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

Cidon, E.U. 2018: Myalgia-arthralgia syndrome induced by docetaxel in oncology: the wolf disguised as a sheep. Sao Paulo Medical Journal 136(3): 270-271

Hatano, T.; Takanashi, M.; Tsuchihashi, H.; Ueno, S-Ichi.; Hayashida, A.; Tsukune, Y.; Kanai, K.; Shimo, Y.; Hattori, N. 2018: Myalgia caused by chronic myositis associated with plasmacytosis: a case report. Bmc Neurology 18(1): 112

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Shi, D.; Ren, A.; Tang, X.; Qi, G.; Xu, Z.; Chai, G.; Hu, R.; Zhou, G.; Kong, Y. 2018: MYB52 Negatively Regulates Pectin Demethylesterification in Seed Coat Mucilage. Plant Physiology 176(4): 2737-2749

Stringlis, I.A.; Yu, K.; Feussner, K.; de Jonge, R.; Van Bentum, S.; Van Verk, M.C.; Berendsen, R.L.; Bakker, P.A.H.M.; Feussner, I.; Pieterse, C.é M.J. 2018: MYB72-dependent coumarin exudation shapes root microbiome assembly to promote plant health. Proceedings of the National Academy of Sciences of the United States of America 115(22): E5213-E5222

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Emert, T. 2018: My Birth Story. Midwifery Today with International Midwife .(121): 48-49

Wong, Y.-L.I.; Kong, D.; Tu, L.; Frasso, R. 2018: "My bitterness is deeper than the ocean": understanding internalized stigma from the perspectives of persons with schizophrenia and their family caregivers. International Journal of Mental Health Systems 12: 14

Chen, J.; Chen, X. 2018: MYBL2 Is Targeted by miR-143-3p and Regulates Breast Cancer Cell Proliferation and Apoptosis. Oncology Research 26(6): 913-922

Shao, M.; Ren, Z.; Zhang, R. 2018: MYBL2 protects against H9c2 injury induced by hypoxia via AKT and NF‑κB pathways. Molecular Medicine Reports 17(3): 4832-4838

Bayley, R.; Blakemore, D.; Cancian, L.; Dumon, S.; Volpe, G.; Ward, C.; Almaghrabi, R.; Gujar, J.; Reeve, N.; Raghavan, M.; Higgs, M.R.; Stewart, G.S.; Petermann, E.; García, P. 2018: MYBL2 Supports DNA Double Strand Break Repair in Hematopoietic Stem Cells. Cancer Research 78(20): 5767-5779

Ding, Q.Q.; Wang, X.T.; Hu, L.Q.; Qi, X.; Ge, L.H.; Xu, W.Y.; Xu, Z.S.; Zhou, Y.B.; Jia, G.Q.; Diao, X.M.; Min, D.H.; Ma, Y.Z.; Chen, M. 2018: MYB-like transcription factor SiMYB42 from foxtail millet (Setaria italica L.) enhances Arabidopsis tolerance to low-nitrogen stress. Yi Chuan 40(4): 327-338

Zhao, H.; Jivraj, S.; Moody, A. 2019: 'My blood pressure is low today, do you have the heating on?' The association between indoor temperature and blood pressure. Journal of Hypertension 37(3): 504-512

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Baraban, E.; Zhang, P.J.; Jaffer, S.; Lubin, D.; Feldman, M.; Bleiweiss, I.J.; Nayak, A. 2018: MYB rearrangement and immunohistochemical expression in adenomyoepithelioma of the breast: a comparison with adenoid cystic carcinoma. Histopathology 73(6): 897-903

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Wang, H.; Dolezal, J.M.; Kulkarni, S.; Lu, J.; Mandel, J.; Jackson, L.E.; Alencastro, F.; Duncan, A.W.; Prochownik, E.V. 2018: Myc and ChREBP transcription factors cooperatively regulate normal and neoplastic hepatocyte proliferation in mice. Journal of Biological Chemistry 293(38): 14740-14757

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Anonymous 2017: MYC Induces Immune Suppression to Promote Lung Tumorigenesis. Cancer Discovery: -

Zou, J.; Zhuang, M.; Yu, X.; Li, N.; Mao, R.; Wang, Z.; Wang, J.; Wang, X.; Zhou, H.; Zhang, L.; Shi, Y. 2018: MYC inhibition increases PD-L1 expression induced by IFN-γ in hepatocellular carcinoma cells. Molecular Immunology 101: 203-209

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Ventelä, S.; Mäkelä, J.-A.; Sears, R.C.; Toppari, J.; Westermarck, J. 2016: MYC is not detected in highly proliferating normal spermatogonia but is coupled with CIP2A in testicular cancers. Matters 2016

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Agarwal, S.; Milazzo, G.; Rajapakshe, K.; Bernardi, R.; Chen, Z.; Barbieri, E.; Koster, J.; Perini, G.; Coarfa, C.; Shohet, J.M. 2018: MYCN acts as a direct co-regulator of p53 in MYCN amplified neuroblastoma. Oncotarget 9(29): 20323-20338

Zhong, X.; Lee, H-Na.; Kim, S.Hyeon.; Park, S-Aye.; Kim, W.; Cha, Y-Nam.; Surh, Y-Joon. 2018: Myc-nick promotes efferocytosis through M2 macrophage polarization during resolution of inflammation. Faseb Journal: Official Publication of the Federation of American Societies for Experimental Biology 32(10): 5312-5325

