Section 66

EurekaMag Full Text Articles Chapter 65,341


Wolff, R.K.; Hoffman, M.D.; Wolff, E.C.; Herrick, J.S.; Sakoda, L.C.; Samowitz, W.S.; Slattery, M.L. 2018: Mutation analysis of adenomas and carcinomas of the colon: Early and late drivers. Genes Chromosomes and Cancer 57(7): 366-376
Shah, N.D.; Shah, P.S.; Panchal, Y.Y.; Katudia, K.H.; Khatri, N.B.; Ray, H.Shankar.P.; Bhatiya, U.R.; Shah, S.C.; Shah, B.S.; Rao, M.V. 2018: Mutation analysis of BRCA1/2 mutations with special reference to polymorphic SNPs in Indian breast cancer patients. Application of Clinical Genetics 11: 59-67
Rubino, E.; Zhang, M.; Mongini, T.; Boschi, S.; Vercelli, L.; Vacca, A.; Govone, F.; Gai, A.; Giordana, M.T.; Grinberg, M.; Rogaeva, E.; Rainero, I. 2018: Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy. Neurobiology of Aging 66: 181.E1-181.E2
Wang, K.Jie.; Zha, X.; Chen, D.Dou.; Zhu, S.Quan. 2018: Mutation Analysis of Families with Autosomal Dominant Congenital Cataract: A Recurrent Mutation in the CRYBA1/A3 Gene Causing Congenital Nuclear Cataract. Current Eye Research 43(3): 304-307
Jiang, L.; Zhang, D.; Xiao, Y.; Wang, Q.; Gong, B.; Guo, X.; Huang, M.; Yang, Z. 2018: Mutation analysis of FBN1 gene in a child with Marfan syndrome. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 35(3): 414-417
Fan, W.L.; Shi, W.W.; Wang, B.B.; Zheng, B.J.; Xue, L.; Tang, X.W.; Guan, M.X. 2017: Mutation analysis of GJB2 gene in 1 822 patients with nonsyndromic hearing loss in Zhejiang Province. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi 31(5): 352-355
Dai, Y.; Wang, C.; Nie, Z.; Han, J.; Chen, T.; Zhao, X.; Ai, C.; Ji, Y.; Gao, T.; Jiang, P. 2018: Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel. Biomedical Reports 8(1): 51-58
Emelyanov, A.K.; Usenko, T.S.; Tesson, C.; Senkevich, K.A.; Nikolaev, M.A.; Miliukhina, I.V.; Kopytova, A.E.; Timofeeva, A.A.; Yakimovsky, A.F.; Lesage, S.; Brice, A.; Pchelina, S.N. 2018: Mutation analysis of Parkinson's disease genes in a Russian data set. Neurobiology of Aging 71: 267.E7-267.E10
Droździok, K.; Kabiesz, J.; Tomsia, M.; Skowronek, R.ł; Rębała, K. 2018: Mutation analysis of short tandem repeats in a population sample from Upper Silesia (southern Poland). Legal Medicine 33: 1-4
Nonose, R.W.; Lezirovitz, K.; de Mello Auricchio, M.T.B.; Batissoco, A.C.; Yamamoto, G.L.; Mingroni-Netto, R.C.él. 2018: Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects. Bmc Medical Genetics 19(1): 73
Tan, Q.; Ku, W.; Zhang, C.; Heyilimu, P.; Tian, Y.; Ke, Y.; Lu, Z. 2018: Mutation analysis of the EBV-lymphoblastoid cell line cautions their use as antigen-presenting cells. Immunology and Cell Biology 96(2): 204-211
Saida, K.; Murase, T.; Ito, M.; Fujii, K.; Takino, H.; Masaki, A.; Kawakita, D.; Ijichi, K.; Tada, Y.; Kusafuka, K.; Iida, Y.; Onitsuka, T.; Yatabe, Y.; Hanai, N.; Hasegawa, Y.; Shinomiya, H.; Nibu, K.-I.; Shimozato, K.; Inagaki, H. 2018: Mutation analysis of the EGFR pathway genes, EGFR, RAS, PIK3CA, BRAF, and AKT1, in salivary gland adenoid cystic carcinoma. Oncotarget 9(24): 17043-17055
Schwarzová, L.; Horinek, A.; Hubacek, J.; Zlatohlavek, L.; Vaclova, M.; Ceska, R.; Vrablik, M. 2018: Mutation analysis of the LDLR gene in Czech hypercholesterolemic patients. Atherosclerosis 263: E234-E234
Heidari, M.M.; Derakhshani, M.; Sedighi, F.; Foruzan-Nia, S.K. 2017: Mutation Analysis of the Mitochondrial tRNA Genes in Iranian Coronary Atherosclerosis Patients. Iranian Journal of Public Health 46(10): 1379-1385
Vieira Neto, E.; Laranjeira, F.; Quelhas, D.; Ribeiro, I.; Seabra, A.; Mineiro, N.; D M Carvalho, L.; Lacerda, L.úc.; G Ribeiro, M.ár. 2018: Mutation analysis of the PAH gene in phenylketonuria patients from Rio de Janeiro, Southeast Brazil. Molecular Genetics and Genomic Medicine 2018
Wang, L.; Wang, X.; He, B.; Cai, N.; Li, W.; Lou, C.; Xin, S.; Wu, Q.; Yu, W.; Qiang, R. 2017: Mutation analysis of the phenylalanine hydroxylase gene and prenatal diagnosis of phenylketonuria in Shaanxi, China. Journal of Pediatric Endocrinology and Metabolism: Jpem 30(12): 1305-1310
Nishiyama, T.; Ishikawa, Y.; Kawashima, N.; Akashi, A.; Adachi, Y.; Hattori, H.; Ushijima, Y.; Kiyoi, H. 2018: Mutation analysis of therapy-related myeloid neoplasms. Cancer Genetics 222-223: 38-45
Yuan, Z.; Jiao, B.; Hou, L.; Xiao, T.; Liu, X.; Wang, J.; Xu, J.; Zhou, L.; Yan, X.; Tang, B.; Shen, L. 2018: Mutation analysis of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis and frontotemporal dementia. Neurobiology of Aging 64: 160.E9-160.E12
Wang, A-Cong.; Zhang, Y-Song.; Wang, B-Song.; Zhao, X-Yu.; Wu, F-Xia.; Zhai, X-Hong.; Sun, J-Xiang.; Mei, S-Yue. 2018: Mutation analysis of the TUBB8 gene in primary infertile women with arrest in oocyte maturation. Gynecological Endocrinology: the Official Journal of the International Society of Gynecological Endocrinology 34(10): 900-904
Hu, T.-M.; Ping, L.-Y.; Hsu, S.-H.; Tsai, H.-Y.; Cheng, M.-C. 2018: Mutation analysis of the WNT7A gene in patients with schizophrenia. Psychiatry Research 265: 246-248
Feng, Y.; Mei, S.Y.; Liu, N.; Guo, R.X. 2018: Mutation analysis of VWF gene in two patients with von Willebrand disease by target sequence capture and high-throughput sequencing technology. Zhonghua Xue Ye Xue Za Zhi 39(3): 242-244
Yu, H.Jin.; Lee, Y.Ju.; Shim, J.Won.; Kim, D.Soo.; Shim, J.Yeon.; Park, M.Soo.; Woo, H.Yeon.; Park, H.; Jung, H.Lim.; Kwon, M.Jung. 2018: Mutation Analysis of X-linked Sideroblastic Anemia in a 12-Month-Old Boy by Massively Parallel Sequencing. Annals of Laboratory Medicine 38(4): 389-392
Lyons, D.M.; Lauring, A.S. 2018: Mutation and Epistasis in Influenza Virus Evolution. Viruses 10(8)
Liu, F.; Yang, Y.; Zheng, Y.; Liang, Y.-H.; Zeng, K. 2018: Mutation and expression of ABCA12 in keratosis pilaris and nevus comedonicus. Molecular Medicine Reports 18(3): 3153-3158
Wang, S.; Luo, Q.; Liu, J.; Liu, L.; Chen, X. 2018: Mutation and fermentation optimization of Bacillus amyloliquefaciens for acetoin production. Sheng Wu Gong Cheng Xue Bao 34(5): 803-811
Boeckx, N.; Op de Beeck, K.; Beyens, M.; Deschoolmeester, V.; Hermans, C.; De Clercq, P.; Garrigou, S.; Normand, C.; Monsaert, E.; Papadimitriou, K.; Laurent-Puig, P.; Pauwels, P.; Van Camp, G.; Taly, V.; Peeters, M. 2018: Mutation and Methylation Analysis of Circulating Tumor DNA can be Used for Follow-up of Metastatic Colorectal Cancer Patients. Clinical Colorectal Cancer 17(2): E369-E379
Yamaguchi, H. 2018: Mutation breeding of ornamental plants using ion beams. Breeding Science 68(1): 71-78
Domingo, E.; Camps, C.; Kaisaki, P.J.; Parsons, M.J.; Mouradov, D.; Pentony, M.M.; Makino, S.; Palmieri, M.; Ward, R.L.; Hawkins, N.J.; Gibbs, P.; Askautrud, H.; Oukrif, D.; Wang, H.; Wood, J.; Tomlinson, E.; Bark, Y.; Kaur, K.; Johnstone, E.C.; Palles, C.; Church, D.N.; Novelli, M.; Danielsen, H.E.; Sherlock, J.; Kerr, D.; Kerr, R.; Sieber, O.; Taylor, J.C.; Tomlinson, I. 2018: Mutation burden and other molecular markers of prognosis in colorectal cancer treated with curative intent: results from the QUASAR 2 clinical trial and an Australian community-based series. Lancet. Gastroenterology and Hepatology 3(9): 635-643
Syama, A.; Sen, S.; Kota, L.N.; Viswanath, B.; Purushottam, M.; Varghese, M.; Jain, S.; Panicker, M.M.; Mukherjee, O. 2018: Mutation burden profile in familial Alzheimer's disease cases from India. Neurobiology of Aging 64: 158.E7-158.E13
De Figueiredo Barros, B.D.; Kupper, B.E.C.; Aguiar Junior, S.; de Mello, C.A.L.; Begnami, M.D.; Chojniak, R.; de Souza, S.J.; Torrezan, G.T.; Carraro, D.M. 2018: Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient with Metastatic Colorectal Cancer. Frontiers in Oncology 8: 306
Kammesheidt, A.; Tonozzi, T.R.; Lim, S.W.; Braunstein, G.D. 2018: Mutation detection using plasma circulating tumor DNA (ctDNA) in a cohort of asymptomatic adults at increased risk for cancer. International Journal of Molecular Epidemiology and Genetics 9(1): 1-12
Sanz-García, F.; Hernando-Amado, S.; Martínez, J.é L. 2018: Mutation-Driven Evolution of Pseudomonas aeruginosa in the Presence of either Ceftazidime or Ceftazidime-Avibactam. Antimicrobial Agents and ChemoTherapy 62(10)
Robert, L.; Ollion, J.; Robert, J.; Song, X.; Matic, I.; Elez, M. 2018: Mutation dynamics and fitness effects followed in single cells. Science 359(6381): 1283-1286
Mugweru, J.; Liu, J.; Makafe, G.; Chiwala, G.; Wang, B.; Wang, C.; Li, X.; Tan, Y.; Yew, W.W.; Tan, S.; Zhang, T. 2018: Mutation EthAW21R confers co-resistance to prothionamide and ethionamide in both Mycobacterium bovis BCG and Mycobacterium tuberculosis H37Rv. Infection and Drug Resistance 11: 891-894
Kretova, O.V.; Gorbacheva, M.A.; Fedoseeva, D.M.; Kravatsky, Y.V.; Chechetkin, V.R.; Tchurikov, N.A. 2018: Mutation Frequencies in HIV-1 Genome in Regions Containing Efficient RNAi Targets as Calculated from Ultra-Deep Sequencing Data. Molekuliarnaia Biologiia 52(3): 460-465
Kretova, O.V.; Gorbacheva, M.A.; Fedoseeva, D.M.; Kravatskya, Y.V.; Chechetkin, V.R.; Tchurikov, N.A. 2018: Mutation Frequencies in RNAi Targets in HIV-1 Genomes Obtained from Blood Plasma of Patients Receiving Anti-Retroviral Therapy. Molekuliarnaia Biologiia 52(4): 591-594
Sicinska, W.; Gront, D.; Sicinski, K. 2018: Mutation goals in the vitamin D receptor predicted by computational methods. Journal of Steroid Biochemistry and Molecular Biology 183: 210-220
Lee, H.H.; Kim, S.Y.; Jung, E.S.; Yoo, J.; Kim, T.-M. 2019: Mutation heterogeneity between primary gastric cancers and their matched lymph node metastases. Gastric Cancer: Official Journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 22(2): 323-334
Bodian, D.L.; Schreiber, J.M.; Vilboux, T.; Khromykh, A.; Hauser, N.S. 2018: Mutation in an alternative transcript of CDKL5 in a boy with early-onset seizures. Cold Spring Harbor Molecular Case Studies 4(3)
Fortuny, C.éc.; Flannery, J.G. 2018: Mutation-Independent Gene Therapies for Rod-Cone Dystrophies. Advances in Experimental Medicine and Biology 1074: 75-81
Cideciyan, A.V.; Sudharsan, R.; Dufour, V.ér.L.; Massengill, M.T.; Iwabe, S.; Swider, M.; Lisi, B.; Sumaroka, A.; Marinho, L.F.; Appelbaum, T.; Rossmiller, B.; Hauswirth, W.W.; Jacobson, S.G.; Lewin, A.S.; Aguirre, G.D.; Beltran, W.A. 2018: Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector. Proceedings of the National Academy of Sciences of the United States of America 115(36): E8547-E8556
Largo, E.; Gladue, D.P.; Torralba, J.; Aguilella, V.M.; Alcaraz, A.; Borca, M.V.; Nieva, J.é L. 2018: Mutation-induced changes of transmembrane pore size revealed by combined ion-channel conductance and single vesicle permeabilization analyses. Biochimica et Biophysica Acta. Biomembranes 1860(5): 1015-1021
Poidevin, M.ël.; Sato, M.; Altinoglu, I.; Delaplace, M.; Sato, C.; Yamaichi, Y. 2018: Mutation in ESBL Plasmid from Escherichia coli O104:H4 Leads Autoagglutination and Enhanced Plasmid Dissemination. Frontiers in Microbiology 9: 130
Sugihara, A.; Nguyen, L.C.; Shamim, H.M.; Iida, T.; Nakase, M.; Takegawa, K.; Senda, M.; Jida, S.; Ueno, M. 2018: Mutation in fission yeast phosphatidylinositol 4-kinase Pik1 is synthetically lethal with defect in telomere protection protein Pot1. Biochemical and Biophysical Research Communications 496(4): 1284-1290
Futterer, J.; Dalby, A.; Lowe, G.C.; Johnson, B.; Simpson, M.A.; Motwani, J.; Williams, M.; Watson, S.P.; Morgan, N.V. 2018: Mutation in GNE is associated with severe congenital thrombocytopenia. Blood 132(17): 1855-1858
Zimenkov, D. 2018: Mutation in luxR Family Transcriptional Regulator Rv0890c Is not a Marker of Linezolid Resistance. Antimicrobial Agents and ChemoTherapy 62(3)
Yao, H.; Ji, C.-C.; Cheng, Y.-J.; Chen, X.-M.; Liu, L.-J.; Fan, J.; Wu, S.-H. 2018: Mutation in KCNE1 associated to early repolarization syndrome by modulation of slowly activating delayed rectifier K+ current. Experimental Cell Research 363(2): 315-320
Cuchanski, M.; Baldwin, K.J. 2018: Mutation in KIF5A c.610C>T Causing Hereditary Spastic Paraplegia with Axonal Sensorimotor Neuropathy. Case Reports in Neurology 10(2): 165-168
Haehner, A.; Hummel, T.; Heinritz, W.; Krueger, S.; Meinhardt, M.; Whitcroft, K.L.; Sabatowski, R.; Gossrau, G. 2018: Mutation in Nav 1.7 causes high olfactory sensitivity. European Journal of Pain 22(10): 1767-1773
Burden, C.J.; Wei, Y. 2018: Mutation in populations governed by a Galton-Watson branching process. Theoretical Population Biology 120: 52-61
Liao, Y.; Bai, Q.; Xu, P.; Wu, T.; Guo, D.; Peng, Y.; Zhang, H.; Deng, X.; Chen, X.; Luo, M.; Ali, A.; Wang, W.; Wu, X. 2018: Mutation in Rice Abscisic Acid2 Results in Cell Death, Enhanced Disease-Resistance, Altered Seed Dormancy and Development. Frontiers in Plant Science 9: 405
Alkhunaizi, E.; Walkiewicz, M.A.; Chitayat, D. 2018: Mutation in the ADNP gene associated with Noonan syndrome features. Clinical Dysmorphology 27(2): 53-57
Krim, E.; Aupy, J.; Clot, F.; Bonnan, M.; Burbaud, P.; Guehl, D. 2018: Mutation in the GCH1 gene with dopa-responsive dystonia and phenotypic variability. Neurology. Genetics 4(2): E231
Lipa, P.; Vinardell, J.é-M.ía.; Kopcińska, J.; Zdybicka-Barabas, A.; Janczarek, M. 2018: Mutation in the pssZ Gene Negatively Impacts Exopolysaccharide Synthesis, Surface Properties, and Symbiosis of Rhizobium leguminosarum bv. trifolii with Clover. Genes 9(7)
Turovskaya, M.V.; Zinchenko, V.P.; Babaev, A.A.; Epifanova, E.A.; Tarabykin, V.S.; Turovsky, E.A. 2018: Mutation in the Sip1 transcription factor leads to a disturbance of the preconditioning of AMPA receptors by episodes of hypoxia in neurons of the cerebral cortex due to changes in their activity and subunit composition. the protective effects of interleukin-10. Archives of Biochemistry and Biophysics 654: 126-135
Rudramurthy, S.M.; Shankarnarayan, S.A.; Dogra, S.; Shaw, D.; Mushtaq, K.; Paul, R.A.; Narang, T.; Chakrabarti, A. 2018: Mutation in the Squalene Epoxidase Gene of Trichophyton interdigitale and Trichophyton rubrum Associated with Allylamine Resistance. Antimicrobial Agents and ChemoTherapy 62(5)
Ganji, V.Kumar.; Biswal, J.K.; Lalzampuia, H.; Basagoudanavar, S.H.; Saravanan, P.; Tamil Selvan, R.P.; Umapathi, V.; Reddy, G.R.; Sanyal, A.; Dechamma, H.J. 2018: Mutation in the VP2 gene of P1-2A capsid protein increases the thermostability of virus-like particles of foot-and-mouth disease virus serotype O. Applied Microbiology and Biotechnology 102(20): 8883-8893
