.; Taylor, V.; Robbins, R.C.; Schrepfer, S. 2009: A novel JAK3 inhibitor, R348, attenuates chronic airway allograft rejection. Transplantation 87(5): 653-659
Billingsley, K.L.; Posadas, J.B.; Moulds, J.M.; Gaur, L.K. 2013: A novel JK null allele associated with typing discrepancies among African Americans. Immunohematology 29(4): 145-148
Horn, T.; Castilho, L.; Moulds, J.M.; Billingsley, K.; Vege, S.; Johnson, N.; Westhoff, C.M. 2012: A novel JKA allele, nt561C>A, associated with silencing of Kidd expression. Transfusion 52(5): 1092-1096
Shi, H.; Yan, X.; Ruan, L.; Xu, X. 2012: A novel JNK from Litopenaeus vannamei involved in white spot syndrome virus infection. Developmental and Comparative Immunology 37(3-4): 421-428
Ito, M.; Nagasawa, M.; Omae, N.; Tsunoda, M.; Ishiyama, J.; Ide, T.; Akasaka, Y.; Murakami, K. 2013: A novel JNK2/SREBP-1c pathway involved in insulin-induced fatty acid synthesis in human adipocytes. Journal of Lipid Research 54(6): 1531-1540
Sun, X.; Xu, Z.; Xie, L.; Lai, R.; Zhu, X.; Zhang, W.; Xie, W. 2009: A novel Janus Kinase 2 mutation involving 14th intron splicing region in a patient with essential thrombocythemia. Leukemia and Lymphoma 50(12): 2089-2091
Pan, M.Y.; Wu, X.H.; Luo, D.B.; Huang, W.; He, Y. 2011: A novel Janus-type AT nucleoside with benzoyl protecting groups forming a pleated-sheet structure. Acta Crystallographica. Section C Crystal Structure Communications 67(Part 5): O175-O178
Palmirotta, R.; Savonarola, A.; Formica, V.; Ludovici, G.; Del Monte, G.; Roselli, M.; Guadagni, F. 2009: A novel K-ras mutation in colorectal cancer. A case report and literature review. Anticancer Research 29(8): 3369-3374
Demos, M.K.; Macri, V.; Farrell, K.; Nelson, T.N.; Chapman, K.; Accili, E.; Armstrong, L. 2009: A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction. Movement Disorders: Official Journal of the Movement Disorder Society 24(5): 778-782
Lassche, S.; Lainez, S.; Bloem, B.R.; van de Warrenburg, B.P.C.; Hofmeijer, J.; Lemmink, H.H.; Hoenderop, J.G.J.; Bindels, R.é J.M.; Drost, G. 2014: A novel KCNA1 mutation causing episodic ataxia type i. Muscle and Nerve 50(2): 289-291
Imbrici, P.; Gualandi, F.; D'Adamo, M.C.; Masieri, M.T.; Cudia, P.; De Grandis, D.; Mannucci, R.; Nicoletti, I.; Tucker, S.J.; Ferlini, A.; Pessia, M. 2008: A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1. Neuroscience 157(3): 577-587
Itoh, H.; Sakaguchi, T.; Ashihara, T.; Ding, W.-G.; Nagaoka, I.; Oka, Y.; Nakazawa, Y.; Yao, T.; Jo, H.; Ito, M.; Nakamura, K.; Ohe, T.; Matsuura, H.; Horie, M. 2009: A novel KCNH2 mutation as a modifier for short QT interval. International Journal of Cardiology 137(1): 83-85
Kuppusamy, M.; Caroccia, B.; Stindl, J.; Bandulik, S.; Lenzini, L.; Gioco, F.; Fishman, V.; Zanotti, G.; Gomez-Sanchez, C.; Bader, M.; Warth, R.; Rossi, G.P. 2014: A novel KCNJ5-insT149 somatic mutation close to, but outside, the selectivity filter causes resistant hypertension by loss of selectivity for potassium. Journal of Clinical Endocrinology and Metabolism 99(9): E1765-E1773