Kong, D.; Zhao, L.; Sun, L.; Fan, S.; Li, H.; Zhao, Y.; Guo, Z.; Lin, L.; Cui, L.; Wang, K.; Chen, W.; Zhang, Y.; Zhou, J.; Li, Y. 2018: MYCN is a novel oncogenic target in adult B-ALL that activates the Wnt/β-catenin pathway by suppressing DKK3. Journal of Cellular and Molecular Medicine 22(7): 3627-3637

Banno, J.M.; Shield, K.; Patel, K.; Sule, A.A. 2017: Mycobacteremia from Crushed Hydromorphone Tablet Injection. Cureus 9(11): E1883

Druszczynska, M.; Wawrocki, S.; Szewczyk, R.; Rudnicka, W. 2017: Mycobacteria-derived biomarkers for tuberculosis diagnosis. Indian Journal of Medical Research 146(6): 700-707

Van Leeuwen, L.M.; Boot, M.; Kuijl, C.; Picavet, D.I.; van Stempvoort, G.; van der Pol, S.M.A.; de Vries, H.E.; van der Wel, N.N.; van der Kuip, M.; van Furth, A.M.; van der Sar, A.M.; Bitter, W. 2018: Mycobacteria employ two different mechanisms to cross the blood-brain barrier. Cellular Microbiology 20(9): E12858

Shah, K.; Atodaria, G.; Patwardhan, M.; Nene, A. 2017: Mycobacteria Intracellulare Spondylodiscitis Presenting as Progressive Consecutive Vertebral Sclerosis: A Case Report. Journal of Orthopaedic Case Reports 7(6): 89-92

Hazbón, M.H.; Rigouts, L.; Schito, M.; Ezewudo, M.; Kudo, T.; Itoh, T.; Ohkuma, M.; Kiss, K.; Wu, L.; Ma, J.; Hamada, M.; Strong, M.; Salfinger, M.; Daley, C.L.; Nick, J.A.; Lee, J.-S.; Rastogi, N.; Couvin, D.; Hurtado-Ortiz, R.; Bizet, C.; Suresh, A.; Rodwell, T.; Albertini, A.; Lacourciere, K.A.; Deheer-Graham, A.; Alexander, S.; Russell, J.E.; Bradford, R.; Riojas, M.A. 2018: Mycobacterial biomaterials and resources for researchers. Pathogens and Disease 76(4)

Mathuram, A.J.; Michael, J.S.; Turaka, V.P.; Jasmine, S.; Carey, R.; Ramya, I. 2018: Mycobacterial blood culture as the only means of diagnosis of disseminated tuberculosis in advanced HIV infection. Tropical Doctor 48(2): 100-102

Mallick, B.; Mandavdhare, H.S.; Aggarwal, S.; Singh, H.; Dutta, U.; Sharma, V. 2018: Mycobacterial chylous ascites: report of three cases and systematic review. Therapeutic Advances in Infectious Disease 5(4): 69-75

Flume, P.A.; Winthrop, K.L. 2018: Mycobacterial Disease: Evolving Concepts. Seminars in Respiratory and Critical Care Medicine 39(3): 269

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Gupta, S.; Rodriguez, G.M. 2018: Mycobacterial extracellular vesicles and host pathogen interactions. Pathogens and Disease 76(4)

Joosten, S.A.; van Meijgaarden, K.E.; Arend, S.M.; Prins, C.; Oftung, F.; Korsvold, G.E.; Kik, S.V.; Arts, R.J.; van Crevel, R.; Netea, M.G.; Ottenhoff, T.H. 2018: Mycobacterial growth inhibition is associated with trained innate immunity. Journal of Clinical Investigation 128(5): 1837-1851

Chao, W.-C.; Yen, C.-L.; Hsieh, C.-Y.; Huang, Y.-F.; Tseng, Y.-L.; Nigrovic, P.A.; Shieh, C.-C. 2017: Mycobacterial infection induces higher interleukin-1β and dysregulated lung inflammation in mice with defective leukocyte NADPH oxidase. Plos one 12(12): E0189453

Naser, A.; Qasem, A.; Naser, S.A. 2018: Mycobacterial infection influences bone biomarker levels in patients with Crohn's disease. Canadian Journal of Physiology and Pharmacology 96(7): 662-667

Liu, Y.-C.; Wu, C.-J.; Ko, P.-S.; Chien, S.-H.; Fan, N.-W.; Wang, H.-Y.; Gau, J.-P.; Liu, C.-J.; Hsiao, L.-T.; Chiou, T.-J.; Liu, C.-Y.; Liu, J.-H. 2020: Mycobacterial infections in adult recipients of allogeneic hematopoietic stem cell transplantation: a cohort study in a high endemic area. Journal of Microbiology Immunology and Infection 53(2): 274-282

Torres-Atencio, I.; Rosero, S.; Ordoñez, C.; Ruiz, M.; Goodridge, A. 2018: Mycobacterial Lipids Induce Calcium Mobilization and Degranulation of Mast Cells. American Journal of Respiratory and Critical Care Medicine 198(6): 813-816

Upadhyay, A.; Kumar, S.; Rooker, S.A.; Koehn, J.T.; Crans, D.C.; McNeil, M.R.; Lott, J.S.; Crick, D.C. 2018: Mycobacterial MenJ: An Oxidoreductase Involved in Menaquinone Biosynthesis. Acs Chemical Biology 13(9): 2498-2507