Minegishi, Y.; Nakaya, N.; Tomarev, S.I. 2018: Mutation in the Zebrafish cct2 Gene Leads to Abnormalities of Cell Cycle and Cell Death in the Retina: a Model of CCT2-Related Leber Congenital Amaurosis. Investigative Ophthalmology and Visual Science 59(2): 995-1004
Skolnikova, E.; Sedova, L.; Krenova, D.; Kren, V.; Seda, O. 2018: Mutation in ZBTB16 gene plays a role in lipid profiles of pregnant rats and their offspring after high-sucrose diet feeding. Atherosclerosis 263: E36-E37
Wei, W.; Xiong, L.; Ye, Y.-N.; Du, M.-Z.; Gao, Y.-Z.; Zhang, K.-Y.; Jin, Y.-T.; Yang, Z.; Wong, P.-C.; Lau, S.K.P.; Kan, B.; Zhu, J.; Woo, P.C.Y.; Guo, F.-B. 2018: Mutation Landscape of Base Substitutions, Duplications, and Deletions in the Representative Current Cholera Pandemic Strain. Genome Biology and Evolution 10(8): 2072-2085
Nishimura, S.; Yamamoto, T.; Nakamura, Y.; Kohno, M.; Hamada, Y.; Sufu, Y.; Fukui, G.; Nanno, T.; Ishiguchi, H.; Kato, T.; Xu, X.; Ono, M.; Oda, T.; Okuda, S.; Kobayashi, S.; Yano, M. 2018: Mutation-linked, excessively tight interaction between the calmodulin binding domain and the C-terminal domain of the cardiac ryanodine receptor as a novel cause of catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm 15(6): 905-914
Bolen, C.R.; McCord, R.; Huet, S.; Frampton, G.M.; Bourgon, R.; Jardin, F.; Dartigues, P.; Punnoose, E.A.; Szafer-Glusman, E.; Xerri, L.; Sujobert, P.; Salles, G.; Venstrom, J.M. 2017: Mutation load and an effector T-cell gene signature may distinguish immunologically distinct and clinically relevant lymphoma subsets. Blood Advances 1(22): 1884-1890
Mukherjee, S.; Roy, M.; Guha, G.; Saha, S.P. 2018: Mutation Location and Cognitive Impairment in Duchenne Muscular Dystrophy. Journal of Neurosciences in Rural Practice 9(3): 410-413
Li, L.; Tian, T.; Zhang, X. 2018: Mutation Mechanisms of Human Breast Cancer. Journal of Computational Biology: a Journal of Computational Molecular Cell Biology 25(4): 396-404
Sun, J.; Kweon, O.; Jin, J.; He, G.-X.; Li, X.; Cerniglia, C.E.; Chen, H. 2017: Mutation network-based understanding of pleiotropic and epistatic mutational behavior of Enterococcus faecalis FMN-dependent azoreductase. Biochemistry and Biophysics Reports 12: 240-244
Monteiro, G.E.R.; Jansen van Vuren, P.; Wichgers Schreur, P.J.; Odendaal, L.; Clift, S.J.; Kortekaas, J.; Paweska, J.T. 2018: Mutation of adjacent cysteine residues in the NSs protein of Rift Valley fever virus results in loss of virulence in mice. Virus Research 249: 31-44
Suligoy, C.M.; Lattar, S.M.; Noto Llana, M.án.; González, C.D.; Alvarez, L.ía.P.; Robinson, D.A.; Gómez, M.I.; Buzzola, F.R.; Sordelli, D.O. 2018: Mutation of Agr Is Associated with the Adaptation of Staphylococcus aureus to the Host during Chronic Osteomyelitis. Frontiers in Cellular and Infection Microbiology 8: 18
Takakura, Y.; Udagawa, H.; Shinjo, A.; Koga, K. 2018: Mutation of a Nicotiana tabacum L. eukaryotic translation-initiation factor gene reduces susceptibility to a resistance-breaking strain of Potato virus Y. Molecular Plant Pathology 19(9): 2124-2133
Mutso, M.; Morro, A.M.; Smedberg, C.; Kasvandik, S.; Aquilimeba, M.; Teppor, M.; Tarve, L.; Lulla, A.; Lulla, V.; Saul, S.; Thaa, B.; McInerney, G.M.; Merits, A.; Varjak, M. 2018: Mutation of CD2AP and SH3KBP1 Binding Motif in Alphavirus nsP3 Hypervariable Domain Results in Attenuated Virus. Viruses 10(5)
Jarchi, S.; Ataei, F.; Hosseinkhani, S. 2018: Mutation of conserved residues K329 and R330 on the surface of firefly luciferase: Effect on proteolytic degradation. International Journal of Biological Macromolecules 115: 324-330
Cabaud, O.; Roubin, R.ég.; Comte, A.; Bascunana, V.; Sergé, A.; Sedjaï, F.; Birnbaum, D.; Rosnet, O.; Acquaviva, C. 2018: Mutation of FOP/FGFR1OP in mice recapitulates human short rib-polydactyly ciliopathy. Human Molecular Genetics 27(19): 3377-3391
Cheng, X.-N.; Shao, M.; Shi, D.-L. 2018: Mutation of frizzled8a delays neural retinal cell differentiation and results in microphthalmia in zebrafish. International Journal of Developmental Biology 62(4-5): 285-291
Bhattacharya, D.; Sinha, K.; Panda, D. 2018: Mutation of G51 in SepF impairs FtsZ assembly promoting ability of SepF and retards the division of Mycobacterium smegmatis cells. Biochemical Journal 475(15): 2473-2489
Chen, Y.; Xiu, W.; Dong, Y.; Wang, J.; Zhao, H.; Su, Y.; Zhou, J.; Zeng, Y.; Li, H.; Wo, J.; Lin, F.; Zhang, H.; Chen, H.; Yang, C.; Zhu, W. 2018: Mutation of glucose-6-phosphate dehydrogenase deficiency in Chinese Han children in eastern Fujian. Medicine 97(30): E11553
Aliès, B.; Borghesani, V.; Noël, S.; Sayen, S.; Guillon, E.; Testemale, D.; Faller, P.; Hureau, C. 2018: Mutations of Histidine 13 to Arginine and Arginine 5 to Glycine Are Responsible for Different Coordination Sites of Zinc(II) to Human and Murine Peptides. Chemistry 24(53): 14233-14241
Wu, S.; Lei, L.; Song, Y.; Liu, M.; Lu, S.; Lou, D.; Shi, Y.; Wang, Z.; He, D. 2018: Mutation of hop-1 and pink-1 attenuates vulnerability of neurotoxicity in C. elegans: the role of mitochondria-associated membrane proteins in Parkinsonism. Experimental Neurology 309: 67-78
Baquedano, M.S.; Guercio, G.; Costanzo, M.; Marino, R.; Rivarola, M.A.; Belgorosky, A. 2018: Mutation of HSD3B2 Gene and Fate of Dehydroepiandrosterone. Vitamins and Hormones 108: 75-123
Zhou, Y.; Wu, R.; Zhao, Q.; Chang, Y.-F.; Wen, X.; Feng, Y.; Huang, X.; Wen, Y.; Yan, Q.; Huang, Y.; Ma, X.; Han, X.; Cao, S. 2018: Mutation of I176R in the e coding region weakens Japanese encephalitis virus neurovirulence, but not its growth rate in BHK-21 cells. Archives of Virology 163(5): 1351-1355
Gao, X.; Yuan, Y.-Y.; Lin, Q.-F.; Xu, J.-C.; Wang, W.-Q.; Qiao, Y.-H.; Kang, D.-Y.; Bai, D.; Xin, F.; Huang, S.-S.; Qiu, S.-W.; Guan, L.-P.; Su, Y.; Wang, G.-J.; Han, M.-Y.; Jiang, Y.; Liu, H.-K.; Dai, P. 2018: Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss. Journal of Medical Genetics 55(5): 298-306
Purkan; Ihsanawati; Natalia, D.; Syah, Y.M.; Retnoningrum, D.S.; Kusuma, H.S. 2016: Mutation of katG in a clinical isolate of Mycobacterium tuberculosis: effects on catalase-peroxidase for isoniazid activation. Ukrainian Biochemical Journal 88(5): 71-81
Liu, N.; Sun, Y.; Wang, P.; Duan, H.; Ge, X.; Li, X.; Pei, Y.; Li, F.; Hou, Y. 2018: Mutation of key amino acids in the polygalacturonase-inhibiting proteins CkPGIP1 and GhPGIP1 improves resistance to Verticillium wilt in cotton. Plant Journal: for Cell and Molecular Biology 96(3): 546-561
Tridgett, M.; Lloyd, J.R.; Kennefick, J.; Moore-Kelly, C.; Dafforn, T.R. 2018: Mutation of M13 Bacteriophage Major Coat Protein for Increased Conjugation to Exogenous Compounds. Bioconjugate Chemistry 29(6): 1872-1875
Martinez-Monseny, A.; Bolasell, M.è; Arjona, C.; Martorell, L.; Yubero, D.; Arsmtrong, J.; Maynou, J.; Fernandez, G.; Del Carmen Salgado, M.; Palau, F.; Serrano, M. 2018: Mutation of PACS1: the milder end of the spectrum. Clinical Dysmorphology 27(4): 148-150
Fu, B.; Xu, T.; Cui, Z.; Ng, H.L.; Wang, K.; Li, J.; Li, Q.X. 2018: Mutation of Phenylalanine-223 to Leucine Enhances Transformation of Benzo[a]pyrene by Ring-Hydroxylating Dioxygenase of Sphingobium sp. FB3 by increasing Accessibility of the Catalytic Site. Journal of Agricultural and Food Chemistry 66(5): 1206-1213
Si, Z.; Liu, H.; Zhu, J.; Chen, J.; Wang, Q.; Fang, L.; Gao, F.; Tian, Y.; Chen, Y.; Chang, L.; Liu, B.; Han, Z.; Zhou, B.; Hu, Y.; Huang, X.; Zhang, T. 2018: Mutation of SELF-PRUNING homologs in cotton promotes short-branching plant architecture. Journal of Experimental Botany 69(10): 2543-2553
Martín-López, J.; Gasparini, P.; Coombes, K.; Croce, C.M.; Boivin, G.P.; Fishel, R. 2018: Mutation of TGFβ-RII eliminates NSAID cancer chemoprevention. Oncotarget 9(16): 12554-12561
Xu, Y.; Li, L.; Ren, H.-T.; Yin, B.; Yuan, J.-G.; Peng, X.-Z.; Qiang, B.-Q.; Cui, L.-Y. 2018: Mutation of the cellular adhesion molecule NECL2 is associated with neuromyelitis optica spectrum disorder. Journal of the Neurological Sciences 388: 133-138
Wu, Q.-Y.; Zhu, Y.-Y.; Wei, F.; Tong, Y.-X.; Cao, J.; Zhou, P.; Li, Z.-Y.; Zeng, L.-Y.; Li, F.; Wang, X.-Y.; Xu, K.-L. 2018: Mutation of the conserved G66 residue in GS region decreased structural stability and activity of arginine kinase. International Journal of Biological Macromolecules 111: 247-254
Pott, A.; Bock, S.; Berger, I.M.; Frese, K.; Dahme, T.; Keßler, M.; Rinné, S.; Decher, N.; Just, S.; Rottbauer, W. 2018: Mutation of the Na+/K+-ATPase Atp1a1a.1 causes QT interval prolongation and bradycardia in zebrafish. Journal of Molecular and Cellular Cardiology 120: 42-52
Zhu, X.; Shen, W.; Huang, J.; Zhang, T.; Zhang, X.; Cui, Y.; Sang, X.; Ling, Y.; Li, Y.; Wang, N.; Zhao, F.; Zhang, C.; Yang, Z.; He, G. 2018: Mutation of the OsSAC1 Gene, which Encodes an Endoplasmic Reticulum Protein with an Unknown Function, Causes Sugar Accumulation in Rice Leaves. Plant and Cell Physiology 59(3): 487-499
Brennan, S.O.; Laurie, A.D. 2018: Mutation of the -RPVR- Propeptide Motif at C-Terminal of the Aα Chain Is Associated with Decreased Fibrinogen Expression. Thrombosis and Haemostasis 118(1): 207-209
Oguma, K.; Ohno, M.; Yoshida, M.; Sentsui, H. 2018: Mutation of the S and 3c genes in genomes of feline coronaviruses. Journal of Veterinary Medical Science 80(7): 1094-1100
Wang, S.; Zhang, Y.-X.; Huang, T.; Sui, J.-N.; Lu, J.; Chen, X.-J.; Wang, K.-K.; Xi, X.-D.; Li, J.-M.; Huang, J.-Y.; Chen, B. 2018: Mutation profile and associated clinical features in Chinese patients with cytogenetically normal acute myeloid leukemia. International Journal of Laboratory Hematology 40(4): 408-418
Zhou, C.; Niu, Y.; Xu, H.; Li, Z.; Wang, T.; Yang, W.; Wang, S.; Wang, D.W.; Liu, J. 2018: Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism. Fertility and Sterility 110(3): 486-495.E5
Zhang, X.H.; Da Wang, J.; Jia, H.Y.; Zhang, J.S.; Li, Y.; Xiong, Y.; Li, J.; Li, X.X.; Huang, Y.; Zhu, G.Y.; Rong, S.S.; Wormstone, M.; Wan, X.H. 2018: Mutation profiles of congenital cataract genes in 21 northern Chinese families. Molecular Vision 24: 471-477
Zhang, Y.; Wang, F.; Chen, X.; Liu, W.; Fang, J.; Wang, M.; Teng, W.; Cao, P.; Liu, H. 2019: Mutation profiling of 16 candidate genes in de novo acute myeloid leukemia patients. Frontiers of Medicine 13(2): 229-237
Schrijver, W.A.M.E.; Selenica, P.; Lee, J.Y.; Ng, C.K.Y.; Burke, K.A.; Piscuoglio, S.; Berman, S.H.; Reis-Filho, J.S.; Weigelt, B.; van Diest, P.J.; Moelans, C.B. 2018: Mutation Profiling of Key Cancer Genes in Primary Breast Cancers and their Distant Metastases. Cancer Research 78(12): 3112-3121
Yu, X.-W.; Huang, D.-H.; Guo, J.-X.; Huang, Y.-Q.; Xie, R.-T.; Cai, J.-F. 2018: Mutation Rate and Clinical Characteristics of CALR, JAK2 V617F and MPL W515K Genes in Patients with Primary Thrombocythemia. Zhongguo Shi Yan Xue Ye Xue Za Zhi 26(3): 866-870
Wu, W.; Ren, W.; Hao, H.; Nan, H.; He, X.; Liu, Q.; Lu, D. 2018: Mutation rates at 42 y chromosomal short tandem repeats in Chinese Han population in Eastern China. International Journal of Legal Medicine 132(5): 1317-1319
Haddix, P.L.; Danderson, C.A. 2018: Mutation Rate Simulation by Dice Roll: Practice with the Drake Equation. Journal of Microbiology and Biology Education 19(2)
Posbergh, C.J.; Kalla, S.E.; Sutter, N.B.; Tennant, B.C.; Huson, H.J. 2018: Mutation responsible for congenital photosensitivity and hyperbilirubinemia in Southdown sheep. American Journal of Veterinary Research 79(5): 538-545
Pfajfer, L.èn.; Mair, N.K.; Jiménez-Heredia, R.úl.; Genel, F.; Gulez, N.; Ardeniz, Öm.ür.; Hoeger, B.; Bal, S.K.ös.; Madritsch, C.; Kalinichenko, A.; Chandra Ardy, R.; Gerçeker, B.ü; Rey-Barroso, J.; Ijspeert, H.; Tangye, S.G.; Simonitsch-Klupp, I.; Huppa, J.B.; van der Burg, M.; Dupré, L.ïc.; Boztug, K. 2018: Mutations affecting the actin regulator WD repeat-containing protein 1 lead to aberrant lymphoid immunity. Journal of Allergy and Clinical Immunology 142(5): 1589-1604.E11
Alred, E.J.; Lodangco, I.; Gallaher, J.; Hansmann, U.H.E. 2018: Mutations Alter RNA-Mediated Conversion of Human Prions. Acs Omega 3(4): 3936-3944
Haybar, H.; Khodadi, E.; Kavianpour, M.; Saki, N. 2018: Mutations and Common Polymorphisms in ADAMTS13 and vWF Genes Responsible for Increasing Risk of Thrombosis. Cardiovascular and Hematological Disorders Drug Targets 18(3): 176-181
Diez-Fernandez, C.; Rüfenacht, V.ér.; Gemperle, C.; Fingerhut, R.; Häberle, J. 2018: Mutations and common variants in the human arginase 1 (ARG1) gene: Impact on patients, diagnostics, and protein structure considerations. Human Mutation 39(8): 1029-1050
Gangat, N.; Mudireddy, M.; Lasho, T.L.; Finke, C.M.; Nicolosi, M.; Szuber, N.; Patnaik, M.M.; Pardanani, A.; Hanson, C.A.; Ketterling, R.P.; Tefferi, A. 2018: Mutations and prognosis in myelodysplastic syndromes: karyotype-adjusted analysis of targeted sequencing in 300 consecutive cases and development of a genetic risk model. American Journal of Hematology 93(5): 691-697
Martinez, E.; Hennessy, D.; Jelfs, P.; Crighton, T.; Chen, S.C.-A.; Sintchenko, V. 2018: Mutations associated with in vitro resistance to bedaquiline in Mycobacterium tuberculosis isolates in Australia. Tuberculosis 111: 31-34
Nukina, K.; Hayashi, A.; Shiomi, Y.; Sugasawa, K.; Ohtsubo, M.; Nishitani, H. 2018: Mutations at multiple CDK phosphorylation consensus sites on Cdt2 increase the affinity of CRL4 Cdt2 for PCNA and its ubiquitination activity in S phase. Genes to Cells: Devoted to Molecular and Cellular Mechanisms 23(3): 200-213
Shen, X.-M.; Brengman, J.M.; Shen, S.; Durmus, H.; Preethish-Kumar, V.; Yuceyar, N.; Vengalil, S.; Nalini, A.; Deymeer, F.; Sine, S.M.; Engel, A.G. 2018: Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunit. Jci Insight 3(2)
Hamer, G.; de Rooij, D.G. 2018: Mutations causing specific arrests in the development of mouse primordial germ cells and gonocytes. Biology of Reproduction 99(1): 75-86
Souza, V.P.; Ikegami, C.íl.M.; Arantes, G.M.; Marana, S.R. 2018: Mutations close to a hub residue affect the distant active site of a GH1 β-glucosidase. Plos one 13(6): E0198696