Hasegawa, K.; Ohno, S.; Ashihara, T.; Itoh, H.; Ding, W.-G.; Toyoda, F.; Makiyama, T.; Aoki, H.; Nakamura, Y.; Delisle, B.P.; Matsuura, H.; Horie, M. 2014: A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels. Heart Rhythm 11(1): 67-75
Patoine, D.; Hasibu, I.; Pilote, S.; Champagne, J.; Drolet, B.; Simard, C. 2011: A novel KCNQ1 variant (L203P) associated with torsades de pointes-related syncope in a Steinert syndrome patient. Canadian Journal of Cardiology 27(2): 263.E5
Fusco, C.; Frattini, D.; Bassi, M.T. 2015: A novel KCNQ3 gene mutation in a child with infantile convulsions and partial epilepsy with centrotemporal spikes. European Journal of Paediatric Neurology: Ejpn: Official Journal of the European Paediatric Neurology Society 19(1): 102-103
Körmöczi, G.ün.F.; Scharberg, E.A.; Gassner, C. 2009: A novel KEL*1,3 allele with weak Kell antigen expression confirming the cis-modifier effect of KEL3. Transfusion 49(4): 733-739
Hu, D.; Sarosh, A.; Dong, Y.-F. 2012: A novel KFCM based fault diagnosis method for unknown faults in satellite reaction wheels. Isa Transactions 51(2): 309-316
Wang, X.; Yang, Y.; Wang, X.; Li, C.; Jia, J. 2014: A novel KIAA0196 (SPG8) mutation in a Chinese family with spastic paraplegia. Chinese Medical Journal 127(10): 1987-1989
Hazan, F.; Ostergaard, P.; Ozturk, T.; Kantekin, E.; Atlihan, F.; Jeffery, S.; Ozkinay, F. 2012: A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family. American Journal of Medical Genetics. Part a 158a (7): 1686-1689
Muglia, M.; Citrigno, L.; D'Errico, E.; Magariello, A.; Distaso, E.; Gasparro, A.A.; Scarafino, A.; Patitucci, A.; Conforti, F.L.; Mazzei, R.; Cortese, R.; Tortelli, R.; Simone, I.L. 2014: A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness. Journal of the Neurological Sciences 343(1-2): 218-220
Tessa, A.; Silvestri, G.; de Leva, M.F.; Modoni, A.; Denora, P.S.; Masciullo, M.; Dotti, M.T.; Casali, C.; Melone, M.A.B.; Federico, A.; Filla, A.; Santorelli, F.M. 2008: A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy. Journal of Neurology 255(7): 1090-1092
Wong, D.W.-S.; Leung, E.L.-H.; Wong, S.K.-M.; Tin, V.P.-C.; Sihoe, A.D.-L.; Cheng, L.-C.; Au, J.S.-K.; Chung, L.-P.; Wong, M.P. 2011: A novel KIF5B-ALK variant in nonsmall cell lung cancer. Cancer 117(12): 2709-2718
Sivori, S.; Falco, M.; Carlomagno, S.; Romeo, E.; Soldani, C.; Bensussan, A.; Viola, A.; Moretta, L.; Moretta, A. 2010: A novel KIR-associated function: evidence that CpG DNA uptake and shuttling to early endosomes is mediated by KIR3DL2. Blood 116(10): 1637-1647
Zhen, J.-X.; Wang, D.-M.; Deng, Z.-H. 2014: A novel KIR2DL3 allele, KIR2DL3*026, found in an individual from a southern Chinese Han population. Tissue Antigens 84(6): 591-592
Zhen, J.-X.; Deng, Z.-H. 2014: A novel KIR2DL3 allele, KIR2DL3*027, identified in an individual from a southern Chinese Han population. Tissue Antigens 84(6): 592-594