Kriel, N.L.; Gallant, J.; van Wyk, N.ël.; van Helden, P.; Sampson, S.L.; Warren, R.M.; Williams, M.J. 2018: Mycobacterial nucleoid associated proteins: An added dimension in gene regulation. Tuberculosis 108: 169-177

Oldenburg, R.; Mayau, V.; Prandi, J.; Arbues, A.; Astarie-Dequeker, C.; Guilhot, C.; Werts, C.; Winter, N.; Demangel, C. 2018: Mycobacterial Phenolic Glycolipids Selectively Disable TRIF-Dependent TLR4 Signaling in Macrophages. Frontiers in Immunology 9: 2

Pradhan, G.; Shrivastva, R.; Mukhopadhyay, S. 2018: Mycobacterial PknG Targets the Rab7l1 Signaling Pathway to Inhibit Phagosome-Lysosome Fusion. Journal of Immunology 201(5): 1421-1433

Jaiswal, S.; Chatterjee, A.; Pandey, S.; Lata, K.; Gadi, R.Kumar.; Manda, R.; Kumar, S.; Reddy, M.Sridhar.; Ramachandran, R.; Srivastava, K.K. 2019: Mycobacterial protein tyrosine kinase, PtkA phosphorylates PtpA at tyrosine residues and the mechanism is stalled by the novel series of inhibitors. Journal of Drug Targeting 27(1): 51-59

Patel, K.; Butala, S.; Khan, T.; Suvarna, V.; Sherje, A.; Dravyakar, B. 2018: Mycobacterial siderophore: a review on chemistry and biology of siderophore and its potential as a target for tuberculosis. European Journal of Medicinal Chemistry 157: 783-790

Van Mechelen, M.; van der Hilst, J.; Gyssens, I.C.; Messiaen, P. 2018: Mycobacterial skin and soft tissue infections: TB or not TB?. Netherlands Journal of Medicine 76(6): 269-274

Sfeir, M.M.; Schuetz, A.; Van Besien, K.; Borczuk, A.C.; Soave, R.; Jenkins, S.G.; Walsh, T.J.; Small, C.B. 2018: Mycobacterial spindle cell pseudotumour: epidemiology and clinical outcomes. Journal of Clinical Pathology 71(7): 626-630

Korabliovienė, J.; Mauricas, M.; Ambrozevičienė, Če.; Valius, M.; Kaupinis, A.; Čaplinskas, S.; Korabliov, P. 2018: Mycobacteria produce proteins involved in biofilm formation and growth-affecting processes. Acta Microbiologica et Immunologica Hungarica 65(3): 405-418

Wallis, R.S.; Good, C.E.; O'Riordan, M.A.; Blumer, J.L.; Jacobs, M.R.; Griffiss, J.M.; Healan, A.; Salata, R.A. 2018: Mycobactericidal activity of bedaquiline plus rifabutin or rifampin in ex vivo whole blood cultures of healthy volunteers: a randomized controlled trial. Plos one 13(5): E0196756

Ko, C-Chung.; Hatfull, G.F. 2018: Mycobacteriophage Fruitloop gp52 inactivates Wag31 (DivIVA) to prevent heterotypic superinfection. Molecular Microbiology 108(4): 443-460

Catalão, M.J.ão.; Pimentel, M. 2018: Mycobacteriophage Lysis Enzymes: Targeting the Mycobacterial Cell Envelope. Viruses 10(8)

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Nunez Breton, J.D.; Hernandez, G.; Simkins, J.; Chaparro, S.V. 2018: Mycobacterium abscessus Left Ventricle Assist Device Driveline Infections: An Emerging Pathogen?. Transplant Infectious Disease: An Official Journal of the Transplantation Society 20(5): E12957

Chiu, Y-Chun.; Yang, S-Chieh.; Wu, C-Hsien.; Chuang, H-Wen.; Tu, Y-Kun.; Ma, C-Hou. 2017: Mycobacterium abscessus Osteomyelitis of the Calcaneus Presenting as Tumor-Mimicking Lesions: A Case Report. Jbjs Case Connector 7(3): E56

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Chongwe, G.; Michelo, C.; Sinkala, E.; Kayamba, V.; Nzayisenga, J.-B.; Drobniewski, F.; Kelly, P. 2018: Mycobacterium avium lysate induces matrix metalloproteinase-1 in intestinal tissue and peripheral blood: Observations from selected hospital based Zambian adults. International Journal of Infectious Diseases: Ijid: Official Publication of the International Society for Infectious Diseases 71: 73-81

Bo, M.; Niegowska, M.; Arru, G.; Sechi, E.; Mariotto, S.; Mancinelli, C.; Farinazzo, A.; Alberti, D.; Gajofatto, A.; Ferrari, S.; Capra, R.; Monaco, S.; Sechi, G.; Sechi, L.A. 2018: Mycobacterium avium subspecies paratuberculosis and myelin basic protein specific epitopes are highly recognized by sera from patients with Neuromyelitis optica spectrum disorder. Journal of Neuroimmunology 318: 97-102

Danelishvili, L.; Rojony, R.; Carson, K.L.; Palmer, A.L.; Rose, S.J.; Bermudez, L.E. 2018: Mycobacterium avium subsp. hominissuis effector MAVA5_06970 promotes rapid apoptosis in secondary-infected macrophages during cell-to-cell spread. Virulence 9(1): 1287-1300