Pagani, I.; Di Pietro, A.; Oteiza, A.; Ghitti, M.; Mechti, N.; Naffakh, N.; Vicenzi, E. 2018: Mutations Conferring Increased Sensitivity to Tripartite Motif 22 Restriction Accumulated Progressively in the Nucleoprotein of Seasonal Influenza a (H1N1) Viruses between 1918 and 2009. Msphere 3(2)
Chen, Y.; Guo, L.; Li, C.-L.; Shan, J.; Xu, H.-S.; Li, J.-Y.; Sun, S.; Hao, S.-J.; Jin, L.; Chai, G.; Zhang, T.-Y. 2018: Mutation screening of Chinese Treacher Collins syndrome patients identified novel TCOF1 mutations. Molecular Genetics and Genomics: Mgg 293(2): 569-577
Lo, F.-S. 2018: Mutation screening of INS and KCNJ11 genes in Taiwanese children with type 1B diabetic onset before the age of 5 years. Journal of the Formosan Medical Association 117(8): 734-737
Shu, S.; Lei, X.; Liu, F.; Cui, B.; Liu, Q.; Ding, Q.; Liu, M.S.; Li, X.G.; Cui, L.; Zhang, X. 2018: Mutation screening of NEK1 in Chinese ALS patients. Neurobiology of Aging 71: 267.E1-267.E4
Che, X.-Q.; Zhao, Q.-H.; Huang, Y.; Li, X.; Ren, R.-J.; Chen, S.-D.; Guo, Q.-H.; Wang, G. 2018: Mutation Screening of the CHCHD2 Gene for Alzheimer's Disease and Frontotemporal Dementia in Chinese Mainland Population. Journal of Alzheimer's Disease: Jad 61(4): 1283-1288
Liu, Y.; Huang, Y.; Hua, R.; Zhao, X.; Yang, W.; Liu, Y.; Zhang, X. 2018: Mutation Screening of the EDA Gene in Seven Chinese Families with X-Linked Hypohidrotic Ectodermal Dysplasia. Genetic Testing and Molecular Biomarkers 22(8): 487-491
Gu, X.; Li, C.; Chen, Y.; Wei, Q.; Cao, B.; Ou, R.; Yuan, X.; Hou, Y.; Zhang, L.; Liu, H.; Wu, Y.; Song, W.; Zhao, B.; Chen, X.; Shang, H.-F. 2019: Mutation screening of the KIF5A gene in Chinese patients with amyotrophic lateral sclerosis. Journal of Neurology Neurosurgery and Psychiatry 90(2): 245-246
Hamid, M.; Ershadi Oskouei, S.; Shariati, G.; Babaei, E.; Galehdari, H.; Saberi, A.; Sedaghat, A. 2018: Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals with Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran. Journal of Pediatric Hematology/Oncology 40(3): 192-195
Gu, X.; Chen, Y.; Wei, Q.; Cao, B.; Ou, R.; Yuan, X.; Hou, Y.; Zhang, L.; Liu, H.; Chen, X.; Shang, H.-F. 2018: Mutation screening of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis/frontotemporal dementia. Neurobiology of Aging 68: 161.E1-161.E3
Jarvis, M.C.; Ebrahimi, D.; Temiz, N.A.; Harris, R.S. 2018: Mutation Signatures Including APOBEC in Cancer Cell Lines. Jnci Cancer Spectrum 2(1)
Cappuyns, E.; Huyghebaert, J.; Vandeweyer, G.; Kooy, R.Frank. 2018: Mutations in ADNP affect expression and subcellular localization of the protein. Cell Cycle 17(9): 1068-1075
Miao, C.; Xiao, L.; Hua, K.; Zou, C.; Zhao, Y.; Bressan, R.A.; Zhu, J.-K. 2018: Mutations in a subfamily of abscisic acid receptor genes promote rice growth and productivity. Proceedings of the National Academy of Sciences of the United States of America 115(23): 6058-6063
Lassuthova, P.; Rebelo, A.P.; Ravenscroft, G.; Lamont, P.J.; Davis, M.R.; Manganelli, F.; Feely, S.M.; Bacon, C.; Brožková, D.Ša.; Haberlova, J.; Mazanec, R.; Tao, F.; Saghira, C.; Abreu, L.; Courel, S.; Powell, E.; Buglo, E.; Bis, D.M.; Baxter, M.F.; Ong, R.W.; Marns, L.; Lee, Y.-C.; Bai, Y.; Isom, D.G.; Barro-Soria, R.é; Chung, K.W.; Scherer, S.S.; Larsson, H.P.; Laing, N.G.; Choi, B.-O.; Seeman, P.; Shy, M.E.; Santoro, L.; Zuchner, S. 2018: Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2. American Journal of Human Genetics 102(3): 505-514
Cannata Serio, M.; Rujano, M.A.; Simons, M. 2018: Mutations in ATP6AP2 cause autophagic liver disease in humans. Autophagy 14(6): 1088-1089
Höben, I.M.; Hjeij, R.; Olbrich, H.; Dougherty, G.W.; Nöthe-Menchen, T.; Aprea, I.; Frank, D.; Pennekamp, P.; Dworniczak, B.; Wallmeier, J.; Raidt, J.; Nielsen, K.G.; Philipsen, M.C.; Santamaria, F.; Venditto, L.; Amirav, I.; Mussaffi, H.; Prenzel, F.; Wu, K.; Bakey, Z.; Schmidts, M.; Loges, N.T.; Omran, H. 2018: Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms. American Journal of Human Genetics 102(5): 973-984
Offenburger, S.-L.; Jongsma, E.; Gartner, A. 2018: Mutations in Caenorhabditis elegans neuroligin-like glit-1, the apoptosis pathway and the calcium chaperone crt-1 increase dopaminergic neurodegeneration after 6-OHDA treatment. Plos Genetics 14(1): E1007106
Higuchi, Y.; Okunushi, R.; Hara, T.; Hashiguchi, A.; Yuan, J.; Yoshimura, A.; Murayama, K.; Ohtake, A.; Ando, M.; Hiramatsu, Y.; Ishihara, S.; Tanabe, H.; Okamoto, Y.; Matsuura, E.; Ueda, T.; Toda, T.; Yamashita, S.; Yamada, K.; Koide, T.; Yaguchi, H.; Mitsui, J.; Ishiura, H.; Yoshimura, J.; Doi, K.; Morishita, S.; Sato, K.; Nakagawa, M.; Yamaguchi, M.; Tsuji, S.; Takashima, H. 2018: Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy. Brain: a Journal of Neurology 141(6): 1622-1636
Vazquez Fonseca, L.; Doimo, M.; Calderan, C.; Desbats, M.A.; Acosta, M.J.; Cerqua, C.; Cassina, M.; Ashraf, S.; Hildebrandt, F.; Sartori, G.; Navas, P.; Trevisson, E.; Salviati, L. 2018: Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function. Human Mutation 39(3): 406-414
Ciftci, S.; Keskin, F.; Abaci, N.; Akyuz, F.; Cakiris, A.; Badur, S.; Kaymakoglu, S.; Ustek, D. 2018: Mutations in Core Gene Region of Hepatitis B Virus in Patients with Chronic Hepatitis B. Clinical Laboratory 2018(3): 10.7754/Clin.Lab.2017.170616
Sun, Z.; Zhou, Q.; Li, H.; Yang, L.; Wu, S.; Sui, R. 2017: Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities. Molecular Vision 23: 977-986
Zhang, C.; Chen, F.; Zhao, Z.; Hu, L.; Liu, H.; Cheng, Z.; Weng, Y.; Chen, P.; Li, Y. 2018: Mutations in CsPID encoding a Ser/Thr protein kinase are responsible for round leaf shape in cucumber (Cucumis sativus L.). TAG. Theoretical and Applied Genetics. Theoretische und Angewandte Genetik 131(6): 1379-1389
Van den Berg, M.P.; Almomani, R.; Biaggioni, I.; van Faassen, M.; van der Harst, P.; Silljé, H.H.W.; Mateo Leach, I.; Hemmelder, M.H.; Navis, G.; Luijckx, G.J.; de Brouwer, A.P.M.; Venselaar, H.; Verbeek, M.M.; van der Zwaag, P.A.; Jongbloed, J.D.H.; van Tintelen, J.P.; Wevers, R.A.; Kema, I.P. 2018: Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome. Circulation Research 122(6): 846-854
Pradhan, M.; Pal, A.; Samanta, A.K.; Banerjee, S.; Samanta, R. 2018: Mutations in cytochrome B gene effects female reproduction of Ghungroo pig. Theriogenology 119: 121-130
Genenncher, B.; Durdevic, Z.; Hanna, K.; Zinkl, D.; Mobin, M.B.; Senturk, N.; Da Silva, B.; Legrand, C.; Carré, C.ém.; Lyko, F.; Schaefer, M. 2018: Mutations in Cytosine-5 tRNA Methyltransferases Impact Mobile Element Expression and Genome Stability at Specific DNA Repeats. Cell Reports 22(7): 1861-1874
Chae, Y.K.; Anker, J.F.; Bais, P.; Namburi, S.; Giles, F.J.; Chuang, J.H. 2018: Mutations in DNA repair genes are associated with increased neo-antigen load and activated T cell infiltration in lung adenocarcinoma. Oncotarget 9(8): 7949-7960
Cunningham, R.L.; Herbert, A.L.; Harty, B.L.; Ackerman, S.D.; Monk, K.R. 2018: Mutations in dock1 disrupt early Schwann cell development. Neural Development 13(1): 17
Kamiya, H.; Makino, T.; Suzuki, T.; Kobayashi, M.; Matsuoka, I. 2018: Mutations induced by 8-oxo-7,8-dihydroguanine in WRN- and DNA polymerase λ-double knockdown cells. Mutagenesis 33(4): 301-310
Overton, N.L.D.; Brakhage, A.A.; Thywißen, A.; Denning, D.W.; Bowyer, P. 2018: Mutations in EEA1 are associated with allergic bronchopulmonary aspergillosis and affect phagocytosis of Aspergillus fumigatus by human macrophages. Plos one 13(3): E0185706
Wei, J.; van der Wekken, A.J.; Saber, A.; Terpstra, M.M.; Schuuring, E.; Timens, W.; Hiltermann, T.J.N.; Groen, H.J.M.; van den Berg, A.; Kok, K. 2018: Mutations in EMT-Related Genes in ALK Positive Crizotinib Resistant Non-Small Cell Lung Cancers. Cancers 10(1)
Modi, B.P.; Teves, M.E.; Pearson, L.N.; Parikh, H.I.; Haymond-Thornburg, H.; Tucker, J.L.; Chaemsaithong, P.; Gomez-Lopez, N.; York, T.P.; Romero, R.; Strauss, J.F. 2017: Mutations in fetal genes involved in innate immunity and host defense against microbes increase risk of preterm premature rupture of membranes (PPROM). Molecular Genetics and Genomic Medicine 5(6): 720-729
Finsterer, J.; Stollberger, C. 2019: Mutations in genes associated with either myopathy or noncompaction. Herz 44(8): 756-758
Rimbara, E.; Mori, S.; Kim, H.; Suzuki, M.; Shibayama, K. 2018: Mutations in Genes Encoding Penicillin-Binding Proteins and Efflux Pumps Play a Role in β-Lactam Resistance in Helicobacter cinaedi. Antimicrobial Agents and ChemoTherapy 62(2)
Amanzougaghene, N.; Fenollar, F.; Diatta, G.; Sokhna, C.; Raoult, D.; Mediannikov, O. 2018: Mutations in GluCl associated with field ivermectin-resistant head lice from Senegal. International Journal of Antimicrobial Agents 52(5): 593-598
Boczonadi, V.; Meyer, K.; Gonczarowska-Jorge, H.; Griffin, H.; Roos, A.; Bartsakoulia, M.; Bansagi, B.; Ricci, G.; Palinkas, F.; Zahedi, R.é P.; Bruni, F.; Kaspar, B.; Lochmüller, H.; Boycott, K.M.; Müller, J.S.; Horvath, R. 2018: Mutations in glycyl-tRNA synthetase impair mitochondrial metabolism in neurons. Human Molecular Genetics 27(12): 2187-2204
Paavo, M.; Zhao, J.; Kim, H.J.; Lee, W.; Zernant, J.; Cai, C.; Allikmets, R.; Tsang, S.H.; Sparrow, J.R. 2018: Mutations in GPR143/OA1 and ABCA4 Inform Interpretations of Short-Wavelength and Near-Infrared Fundus Autofluorescence. Investigative Ophthalmology and Visual Science 59(6): 2459-2469
Gambaryan, A.S.; Lomakina, N.F.; Boravleva, E.Y.; Mochalova, L.V.; Sadykova, G.K.; Prilipov, A.G.; Matrosovich, T.Y.; Matrosovich, M.N. 2018: Mutations in Hemagglutinin and Polymerase Alter the Virulence of Pandemic A(H1N1) Influenza Virus. Molekuliarnaia Biologiia 52(4): 644-658
Yin, F.; Xie, Y.; Fan, H.; Zhang, J.; Guo, Z. 2017: Mutations in hepatitis B virus polymerase are associated with the postoperative survival of hepatocellular carcinoma patients. Plos one 12(12): E0189730
Moghbeli, M.; Naghibzadeh, B.; Ghahraman, M.; Fatemi, S.; Taghavi, M.; Vakili, R.; Abbaszadegan, M.R. 2018: Mutations in HNF1A Gene are not a Common Cause of Familial Young-Onset Diabetes in Iran. Indian Journal of Clinical Biochemistry: Ijcb 33(1): 91-95
Yu, Z.; Tang, P.L.; Wang, J.; Bao, S.; Shieh, J.T.; Leung, A.W.; Zhang, Z.; Gao, F.; Wong, S.Y.; Hui, A.L.; Gao, Y.; Dung, N.; Zhang, Z.-G.; Fan, Y.; Zhou, X.; Zhang, Y.; Wong, D.S.; Sham, P.C.; Azhar, A.; Kwok, P.-Y.; Tam, P.P.; Lian, Q.; Cheah, K.S.; Wang, B.; Song, Y.-Q. 2018: Mutations in Hnrnpa1 cause congenital heart defects. Jci Insight 3(2)
Norquist, B.M.; Brady, M.F.; Harrell, M.I.; Walsh, T.; Lee, M.K.; Gulsuner, S.; Bernards, S.S.; Casadei, S.; Burger, R.A.; Tewari, K.S.; Backes, F.; Mannel, R.S.; Glaser, G.; Bailey, C.; Rubin, S.; Soper, J.; Lankes, H.A.; Ramirez, N.C.; King, M.C.; Birrer, M.J.; Swisher, E.M. 2018: Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group Study. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 24(4): 777-783
Biryukov, J.; Myers, J.C.; McLaughlin-Drubin, M.E.; Griffin, H.M.; Milici, J.; Doorbar, J.; Meyers, C. 2017: Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation. Viruses 9(12)
Müller, N.A.; Zhang, L.; Koornneef, M.; Jiménez-Gómez, J.é M. 2018: Mutations in EID1 and LNK2 caused light-conditional clock deceleration during tomato domestication. Proceedings of the National Academy of Sciences of the United States of America 115(27): 7135-7140
Rudat, A.K.; Pokhrel, A.; Green, T.J.; Gray, M.J. 2018: Mutations in Escherichia coli Polyphosphate Kinase that Lead to Dramatically Increased in Vivo Polyphosphate Levels. Journal of Bacteriology 200(6)
Kim, S.-Y.; Jhun, B.W.; Moon, S.M.; Shin, S.H.; Jeon, K.; Kwon, O.J.; Yoo, I.Y.; Huh, H.J.; Ki, C.-S.; Lee, N.Y.; Shin, S.J.; Daley, C.L.; Suh, G.Y.; Koh, W.-J. 2018: Mutations in gyrA and gyrB in Moxifloxacin-Resistant Mycobacterium avium Complex and Mycobacterium abscessus Complex Clinical Isolates. Antimicrobial Agents and ChemoTherapy 62(9)
Khandelwal, P.; Birla, S.; Bhatia, D.; Puraswani, M.; Saini, H.; Sinha, A.; Hari, P.; Sharma, A.; Bagga, A. 2018: Mutations in membrane cofactor protein (CD46) gene in Indian children with hemolytic uremic syndrome. Clinical Kidney Journal 11(2): 198-203
Su, W.-H.; Jou, Y.-S.; Zhang, J.-H.; Ho, C.-M.; Tai, D.-I. 2018: Mutations in NOTCH1 and nucleotide excision repair genes are correlated with prognosis of hepatitis B virus-associated hepatocellular carcinoma. Journal of Cancer 9(15): 2678-2686
Pandey, N.; Rashid, T.; Jalvi, R.; Sharma, M.; Rangasayee, R.; Andrabi, K.I.; Anand, A. 2017: Mutations in OTOF, CLDN14 and SLC26A4 genes as major causes of hearing impairment in Dhadkai village, Jammu and Kashmir, India. Indian Journal of Medical Research 146(4): 489-497
Heinen, C.A.; de Vries, E.M.; Alders, M.ël.; Bikker, H.; Zwaveling-Soonawala, N.; van den Akker, E.L.T.; Bakker, B.; Hoorweg-Nijman, G.; Roelfsema, F.; Hennekam, R.C.; Boelen, A.; van Trotsenburg, A.S.P.; Fliers, E. 2018: Mutations in IRS4 are associated with central hypothyroidism. Journal of Medical Genetics 55(10): 693-700
Bellanné-Chantelot, C.; Schmaltz-Panneau, B.; Marty, C.; Fenneteau, O.; Callebaut, I.; Clauin, S.év.; Docet, A.él.; Damaj, G.-L.; Leblanc, T.; Pellier, I.; Stoven, C.éc.; Souquere, S.; Antony-Debré, I.éa.; Beaupain, B.; Aladjidi, N.; Barlogis, V.; Bauduer, F.éd.ér.; Bensaid, P.; Boespflug-Tanguy, O.; Berger, C.; Bertrand, Y.; Carausu, L.; Fieschi, C.; Galambrun, C.; Schmidt, A.; Journel, H.; Mazingue, F.ço.; Nelken, B.; Quah, T.C.; Oksenhendler, E.; Ouachée, M.; Pasquet, M.èn.; Saada, V.ér.; Suarez, F.; Pierron, G.ér.; Vainchenker, W.; Plo, I.; Donadieu, J. 2018: Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome. Blood 132(12): 1318-1331
Alimirzaie, S.; Mohamadkhani, A.; Masoudi, S.; Sellars, E.; Boffetta, P.; Malekzadeh, R.; Akbari, M.R.; Pourshams, A. 2018: Mutations in Known and Novel cancer Susceptibility Genes in Young Patients with Pancreatic Cancer. Archives of Iranian Medicine 21(6): 228-233
Patel, N.; Alkuraya, H.; Alzahrani, S.S.; Nowailaty, S.R.; Seidahmed, M.Z.; Alhemidan, A.; Ben-Omran, T.; Ghazi, N.G.; Al-Aqeel, A.; Al-Owain, M.; Alzaidan, H.I.; Faqeih, E.; Kurdi, W.; Rahbeeni, Z.; Ibrahim, N.; Abdulwahab, F.; Hashem, M.; Shaheen, R.; Abouelhoda, M.; Monies, D.; Khan, A.O.; Aldahmesh, M.A.; Alkuraya, F.S. 2018: Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophies. Clinical Genetics 94(6): 554-563