Zhao, J.; Zhen, J.-X.; Deng, Z.-H. 2014: A novel KIR2DL3 variant allele, KIR2DL3*031, identified from a southern Chinese Han individual. Tissue Antigens 84(4): 429-430
Zhen, J.-X.; Xu, Y.-P.; Deng, Z.-H. 2014: A novel KIR2DL3*00110 allele identified in a southern Chinese Han individual. Tissue Antigens 84(4): 424-426
Yindom, L.-M.; Wang, L.; Dong, T.; Rowland-Jones, S.L. 2014: A novel KIR3DL1*0070104 allele found in individuals from Asia. Tissue Antigens 83(3): 204-206
Yindom, L.-M.; de Silva, T.I.; Rowland-Jones, S.L. 2014: A novel KIR3DL1*0200102 allele isolated from a West African donor by sequence-based typing. Tissue Antigens 83(4): 305-306
Yindom, L.-M.; Wang, L.; Xu, K.; Dong, T.; Rowland-Jones, S.L. 2014: A novel KIR3DS1*0130107 allele isolated by sequencing from an Asian donor. International Journal of Immunogenetics 41(3): 267-268
Yang, B.; Yang, Q.; Yan, H.; Sun, T.; Wu, N. 2013: A novel KIT frame-shift mutation in a large Chinese family with variably severe phenotypes of piebaldism. Journal of Dermatology 40(2): 126-127
Yin, X.-Y.; Ren, Y.-Q.; Yang, S.; Xu, S.-X.; Zhou, F.-S.; Du, W.-H.; Lin, D.; Wang, P.-G.; Zhang, S.-M.; Zhang, X.-J. 2009: A novel KIT missense mutation in one Chinese family with piebaldism. Archives of Dermatological Research 301(5): 387-389
Smrž, D.; Bandara, G.; Zhang, S.; Mock, B.A.; Beaven, M.A.; Metcalfe, D.D.; Gilfillan, A.M. 2013: A novel KIT-deficient mouse mast cell model for the examination of human KIT-mediated activation responses. Journal of Immunological Methods 390(1-2): 52-62
Shi, M.; Cui, J.; Du, J.; Wei, D.; Jia, Z.; Zhang, J.; Zhu, Z.; Gao, Y.; Xie, K. 2014: A novel KLF4/LDHA signaling pathway regulates aerobic glycolysis in and progression of pancreatic cancer. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 20(16): 4370-4380
He, Z.; Cai, J.; Lim, J.-W.; Kroll, K.; Ma, L. 2011: A novel KRAB domain-containing zinc finger transcription factor ZNF431 directly represses Patched1 transcription. Journal of Biological Chemistry 286(9): 7279-7289
Lee, Y.-W.; Lee, S.-T.; Cha, J.-G.; Park, J.-H.; Jeon, B.R.; Lee, Y.K.; Kim, J.-W.; Ki, C.-S. 2010: A novel KRIT1 gene mutation in a patient with cerebral and multiple spinal cavernous malformations. Annals of Clinical and Laboratory Science 40(3): 290-294
Deng, W.; Yuan, P.; Lai, W.; Chen, M.; Wang, Y.; Dai, S. 2011: A novel KRT5 mutation, p.Lys199Asn, is associated with three subtypes of epidermolysis bullosa simplex phenotypes in a single Chinese family. Journal of Dermatological Science 64(3): 241-243
Li, R.; Wang, H.; Jiang, Y.; Yu, Y.; Wang, L.; Zhou, M.; Zhang, Y.; Chen, T.; Shaw, C. 2012: A novel Kazal-type trypsin inhibitor from the skin secretion of the Central American red-eyed leaf frog, Agalychnis callidryas. Biochimie 94(6): 1376-1381
Takabayashi, S.; Nishikawa, T.; Katoh, H. 2012: A novel Kit gene mutation in CF1 mice involved in the extracellular domain of the KIT protein. Experimental Animals 61(4): 435-444