Klotz, D.; Barth, S.A.; Baumgärtner, W.; Hewicker-Trautwein, M. 2018: Mycobacterium avium subsp. hominissuis Infection in a Domestic Rabbit, Germany. Emerging Infectious Diseases 24(3): 596-598

Galiero, A.; Leo, S.; Garbarino, C.; Arrigoni, N.; Russo, S.; Giacomelli, S.; Bianchi, A.; Trevisiol, K.; Idrizi, I.; Daka, G.; Fratini, F.; Turchi, B.; Cerri, D.; Ricchi, M. 2018: Mycobacterium aviumsubsp. paratuberculosis isolated from wild red deer (Cervus elaphus) in Northern Italy. Veterinary Microbiology 217: 167-172

Encinas, M.; Marfil, M.J.; Garbaccio, S.; Barandiaran, S.; Huertas, P.; Morsella, C.; Macías, A.; Magnano, G.; Zapata, L.; Bigi, F.; Cataldi, A.; Paolicchi, F.; Zumárraga, M.; Eirin, M.E. 2018: Mycobacterium bovis ESAT-6, CFP-10 and EspC antigens show high conservation among field isolates. Tuberculosis 111: 143-146

Michelet, L.; De Cruz, K.; Hénault, S.; Tambosco, J.; Richomme, C.él.; Réveillaud, Éd.; Gares, H.él.èn.; Moyen, J.-L.; Boschiroli, M.ía.L. 2018: Mycobacterium bovis Infection of Red Fox, France. Emerging Infectious Diseases 24(6): 1150-1153

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Cheng, V.C.C.; Wong, S.C.; Chen, J.H.K.; Wong, S.C.Y.; Yuen, K.Y. 2018: Mycobacterium chimaera-contaminated heater-cooler devices: the inner surface as the missing link?. Journal of Hospital Infection 100(3): E157-E158

Scriven, J.E.; Scobie, A.; Verlander, N.Q.; Houston, A.; Collyns, T.; Cajic, V.; Kon, O.M.; Mitchell, T.; Rahama, O.; Robinson, A.; Withama, S.; Wilson, P.; Maxwell, D.; Agranoff, D.; Davies, E.; Llewelyn, M.; Soo, S.-S.; Sahota, A.; Cooper, M.A.; Hunter, M.; Tomlins, J.; Tiberi, S.; Kendall, S.; Dedicoat, M.; Alexander, E.; Fenech, T.; Zambon, M.; Lamagni, T.; Smith, E.G.; Chand, M. 2018: Mycobacterium chimaera infection following cardiac surgery in the United Kingdom: clinical features and outcome of the first 30 cases. Clinical Microbiology and Infection: the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases 24(11): 1164-1170

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Vutescu, E.Stefan.; Koenig, K.M. 2017: Mycobacterium cosmeticum Infection After Total Knee Arthroplasty: A Case Report. Jbjs Case Connector 7(1): E3

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Yokoyama, A.; Kage, H.; Ohama, Y.; Sato, T.; Miyashita, N.; Noguchi, S.; Okugawa, S.; Yamauchi, Y.; Moriya, K.; Nagase, T. 2018: Mycobacterium heckeshornense lung infection diagnosed by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS). Journal of Infection and Chemotherapy: Official Journal of the Japan Society of ChemoTherapy 24(9): 763-765

McNeil, E.P.; Goldfarb, N.; Hannon, G.R.; Miller, D.D.; Farah, R.S. 2019: Mycobacterium immunogenum folliculitis on the lower extremities of a healthy young adult. Clinical and Experimental Dermatology 44(3): 328-330

Becker, Sören.L.; Halfmann, A.; Schilling, L.; Mawlood, D.A.; Janssen, E.; Reischl, U.; Vogt, T.; Müller, C.Sl. 2018: Mycobacterium iranicum infection in a patient with fish tank granuloma: a first case report. European Journal of Dermatology: Ejd 28(2): 238-239

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Miqueleiz-Zapatero, A.; Santa Olalla-Peralta, C.; Guerrero-Torres, M.ía.D.; Cardeñoso-Domingo, L.; Hernández-Milán, B.én.; Domingo-García, D. 2018: Mycobacterium lentiflavum as the main cause of lymphadenitis in pediatric population. Enfermedades Infecciosas y Microbiologia Clinica 36(10): 640-643

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Johansen, M.D.; Kasparian, J.A.; Hortle, E.; Britton, W.J.; Purdie, A.C.; Oehlers, S.H. 2018: Mycobacterium marinum infection drives foam cell differentiation in zebrafish infection models. Developmental and Comparative Immunology 88: 169-172

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Chen, Z.; Shao, X.-Y.; Wang, C.; Hua, M.-H.; Wang, C.-N.; Wang, X.; Wang, Q.-J.; Yao, J.-Y.; Fan, Y.-H.; Qin, Y.-W. 2018: Mycobacterium marinum Infection in Zebrafish and Microglia Imitates the Early Stage of Tuberculous Meningitis. Journal of Molecular Neuroscience: Mn 64(2): 321-330