Bai, B.; Shan, L.; Xie, B.; Huang, X.; Mao, W.; Wang, X.; Wang, D.; Zhu, H. 2018: Mutations in KRAS codon 12 predict poor survival in Chinese patients with metastatic colorectal cancer. Oncology Letters 15(3): 3161-3166
Breuss, M.W.; Nguyen, A.; Song, Q.; Nguyen, T.; Stanley, V.; James, K.N.; Musaev, D.; Chai, G.; Wirth, S.A.; Anzenberg, P.; George, R.D.; Johansen, A.; Ali, S.; Zia-Ur-Rehman, M.; Sultan, T.; Zaki, M.S.; Gleeson, J.G. 2018: Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome. American Journal of Human Genetics 103(2): 296-304
Lewis, P.A. 2018: Mutations in LRRK2 amplify cell-to-cell protein aggregate propagation: a hypothesis. Acta Neuropathologica 135(6): 973-976
Espino Guarch, M.; Font-Llitjós, M.; Murillo-Cuesta, S.; Errasti-Murugarren, E.; Celaya, A.M.; Girotto, G.; Vuckovic, D.; Mezzavilla, M.; Vilches, C.; Bodoy, S.; Sahún, I.; González, L.; Prat, E.; Zorzano, A.; Dierssen, M.; Varela-Nieto, I.; Gasparini, P.; Palacín, M.; Nunes, V. 2018: Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss. Elife 7
Comisso, M.; Hadchouel, A.; de Blic, J.; Mirande, M. 2018: Mutations in MARS identified in a specific type of pulmonary alveolar proteinosis alter methionyl-tRNA synthetase activity. Febs Journal 285(14): 2654-2661
Al-Khersan, H.; Kwong, A.; Grassi, M.A. 2019: Mutations in MERTK are not associated with age-related macular degeneration. International Ophthalmology 39(1): 63-67
Leng, Y.; Yan, L.; Feng, H.; Chen, C.; Wang, S.; Luo, Y.; Cao, L. 2018: Mutations in mevalonate pathway genes in patients with familial or sporadic porokeratosis. Journal of Dermatology 45(7): 862-866
Dazzo, E.; Rehberg, K.; Michelucci, R.; Passarelli, D.; Boniver, C.; Vianello Dri, V.; Striano, P.; Striano, S.; Pasterkamp, R.J.; Nobile, C. 2018: Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsy. Annals of Neurology 83(3): 483-493
Chen, K.S.; Stroup, E.K.; Budhipramono, A.; Rakheja, D.; Nichols-Vinueza, D.; Xu, L.; Stuart, S.H.; Shukla, A.A.; Fraire, C.; Mendell, J.T.; Amatruda, J.F. 2018: Mutations in microRNA processing genes in Wilms tumors derepress the IGF2 regulator PLAG1. Genes and Development 32(15-16): 996-1007
Hopkins, J.F.; Denroche, R.E.; Aguiar, J.A.; Notta, F.; Connor, A.A.; Wilson, J.M.; Stein, L.D.; Gallinger, S.; Boutros, P.C. 2018: Mutations in Mitochondrial DNA from Pancreatic Ductal Adenocarcinomas Associate with Survival Times of Patients and Accumulate as Tumors Progress. Gastroenterology 154(6): 1620-1624.E5
Churchward, C.P.; Calder, A.; Snyder, L.A.S. 2018: Mutations in Neisseria gonorrhoeae grown in sub-lethal concentrations of monocaprin do not confer resistance. Plos one 13(4): E0195453
Miao, J.; Chi, Y.; Lin, D.; Tyler, B.M.; Liu, X. 2018: Mutations in ORP1 Conferring Oxathiapiprolin Resistance Confirmed by Genome Editing using CRISPR/Cas9 in Phytophthora capsici and P. sojae. Phytopathology 108(12): 1412-1419
Williams, C.J.; Qazi, U.; Bernstein, M.; Charniak, A.; Gohr, C.; Mitton-Fitzgerald, E.; Ortiz, A.; Cardinal, L.; Kaell, A.T.; Rosenthal, A.K. 2018: Mutations in osteoprotegerin account for the CCAL1 locus in calcium pyrophosphate deposition disease. Osteoarthritis and Cartilage 26(6): 797-806
Hamasuna, R.; Le, P.T.; Kutsuna, S.; Furubayashi, K.; Matsumoto, M.; Ohmagari, N.; Fujimoto, N.; Matsumoto, T.; Jensen, J.S. 2018: Mutations in ParC and GyrA of moxifloxacin-resistant and susceptible Mycoplasma genitalium strains. Plos one 13(6): E0198355
Ruiz-García, R.; Vargas-Hernández, A.; Chinn, I.K.; Angelo, L.S.; Cao, T.N.; Coban-Akdemir, Z.; Jhangiani, S.N.; Meng, Q.; Forbes, L.R.; Muzny, D.M.; Allende, L.M.; Ehlayel, M.S.; Gibbs, R.A.; Lupski, J.R.; Uzel, G.; Orange, J.S.; Mace, E.M. 2018: Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatment. Journal of Allergy and Clinical Immunology 142(2): 605-617.E7
Broekaert, I.J.; Becker, K.; Gottschalk, I.; Körber, F.; Dötsch, J.ör.; Thiele, H.; Altmüller, J.; Nürnberg, P.; Hünseler, C.; Cirak, S. 2018: Mutations in plasmalemma vesicle-associated protein cause severe syndromic protein-losing enteropathy. Journal of Medical Genetics 55(9): 637-640
Zhu, F.; Liu, C.; Wang, F.; Yang, X.; Zhang, J.; Wu, H.; Zhang, Z.; He, X.; Zhang, Z.; Zhou, P.; Wei, Z.; Shang, Y.; Wang, L.; Zhang, R.; Ouyang, Y.-C.; Sun, Q.-Y.; Cao, Y.; Li, W. 2018: Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome. American Journal of Human Genetics 103(2): 188-199
Vögtle, F-Nora.; Brändl, Börn.; Larson, A.; Pendziwiat, M.; Friederich, M.W.; White, S.M.; Basinger, A.; Kücükköse, C.; Muhle, H.; Jähn, J.A.; Keminer, O.; Helbig, K.L.; Delto, C.F.; Myketin, L.; Mossmann, D.; Burger, N.; Miyake, N.; Burnett, A.; van Baalen, A.; Lovell, M.A.; Matsumoto, N.; Walsh, M.; Yu, H-Chun.; Shinde, D.N.; Stephani, U.; Van Hove, J.L.K.; Müller, F-Josef.; Helbig, I. 2018: Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood. American Journal of Human Genetics 102(4): 557-573
Zaman, T.; Helbig, I.; Božović, I.B.ć; DeBrosse, S.D.; Bergqvist, A.C.; Wallis, K.; Medne, L.; Maver, A.š; Peterlin, B.; Helbig, K.L.; Zhang, X.; Goldberg, E.M. 2018: Mutations in SCN3A cause early infantile epileptic encephalopathy. Annals of Neurology 83(4): 703-717
Zaw, M.T.; Emran, N.A.; Lin, Z. 2018: Mutations inside rifampicin-resistance determining region of rpoB gene associated with rifampicin-resistance in Mycobacterium tuberculosis. Journal of Infection and Public Health 11(5): 605-610
Zhao, W.; Zhang, S.-C.; Huang, W.-K.; Li, X.-L. 2018: Mutations in Smad-interacting protein 1 gene are responsible for absence of its expression in Hirschsprung's disease. Clinical and Experimental Medicine 18(3): 445-451
Huq, A.J.; Walsh, M.; Rajagopalan, B.; Finlay, M.; Trainer, A.H.; Bonnet, F.; Sevenet, N.; Winship, I.M. 2018: Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same. Familial Cancer 17(4): 601-606
Danis, D.; Brennerova, K.; Skopkova, M.; Kurdiova, T.; Ukropec, J.; Stanik, J.; Kolnikova, M.; Gasperikova, D. 2018: Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients. Endocrine Regulations 52(2): 110-118
Pizzino, A.; Whitehead, M.; Sabet Rasekh, P.; Murphy, J.; Helman, G.; Bloom, M.; Evans, S.H.; Murnick, J.G.; Conry, J.; Taft, R.J.; Simons, C.; Vanderver, A.; Adang, L.A. 2018: Mutations in SZT2 result in early-onset epileptic encephalopathy and leukoencephalopathy. American Journal of Medical Genetics. Part a 176(6): 1443-1448
Zakirova, Z.; Fanutza, T.; Bonet, J.; Readhead, B.; Zhang, W.; Yi, Z.; Beauvais, G.; Zwaka, T.P.; Ozelius, L.J.; Blitzer, R.D.; Gonzalez-Alegre, P.; Ehrlich, M.E. 2018: Mutations in THAP1/DYT6 reveal that diverse dystonia genes disrupt similar neuronal pathways and functions. Plos Genetics 14(1): E1007169
Ohshima, Y.; Taguchi, K.; Mizuta, I.; Tanaka, M.; Tomiyama, T.; Kametani, F.; Yabe-Nishimura, C.; Mizuno, T.; Tokuda, T. 2018: Mutations in the β-amyloid precursor protein in familial Alzheimer's disease increase Aβ oligomer production in cellular models. Heliyon 4(1): E00511
Liang, S.; Qi, Y.; Zhao, J.; Li, Y.; Wang, R.; Shao, J.; Liu, X.; An, L.; Yu, F. 2017: Mutations in the Arabidopsis AtMRS2-11/AtMGT10/VAR5 Gene Cause Leaf Reticulation. Frontiers in Plant Science 8: 2007
Vasileiou, G.; Vergarajauregui, S.; Endele, S.; Popp, B.; Büttner, C.; Ekici, A.B.; Gerard, M.; Bramswig, N.C.; Albrecht, B.; Clayton-Smith, J.; Morton, J.; Tomkins, S.; Low, K.; Weber, A.; Wenzel, M.; Altmüller, J.; Li, Y.; Wollnik, B.; Hoganson, G.; Plona, M.-R.ée.; Cho, M.T.; Thiel, C.T.; Lüdecke, H.-J.; Strom, T.M.; Calpena, E.; Wilkie, A.O.M.; Wieczorek, D.; Engel, F.B.; Reis, A.é 2018: Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome. American Journal of Human Genetics 102(3): 468-479
Dostálková, A.žb.ět.; Kaufman, F.; Křížová, I.; Kultová, A.; Strohalmová, K.ín.; Hadravová, R.; Ruml, T.áš; Rumlová, M. 2018: Mutations in the Basic Region of the Mason-Pfizer Monkey Virus Nucleocapsid Protein Affect Reverse Transcription, Genomic RNA Packaging, and the Virus Assembly Site. Journal of Virology 92(10)
Augusciak-Duma, A.; Witecka, J.; Sieron, A.L.; Janeczko, M.; Pietrzyk, J.J.; Ochman, K.; Galicka, A.; Borszewska-Kornacka, M.K.; Pilch, J.; Jakubowska-Pietkiewicz, E. 2018: Mutations in the COL1A1 and COL1A2 genes associated with osteogenesis imperfecta (OI) types i or IIi. Acta Biochimica Polonica 65(1): 79-86
Korobko, I.V.; Shepelev, M.V. 2018: Mutations in the Effector Domain of RhoV GTPase Impair its Binding to Pak1 Protein Kinase. Molekuliarnaia Biologiia 52(4): 692-698
Cox, L.L.; Cox, T.C.; Moreno Uribe, L.M.; Zhu, Y.; Richter, C.T.; Nidey, N.; Standley, J.M.; Deng, M.; Blue, E.; Chong, J.X.; Yang, Y.; Carstens, R.P.; Anand, D.; Lachke, S.A.; Smith, J.D.; Dorschner, M.O.; Bedell, B.; Kirk, E.; Hing, A.V.; Venselaar, H.; Valencia-Ramirez, L.C.; Bamshad, M.J.; Glass, I.A.; Cooper, J.A.; Haan, E.; Nickerson, D.A.; van Bokhoven, H.; Zhou, H.; Krahn, K.N.; Buckley, M.F.; Murray, J.C.; Lidral, A.C.; Roscioli, T. 2018: Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate. American Journal of Human Genetics 102(6): 1143-1157
Gelsomino, L.; Panza, S.; Giordano, C.; Barone, I.; Gu, G.; Spina, E.; Catalano, S.; Fuqua, S.; Andò, S. 2018: Mutations in the estrogen receptor alpha hormone binding domain promote stem cell phenotype through notch activation in breast cancer cell lines. Cancer Letters 428: 12-20
Sukenik Halevy, R.; Chien, H.-C.; Heinz, B.; Bamshad, M.J.; Nickerson, D.A.; Kircher, M.; Ahituv, N. 2018: Mutations in the fourth β-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers. Human Mutation 39(6): 811-815
Weisschuh, N.; Stingl, K.; Audo, I.; Biskup, S.; Bocquet, B.éa.; Branham, K.; Burstedt, M.S.; De Baere, E.; De Vries, M.J.; Golovleva, I.; Green, A.; Heckenlively, J.; Leroy, B.P.; Meunier, I.; Traboulsi, E.; Wissinger, B.; Kohl, S. 2018: Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsia. Human Mutation 39(10): 1366-1371
Dunn, B.S.; Rush, L.; Lu, J.-Y.; Xu, T. 2018: Mutations in the Drosophila tricellular junction protein M6 synergize with RasV12 to induce apical cell delamination and invasion. Proceedings of the National Academy of Sciences of the United States of America 115(33): 8358-8363
Nguyen, K.V.; Nguyen, T.V.; Nguyen, H.T.T.; Le, D.V. 2018: Mutations in the gyrA, parC, and mexR genes provide functional insights into the fluoroquinolone-resistant Pseudomonas aeruginosa isolated in Vietnam. Infection and Drug Resistance 11: 275-282
Liu, L.; Xie, T.; Peng, P.; Qiu, H.; Zhao, J.; Fang, J.; Patil, S.B.; Wang, Y.; Fang, S.; Chu, J.; Yuan, S.; Zhang, W.; Li, X. 2018: Mutations in the MIT3 gene encoding a caroteniod isomerase lead to increased tiller number in rice. Plant Science: An International Journal of Experimental Plant Biology 267: 1-10
Chen, A.; Tiosano, D.; Guran, T.; Baris, H.N.; Bayram, Y.; Mory, A.; Shapiro-Kulnane, L.; Hodges, C.A.; Akdemir, Z.C.; Turan, S.; Jhangiani, S.N.; van den Akker, F.; Hoppel, C.L.; Salz, H.K.; Lupski, J.R.; Buchner, D.A. 2018: Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency. Human Molecular Genetics 27(11): 1913-1926
Palagano, E.; Zuccarini, G.; Prontera, P.; Borgatti, R.; Stangoni, G.; Elisei, S.; Mantero, S.; Menale, C.; Forlino, A.; Uva, P.; Oppo, M.; Vezzoni, P.; Villa, A.; Merlo, G.R.; Sobacchi, C. 2018: Mutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1. Bone 114: 125-136
Hashemi, H.; Condurat, A.-L.; Stroh-Dege, A.; Weiss, N.; Geiss, C.; Pilet, J.; Cornet Bartolomé, C.; Rommelaere, J.; Salomé, N.; Dinsart, C. 2018: Mutations in the Non-Structural Protein-Coding Sequence of Protoparvovirus H-1PV Enhance the Fitness of the Virus and Show Key Benefits Regarding the Transduction Efficiency of Derived Vectors. Viruses 10(4)
Li, W.; Gumpper, R.H.; Uddin, Y.; Schmidt-Krey, I.; Luo, M. 2018: Complementary Mutations in the N and L Proteins for Restoration of Viral RNA Synthesis. Journal of Virology 92(22)
Tamura, K.; Yu, J.; Hata, T.; Suenaga, M.; Shindo, K.; Abe, T.; MacGregor-Das, A.; Borges, M.; Wolfgang, C.L.; Weiss, M.J.; He, J.; Canto, M.I.; Petersen, G.M.; Gallinger, S.; Syngal, S.; Brand, R.E.; Rustgi, A.; Olson, S.H.; Stoffel, E.; Cote, M.L.; Zogopoulos, G.; Potash, J.B.; Goes, F.S.; McCombie, R.W.; Zandi, P.P.; Pirooznia, M.; Kramer, M.; Parla, J.; Eshleman, J.R.; Roberts, N.J.; Hruban, R.H.; Klein, A.P.; Goggins, M. 2018: Mutations in the pancreatic secretory enzymes CPA1 and CPB1 are associated with pancreatic cancer. Proceedings of the National Academy of Sciences of the United States of America 115(18): 4767-4772
Tjhin, E.T.; Spry, C.; Sewell, A.L.; Hoegl, A.; Barnard, L.; Sexton, A.E.; Siddiqui, G.; Howieson, V.M.; Maier, A.G.; Creek, D.J.; Strauss, E.; Marquez, R.; Auclair, K.; Saliba, K.J. 2018: Mutations in the pantothenate kinase of Plasmodium falciparum confer diverse sensitivity profiles to antiplasmodial pantothenate analogues. Plos Pathogens 14(4): E1006918
Zhong, G.; Le, M.Q.; Lopes, T.J.S.; Halfmann, P.; Hatta, M.; Fan, S.; Neumann, G.; Kawaoka, Y. 2018: Mutations in the PA Protein of Avian H5N1 Influenza Viruses Affect Polymerase Activity and Mouse Virulence. Journal of Virology 92(4)
Brereton, E.; Fassi, E.; Araujo, G.C.; Dodd, J.; Telegrafi, A.; Pathak, S.J.; Shinawi, M. 2018: Mutations in the PH Domain of DNM1 are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities. Molecular Genetics and Genomic Medicine 6(2): 294-300
Shi, T.-W.; Bai, N.; Zhang, J.-A.; Lu, F.; Chen, X.-B.; Kong, X.-D.; Yu, J.-B. 2018: Mutations in the γ-secretase genes PSEN1, PSENEN, and NCSTN in a family with acne inversa. European Journal of Dermatology: Ejd 28(3): 374-376
Shahmarvand, N.; Nagy, A.; Shahryari, J.; Ohgami, R.S. 2018: Mutations in the signal transducer and activator of transcription family of genes in cancer. Cancer Science 109(4): 926-933
Norppa, A.J.; Kauppala, T.M.; Heikkinen, H.A.; Verma, B.; Iwaï, H.; Frilander, M.J. 2018: Mutations in the U11/U12-65K protein associated with isolated growth hormone deficiency lead to structural destabilization and impaired binding of U12 snRNA. Rna 24(3): 396-409
Held, K.; Gruss, F.; Aloi, V.D.; Janssens, A.; Ulens, C.; Voets, T.; Vriens, J. 2018: Mutations in the voltage-sensing domain affect the alternative ion permeation pathway in the TRPM3 channel. Journal of Physiology 596(12): 2413-2432