Fu, W.-F.; Li, H.-J.; Wang, D.-H.; Zhou, L.-J.; Li, L.; Gan, X.; Xu, Q.-Q.; Song, H.-B. 2009: A novel Kolbe reaction pathway for a selective one- and two-electron reduction of azo compounds. Chemical Communications 37: 5524-5526
Kino, K.; Arai, T.; Tateiwa, D. 2010: A novel L-amino acid ligase from Bacillus subtilis NBRC3134 catalyzed oligopeptide synthesis. Bioscience Biotechnology and Biochemistry 74(1): 129-134
Kino, K.; Kotanaka, Y.; Arai, T.; Yagasaki, M. 2009: A novel L-amino acid ligase from Bacillus subtilis NBRC3134, a microorganism producing peptide-antibiotic rhizocticin. Bioscience Biotechnology and Biochemistry 73(4): 901-907
Yang, C.-A.; Cheng, C.-H.; Lo, C.-T.; Liu, S.-Y.; Lee, J.-W.; Peng, K.-C. 2011: A novel L-amino acid oxidase from Trichoderma harzianum ETS 323 associated with antagonism of Rhizoctonia solani. Journal of Agricultural and Food Chemistry 59(9): 4519-4526
Choi, H.-I.; Park, J.-I.; Kim, H.-J.; Kim, D.-W.; Kim, S.-S. 2009: A novel L-ascorbic acid and peptide conjugate with increased stability and collagen biosynthesis. Bmb Reports 42(11): 743-746
Li, Y.; Kawakami, N.; Ogola, H.J.O.; Ashida, H.; Ishikawa, T.; Shibata, H.; Sawa, Y. 2011: A novel L-aspartate dehydrogenase from the mesophilic bacterium Pseudomonas aeruginosa PAO1: molecular characterization and application for L-aspartate production. Applied Microbiology and Biotechnology 90(6): 1953-1962
Michelow, I.C.; Dong, M.; Mungall, B.A.; Yantosca, L.M.; Lear, C.; Ji, X.; Karpel, M.; Rootes, C.L.; Brudner, M.; Houen, G.; Eisen, D.P.; Kinane, T.B.; Takahashi, K.; Stahl, G.L.; Olinger, G.G.; Spear, G.T.; Ezekowitz, R.A.B.; Schmidt, E.V. 2010: A novel L-ficolin/mannose-binding lectin chimeric molecule with enhanced activity against Ebola virus. Journal of Biological Chemistry 285(32): 24729-24739
Ogawa, J.; Kodera, T.; Smirnov, S.V.; Hibi, M.; Samsonova, N.N.; Koyama, R.; Yamanaka, H.; Mano, J.; Kawashima, T.; Yokozeki, K.; Shimizu, S. 2011: A novel L-isoleucine metabolism in Bacillus thuringiensis generating (2S,3R,4S)-4-hydroxyisoleucine, a potential insulinotropic and anti-obesity amino acid. Applied Microbiology and Biotechnology 89(6): 1929-1938
Metz, B.; Mojzita, D.; Herold, S.; Kubicek, C.P.; Richard, P.; Seiboth, B. 2013: A novel L-xylulose reductase essential for L-arabinose catabolism in Trichoderma reesei. Biochemistry 52(14): 2453-2460
Rahbari, R.; Sheahan, T.; Modes, V.; Collier, P.; Macfarlane, C.; Badge, R.M. 2009: A novel L1 retrotransposon marker for Hela cell line identification. Biotechniques 46(4): 277-284
Bogusławska, D.ża.M.; Heger, E.żb.; Listowski, M.; Wasiński, D.; Kuliczkowski, K.; Machnicka, B.; Sikorski, A.F. 2014: A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?. British Journal of Haematology 167(2): 269-271
Piccione, M.; Matina, F.; Fichera, M.; Lo Giudice, M.; Damiani, G.; Jakil, M.C.; Corsello, G. 2010: A novel L1CAM mutation in a fetus detected by prenatal diagnosis. European Journal of Pediatrics 169(4): 415-419