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Matsuda, S.; Suzuki, S.; Morimoto, K.; Aono, A.; Nishio, K.; Asakura, T.; Sasaki, Y.; Namkoong, H.; Nishimura, T.; Ogata, H.; Hasegawa, N.; Kurashima, A.; Ishii, M.; Tatsumi, K.; Mitarai, S.; Goto, H. 2018: Mycobacterium triplex pulmonary disease with acquired macrolide resistance in immunocompetent patients. Clinical Microbiology and Infection: the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases 24(6): 671-672

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Zhang, W.; Niu, C.; Fu, R-Yang.; Peng, Z-Yu. 2018: Mycobacterium tuberculosis H37Rv infection regulates alternative splicing in Macrophages. Bioengineered 9(1): 203-208

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Etna, M.P.; Sinigaglia, A.; Grassi, A.; Giacomini, E.; Romagnoli, A.; Pardini, M.; Severa, M.; Cruciani, M.; Rizzo, F.; Anastasiadou, E.; Di Camillo, B.; Barzon, L.; Fimia, G.M.; Manganelli, R.; Coccia, E.M. 2018: Mycobacterium tuberculosis-induced miR-155 subverts autophagy by targeting ATG3 in human dendritic cells. Plos Pathogens 14(1): E1006790

Reece, S.T.; Vogelzang, A.; Tornack, J.; Bauer, W.; Zedler, U.; Schommer-Leitner, S.; Stingl, G.; Melchers, F.; Kaufmann, S.H.E. 2018: Mycobacterium tuberculosis-Infected Hematopoietic Stem and Progenitor Cells Unable to Express Inducible Nitric Oxide Synthase Propagate Tuberculosis in Mice. Journal of Infectious Diseases 217(10): 1667-1671

Wang, X.; Wu, Y.; Jiao, J.; Huang, Q. 2018: Mycobacterium tuberculosis infection induces IL-10 gene expression by disturbing histone deacetylase 6 and histonedeacetylase 11 equilibrium in macrophages. Tuberculosis 108: 118-123

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Castro-Garza, J.; Luévano-Martínez, M.L.; Villarreal-Treviño, L.; Gosálvez, J.; Fernández, J.é L.; Dávila-Rodríguez, M.I.; García-Vielma, C.; González-Hernández, S.; Cortés-Gutiérrez, E.I. 2018: Mycobacterium tuberculosis promotes genomic instability in macrophages. Memorias do Instituto Oswaldo Cruz 113(3): 161-166

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Yang, J.D.; Mott, D.; Sutiwisesak, R.; Lu, Y.-J.; Raso, F.; Stowell, B.; Babunovic, G.H.; Lee, J.; Carpenter, S.M.; Way, S.S.; Fortune, S.M.; Behar, S.M. 2018: Mycobacterium tuberculosis-specific CD4+ and CD8+ T cells differ in their capacity to recognize infected macrophages. Plos Pathogens 14(5): E1007060

Mishra, A.; Surolia, A. 2018: Mycobacterium tuberculosis: Surviving and Indulging in an Unwelcoming Host. Iubmb Life 70(9): 917-925

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Douine, M.; Gozlan, R.; Nacher, M.; Dufour, J.; Reynaud, Y.; Elguero, E.; Combe, M.; Velvin, C.J.; Chevillon, C.; Berlioz-Arthaud, A.; Labbé, S.; Sainte-Marie, D.; Guégan, J-François.; Pradinaud, R.; Couppié, P. 2017: Mycobacterium ulcerans infection (Buruli ulcer) in French Guiana, South America, 1969-2013: an epidemiological study. Lancet. Planetary health 1(2): e65-e73

Fonken, L.K.; Frank, M.G.; D'Angelo, H.M.; Heinze, J.D.; Watkins, L.R.; Lowry, C.A.; Maier, S.F. 2018: Mycobacterium vaccae immunization protects aged rats from surgery-elicited neuroinflammation and cognitive dysfunction. Neurobiology of Aging 71: 105-114

Hirama, T.; Marchand-Austin, A.; Ma, J.; Alexander, D.C.; Brode, S.K.; Marras, T.K.; Jamieson, F.B. 2018: Mycobacterium xenopi Genotype Associated with Clinical Phenotype in Lung Disease. Lung 196(2): 213-217

Kovalchuk, A.; Mukrimin, M.; Zeng, Z.; Raffaello, T.; Liu, M.; Kasanen, R.; Sun, H.; Asiegbu, F.O. 2018: Mycobiome analysis of asymptomatic and symptomatic Norway spruce trees naturally infected by the conifer pathogens Heterobasidion spp. Environmental Microbiology Reports 10(5): 532-541

Hu, W.; Strom, N.; Haarith, D.; Chen, S.; Bushley, K.E. 2018: Mycobiome of Cysts of the Soybean Cyst Nematode Under Long Term Crop Rotation. Frontiers in Microbiology 9: 386

Adekoya, I.; Obadina, A.; Adaku, C.C.; De Boevre, M.; Okoth, S.; De Saeger, S.; Njobeh, P. 2018: Mycobiota and co-occurrence of mycotoxins in South African maize-based opaque beer. International Journal of Food Microbiology 270: 22-30

Gazis, R.; Poplawski, L.; Klingeman, W.; Boggess, S.L.; Trigiano, R.N.; Graves, A.D.; Seybold, S.J.; Hadziabdic, D. 2018: Mycobiota associated with insect galleries in walnut with thousand cankers disease reveals a potential natural enemy against Geosmithia morbida. Fungal Biology 122(4): 241-253