Martin, C.-A.; Sarlós, K.; Logan, C.V.; Thakur, R.S.; Parry, D.A.; Bizard, A.H.; Leitch, A.; Cleal, L.; Ali, N.S.; Al-Owain, M.A.; Allen, W.; Altmüller, J.; Aza-Carmona, M.; Barakat, B.A.Y.; Barraza-García, J.; Begtrup, A.; Bogliolo, M.; Cho, M.T.; Cruz-Rojo, J.; Dhahrabi, H.A.M.; Elcioglu, N.H.; Gorman, G.ái.S.; Jobling, R.; Kesterton, I.; Kishita, Y.; Kohda, M.; Le Quesne Stabej, P.; Malallah, A.J.; Nürnberg, P.; Ohtake, A.; Okazaki, Y.; Pujol, R.; Ramirez, M.J.é; Revah-Politi, A.; Shimura, M.; Stevens, P.; Taylor, R.W.; Turner, L.; Williams, H.; Wilson, C.; Yigit, G.ök.; Zahavich, L.; Alkuraya, F.S.; Surralles, J.; Iglesias, A.; Murayama, K.; Wollnik, B.; Dattani, M.; Heath, K.E.; Hickson, I.D.; Jackson, A.P. 2018: Mutations in TOP3A Cause a Bloom Syndrome-like Disorder. American Journal of Human Genetics 103(2): 221-231
Luscan, R.; Mechaussier, S.; Paul, A.; Tian, G.; Gérard, X.; Defoort-Dellhemmes, S.; Loundon, N.; Audo, I.; Bonnin, S.; LeGargasson, J.-F.ço.; Dumont, J.; Goudin, N.; Garfa-Traoré, M.; Bras, M.; Pouliet, A.; Bessières, B.; Boddaert, N.; Sahel, J.é-A.; Lyonnet, S.; Kaplan, J.; Cowan, N.J.; Rozet, J.-M.; Marlin, S.; Perrault, I. 2017: Mutations in TUBB4B Cause a Distinctive Sensorineural Disease. American Journal of Human Genetics 101(6): 1006-1012
De Campos, S.B.; Lardi, M.; Gandolfi, A.; Eberl, L.; Pessi, G. 2017: Mutations in two Paraburkholderia phymatum Type Vi Secretion Systems Cause Reduced Fitness in Interbacterial Competition. Frontiers in Microbiology 8: 2473
Zhang, Q.; Chen, J.; Qin, Y.; Wang, J.; Zhou, L. 2018: Mutations in voltage-gated L-type calcium channel: implications in cardiac arrhythmia. Channels 12(1): 201-218
Carmona-Antoñanzas, G.; Helgesen, K.O.; Humble, J.L.; Tschesche, C.; Bakke, M.J.; Gamble, L.; Bekaert, M.ël.; Bassett, D.I.; Horsberg, T.E.; Bron, J.E.; Sturm, A. 2019: Mutations in voltage-gated sodium channels from pyrethroid resistant salmon lice (Lepeophtheirus salmonis). Pest Management Science 75(2): 527-536
Portnoi, M.-F.; Dumargne, M.-C.; Rojo, S.; Witchel, S.F.; Duncan, A.J.; Eozenou, C.; Bignon-Topalovic, J.; Yatsenko, S.A.; Rajkovic, A.; Reyes-Mugica, M.; Almstrup, K.; Fusee, L.; Srivastava, Y.; Chantot-Bastaraud, S.; Hyon, C.; Louis-Sylvestre, C.; Validire, P.; de Malleray Pichard, C.; Ravel, C.; Christin-Maitre, S.; Brauner, R.; Rossetti, R.; Persani, L.; Charreau, E.H.; Dain, L.; Chiauzzi, V.A.; Mazen, I.; Rouba, H.; Schluth-Bolard, C.; MacGowan, S.; McLean, W.H.I.; Patin, E.; Rajpert-De Meyts, E.; Jauch, R.; Achermann, J.C.; Siffroi, J.-P.; McElreavey, K.; Bashamboo, A. 2018: Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies. Human Molecular Genetics 27(7): 1228-1240
Seong, E.; Insolera, R.; Dulovic, M.; Kamsteeg, E.-J.; Trinh, J.; Brüggemann, N.; Sandford, E.; Li, S.; Ozel, A.B.; Li, J.Z.; Jewett, T.; Kievit, A.J.A.; Münchau, A.; Shakkottai, V.; Klein, C.; Collins, C.A.; Lohmann, K.; van de Warrenburg, B.P.; Burmeister, M. 2018: Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects. Annals of Neurology 83(6): 1075-1088
Braun, D.A.; Shril, S.; Sinha, A.; Schneider, R.; Tan, W.; Ashraf, S.; Hermle, T.; Jobst-Schwan, T.; Widmeier, E.; Majmundar, A.J.; Daga, A.; Warejko, J.K.; Nakayama, M.; Schapiro, D.; Chen, J.; Airik, M.; Rao, J.; Schmidt, J.M.; Hoogstraten, C.A.; Hugo, H.; Meena, J.; Lek, M.; Laricchia, K.M.; Bagga, A.; Hildebrandt, F. 2018: Mutations in WDR4 as a new cause of Galloway-Mowat syndrome. American Journal of Medical Genetics. Part a 176(11): 2460-2465
O'Connor, E.; Vandrovcova, J.; Bugiardini, E.; Chelban, V.; Manole, A.; Davagnanam, I.; Wiethoff, S.; Pittman, A.; Lynch, D.S.; Efthymiou, S.; Marino, S.; Manzur, A.Y.; Roberts, M.; Hanna, M.G.; Houlden, H.; Matthews, E.; Wood, N.W. 2018: Mutations in XRCC1 cause cerebellar ataxia and peripheral neuropathy. Journal of Neurology Neurosurgery and Psychiatry 89(11): 1230-1232
Lu, D.; Song, J.; Sun, Y.; Qi, F.; Liu, L.; Jin, Y.; McNutt, M.A.; Yin, Y. 2018: Mutations of deubiquitinase OTUD1 are associated with autoimmune disorders. Journal of Autoimmunity 94: 156-165
Yao, Y.; Enkhtsetseg, S.; Odsbu, I.; Fan, L.; Morigen, M. 2018: Mutations of DnaA-boxes in the oriR region increase replication frequency of the MiniR1-1 plasmid. Bmc Microbiology 18(1): 27
Liao, D.; Liao, Q.; Huang, C.; Bi, F. 2018: Mutations of G38R and D40G cause amyotrophic lateral sclerosis by reducing Annexin A11 protein stability. Zhong Nan da Xue Xue Bao. Yi Xue Ban 43(6): 577-582
Tavanaee Sani, A.; Ashna, H.; Kaffash, A.; Khaledi, A.; Ghazvini, K. 2018: Mutations of rpob Gene Associated with Rifampin Resistance among Mycobacterium Tuberculosis Isolated in Tuberculosis Regional Reference Laboratory in Northeast of Iran during 2015-2016. Ethiopian journal of health sciences 28(3): 299-304
Huang, D.; Sun, W.; Zhou, Y.; Li, P.; Chen, F.; Chen, H.; Xia, D.; Xu, E.; Lai, M.; Wu, Y.; Zhang, H. 2018: Mutations of key driver genes in colorectal cancer progression and metastasis. Cancer Metastasis Reviews 37(1): 173-187
Pandey, S.; Bourn, J.; Cekanova, M. 2018: Mutations of p53 decrease sensitivity to the anthracycline treatments in bladder cancer cells. Oncotarget 9(47): 28514-28531
Jia, X.-s.; Zhou, S.-m.; Xu, M.-x.; Yang, Y.; Wu, K. 2016: Mutations of Plasmodium falciparum Multidrug Resistance 1 Gene in Imported Plasmodium falciparum in Wuhan. Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi 34(6): 489-492
Mader, S.; Brimberg, L.; Soltys, J.N.; Bennett, J.L.; Diamond, B. 2018: Mutations of Recombinant Aquaporin-4 Antibody in the Fc Domain Can Impair Complement-Dependent Cellular Cytotoxicity and Transplacental Transport. Frontiers in Immunology 9: 1599
Isakova, J.; Sovkhozova, N.; Vinnikov, D.; Goncharova, Z.; Talaibekova, E.; Aldasheva, N.; Aldashev, A. 2018: Mutations of rpoB, katG, inhA and ahp genes in rifampicin and isoniazid-resistant Mycobacterium tuberculosis in Kyrgyz Republic. Bmc Microbiology 18(1): 22
Yoshikawa, A.; Nishimura, F.; Inai, A.; Eriguchi, Y.; Nishioka, M.; Takaya, A.; Tochigi, M.; Kawamura, Y.; Umekage, T.; Kato, K.; Sasaki, T.; Ohashi, Y.; Iwamoto, K.; Kasai, K.; Kakiuchi, C. 2018: Mutations of the glycine cleavage system genes possibly affect the negative symptoms of schizophrenia through metabolomic profile changes. Psychiatry and Clinical Neurosciences 72(3): 168-179
Lehrer, S.; Rheinstein, P.H.; Rosenzweig, K.E. 2018: Mutations of the PDE5A Gene Confer a Survival Advantage in Patients with Colon Cancer. Cancer Prevention Research 11(7): 439-440
Lenzini, L.; Prisco, S.; Gallina, M.; Kuppusamy, M.; Rossi, G.P. 2018: Mutations of the Twik-Related Acid-Sensitive K+ Channel 2 Promoter in Human Primary Aldosteronism. Endocrinology 159(3): 1352-1359
Krenn, M.; Salzer, E.; Simonitsch-Klupp, I.; Rath, J.; Wagner, M.; Haack, T.B.; Strom, T.M.; Schänzer, A.; Kilimann, M.W.; Schmidt, R.L.J.; Schmetterer, K.G.; Zimprich, A.; Boztug, K.; Hahn, A.; Zimprich, F. 2018: Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype-phenotype spectrum. Journal of Neurology 265(2): 394-401
Otten, A.B.C.; Sallevelt, S.C.E.H.; Carling, P.J.; Dreesen, J.C.F.M.; Drüsedau, M.; Spierts, S.; Paulussen, A.D.C.; de Die-Smulders, C.E.M.; Herbert, M.; Chinnery, P.F.; Samuels, D.C.; Lindsey, P.; Smeets, H.J.M. 2018: Mutation-specific effects in germline transmission of pathogenic mtDNA variants. Human Reproduction 33(7): 1331-1341
Jiang, Y.; Gao, S.; Wu, L.; Jin, X.; Deng, T.; Wang, L.; Huang, S.; Gao, X.; Chen, J.; Han, D.; Gao, H.; Dai, P. 2018: Mutation spectra and founder effect of TMC1 in patients with non-syndromic deafness in Xiamen area, China. American Journal of Medical Genetics. Part B Neuropsychiatric Genetics: the Official Publication of the International Society of Psychiatric Genetics 177(3): 301-307
Mohammed, F.; Elshafey, A.; Al-Balool, H.; Alaboud, H.; Al Ben Ali, M.; Baqer, A.; Bastaki, L. 2018: Mutation spectrum analysis of Duchenne/Becker muscular dystrophy in 68 families in Kuwait: the era of personalized medicine. Plos one 13(5): E0197205
Han, Y.; Lin, Y.; Sun, Q.; Wang, S.; Gao, Y.; Shao, L. 2017: Mutation spectrum of Chinese patients with Bartter syndrome. Oncotarget 8(60): 101614-101622
Bhattacharya, S.; Khadilkar, S.V.; Nalini, A.; Ganapathy, A.; Mannan, A.U.; Majumder, P.P.; Bhattacharya, A. 2018: Mutation Spectrum of GNE Myopathy in the Indian Sub-Continent. Journal of Neuromuscular Diseases 5(1): 85-92
Wang, R.; Shen, N.; Ye, J.; Han, L.; Qiu, W.; Zhang, H.; Liang, L.; Sun, Y.; Fan, Y.; Wang, L.; Wang, Y.; Gong, Z.; Liu, H.; Wang, J.; Yan, H.; Blau, N.; Gu, X.; Yu, Y. 2018: Mutation spectrum of hyperphenylalaninemia candidate genes and the genotype-phenotype correlation in the Chinese population. Clinica Chimica Acta; International Journal of Clinical Chemistry 481: 132-138
Smaragda, K.; Vassiliki, K.; George, K.; Polixeni, S.; Christoforos, G.; Anastasios, A.; Minas, A.I.; Stavrenia, K.; Theoni, P.; Ioannis, D.; Miltiadis, T.K. 2018: Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles. Journal of Ophthalmology 2018: 5706142
Tang, M.; Sun, L.; Hu, A.; Yuan, M.; Yang, Y.; Peng, X.; Ding, X. 2017: Mutation Spectrum of the LRP5, NDP, and TSPAN12 Genes in Chinese Patients with Familial Exudative Vitreoretinopathy. Investigative Ophthalmology and Visual Science 58(13): 5949-5957
Hirokawa, Y.; Kanesaki, Y.; Arai, S.; Saruta, F.; Hayashihara, K.; Murakami, A.; Shimizu, K.; Honda, H.; Yoshikawa, H.; Hanai, T. 2018: Mutations responsible for alcohol tolerance in the mutant of Synechococcus elongatus PCC 7942 (SY1043) obtained by single-cell screening system. Journal of Bioscience and Bioengineering 125(5): 572-577
Liu, K.; He, L.; Liu, Z.; Xu, J.; Liu, Y.; Kuang, Q.; Wen, Z.; Li, M. 2017: Mutation status coupled with RNA-sequencing data can efficiently identify important non-significantly mutated genes serving as diagnostic biomarkers of endometrial cancer. Bmc Bioinformatics 18(Suppl 14): 472
Cundy, T.; Dray, M.; Delahunt, J.; Hald, J.D.; Langdahl, B.; Li, C.; Szybowska, M.; Mohammed, S.; Duncan, E.L.; McInerney-Leo, A.M.; Wheeler, P.G.; Roschger, P.; Klaushofer, K.; Rai, J.; Weis, M.; Eyre, D.; Schwarze, U.; Byers, P.H. 2018: Mutations that Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type i Procollagen Are Associated with a Unique Osteogenesis Imperfecta Phenotype. Journal of Bone and Mineral Research: the Official Journal of the American Society for Bone and Mineral Research 33(7): 1260-1271
Sanyal, S.; Molnarova, L.; Richterova, J.; Huraiova, B.; Benko, Z.; Polakova, S.; Cipakova, I.; Sevcovicova, A.; Gaplovska-Kysela, K.; Mechtler, K.; Cipak, L.; Gregan, J. 2018: Mutations that prevent methylation of cohesin render sensitivity to DNA damage in S. pombe. Journal of Cell Science 131(13)
Singh, M.; Inoue, K.; Pushkarev, A.; Béjà, O.; Kandori, H. 2018: Mutation Study of Heliorhodopsin 48C12. Biochemistry 57(33): 5041-5049
Wang, X.; Liu, X.; Huang, L.; Fang, S.; Jia, X.; Xiao, X.; Li, S.; Guo, X. 2018: Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome. Current Eye Research 43(11): 1334-1341
Liu, K.; Xie, M.; Lu, X.; Yu, H.; Wang, H.; Xu, Y.; Yang, Q.; Lin, Y.; Ma, Q. 2018: Mutations within the major hydrophilic region (MHR) of Hepatitis B virus from individuals with simultaneous HBsAg and anti-HBs in Guangzhou, Southern China. Journal of Medical Virology 90(8): 1337-1342
Hotz, A.; Bourrat, E.; Küsel, J.; Oji, V.; Alter, S.; Hake, L.; Korbi, M.; Ott, H.; Hausser, I.; Zimmer, A.D.; Fischer, J. 2018: Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis. Human Mutation 39(10): 1305-1313
Vuillaume, M-Laure.; Moizard, M-Pierre.; Rossignol, S.; Cottereau, E.; Vonwill, S.; Alessandri, J-Luc.; Busa, T.; Colin, E.; Gérard, M.; Giuliano, F.; Lambert, L.; Lefevre, M.; Kotecha, U.; Nampoothiri, S.; Netchine, Iène.; Raynaud, M.; Brioude, Fédéric.; Toutain, A. 2018: Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. Human Mutation 39(6): 790-805
Anand, D.; Agrawal, S.A.; Slavotinek, A.; Lachke, S.A. 2018: Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects. Human Mutation 39(4): 471-494
Wen, F.; Blackmon, S.; Olivier, A.K.; Li, L.; Guan, M.; Sun, H.; Wang, P.G.; Wan, X.-F. 2018: Mutation W222L at the Receptor Binding Site of Hemagglutinin could Facilitate Viral Adaption from Equine Influenza A(H3N8) Virus to Dogs. Journal of Virology 92(18)
Han, S-Ki.; Qi, X.; Sugihara, K.; Dang, J.H.; Endo, T.A.; Miller, K.L.; Kim, E-Deok.; Miura, T.; Torii, K.U. 2018: MUTE Directly Orchestrates Cell-State Switch and the Single Symmetric Division to Create Stomata. Developmental Cell 45(3): 303-315.E5
Kulandaisamy, A.; Binny Priya, S.; Sakthivel, R.; Tarnovskaya, S.; Bizin, I.; Hönigschmid, P.; Frishman, D.; Gromiha, M.M. 2018: MutHTP: mutations in human transmembrane proteins. Bioinformatics 34(13): 2325-2326
Sachdeva, K.; Upadhyay, A. 2017: Mutilating Lesions of Face. Indian Journal of Otolaryngology and Head and Neck Surgery: Official Publication of the Association of Otolaryngologists of India 69(4): 527-534
Winn, R.T.; Brass, D.; Meggitt, S.J. 2018: Mutilating male genital Crohn's without gastrointestinal involvement. Journal of the European Academy of Dermatology and Venereology: Jeadv 32(9): E355-E357
Khanna, K.; Bajpai, M.; Gupta, A.; Goel, P. 2017: 'Mutiny on the crown': two cases of rare cephalic malformations. BMJ Case Reports
Verrier, F.; Dubois d'Enghien, C.; Gauthier-Villars, M.; Bonadona, V.ér.; Faure-Conter, C.éc.; Dijoud, F.éd.ér.; Stoppa-Lyonnet, D.; Houdayer, C.; Golmard, L. 2018: Mutiple DICER1-related lesions associated with a germline deep intronic mutation. Pediatric Blood and Cancer 65(6): E27005
Balasubramaniam, C.; Subramaniam, V.; Balasubramaniam, V. 1993: Mutism following posterior fossa surgery for medulloblastoma. Neurology India 41(3): 173-175
Chen, C-Ho.; Lin, Y-Song.; Wu, S-Jung.; Mi, F-Long. 2018: Mutlifunctional nanoparticles prepared from arginine-modified chitosan and thiolated fucoidan for oral delivery of hydrophobic and hydrophilic drugs. Carbohydrate Polymers 193: 163-172
Makovický, P.; Caja, F.; Vodicková, L.; Makovický, P.; Cervinková, M.; Juhász, A.; Samasca, G.; Vodicka, P. 2016: MutL protein homologue 1(MLH1) in colon adenocarcinomas of the dog: minireview. Ceskoslovenska Fysiologie 65(2): 88-93
Rasila, T.S.; Pulkkinen, E.; Kiljunen, S.; Haapa-Paananen, S.; Pajunen, M.I.; Salminen, A.; Paulin, L.; Vihinen, M.; Rice, P.A.; Savilahti, H. 2018: Mu transpososome activity-profiling yields hyperactive MuA variants for highly efficient genetic and genome engineering. Nucleic Acids Research 46(9): 4649-4661