Arikoglu, T.; Yarali, N.; Kara, A.; Bay, A.; Bozkaya, I.O.; Tunc, B.; Percy, M.J. 2009: A novel L218P mutation in NADH-cytochrome b5 reductase associated with type I recessive congenital methemoglobinemia. Pediatric Hematology and Oncology 26(5): 381-385
Del Grande, A.; Luigetti, M.; Conte, A.; Mancuso, I.; Lattante, S.; Marangi, G.; Stipa, G.; Zollino, M.; Sabatelli, M. 2011: A novel L67P SOD1 mutation in an Italian ALS patient. Amyotrophic Lateral Sclerosis: Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 12(2): 150-152
Mazzucchelli, I.; Garofoli, F.; Decembrino, L.; Castiglia, D.; Tadini, G.; Bellingeri, A.; Borghesi, A.; Tzialla, C.; Manzoni, P.; Stronati, M. 2011: A novel LAMA3 mutation in a newborn with junctional epidermolysis bullosa herlitz type. Neonatology 99(3): 188-191
Rezk, N.L.; White, N.R.; Jennings, S.H.; Kashuba, A.D.M. 2009: A novel LC-ESI-MS method for the simultaneous determination of etravirine, darunavir and ritonavir in human blood plasma. Talanta 79(5): 1372-1378
Koivumäki, T.; Gürbüz, G.ök.; Poutanen, M.; Heinonen, M. 2012: A novel LC-MS application to investigate oxidation of peptides isolated from β-lactoglobulin. Journal of Agricultural and Food Chemistry 60(27): 6799-6805
Plumb, R.S.; Mather, J.; Little, D.; Rainville, P.D.; Twohig, M.; Harland, G.; Kenny, D.J.; Nicholson, J.K.; Wilson, I.D.; Kass, I.J. 2010: A novel LC-MS approach for the detection of metabolites in DMPK studies. Bioanalysis 2(10): 1767-1778
Xu, Z.; Gao, S.; Cai, F.; Zhang, F.; Jiang, W.; Liu, X.; Chen, W. 2014: A novel LC-MS/MS method for determination of tissue distribution and excretion of timosaponin B-Ii in rat biological matrices. Biomedical Chromatography: Bmc 28(7): 1011-1016
Matta, M.K.; Burugula, L.; Pilli, N.R.; Inamadugu, J.K.; J V L N, S.R. 2012: A novel LC-MS/MS method for simultaneous quantification of tenofovir and lamivudine in human plasma and its application to a pharmacokinetic study. Biomedical Chromatography: Bmc 26(10): 1202-1209
Johnson, C.; Edison, B.; Brouda, I.; Green, B. 2009: A novel LCD (coal tar) solution for psoriasis does not discolor naturally light or color-processed hair in an exaggerated exposure test model. Journal of Cosmetic Dermatology 8(3): 211-215
Ciotti, P.; Luigetti, M.; Geroldi, A.; Capponi, S.; Pezzini, I.; Gulli, R.; Pazzaglia, C.; Padua, L.; Massa, R.; Mandich, P.; Bellone, E. 2014: A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease. Journal of the Neurological Sciences 343(1-2): 183-186
Luigetti, M.; Fabrizi, G.M.; Taioli, F.; Del Grande, A.; Lo Monaco, M. 2014: A novel LITAF/SIMPLE variant within a family with minimal demyelinating Charcot-Marie-Tooth disease. Neurological Sciences: Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 35(12): 2005-2007
Kim, H.Y.; Ki, C.-S.; Kang, S.-J.; Khang, S.K.; Koh, S.-H.; Kim, D.-W.; Kim, S.H.; Sung, I.-H. 2008: A novel LMNA gene mutation Leu162Pro and the associated clinical characteristics in a family with autosomal-dominant emery-dreifuss muscular dystrophy. Muscle and Nerve 38(4): 1336-1339