Xing, H.-Q.; Ma, J.-C.; Xu, B.-L.; Zhang, S.-W.; Wang, J.; Cao, L.; Yang, X.-M. 2018: Mycobiota of maize seeds revealed by rDNA-ITS sequence analysis of samples with varying storage times. Microbiologyopen 7(6): E00609

Jedidi, I.; Soldevilla, C.; Lahouar, A.; Marín, P.; González-Jaén, M.ía.T.; Said, S. 2018: Mycoflora isolation and molecular characterization of Aspergillus and Fusarium species in Tunisian cereals. Saudi Journal of Biological Sciences 25(5): 868-874

Kortei, N.K.; Odamtten, G.T.; Obodai, M.; Wiafe-Kwagyan, M. 2018: Mycofloral profile and the radiation sensitivity (D10 values) of solar dried and gamma irradiated Pleurotus ostreatus (Jacq.Ex. Fr.) Kummer fruitbodies stored in two different packaging materials. Food Science and Nutrition 6(1): 180-188

Leslie, J.F.; Lattanzio, V.; Audenaert, K.; Battilani, P.; Cary, J.; Chulze, S.N.; De Saeger, S.; Gerardino, A.; Karlovsky, P.; Liao, Y-Cai.; Maragos, C.M.; Meca, G.; Medina, A.; Moretti, A.; Munkvold, G.; Mulè, G.; Njobeh, P.; Pecorelli, I.; Perrone, G.; Pietri, A.; Palazzini, J.M.; Proctor, R.H.; Rahayu, E.S.; Ramírez, M.L.; Samson, R.; Stroka, Jörg.; Sulyok, M.; Sumarah, M.; Waalwijk, C.; Zhang, Q.; Zhang, H.; Logrieco, A.F. 2018: MycoKey Round Table Discussions of Future Directions in Research on Chemical Detection Methods, Genetics and Biodiversity of Mycotoxins. Toxins 10(3)

Bedada, T.L.; Dera, F.A.; Edicho, R.M.; Gebre, S.G.; Asefa, Y.B.; Sima, W.G.; Maheder, R.F.; Negassi, T.Y.; Biegna, A.G. 2018: Mycological and Bacteriological Quality and Safety of Bottled Water in Ethiopia. Open Microbiology Journal 12: 200-208

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Goebel, A.; Jacob, A.; Frank, B.; Sacco, P.; Alexander, G.; Philips, C.; Bassett, P.; Moots, R. 2018: Mycophenolate for persistent complex regional pain syndrome, a parallel, open, randomised, proof of concept trial. Scandinavian Journal of Pain 18(1): 29-37

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Avasare, R.S.; Canetta, P.A.; Bomback, A.S.; Marasa, M.; Caliskan, Y.; Ozluk, Y.; Li, Y.; Gharavi, A.G.; Appel, G.B. 2018: Mycophenolate Mofetil in Combination with Steroids for Treatment of C3 Glomerulopathy: a Case Series. Clinical Journal of the American Society of Nephrology: Cjasn 13(3): 406-413

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Huang, S.-W.; Chen, H.; Lu, M.-L.; Wang, J.-L.; Xie, R.-L.; Zhao, B.; Chen, Y.; Xu, Z.-W.; Fei, J.; Mao, E.-Q.; Chen, E.-Z. 2018: Mycophenolate Mofetil Protects Septic Mice via the Dual Inhibition of Inflammatory Cytokines and PD-1. Inflammation 41(3): 1008-1020

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Ssepuuya, G.; Van Poucke, C.; Ediage, E.Njumbe.; Mulholland, C.; Tritscher, A.; Verger, P.; Kenny, M.; Bessy, C.; De Saeger, S. 2018: Mycotoxin contamination of sorghum and its contribution to human dietary exposure in four sub-Saharan countries. Food Additives and Contaminants. Part A Chemistry Analysis Control Exposure and Risk Assessment 35(7): 1384-1393

Liew, W.-P.-P.; Mohd-Redzwan, S. 2018: Mycotoxin: its Impact on Gut Health and Microbiota. Frontiers in Cellular and Infection Microbiology 8: 60

Gajęcka, M.; Waśkiewicz, A.; Zielonka, Łu.; Goliński, P.; Rykaczewska, A.; Lisieska-Żołnierczyk, S.; Gajęcki, M.T. 2018: Mycotoxin levels in the digestive tissues of immature gilts exposed to zearalenone and deoxynivalenol. Toxicon: Official Journal of the International Society on Toxinology 153: 1-11

Wu, T.-S.; Yang, J.-J.; Wang, Y.-W.; Yu, F.-Y.; Liu, B.-H. 2016: Mycotoxin ochratoxin a disrupts renal development via a miR-731/prolactin receptor axis in zebrafish. Toxicology Research 5(2): 519-529

Nguyen, T.T.T.; Kim, J.; Jeon, S.J.; Lee, C.W.; Magan, N.; Lee, H.B. 2018: Mycotoxin production of Alternaria strains isolated from Korean barley grains determined by LC-MS/MS. International Journal of Food Microbiology 268: 44-52

Osweiler, G.D. 2001: Mycotoxins. Veterinary Clinics of North America. Equine Practice 17(3): 547-566 Viii

