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

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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

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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

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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

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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

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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

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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

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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

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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

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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