Botto, N.; Vittorini, S.; Colombo, M.Giovanna.; Biagini, A.; Paradossi, U.; Aquaro, G.; Andreassi, M.Grazia. 2010: A novel LMNA mutation (R189W) in familial dilated cardiomyopathy: evidence for a 'hot spot' region at exon 3: a case report. Cardiovascular Ultrasound 8: 9
Mao, Y.; Zhang, D.-W.; Wen, J.; Cao, Q.; Chen, R.-J.; Zhu, J.; Feng, Z.-Q. 2012: A novel LMP1 antibody synergizes with mitomycin C to inhibit nasopharyngeal carcinoma growth in vivo through inducing apoptosis and downregulating vascular endothelial growth factor. International Journal of Molecular Sciences 13(2): 2208-2218
Oshimo, T.; Fukai, K.; Higashi, N.; Kitano, T.; Imai, Y.; Shintaku, H.; Ishii, M. 2008: A novel LMX1B nonsense mutation in a family with nail-patella syndrome. Journal of Dermatological Science 52(1): 57-60
Bankston, J.R.; Sampson, K.J.; Kateriya, S.; Glaaser, I.W.; Malito, D.L.; Chung, W.K.; Kass, R.S. 2007: A novel LQT-3 mutation disrupts an inactivation gate complex with distinct rate-dependent phenotypic consequences. Channels 1(4): 273-280
Wang, L.; Guo, J.-f.; Nie, L.-l.; Xu, Q.; Zuo, X.; Sun, Q.-y.; Yan, X.-x.; Tang, B.-s. 2010: A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease. Neuroscience Letters 468(3): 198-201
Haubenberger, D.; Bonelli, S.; Hotzy, C.; Leitner, P.; Lichtner, P.; Samal, D.; Katzenschlager, R.; Djamshidian, A.; Brücke, T.; Steffelbauer, M.; Bancher, C.; Grossmann, J.; Ransmayr, G.; Strom, T.M.; Meitinger, T.; Gasser, T.; Auff, E.; Zimprich, A. 2007: A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease. Movement Disorders: Official Journal of the Movement Disorder Society 22(11): 1640-1643
Pesquero, N.C.; Gongora-Rubio, M.ár.R.; Yamanaka, H. 2013: A novel LTCC electrochemical cell construction and characterization: a detection compartment for portable devices. Analyst 138(15): 4298-4304
Kwon, J.; Cho, H.J.; Han, S.H.; No, J.G.; Kwon, J.Y.; Kim, H. 2010: A novel LZAP-binding protein, NLBP, inhibits cell invasion. Journal of Biological Chemistry 285(16): 12232-12240
Chen, W.-X.; Liu, Q.-P.; Zhuang, G.-L.; Zhou, S.-J. 2013: A novel La(III)-based metal-organic framework (MOF) with a new topology: poly[diaquabis(μ5-2,5-dioxopiperazine-1,4-diacetato)(μ2-oxalato)dilanthanum(III). Acta Crystallographica. Section C Crystal Structure Communications 69(Part 1): 5-7
Ruiz-Barba, J.é L.; Jiménez-Díaz, R. 2012: A novel Lactobacillus pentosus-paired starter culture for Spanish-style green olive fermentation. Food Microbiology 30(1): 253-259
Watson, E.; Clark, E.M.; Alberdi, M.P.; Inglis, N.F.; Porter, M.; Imrie, L.; McLean, K.; Manson, E.; Lainson, A.; Smith, D.G.E. 2011: A novel Lawsonia intracellularis autotransporter protein is a prominent antigen. Clinical and Vaccine Immunology: Cvi 18(8): 1282-1287
Bringmann, G.; Thomale, K.; Bischof, S.; Schneider, C.; Schultheis, M.; Schwarz, T.; Moll, H.; Schurigt, U. 2013: A novel Leishmania major amastigote assay in 96-well format for rapid drug screening and its use for discovery and evaluation of a new class of leishmanicidal quinolinium salts. Antimicrobial Agents and ChemoTherapy 57(7): 3003-3011