Pascari, X.; Ramos, A.J.; Marín, S.; Sanchís, V. 2018: Mycotoxins and beer. Impact of beer production process on mycotoxin contamination. a review. Food Research International 103: 121-129

Broom, L. 2015: Mycotoxins and the intestine. Animal Nutrition 1(4): 262-265

Wen, J.; Mu, P.; Deng, Y. 2016: Mycotoxins: cytotoxicity and biotransformation in animal cells. Toxicology Research 5(2): 377-387

Shao, M.; Li, L.; Gu, Z.; Yao, M.; Xu, D.; Fan, W.; Yan, L.; Song, S. 2018: Mycotoxins in commercial dry pet food in China. Food Additives and Contaminants. Part B Surveillance 11(4): 237-245

Pizzolato Montanha, F.; Anater, A.; Burchard, J.F.; Luciano, F.B.; Meca, G.; Manyes, L.; Pimpão, C.áu.T. 2018: Mycotoxins in dry-cured meats: a review. Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research Association 111: 494-502

Khezri, A.; Herranz-Jusdado, J.G.; Ropstad, E.; Fraser, T.Wk. 2018: Mycotoxins induce developmental toxicity and behavioural aberrations in zebrafish larvae. Environmental Pollution 242(Pt A): 500-506

Zhang, K.; Flannery, B.M.; Oles, C.J.; Adeuya, A. 2018: Mycotoxins in infant/toddler foods and breakfast cereals in the US retail market. Food Additives and Contaminants. Part B Surveillance 11(3): 183-190

Liu, X.-L.; Wu, R.-Y.; Sun, X.-F.; Cheng, S.-F.; Zhang, R.-Q.; Zhang, T.-Y.; Zhang, X.-F.; Zhao, Y.; Shen, W.; Li, L. 2018: Mycotoxin zearalenone exposure impairs genomic stability of swine follicular granulosa cells in vitro. International Journal of Biological Sciences 14(3): 294-305

Muthulakshmi, S.; Hamideh, P.F.; Habibi, H.R.; Maharajan, K.; Kadirvelu, K.; Mudili, V. 2018: Mycotoxin zearalenone induced gonadal impairment and altered gene expression in the hypothalamic-pituitary-gonadal axis of adult female zebrafish (Danio rerio). Journal of Applied Toxicology: Jat 38(11): 1388-1397

Qu, J.; Zhao, X.; Wang, J.; Liu, X.; Yan, Y.; Liu, L.; Cai, H.; Qu, H.; Lu, N.; Sun, Y.; Wang, F.; Wang, J.; Zhang, J. 2017: MYC overexpression with its prognostic and clinicopathological significance in breast cancer. Oncotarget 8(55): 93998-94008

Sharma, M.; Guleria, S.; Singh, K.; Chauhan, A.; Kulshrestha, S. 2018: Mycovirus associated hypovirulence, a potential method for biological control of Fusarium species. Virusdisease 29(2): 134-140

Mochama, P.; Jadhav, P.; Neupane, A.; Lee Marzano, S.-Y. 2018: Mycoviruses as Triggers and Targets of RNA Silencing in White Mold Fungus Sclerotinia sclerotiorum. Viruses 10(4)

Macek, P.; Cliff, M.J.; Embrey, K.J.; Holdgate, G.A.; Nissink, J.W.M.; Panova, S.; Waltho, J.P.; Davies, R.A. 2018: Myc phosphorylation in its basic helix-loop-helix region destabilizes transient α-helical structures, disrupting Max and DNA binding. Journal of Biological Chemistry 293(24): 9301-9310

Ohanian, M.; Rozovski, U.; Kanagal-Shamanna, R.; Abruzzo, L.V.; Loghavi, S.; Kadia, T.; Futreal, A.; Bhalla, K.; Zuo, Z.; Huh, Y.O.; Post, S.M.; Ruvolo, P.; Garcia-Manero, G.; Andreeff, M.; Kornblau, S.; Borthakur, G.; Hu, P.; Medeiros, L.Jeffrey.; Takahashi, K.; Hornbaker, M.J.; Zhang, J.; Nogueras-González, G.M.; Huang, X.; Verstovsek, S.; Estrov, Z.; Pierce, S.; Ravandi, F.; Kantarjian, H.M.; Bueso-Ramos, C.E.; Cortes, J.E. 2019: MYC protein expression is an important prognostic factor in acute myeloid leukemia. Leukemia and Lymphoma 60(1): 37-48

Ambrosio, M.R.; Lazzi, S.; Bello, G.L.; Santi, R.; Porro, L.D.; de Santi, M.M.; Guazzo, R.; Mundo, L.; Rigacci, L.; Kovalchuck, S.; Onyango, N.; Fabbri, A.; Cencini, E.; Zinzani, P.L.; Zaja, F.; Angrilli, F.; Stelitano, C.; Cabras, M.G.; Spataro, G.; Bob, R.; Menter, T.; Granai, M.; Cevenini, G.; Naresh, K.N.; Stein, H.; Sabattini, E.; Leoncini, L. 2019: MYC protein expression scoring and its impact on the prognosis of aggressive B-cell lymphoma patients. Haematologica 104(1): E25-E28

Møller, H.E.H.; Preiss, B.S.; Pedersen, P.; Østergaard, B.; Frederiksen, M.; Abildgaard, N.; Møller, M.B. 2018: Myc protein overexpression is a feature of progression and adverse prognosis in multiple myeloma. European Journal of Haematology 2018