Chen, S.; Huang, T.; Wen, T.; Li, H.; Xu, M.; Gu, J. 2018: MutScan: fast detection and visualization of target mutations by scanning FASTQ data. Bmc Bioinformatics 19(1): 16
Hanne, J.; Britton, B.M.; Park, J.; Liu, J.; Martín-López, J.; Jones, N.; Schoffner, M.; Klajner, P.; Bundschuh, R.; Lee, J.-B.; Fishel, R. 2018: MutS homolog sliding clamps shield the DNA from binding proteins. Journal of Biological Chemistry 293(37): 14285-14294
Singh, G.; Bhat, B.; Jayadev, M.S.K.; Madhusudhan, C.; Singh, A. 2018: MutTCPdb: a comprehensive database for genomic variants of a tropical country neglected disease-tropical calcific pancreatitis. Database: the Journal of Biological Databases and Curation 2018
Versano, Z.; Shany, E.; Freedman, S.; Tuval-Kochen, L.; Leitner, M.; Paglin, S.; Toren, A.; Yalon, M. 2018: MutT homolog 1 counteracts the effect of anti-neoplastic treatments in adult and pediatric glioblastoma cells. Oncotarget 9(44): 27547-27563
Li, J.; Yang, C.-C.; Tian, X.-Y.; Li, Y.-X.; Cui, J.; Chen, Z.; Deng, Z.-L.; Chen, F.-J.; Hayakawa, H.; Sekiguchi, M.; Cai, J.-P. 2017: MutT-related proteins are novel progression and prognostic markers for colorectal cancer. Oncotarget 8(62): 105714-105726
Cieślik, P.; Woźniak, M.; Rook, J.M.; Tantawy, M.N.; Conn, P.J.; Acher, F.; Tokarski, K.; Kusek, M.; Pilc, A.; Wierońska, J.M. 2018: Mutual activation of glutamatergic mGlu4 and muscarinic M4 receptors reverses schizophrenia-related changes in rodents. Psychopharmacology 235(10): 2897-2913
Boukahil, I.; Czuprynski, C.J. 2018: Mutual antagonism between Mannheimia haemolytica and Pasteurella multocida when forming a biofilm on bovine bronchial epithelial cells in vitro. Veterinary Microbiology 216: 218-222
Green, P.A.; Patek, S.N. 2018: Mutual assessment during ritualized fighting in mantis shrimp (Stomatopoda). PROCEEDINGS. Biological Sciences 285(1871)
Sadeghnezhad, M.; Heshmati Nabavi, F.; Najafi, F.; Kareshki, H.; Esmaily, H. 2018: Mutual benefits in academic-service partnership: An integrative review. Nurse Education Today 68: 78-85
Nilendu, P.; Sarode, S.C.; Jahagirdar, D.; Tandon, I.; Patil, S.; Sarode, G.S.; Pal, J.K.; Sharma, N.K. 2018: Mutual concessions and compromises between stromal cells and cancer cells: driving tumor development and drug resistance. Cellular Oncology 41(4): 353-367
DSouza, A.M.; Abidin, A.Z.; Chockanathan, U.; Schifitto, G.; Wismüller, A. 2018: Mutual connectivity analysis of resting-state functional MRi data with local models. Neuroimage 178: 210-223
Wang, S.; Xiao, J.; Wan, L.; Zhou, Z.; Wang, Z.; Song, C.; Zhou, Y.; Cao, X. 2018: Mutual Dependence of Nitrogen and Phosphorus as Key Nutrient Elements: one Facilitates Dolichospermum flos-aquae to Overcome the Limitations of the other. Environmental Science and Technology 52(10): 5653-5661
Foster, C.T.; Gualdrini, F.; Treisman, R. 2017: Mutual dependence of the MRTF-SRF and YAP-TEAD pathways in cancer-associated fibroblasts is indirect and mediated by cytoskeletal dynamics. Genes and Development 31(23-24): 2361-2375
Kim, S.-W.; Lee, Y.K.; Hong, J.H.; Park, J.-Y.; Choi, Y.-A.; Lee, D.U.; Choi, J.; Sym, S.J.; Kim, S.-H.; Khang, D. 2018: Mutual Destruction of Deep Lung Tumor Tissues by Nanodrug-Conjugated Stealth Mesenchymal Stem Cells. Advanced Science 5(5): 1700860
Liu, C.-B.; Zhang, L.; Wu, Q.; Qu, G.-B.; Yin, Y.-G.; Hu, L.-G.; Shi, J.-B.; Jiang, G.-B. 2018: Mutual detoxification of mercury and selenium in unicellular Tetrahymena. Journal of Environmental Sciences 68: 143-150
Wang, X.; Wang, X.; Di, Q.; Zhao, H.; Liang, B.; Yang, J. 2017: Mutual Effects of Fluorine Dopant and Oxygen Vacancies on Structural and Luminescence Characteristics of F Doped SnO₂ Nanoparticles. Materials 10(12)
Corso, G.; Bonanni, B.; Veronesi, P.; Galimberti, V. 2018: Mutual exclusion of CDH1 and BRCA germline mutations in the pathway of hereditary breast cancer. Archives of Gynecology and Obstetrics 297(4): 1067-1068
Shao, X.; Cui, X.; Yu, X.; Cai, W. 2018: Mutual factor analysis for quantitative analysis by temperature dependent near infrared spectra. Talanta 183: 142-148
Maurer, C.; Vosseler, B.; Senn, B.; Gattinger, H. 2018: Mutual guiding and following of movement - the interaction process in mobilisation based on the example of kinaesthetics: a qualitative study. Pflege 31(3): 145-154
Luebbert, C.; Wessner, M.; Sadowski, G. 2018: Mutual Impact of Phase Separation/Crystallization and Water Sorption in Amorphous Solid Dispersions. Molecular Pharmaceutics 15(2): 669-678
Kamradt, T.; Amling, M.; Dankbar, B.; Dudeck, A.; Gunzer, M.; Ignatius, A.; Krönke, G.; Kubatzky, K.; Pap, T.; Prinz, I.; Schett, G.; Schinke, T.; Tuckermann, J.; Waisman, A. 2018: Mutual influence of immune system and bones. Zeitschrift für Rheumatologie 77(Suppl 1): 8-11
Hori, T.; Kamino, T.; Yoshimoto, Y.; Takagi, S.; Kinefuchi, I. 2018: Mutual influence of molecular diffusion in gas and surface phases. Physical Review e 97(1-1): 013101
Peretti, M.; Raciti, F.M.; Carlini, V.; Verduci, I.; Sertic, S.; Barozzi, S.; Garré, M.; Pattarozzi, A.; Daga, A.; Barbieri, F.; Costa, A.; Florio, T.; Mazzanti, M. 2018: Mutual Influence of ROS, pH, and CLIC1 Membrane Protein in the Regulation of G1-S Phase Progression in Human Glioblastoma Stem Cells. Molecular Cancer Therapeutics 17(11): 2451-2461
Grigorenko, V.; Uporov, I.; Rubtsova, M.; Andreeva, I.; Shcherbinin, D.; Veselovsky, A.; Serova, O.; Ulyashova, M.; Ishtubaev, I.; Egorov, A. 2018: Mutual influence of secondary and key drug-resistance mutations on catalytic properties and thermal stability of TEM-type β-lactamases. Febs Open Bio 8(1): 117-129
Sun, C.; Yang, F.; Wang, C.; Wang, Z.; Zhang, Y.; Ming, D.; Du, J. 2018: Mutual Information-Based Brain Network Analysis in Post-stroke Patients with Different Levels of Depression. Frontiers in Human Neuroscience 12: 285
Fayard, N.; Goetschy, A.; Pierrat, R.; Carminati, R. 2018: Mutual Information between Reflected and Transmitted Speckle Images. Physical Review Letters 120(7): 073901
Lin, L-Hui.; Chen, T-Jer. 2018: Mutual Information Correlation with Human Vision in Medical Image Compression. Current Medical Imaging Reviews 14(1): 64-70
von Wegner, F.; Laufs, H.; Tagliazucchi, E. 2018: Mutual information identifies spurious Hurst phenomena in resting state EEG and fMRI data. Physical Review e 97(2-1): 022415
Becker, S. 1996: Mutual information maximization: models of cortical self-organization. Network 7(1): 7-31
Koyama, M.; Pujala, A. 2018: Mutual inhibition of lateral inhibition: a network motif for an elementary computation in the brain. Current Opinion in Neurobiology 49: 69-74
Barral-Fraga, L.; Martiñá-Prieto, D.; Barral, M.ía.T.; Morin, S.; Guasch, H. 2018: Mutual interaction between arsenic and biofilm in a mining impacted river. Science of the Total Environment 636: 985-998
Vollmer, M.; Esders, S.; Farquharson, F.M.; Neugart, S.; Duncan, S.H.; Schreiner, M.; Louis, P.; Maul, R.; Rohn, S. 2018: Mutual Interaction of Phenolic Compounds and Microbiota: Metabolism of Complex Phenolic Apigenin-C- and Kaempferol-O-Derivatives by Human Fecal Samples. Journal of Agricultural and Food Chemistry 66(2): 485-497
Avsievich, T.; Popov, A.; Bykov, A.; Meglinski, I. 2018: Mutual interaction of red blood cells assessed by optical tweezers and scanning electron microscopy imaging. Optics Letters 43(16): 3921-3924
Nanić, L.; Vidaček, N.Šk.; Ravlić, S.; Šatović, E.; Huzak, M.; Rubelj, I. 2018: Mutual interactions between telomere heterogeneity and cell culture growth dynamics shape stochasticity of cell aging. Biogerontology 19(1): 23-31
Zhang, R.; Thabet, A.; Hiob, L.; Zheng, W.; Daugschies, A.; Bangoura, B. 2018: Mutual interactions of the apicomplexan parasites Toxoplasma gondii and Eimeria tenella with cultured poultry macrophages. Parasites and Vectors 11(1): 453
De Bruin, N.; Ferreirós, N.; Schmidt, M.; Hofmann, M.; Angioni, C.; Geisslinger, G.; Parnham, M.J. 2018: Mutual inversion of flurbiprofen enantiomers in various rat and mouse strains. Chirality 30(5): 632-641
Parker, M.A. 1999: Mutualism in Metapopulations of Legumes and Rhizobia. American Naturalist 153(S5): S48-S60
Hu, L.-Y.; Li, D.; Sun, K.; Cao, W.; Fu, W.-Q.; Zhang, W.; Dai, C.-C. 2018: Mutualistic fungus Phomopsis liquidambari increases root aerenchyma formation through auxin-mediated ethylene accumulation in rice (Oryza sativa L.). Plant Physiology and Biochemistry (Paris) 130: 367-376
Koch, S.; Hägglund, M. 2017: Mutual Learning and Exchange of Health Informatics Experiences from Around the World - Evaluation of a Massive Open Online Course in eHealth. Studies in Health Technology and Informatics 245: 753-757
Ren, Y.; Jiao, L.; Yang, S.; Wang, S. 2018: Mutual Learning Between Saliency and Similarity: Image Cosegmentation via Tree Structured Sparsity and Tree Graph Matching. IEEE Transactions on Image Processing: a Publication of the IEEE Signal Processing Society 27(9): 4690-4704
Levin, E.D.; Wells, C.; Slade, S.; Rezvani, A.H. 2018: Mutually augmenting interactions of dextromethorphan and sazetidine-A for reducing nicotine self-administration in rats. Pharmacology Biochemistry and Behavior 166: 42-47
Jin, Y.; Dong, H.; Shi, Y.; Bian, L. 2018: Mutually exclusive alternative splicing of pre-mRNAs. Wiley Interdisciplinary Reviews. Rna 9(3): E1468
Arzumanyan, G.A.; Gabriel, K.N.; Ravikumar, A.; Javanpour, A.A.; Liu, C.C. 2018: Mutually Orthogonal DNA Replication Systems in Vivo. Acs Synthetic Biology 7(7): 1722-1729
Sawyer, J.C.; Miller, T.M.; Sweeny, B.C.; Ard, S.G.; Viggiano, A.A.; Shuman, N.S. 2018: Mutual neutralization of H+ and D+ with the atomic halide anions Cl-,Br-, and i. Journal of Chemical Physics 149(4): 044303
Lynch, H.Fernandez.; Gelinas, L.; Largent, E.A. 2018: Mutual Obligations in Research and Withholding Payment From Deceptive Participants. American Journal of Bioethics: Ajob 18(4): 85-87
Li, S.; Liu, J.; Lu, Y.; Zhu, L.; Li, C.; Hu, L.; Li, J.; Jiang, J.; Low, S.; Liu, Q. 2018: Mutual promotion of electrochemical-localized surface plasmon resonance on nanochip for sensitive sialic acid detection. Biosensors and Bioelectronics 117: 32-39
Flexer, A.; Stevens, J. 2018: Mutual proximity graphs for improved reachability in music recommendation. Journal of new Music Research 47(1): 17-28
Titone, R.; Zhu, M.; Robertson, D.M. 2019: Mutual regulation between IGF-1R and IGFBP-3 in human corneal epithelial cells. Journal of Cellular Physiology 234(2): 1426-1441
Yu, Z-Wei.; Xu, Y-Qin.; Zhang, X-Juan.; Pan, J-Rong.; Xiang, H-Xia.; Gu, X-Hong.; Ji, S-Bao.; Qian, J. 2019: Mutual regulation between miR-21 and the TGFβ/Smad signaling pathway in human bronchial fibroblasts promotes airway remodeling. Journal of Asthma: Official Journal of the Association for the Care of Asthma 56(4): 341-349
Wang, X.; Huai, G.; Wang, H.; Liu, Y.; Qi, P.; Shi, W.; Peng, J.; Yang, H.; Deng, S.; Wang, Y. 2018: Mutual regulation of the Hippo/Wnt/LPA/TGF‑β signaling pathways and their roles in glaucoma (Review). International Journal of Molecular Medicine 41(3): 1201-1212
Gratuze, M.; Joly-Amado, A.él.; Vieau, D.; Buée, L.; Blum, D. 2018: Mutual Relationship between Tau and Central Insulin Signalling: Consequences for AD and Tauopathies?. Neuroendocrinology 107(2): 181-195
Herr, M.M.; Schonfeld, S.J.; Dores, G.ça.M.; Withrow, D.R.; Tucker, M.A.; Curtis, R.E.; Morton, L.M. 2018: Mutual Risks of Cutaneous Melanoma and Specific Lymphoid Neoplasms: Second Cancer Occurrence and Survival. Journal of the National Cancer Institute 110(11): 1248-1258
Liu, K.; Zhang, C.; Li, B.; Xie, W.; Zhang, J.; Nie, X.; Tan, P.; Zheng, L.; Wu, S.; Qin, Y.; Cui, J.; Zhi, F. 2018: Mutual Stabilization between TRIM9 Short Isoform and MKK6 Potentiates p38 Signaling to Synergistically Suppress Glioblastoma Progression. Cell Reports 23(3): 838-851
Li, Q.; Lin, Y.; Chen, Y.; Loke, A.Y. 2018: Mutual Support and Challenges Among Chinese Couples Living with Colorectal Cancer: a Qualitative Study. Cancer Nursing 41(5): E50-E60
Yang, W.-P.; Liu, C.-W.; Sung, S.-F. 2018: Mutual Support Beyond Suffering and Mortality-Spiritual Care for Families of Terminal Cancer Patients. Hu Li Za Zhi Journal of Nursing 65(3): 22-27
Cipolletta, S.; Gammino, G.R.; Francescon, P.; Palmieri, A. 2018: Mutual support groups for family caregivers of people with amyotrophic lateral sclerosis in Italy: a pilot study. Health and Social Care in the Community 26(4): 556-563
Panella, M.; Mosca, N.; Di Palo, A.; Potenza, N.; Russo, A. 2018: Mutual suppression of miR-125a and Lin28b in human hepatocellular carcinoma cells. Biochemical and Biophysical Research Communications 500(3): 824-827
Tasca, D.S.; Sánchez, P.; Walborn, S.P.; Rudnicki, Łu. 2018: Mutual Unbiasedness in Coarse-Grained Continuous Variables. Physical Review Letters 120(4): 040403
Caves, E.M.; Green, P.A.; Johnsen, S.ön. 2018: Mutual visual signalling between the cleaner shrimp Ancylomenes pedersoni and its client fish. PROCEEDINGS. Biological Sciences 285(1881)
Zhang, S.; Guo, H.; Chen, D.; Chen, X.; Jin, Q. 2018: MUTYH and ORAI1 polymorphisms are associated with susceptibility to osteoarthritis in the Chinese Han population. Journal of International Medical Research 46(6): 2292-2300
Iness, A.N.; Litovchick, L. 2018: MuvB: a Key to Cell Cycle Control in Ovarian Cancer. Frontiers in Oncology 8: 223
Burkholder, A.B.; Lujan, S.A.; Lavender, C.A.; Grimm, S.A.; Kunkel, T.A.; Fargo, D.C. 2018: Muver, a computational framework for accurately calling accumulated mutations. Bmc Genomics 19(1): 345
Saluzzo, S. 2018: MUW researcher of the month. Wiener Klinische Wochenschrift: -
Anonymous 1899: Muzzling and Rabies. Hospital 26(665): 205
Anonymous 1897: Muzzling or Rabies. Hospital 23(586): 195-196
Anonymous 1912: Muzzling the School Doctor. Hospital 51(1333): 420
Rouwendal, J. 2018: M. Van Acker: From flux to frame. Designing infrastructure and shaping urbanization in Belgium: Leuven University Press, Leuven, 2014, p. 464, 9789058679581. Journal of Housing and the Built Environment 32(1): 185-186
Anonymous 1835: M. Velpeau on Puerperal Convulsions. Medico-chirurgical review 23(45): 61-68