Wong, K.-S.; Cheung, M.-K.; Au, C.-H.; Kwan, H.-S. 2013: A novel Lentinula edodes laccase and its comparative enzymology suggest guaiacol-based laccase engineering for bioremediation. Plos one 8(6): E66426
Wang, S.; Chai, Z.; Zhou, S.; Wang, S.; Zhu, X.; Wei, Y. 2013: A novel Lewis acid catalyzed [3 + 3]-annulation strategy for the syntheses of tetrahydro-β-carbolines and tetrahydroisoquinolines. Organic Letters 15(11): 2628-2631
Geldenhuys, W.J.; Aring, D.; Sadana, P. 2014: A novel Lipoprotein lipase (LPL) agonist rescues the enzyme from inhibition by angiopoietin-like 4 (ANGPTL4). Bioorganic and Medicinal Chemistry Letters 24(9): 2163-2167
Van Pijkeren, J.P.; Morrissey, D.; Monk, I.R.; Cronin, M.; Rajendran, S.; O'Sullivan, G.C.; Gahan, C.G.M.; Tangney, M. 2010: A novel Listeria monocytogenes-based DNA delivery system for cancer gene therapy. Human Gene Therapy 21(4): 405-416
Liu, J.; Li, Q.-J.; Zhang, W. 2010: A novel Locally Linear Embedding and Wavelet Transform based encoding method for prediction of MHC-Ii binding affinity. Interdisciplinary Sciences Computational Life Sciences 2(2): 145-150
Gizeli, E.; Stevenson, A.C.; Goddard, N.J.; Lowe, C.R. 1992: A novel Love-plate acoustic sensor utilizing polymer overlayers. IEEE Transactions on Ultrasonics Ferroelectrics and Frequency Control 39(5): 657-659
Hosseini, M.; Ganjali, M.R.; Rafiei-Sarmazdeh, Z.; Faridbod, F.; Goldooz, H.; Badiei, A.; Nourozi, P.; Ziarani, G.M. 2013: A novel Lu3+ fluorescent nano-chemosensor using new functionalized mesoporous structures. Analytica Chimica Acta 771: 95-101
Nakhro, K.; Park, J.-M.; Kim, Y.J.; Yoon, B.R.; Yoo, J.H.; Koo, H.; Choi, B.-O.; Chung, K.W. 2013: A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2L. Neuromuscular Disorders: Nmd 23(8): 656-663
Xu, X.-g.; Hong, X.-z.; Liu, Y.; Zhu, F.-m.; Lv, H.-j.; Yan, L.-x. 2009: A novel M142T mutation in the B glycosyltransferase gene associated with B3 variant in Chinese. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 26(3): 254-257
Matos, T.D.; Caria, H.; Simões-Teixeira, H.; Aasen, T.; Dias, O.; Andrea, M.; Kelsell, D.P.; Fialho, G. 2008: A novel M163L mutation in connexin 26 causing cell death and associated with autosomal dominant hearing loss. Hearing Research 240(1-2): 87-92
Leclerc, D.; Rivest, M.; Babin, C.; López-Macias, C.; Savard, P. 2013: A novel M2e based flu vaccine formulation for dogs. Plos one 8(10): E77084
Miller, P.C.; Clarke, J.; Koru-Sengul, T.; Brinkman, J.; El-Ashry, D. 2015: A novel MAPK-microRNA signature is predictive of hormone-therapy resistance and poor outcome in ER-positive breast cancer. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 21(2): 373-385
Lladó, A.; Ezquerra, M.; Sánchez-Valle, R.; Rami, L.; Tolosa, E.; Molinuevo, J.L. 2007: A novel MAPT mutation (P301T) associated with familial frontotemporal dementia. European Journal of Neurology 14(8): E9-10