Walter, V.; Du, Y.; Danilova, L.; Hayward, M.C.; Hayes, D.N. 2018: MVisAGe Identifies Concordant and Discordant Genomic Alterations of Driver Genes in Squamous Tumors. Cancer Research 78(12): 3375-3385
Klawohn, S.; Kaupp, M.; Karton, A. 2018: MVO-10: a Gas-Phase Oxide Benchmark for Localization/Delocalization in Mixed-Valence Systems. Journal of Chemical Theory and Computation 14(7): 3512-3523
Iglehart, B. 2018: MVO Automation Platform: Addressing Unmet Needs in Clinical Laboratories with Microcontrollers, 3D Printing, and Open-Source Hardware/Software. Slas Technology 23(5): 423-431
Gao, N.L.; Zhang, C.; Zhang, Z.; Hu, S.; Lercher, M.J.; Zhao, X.-M.; Bork, P.; Liu, Z.; Chen, W.-H. 2018: MVP: a microbe-phage interaction database. Nucleic Acids Research 46(D1): D700-D707
Lintel, N.J.; Luebker, S.A.; Lele, S.M.; Koepsell, S.A. 2018: MVP immunohistochemistry is a useful adjunct in distinguishing leiomyosarcoma from leiomyoma and leiomyoma with bizarre nuclei. Human Pathology 73: 122-127
Bergallo, M.; Galliano, I.; Montanari, P.; Rassu, M.; Daprà, V.; Merlino, C.; Tovo, P.-A. 2023: MW Polyomavirus in diarrheal Italian infants. Minerva Pediatrics 75(3): 327-330
Aragão, D.; Aishima, J.; Cherukuvada, H.; Clarken, R.; Clift, M.; Cowieson, N.P.; Ericsson, D.J.; Gee, C.L.; Macedo, S.; Mudie, N.; Panjikar, S.; Price, J.R.; Riboldi-Tunnicliffe, A.; Rostan, R.; Williamson, R.; Caradoc-Davies, T.T. 2018: MX2: a high-flux undulator microfocus beamline serving both the chemical and macromolecular crystallography communities at the Australian Synchrotron. Journal of Synchrotron Radiation 25(Part 3): 885-891
Jaguva Vasudevan, A.A.; Bähr, A.; Grothmann, R.; Singer, A.; Häussinger, D.; Zimmermann, A.; Münk, C. 2018: MXB inhibits murine cytomegalovirus. Virology 522: 158-167
Kumagai, S.; Takaishi, S.; Gao, M.; Iguchi, H.; Breedlove, B.K.; Yamashita, M. 2018: MX-Chain Compounds with ReO4 Counterions: Exploration of the Robin-Day Class I-Ii Boundary. Inorganic Chemistry 57(7): 3775-3781
Dudnyk, A.; Burman, M.; Kulyk, L.; Rzhepishevska, O. 2018: M/XDR-TB treatment perspective: how to avoid mountains of pills via digital technologies. Respirology 23(6): 636-637
Okubo, M.; Sugahara, A.; Kajiyama, S.; Yamada, A. 2018: MXene as a Charge Storage Host. Accounts of Chemical Research 51(3): 591-599
Niu, S.; Wang, Z.; Yu, M.; Yu, M.; Xiu, L.; Wang, S.; Wu, X.; Qiu, J. 2018: MXene-Based Electrode with Enhanced Pseudocapacitance and Volumetric Capacity for Power-Type and Ultra-Long Life Lithium Storage. Acs Nano 12(4): 3928-3937
Yang, X.; Gao, N.; Zhou, S.; Zhao, J. 2018: MXene nanoribbons as electrocatalysts for the hydrogen evolution reaction with fast kinetics. Physical Chemistry Chemical Physics: Pccp 20(29): 19390-19397
Zhang, Y.-Z.; Lee, K.H.; Anjum, D.H.; Sougrat, R.; Jiang, Q.; Kim, H.; Alshareef, H.N. 2018: MXenes stretch hydrogel sensor performance to new limits. Science Advances 4(6): Eaat 0098
Case, H.B.; Dickenson, N.E. 2018: MxiN Differentially Regulates Monomeric and Oligomeric Species of the Shigella Type Three Secretion System ATPase Spa47. Biochemistry 57(15): 2266-2277
Gibbens, N. 2018: My 10 years as UK chief vet. Veterinary Record 182(9): 265
Mohanty, B.D. 2018: My 3 Rules. Journal of Graduate Medical Education 10(1): 97-98
Mohan, V. 2018: My 40-year journey in diabetes research: the power of collaboration. Perspectives in Clinical Research 9(3): 113-122
Hovius, S.E.R. 2018: My 40-year perspective on hand surgery. Journal of Hand Surgery European Volume 43(4): 351-361
Anonymous 1918: Myalgia: A Clinical Study. Hospital 63(1652): 369-370
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Rand, T.A.; Sutou, K.; Tanabe, K.; Jeong, D.; Nomura, M.; Kitaoka, F.; Tomoda, E.; Narita, M.; Nakamura, M.; Nakamura, M.; Watanabe, A.; Rulifson, E.; Yamanaka, S.; Takahashi, K. 2018: MYC Releases Early Reprogrammed Human Cells from Proliferation Pause via Retinoblastoma Protein Inhibition. Cell Reports 23(2): 361-375
Lu, Y.; Hu, Z.; Mangala, L.S.; Stine, Z.E.; Hu, X.; Jiang, D.; Xiang, Y.; Zhang, Y.; Pradeep, S.; Rodriguez-Aguayo, C.; Lopez-Berestein, G.; DeMarzo, A.M.; Sood, A.K.; Zhang, L.; Dang, C.V. 2018: MYC Targeted Long Noncoding RNA DANCR Promotes Cancer in Part by Reducing p21 Levels. Cancer Research 78(1): 64-74
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Li, X-Li.; Xu, P-Cheng.; Chen, T.; Yan, T-Kun.; Jiang, J-Qing.; Jia, J-Ya.; Wei, L.; Shang, W-Ya.; Hu, S-Yi. 2017: Myeloperoxidase-antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis developed from ANCA negative renal limited vasculitis: A case report. Medicine 96(51): E9128
Khan, A.A.; Alsahli, M.A.; Rahmani, A.H. 2018: Myeloperoxidase as an Active Disease Biomarker: Recent Biochemical and Pathological Perspectives. Medical Sciences 6(2)
Ollikainen, E.; Tulamo, R.; Lehti, S.; Hernesniemi, J.; Niemelä, M.; Kovanen, P.T.; Frösen, J. 2018: Myeloperoxidase Associates with Degenerative Remodeling and Rupture of the Saccular Intracranial Aneurysm Wall. Journal of Neuropathology and Experimental Neurology 77(6): 461-468
Delporte, C.éd.; Zouaoui Boudjeltia, K.; Furtmüller, P.G.; Maki, R.A.; Dieu, M.; Noyon, C.; Soudi, M.; Dufour, D.; Coremans, C.; Nuyens, V.; Reye, F.; Rousseau, A.; Raes, M.; Moguilevsky, N.; Vanhaeverbeek, M.; Ducobu, J.; Nève, J.; Robaye, B.; Vanhamme, L.; Reynolds, W.F.; Obinger, C.; Van Antwerpen, P. 2018: Myeloperoxidase-catalyzed oxidation of cyanide to cyanate: a potential carbamylation route involved in the formation of atherosclerotic plaques?. Journal of Biological Chemistry 293(17): 6374-6386
Rastogi, P.; Sharma, S.; Sreedharanunni, S.; Sharma, P.; Sachdeva, M.Updesh.Singh.; Jain, R.; Naseem, S.; Trehan, A.; Varma, N. 2018: Myeloperoxidase Deficient Acute Promyelocytic Leukemia: Report of Two Cases. Indian Journal of Hematology and Blood Transfusion: An Official Journal of Indian Society of Hematology and Blood Transfusion 34(2): 372-374
Meyer, N.J.; Reilly, J.P.; Feng, R.; Christie, J.D.; Hazen, S.L.; Albert, C.J.; Franke, J.D.; Hartman, C.L.; McHowat, J.; Ford, D.A. 2017: Myeloperoxidase-derived 2-chlorofatty acids contribute to human sepsis mortality via acute respiratory distress syndrome. Jci Insight 2(23)
Zeng, L.; Mathew, A.V.; Byun, J.; Atkins, K.B.; Brosius, F.C.; Pennathur, S. 2018: Myeloperoxidase-derived oxidants damage artery wall proteins in an animal model of chronic kidney disease-accelerated atherosclerosis. Journal of Biological Chemistry 293(19): 7238-7249
Chen, S-Fang.; Wang, F-Mei.; Li, Z-Ying.; Yu, F.; Chen, M.; Zhao, M-Hui. 2018: Myeloperoxidase influences the complement regulatory activity of complement factor H. Rheumatology 57(12): 2213-2224
Chami, B.; Martin, N.J.J.; Dennis, J.M.; Witting, P.K. 2018: Myeloperoxidase in the inflamed colon: a novel target for treating inflammatory bowel disease. Archives of Biochemistry and Biophysics 645: 61-71
Beckmann, L.; Dicke, C.; Spath, B.; Lehr, C.; Sievers, B.; Klinke, A.; Baldus, S.; Rudolph, V.; Langer, F. 2017: Myeloperoxidase Is a Negative Regulator of Phospholipid-Dependent Coagulation. Thrombosis and Haemostasis 117(12): 2300-2311
Aratani, Y. 2018: Myeloperoxidase: its role for host defense, inflammation, and neutrophil function. Archives of Biochemistry and Biophysics 640: 47-52
Kimak, E.żb.; Zięba, B.; Duma, D.; Solski, J. 2018: Myeloperoxidase level and inflammatory markers and lipid and lipoprotein parameters in stable coronary artery disease. Lipids in Health and Disease 17(1): 71
Wang, G.; Mathew, A.Vachaparampil.; Yu, H.; Li, L.; He, L.; Gao, W.; Liu, X.; Guo, Y.; Byun, J.; Zhang, J.; Chen, Y.Eugene.; Pennathur, S. 2018: Myeloperoxidase mediated HDL oxidation and HDL proteome changes do not contribute to dysfunctional HDL in Chinese subjects with coronary artery disease. Plos one 13(3): E0193782
Chen, X.; Duong, M.-N.; Nicholls, S.J.; Bursill, C. 2018: Myeloperoxidase modification of high-density lipoprotein suppresses human endothelial cell proliferation and migration via inhibition of ERK1/2 and Akt activation. Atherosclerosis 273: 75-83
Tseng, A.; Kim, K.; Li, J.; Cho, J. 2018: Myeloperoxidase Negatively Regulates Neutrophil-Endothelial Cell Interactions by Impairing αMβ2 Integrin Function in Sterile Inflammation. Frontiers in Medicine 5: 134
Khalil, A.; Medfai, H.; Poelvoorde, P.; Kazan, M.F.; Delporte, C.; Van Antwerpen, P.; El-Makhour, Y.; Biston, P.; Delrée, P.; Badran, B.; Vanhamme, L.; Boudjeltia, K.Z. 2018: Myeloperoxidase promotes tube formation, triggers ERK1/2 and Akt pathways and is expressed endogenously in endothelial cells. Archives of Biochemistry and Biophysics 654: 55-69
Rodriguez-Palacios, A.; Cominelli, F. 2019: Myeloperoxidases and Proteobacteria: Reliable Interspecies Biomarkers to Identify and Monitor Pro-inflammatory Diets in Humans. Inflammatory Bowel Diseases 25(2): E1-E2
Herder, C.; Kannenberg, J.M.; Huth, C.; Carstensen-Kirberg, M.; Rathmann, W.; Koenig, W.; Strom, A.; Bönhof, G.J.; Heier, M.; Thorand, B.; Peters, A.; Roden, M.; Meisinger, C.; Ziegler, D. 2018: Myeloperoxidase, superoxide dismutase-3, cardiometabolic risk factors, and distal sensorimotor polyneuropathy: the KORA F4/FF4 study. Diabetes/Metabolism Research and Reviews 34(5): E3000
Shomali, W.; Gotlib, J. 2018: Myelophthisic marrow involved by breast cancer and acute myeloid leukemia. Blood 131(9): 1036
Mitroulis, I.; Kalafati, L.; Hajishengallis, G.; Chavakis, T. 2018: Myelopoiesis in the Context of Innate Immunity. Journal of Innate Immunity 10(5-6): 365-372
Young, K.M. 1985: Myeloproliferative disorders. Veterinary Clinics of North America. Small Animal Practice 15(4): 769-781
Nangalia, J.; Green, A.R. 2017: Myeloproliferative neoplasms: from origins to outcomes. Blood 130(23): 2475-2483
Tafesh, L.; Musgrave, K.; Roberts, W.; Plews, D.; Carey, P.; Biss, T. 2019: Myeloproliferative Neoplasms in Children and Adolescents and Thrombosis at Unusual Sites: the Role of Driver Mutations. Journal of Pediatric Hematology/Oncology 41(6): 490-493
Andersen, M.A.; Bjerrum, O.W.; Ranjan, A.; Skov, V.; Kruse, T.A.; Thomassen, M.; Skytthe, A.; Hasselbalch, H.C.; Christensen, K. 2018: Myeloproliferative Neoplasms in Danish Twins. Acta Haematologica 139(3): 195-198
Anonymous 2018: Myeloproliferative Neoplasms May Be Sensitive to Dual BET/JAK Inhibition. Cancer discovery 8(2): OF10
Kamiunten, A.; Shide, K.; Shimoda, K. 2018: Myeloproliferative neoplasms: recent progresses in therapy. Japanese Journal of Clinical Hematology 59(6): 741-746
Qin, C.; Zhang, W-Hao.; Yang, D-Gang.; Yang, M-Liang.; Du, L-Jie.; Li, J-Jun. 2018: Myelotomy promotes locomotor recovery in rats subjected to spinal cord injury: A meta-analysis of six randomized controlled trials. Neural Regeneration Research 13(6): 1096-1106
Cramer, E.Paula. 2018: My Entrance, Her Exit. JournalofSocialWorkinEnd-Of-LifeandPalliativeCare 14(2-3): 127
D'Amour, R. 2016: My experience as a Quarantine Officer welcoming Syrian refugees. Canada Communicable Disease Report 42(Suppl. 2): S11-S12
Fox, K. 2018: My experience of being a doctor with psychosis. British Journal of General Practice: the Journal of the Royal College of General Practitioners 68(666): 30
Hind, W. 1901: My Experience of Suprapubic Lithotomy. Hospital 30(761): 61-62
Anonymous 1914: My Experiences in a Field Ambulance. Hospital 57(1479): 85-87
Gore, R. 2018: My Eye Pressure Is Up Again!. Journal of Pediatric Ophthalmology and Strabismus 55(4): 215
Kim, G.; Kim, T. 2018: My Family's Struggle With Dementia: Trying to Hit the High Notes. Family Medicine 50(4): 304-305
Arntzen, E. 2017: My father found the way to the best death. Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 137(9): 640
Rezak, M. 2018: My Father, my Patient. Narrative Inquiry in Bioethics 8(1): 22-25
Ciance, K.L. 2018: My father, the "treatment truck," and the road to recovery. Nursing 48(9): 48
Prunet, Nël. 2019: My favourite flowering image: an Arabidopsis inflorescence expressing fluorescent reporters for the APETALA3 and SUPERMAN genes. Journal of Experimental Botany 70(21): E6499-E6501
Anonymous 1918: My Fellow-Probationer. Hospital 65(1694): 166
Anonymous 1914: My First Christmas in Hospital. Hospital 55(1436): 373
Nobbs, A.; Nobbs, A. 2018: My first experiences of nurse leadership. British Journal of Nursing 27(10): 572-573
Cory, S. 2018: MyGrief.ca. Annals of Palliative Medicine 7(Suppl 1): Ab017
Samelson-Jones, B.J.; Kramer, P.M.; Chicka, M.; Gunning, W.T.; Lambert, M.P. 2018: MYH9-macrothrombocytopenia caused by a novel variant (E1421K) initially presenting as apparent neonatal alloimmune thrombocytopenia. Pediatric Blood and Cancer 65(4)
Marques, M.I.ês.; Carrington Queiró, L.ís.; Prior, A.R.; Lopo Tuna, M. 2018: MYH9-related disorders: a rare cause of neonatal thrombocytopaenia. BMJ Case Reports
Zaninetti, C.; De Rocco, D.; Giangregorio, T.; Bozzi, V.; Demeter, J.; Leoni, P.; Noris, P.; Ryhänen, S.; Barozzi, S.; Pecci, A.; Savoia, A. 2019: MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder. Hamostaseologie 39(1): 87-94
Pecci, A.; Ma, X.; Savoia, A.; Adelstein, R.S. 2018: MYH9: Structure, functions and role of non-muscle myosin IIA in human disease. Gene 664: 152-167
Shields, D. 2017: My Healing Journey. Beginnings 37(1): 20
Zhang, X.; Deng, Z.; Parvinzamir, F.; Dong, F. 2018: MyHealthAvatar lifestyle management support for cancer patients. Ecancermedicalscience 12: 849
Mendelson, D.; Wolf, G. 2016: "My [Electronic] Health Record" – Cui Bono (for Whose Benefit)?. Journal of Law and Medicine 24(2): 283-296
Dowd, A.J.; Jackson, C.; Tang, K.T.Y.; Nielsen, D.; Clarkin, D.H.; Culos-Reed, S.N. 2018: MyHealthyGut: development of a theory-based self-regulatory app to effectively manage celiac disease. Mhealth 4: 19
Fabian, K.; Fannoh, J.; Washington, G.G.; Geninyan, W.B.; Nyachienga, B.; Cyrus, G.; Hallowanger, J.N.; Beste, J.; Rao, D.; Wagenaar, B.H. 2018: "My Heart die in Me": Idioms of Distress and the Development of a Screening Tool for Mental Suffering in Southeast Liberia. Culture Medicine and Psychiatry 42(3): 684-703
Covert, E. 2018: My Heart Failure Journey. JACC. Heart Failure 6(3): 260-261
Meyer, A.L.; Garbade, J. 2018: My HeartWare implantation technique: tricks and pitfalls. Interactive Cardiovascular and Thoracic Surgery 27(6): 943-945
Tufts, K.A.; Wessell, J. 2018: My how times have changed…interprofessional collaboration is in the house. Journal of the Association of Nurses in Aids Care: Janac 29(4): 619-620
Nomura, R.; Miyai, K.; Nishimura, G.; Kashimada, K.; Morio, T. 2017: Myhre syndrome: Age-dependent progressive phenotype. Pediatrics International: Official Journal of the Japan Pediatric Society 59(11): 1205-1206
Johnson, H.M.; LaMantia, J.N.; Brown, C.M.; Warner, R.C.; Zeller, L.M.; Haggart, R.C.; Stonewall, K.; Lauver, D.R. 2017: My Hypertension Education and Reaching Target (MyHEART): Development and Dissemination of a Patient-Centered Website for Young Adults with Hypertension. Jmir Cardio 1(2)
Jakhar, D.; Misra, A.; Dabas, S. 2018: Myiasis under Dermatoscope: the Hidden Story. Indian Dermatology Online Journal 9(3): 220-221
Anonymous 1913: My Impression of the Hospital: The Unaided Composition of a Patient Aged Eleven. Hospital 55(1435): 340
Hirschberg, C.B. 2018: My journey in the discovery of nucleotide sugar transporters of the Golgi apparatus. Journal of Biological Chemistry 293(33): 12653-12662
Jupiter, J. 2018: My journey through the elbow. Journal of Shoulder and Elbow Surgery 27(12): 2292-2294
Xie, X.; Wang, X.; Liao, W.; Fei, R.; Wu, N.; Cong, X.; Chen, Q.; Wei, L.; Wang, Y.; Chen, H. 2018: MYL6B, a myosin light chain, promotes MDM2-mediated p53 degradation and drives HCC development. Journal of Experimental and Clinical Cancer Research: Cr 37(1): 28
Sadayappan, S.; Sadayappan, S. 2018: My Life, my Heart, and My(osin) Binding Protein-C. Circulation Research 122(7): 918-920
Bennett, N. 2018: My light bulb moment. British Journal of Nursing 27(4): 184
Lin, J.; He, Y.; Chen, L.; Chen, X.; Zang, S.; Lin, W. 2018: MYLK promotes hepatocellular carcinoma progression through regulating cytoskeleton to enhance epithelial-mesenchymal transition. Clinical and Experimental Medicine 18(4): 523-533
Brüggemann, N.; Steffen, A. 2018: Mylohyoid hemispasm in a patient with hypoglossal nerve stimulation. Clinical Case Reports 6(8): 1657-1658
Lee, K.M.; Joo, M.C.; Yu, Y.M.; Kim, M.-S. 2018: Mylohyoid motor evoked potentials can effectively predict persistent dysphagia 3 months poststroke. Neurogastroenterology and Motility: the Official Journal of the European Gastrointestinal Motility Society 30(7): E13323
Gelman, S. 2018: Classic Papers Revisited: My Love Affair with the Venous System. Anesthesiology 129(2): 329-332
Dolan, J. 2018: My LVAD Gave me a New Lease on Life. JACC. Heart Failure 6(4): 343
Clarfield, A.M. 2018: My Medicine, my body: the Serious Physician becomes a Serious Patient. Israel Medical Association Journal: Imaj 20(1): 66
Mermel, L.A. 2017: My Mentor. Wmj: Official Publication of the State Medical Society of Wisconsin 116(5): 189
Heiphetz, L.; Lane, J.D.; Waytz, A.; Young, L.L. 2018: My mind, your mind, and God's mind: how children and adults conceive of different agents' moral beliefs. British Journal of Developmental Psychology 36(3): 467-481
Weller, L.; Schwarz, K.A.; Kunde, W.; Pfister, R. 2018: My mistake? Enhanced error processing for commanded compared to passively observed actions. Psychophysiology 55(6): E13057
Lundebjerg, N.E. 2018: My Mom is Dead (and that is OK). Journal of the American Geriatrics Society 66(3): 629-630
Felson, B. 1976: My most unforgettable patient. Seminars in Roentgenology 11(2): 77-79
Due, K. 2018: My mother, Ngandi. Medical Journal of Australia 209(1): 10
Mackworth-Young, C.R.; Bond, V.; Wringe, A.; Konayuma, K.; Clay, S.; Chiiya, C.; Chonta, M.; Sievwright, K.; Stangl, A.L. 2017: "My mother told me that i should not": a qualitative study exploring the restrictions placed on adolescent girls living with HIV in Zambia. Journal of the International Aids Society 20(4)
Anonymous 1912: My Motor-Cycling Experiences: By a Country Practitioner. Hospital 52(1348): 154
Shokuhfar, T.; Hurley, M.C.; Al-Smadi, A.; Ansari, S.A.; Potts, M.B.; Jahromi, B.S.; Alden, T.D.; Shaibani, A. 2018: MynxGrip vascular closure device use in pediatric neurointerventional procedures. Journal of Neurosurgery. Pediatrics 21(5): 466-470
Ben-Dor, I.; Craig, P.; Torguson, R.; Rogers, T.; Buchanan, K.D.; Pokharel, S.; Gai, J.; Okubagzi, P.G.; Satler, L.F.; Pichard, A.D.; Baker, N.C.; Waksman, R. 2018: MynxGrip® vascular closure device versus manual compression for hemostasis of percutaneous transfemoral venous access closure: Results from a prospective multicenter randomized study. Cardiovascular Revascularization Medicine: Including Molecular Interventions 19(4): 418-422
Teixeira, M.M. 2018: Myo1f is critical for neutrophil migration in vivo. Blood 131(17): 1879-1880
Zhao, X.; Zhang, W.; Ji, W. 2018: MYO5A inhibition by miR-145 acts as a predictive marker of occult neck lymph node metastasis in human laryngeal squamous cell carcinoma. Oncotargets and Therapy 11: 3619-3635
Dhekne, H.S.; Pylypenko, O.; Overeem, A.W.; Zibouche, M.; Ferreira, R.J.; van der Velde, K.Joeri.; Rings, E.H.H.M.; Posovszky, C.; van der Sluijs, P.; Swertz, M.A.; Houdusse, A.; van IJzendoorn, S.C.D. 2018: MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Human Mutation 39(3): 333-344
O'Connor, E.; Phan, V.; Cordts, I.; Cairns, G.; Hettwer, S.; Cox, D.; Lochmüller, H.; Roos, A. 2018: MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretion. Human Molecular Genetics 27(8): 1434-1446
Mustonen, A.-M.; Määttänen, M.; Kärjä, V.; Puukka, K.; Aho, J.; Saarela, S.; Nieminen, P. 2018: Myo- and cardiotoxic effects of the wild winter mushroom ( Flammulina velutipes) on mice. Experimental Biology and Medicine 243(7): 639-644
Sampath, S.C.; Sampath, S.C.; Millay, D.P. 2018: Myoblast fusion confusion: the resolution begins. Skeletal Muscle 8(1): 3
Duplanty, A.A.; Siggins, R.W.; Allerton, T.; Simon, L.; Molina, P.E. 2018: Myoblast mitochondrial respiration is decreased in chronic binge alcohol administered simian immunodeficiency virus-infected antiretroviral-treated rhesus macaques. Physiological Reports 6(5)
Testa, S.; D'Addabbo, P.; Fornetti, E.; Belli, R.; Fuoco, C.; Bernardini, S.; Cannata, S.; Frezza, D.; Gargioli, C. 2018: Myoblast Myogenic Differentiation but not Fusion Process Is Inhibited via MyoD Tetraplex Interaction. Oxidative Medicine and Cellular Longevity 2018: 7640272
Scharf, M.; Oezdemir, D.; Schmid, A.; Kemmler, W.; von Stengel, S.; May, M.S.; Uder, M.; Lell, M.M. 2017: Myocardial adaption to HI(R)T in previously untrained men with a randomized, longitudinal cardiac MR imaging study (Physical adaptions in Untrained on Strength and Heart trial, PUSH-trial). Plos one 12(12): E0189204
Sawmiller, D.R.; Fenton, R.A.; Dobson, J.G. 1998: Myocardial adenosine A1-receptor sensitivity during juvenile and adult stages of maturation. American Journal of Physiology. Heart and Circulatory Physiology 274(2): H627-H635
Merante, F.; Mickle, D.A.G.; Weisel, R.D.; Li, R-Ke.; Tumiati, L.C.; Rao, V.; Williams, W.G.; Robinson, B.H. 2018: Myocardial aerobic metabolism is impaired in a cell culture model of cyanotic heart disease. American Journal of Physiology. Heart and Circulatory Physiology 275(5): H1673-H1681
Izumi, Y.; Saito, T.; Sato, S.; Shimizu, W. 2018: Myocardial alterations in a patient with mucopolysaccharidosis type IS. European Heart Journal 39(20): 1863
Li, Y.Y.; Zhu, W.R.; Chai, K.; Yang, J.F.; Fang, F.; He, S.R.; Yang, C.Q.; Wang, H. 2018: Myocardial amyloid deposition in patients aged over 85 years with heart failure and preserved ejection fraction. Zhonghua Xin Xue Guan Bing Za Zhi 46(6): 438-443
Kim, K.Hoo.; Nakaoka, Y.; Augustin, H.G.; Koh, G.Young. 2018: Myocardial Angiopoietin-1 Controls Atrial Chamber Morphogenesis by Spatiotemporal Degradation of Cardiac Jelly. Cell Reports 23(8): 2455-2466
Ramsey, B.C.; Fentanes, E.; Choi, A.D.; Branch, K.R.; Thomas, D.M. 2018: Myocardial Assessment with Cardiac CT: Ischemic Heart Disease and Beyond. Current Cardiovascular Imaging Reports 11(7): 16
Davis, L.E.; Hohimer, A.Roger.; Morton, M.J. 2018: Myocardial blood flow and coronary reserve in chronically anemic fetal lambs. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology 277(1): R306-R313
Tsj, O.; Rjj, K.; Jh, C.; M, W.; Fm, v.d.Z. 2018: Myocardial blood flow and myocardial flow reserve values in 13N-ammonia myocardial perfusion PET/CT using a time-efficient protocol in patients without coronary artery disease. European Journal of Hybrid Imaging 2(1): 11
Takala, T.O.; Nuutila, P.; Katoh, C.; Luotolahti, M.; Bergman, Jörgen.; Mäki, M.; Oikonen, V.; Ruotsalainen, U.; Grönroos, T.; Haaparanta, M.; Kapanen, J.; Knuuti, J. 2018: Myocardial blood flow, oxygen consumption, and fatty acid uptake in endurance athletes during insulin stimulation. American Journal of Physiology. Endocrinology and Metabolism 277(4): E585-E590
Torii, S.; Virmani, R.; Finn, A. 2018: Myocardial Bridge and the Progression of Atherosclerotic Plaque in the Proximal Segment. Arteriosclerosis Thrombosis and Vascular Biology 38(6): 1250-1251
Miakinkova, L.O.; Teslenko, Y.V.; Tsyhanenko, I.V. 2018: Myocardial bridge as the only cause of acute coronary syndrome among the young patients. Wiadomosci Lekarskie 71(3 Part 1): 607-611
Paraskevas, G.; Koutsouflianiotis, K.; Iliou, K. 2017: Myocardial bridge over the left anterior descending coronary artery: A case report and review of the literature. Journal of Research in Medical Sciences: the Official Journal of Isfahan University of Medical Sciences 22: 113
Jukić, M.; Pavić, L.; Bitunjac, I.; Jukić, T.; Milošević, M.; Lovrić, D.; Lovrić Benčić, M. 2017: Myocardial bridging as one of the causes of atypical chest pain in young women. Egyptian Heart Journal:: Official Bulletin of the Egyptian Society of Cardiology 69(4): 235-239
Triantafyllis, A.S.; de Ridder, S.; Teeuwen, K.; Otterspoor, L.C. 2018: Myocardial bridging, a trigger for Takotsubo syndrome. Netherlands Heart Journal: Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 26(11): 573-574
Monnier-Cholley, L.; Roux, A.; Pacanowski, J.ér.ôm.; Arrivé, L. 2018: Myocardial calcifications following sepsis. Intensive Care Medicine 44(6): 981-982
Fish, K.M.; Hajjar, R.J. 2018: Myocardial Cannabinoid Receptor Imaging in Obesity. JACC. Cardiovascular Imaging 11(2 Part 2): 333-335
Ling, S.; Li, Y.; Zhong, G.; Zheng, Y.; Xu, Q.; Zhao, D.; Sun, W.; Jin, X.; Li, H.; Li, J.; Sun, H.; Cao, D.; Song, J.; Liu, C.; Yuan, X.; Wu, X.; Zhao, Y.; Liu, Z.; Li, Q.; Li, Y. 2018: Myocardial CKIP-1 Overexpression Protects from Simulated Microgravity-Induced Cardiac Remodeling. Frontiers in Physiology 9: 40
Berger, F.; Hansi, C.; Niemann, T. 2018: Myocardial Clefts - Incidental Findings in Parainfectious Myocarditis. Praxis 107(11): 599-602
Branch, K.R.; Haley, R.D.; Bittencourt, M.S.; Patel, A.R.; Hulten, E.; Blankstein, R. 2017: Myocardial computed tomography perfusion. Cardiovascular Diagnosis and Therapy 7(5): 452-462
Chilton, R.; Lin, C.; Gallegos, K.M.; Pham, S. 2018: Myocardial considerations in type 2 diabetes: 2018. Journal of Diabetes 10(10): 784-788
Mora, V.; Roldán, I.; Romero, E.; Saurí, Aó.; Romero, D.; Pérez-Gozalbo, J.; Ugalde, N.; Bertolín, J.; Rodriguez-Israel, M.; Delgado, C.Pérez-Olivares.; Lowenstein, J.A. 2018: Myocardial Contraction during the Diastolic Isovolumetric Period: Analysis of Longitudinal Strain by Means of Speckle Tracking Echocardiography. Journal of cardiovascular development and disease 5(3)
Matthews, S.D.; Rubin, J.; Cohen, L.P.; Maurer, M.S. 2018: Myocardial Contraction Fraction: a Volumetric Measure of Myocardial Shortening Analogous to Strain. Journal of the American College of Cardiology 71(2): 255-256
Rubin, J.; Steidley, D.E.; Carlsson, M.; Ong, M.-L.; Maurer, M.S. 2018: Myocardial Contraction Fraction by M-Mode Echocardiography Is Superior to Ejection Fraction in Predicting Mortality in Transthyretin Amyloidosis. Journal of Cardiac Failure 24(8): 504-511
Stolmeijer, R.T.; Lameijer, H. 2017: Myocardial contusion following trauma. Nederlands Tijdschrift Voor Geneeskunde 161: D1766
Murakami, Y.; Zhang, J.; Eijgelshoven, M.H.J.; Chen, W.; Carlyle, W.C.; Zhang, Y.; Gong, G.; Bache, R.J. 2018: Myocardial creatine kinase kinetics in hearts with postinfarction left ventricular remodeling. American Journal of Physiology. Heart and Circulatory Physiology 276(3): H892-H900
Di Bella, G.; Pizzino, F. 2018: Myocardial Deformation Analysis and Late-Gadolinium Enhancement: Important Markers of Cardiac Amyloidosis Involvement that can Masquerade as a False-Negative Diagnosis. Circulation Journal: Official Journal of the Japanese Circulation Society 82(10): 2687
Dores, H.él.; Mendes, L.íg.; Dinis, P.; Cardim, N.; Monge, J.é C.; Santos, J.é F. 2018: Myocardial deformation and volume of exercise: a new overlap between pathology and athlete's heart?. International Journal of Cardiovascular Imaging 34(12): 1869-1875
Ohta, Y.; Kitao, S.; Yunaga, H.; Fujii, S.; Mukai, N.; Yamamoto, K.; Ogawa, T. 2018: Myocardial Delayed Enhancement CT for the Evaluation of Heart Failure: Comparison to MRi. Radiology 288(3): 682-691
El-Battrawy, I.; Borggrefe, M.; Akin, I. 2018: Myocardial Dysfunction Following Brain Death. Journal of the American College of Cardiology 71(3): 368
Karnad, D.R.; Saseedharan, S. 2017: Myocardial Dysfunction in Sepsis and Septic Shock. Journal of the Association of Physicians of India 65(12): 11-12
Kumar, A.; Haery, C.; Parrillo, J.E. 2000: Myocardial dysfunction in septic shock. Critical Care Clinics 16(2): 251-287
Maddaford, T.G.; Pierce, G.N. 1997: Myocardial dysfunction is associated with activation of Na+/H+exchange immediately during reperfusion. American Journal of Physiology. Heart and Circulatory Physiology 273(5): H2232-H2239
Pineton de Chambrun, M.; Mathian, A.; Luyt, C.-E.; Combes, A.; Amoura, Z. 2018: Myocardial dysfunction is frequent in systemic capillary-leak syndrome (Clarkson disease) severe episodes. Journal of Allergy and Clinical Immunology 141(4): 1539-1540
Kotecha, T.; Martinez-Naharro, A.; Treibel, T.A.; Francis, R.; Nordin, S.; Abdel-Gadir, A.; Knight, D.S.; Zumbo, G.; Rosmini, S.; Maestrini, V.; Bulluck, H.; Rakhit, R.D.; Wechalekar, A.D.; Gilbertson, J.; Sheppard, M.N.; Kellman, P.; Gillmore, J.D.; Moon, J.C.; Hawkins, P.N.; Fontana, M. 2018: Myocardial Edema and Prognosis in Amyloidosis. Journal of the American College of Cardiology 71(25): 2919-2931
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