Villa, C.; Ghezzi, L.; Pietroboni, A.M.; Fenoglio, C.; Cortini, F.; Serpente, M.; Cantoni, C.; Ridolfi, E.; Marcone, A.; Benussi, L.; Ghidoni, R.; Jacini, F.; Arighi, A.; Fumagalli, G.G.; Mandelli, A.; Binetti, G.; Cappa, S.; Bresolin, N.; Scarpini, E.; Galimberti, D. 2011: A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia. Journal of Alzheimer's Disease: Jad 26(1): 19-26
Iyer, A.; Lapointe, N.E.; Zielke, K.; Berdynski, M.; Guzman, E.; Barczak, A.; Chodakowska-Żebrowska, M.łg.; Barcikowska, M.; Feinstein, S.; Zekanowski, C. 2013: A novel MAPT mutation, G55R, in a frontotemporal dementia patient leads to altered Tau function. Plos one 8(9): E76409
Herr, R.; Wöhrle, F.U.; Danke, C.; Berens, C.; Brummer, T. 2011: A novel MCF-10A line allowing conditional oncogene expression in 3D culture. Cell Communication and Signaling: Ccs 9: 17
Keyomarsi, K. 2008: A novel MCM-2 fragment with potential biological function in senescence. Cell Cycle 7(22): 3480
Gavvovidis, I.; Rost, I.; Trimborn, M.; Kaiser, F.J.; Purps, J.; Wiek, C.; Hanenberg, H.; Neitzel, H.; Schindler, D. 2012: A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cells. Plos one 7(8): E40387
Halwachs, S.; Wassermann, L.; Honscha, W. 2014: A novel MDCKIi in vitro model for assessing ABCG2-drug interactions and regulation of ABCG2 transport activity in the caprine mammary gland by environmental pollutants and pesticides. Toxicology in Vitro: An International Journal Published in Association with Bibra 28(3): 432-441
Johnston, T.H.; Millar, Z.; Huot, P.; Wagg, K.; Thiele, S.; Salomonczyk, D.; Yong-Kee, C.J.; Gandy, M.N.; McIldowie, M.; Lewis, K.D.; Gomez-Ramirez, J.; Lee, J.; Fox, S.H.; Martin-Iverson, M.; Nash, J.E.; Piggott, M.J.; Brotchie, J.M. 2012: A novel MDMA analogue, UWA-101, that lacks psychoactivity and cytotoxicity, enhances L-DOPA benefit in parkinsonian primates. FASEB Journal 26(5): 2154-2163
Crouthamel, M.H.; Wu, D.; Yang, Z.; Ho, R.J.Y. 2010: A novel MDR1 GT1292-3TG (Cys431Leu) genetic variation and its effect on P-glycoprotein biologic functions. Aaps Journal 12(4): 548-555
Braga, E.; Loginov, W.; Khodyrev, D.; Pronina, I.; Kazubskaya, T.; Bogatyrova, O.; Kashuba, V.I.; Senchenko, V.N.; Klein, G.; Lerman, M.I.; Kisselev, L.L.; Zabarovsky, E.R. 2011: A novel MECA3 region in human 3p21.3 harboring putative tumor suppressor genes and oncogenes. Experimental Oncology 33(1): 33-41
Khajuria, R.; Gupta, N.; Sapra, S.; Gulati, S.; Ghosh, M.; Kalra, V.; Kabra, M. 2011: A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosis. Journal of Child Neurology 26(2): 209-213
Fendri-Kriaa, N.èn.; Abdelkafi, Z.; Rebeh, I.B.; Kamoun, F.; Triki, C.; Fakhfakh, F. 2009: A novel MECP2 gene mutation in a Tunisian patient with Rett syndrome. Genetic Testing and Molecular Biomarkers 13(1): 109-113
Jülich, K.; Horn, D.; Burfeind, P.; Erler, T.; Auber, B. 2009: A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism. Journal of Pediatrics 155(1): 140-143