Groulx, J.-F.ço.; Boudjadi, S.; Beaulieu, J.-F.ço. 2018: MYC Regulates α6 Integrin Subunit Expression and Splicing Under its Pro-Proliferative ITGA6A Form in Colorectal Cancer Cells. Cancers 10(2)

Malpeli, G.; Barbi, S.; Tosadori, G.; Greco, C.; Zupo, S.; Pedron, S.; Brunelli, M.; Bertolaso, A.; Scupoli, M.T.; Krampera, M.; Kamga, P.T.; Croce, C.M.; Calin, G.A.; Scarpa, A.; Zamò, A. 2018: MYC-related micro RNAs signatures in non-Hodgkin B-cell lymphomas and their relationships with core cellular pathways. Oncotarget 9(51): 29753-29771

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

Heightman, A.J. 2017: My Curtain Call: An inside look at a hospital stay for chest pain. Jems: a Journal of Emergency Medical Services 42(2): 10-14

Block, M.S.; Vierkant, R.A.; Rambau, P.F.; Winham, S.J.; Wagner, P.; Traficante, N.; Tołoczko, A.; Tiezzi, D.G.; Taran, F.A.; Sinn, P.; Sieh, W.; Sharma, R.; Rothstein, J.H.; Ramón Y Cajal, T.; Paz-Ares, L.; Oszurek, O.; Orsulic, S.; Ness, R.B.; Nelson, G.; Modugno, F.; Menkiszak, J.; McGuire, V.; McCauley, B.M.; Mack, M.; Lubiński, J.; Longacre, T.A.; Li, Z.; Lester, J.; Kennedy, C.J.; Kalli, K.R.; Jung, A.Y.; Johnatty, S.E.; Jimenez-Linan, M.; Jensen, A.; Intermaggio, M.P.; Hung, J.; Herpel, E.; Hernandez, B.Y.; Hartkopf, A.D.; Harnett, P.R.; Ghatage, P.; García-Bueno, J.é M.; Gao, B.; Fereday, S.; Eilber, U.; Edwards, R.P.; de Sousa, C.B.; de Andrade, J.M.; Chudecka-Głaz, A.; Chenevix-Trench, G.; Cazorla, A.; Brucker, S.Y.; Alsop,; 2018: MyD88 and TLR4 Expression in Epithelial Ovarian Cancer. Mayo Clinic Proceedings 93(3): 307-320

Di Padova, F.; Quesniaux, V.F.J.; Ryffel, B. 2018: MyD88 as a therapeutic target for inflammatory lung diseases. Expert Opinion on Therapeutic Targets 22(5): 401-408

Aggarwal, V.; Das, A.; Bal, A.; Srinivasan, R.; Das, R.; Prakash, G.; Malhotra, P.; Varma, S. 2019: MYD88, CARD11, and CD79B Oncogenic Mutations are Rare Events in the Indian Cohort of De Novo Nodal Diffuse Large B-Cell Lymphoma. Applied Immunohistochemistry and Molecular Morphology: Aimm 27(4): 311-318

Reins, R.Y.; Lema, C.; Courson, J.; Kunnen, C.M.E.; Redfern, R.L. 2018: MyD88 Deficiency Protects Against Dry Eye-Induced Damage. Investigative Ophthalmology and Visual Science 59(7): 2967-2976

Gallot, Y.S.; Straughn, A.R.; Bohnert, K.R.; Xiong, G.; Hindi, S.M.; Kumar, A. 2018: MyD88 is required for satellite cell-mediated myofiber regeneration in dystrophin-deficient mdx mice. Human Molecular Genetics 27(19): 3449-3463

Delitto, A.E.; Rocha, F.; Decker, A.M.; Amador, B.; Sorenson, H.L.; Wallet, S.M. 2018: MyD88-mediated innate sensing by oral epithelial cells controls periodontal inflammation. Archives of Oral Biology 87: 125-130

Guerrera, M.L.; Tsakmaklis, N.; Xu, L.; Yang, G.; Demos, M.; Kofides, A.; Chan, G.G.; Manning, R.J.; Liu, X.; Chen, J.G.; Munshi, M.; Patterson, C.J.; Castillo, J.J.; Dubeau, T.; Gustine, J.; Carrasco, R.D.; Arcaini, L.; Varettoni, M.; Cazzola, M.; Treon, S.P.; Hunter, Z.R. 2018: MYD88 mutated and wild-type Waldenström's Macroglobulinemia: characterization of chromosome 6q gene losses and their mutual exclusivity with mutations in CXCR4. Haematologica 103(9): E408-E411

Takano, S.; Hattori, K.; Ishikawa, E.; Narita, Y.; Iwadate, Y.; Yamaguchi, F.; Nagane, M.; Akimoto, J.; Oka, H.; Tanaka, S.; Sakata, M.; Matsuda, M.; Yamamoto, T.; Chiba, S.; Matsumura, A. 2018: MyD88 Mutation in Elderly Predicts Poor Prognosis in Primary Central Nervous System Lymphoma: Multi-Institutional Analysis. World Neurosurgery 112: E69-E73

Wang, Y.L. 2018: MYD88 Mutations and Sensitivity to Ibrutinib Therapy. Journal of Molecular Diagnostics: Jmd 20(2): 264-266

Mandraju, R.; Jain, A.; Gao, Y.; Ouyang, Z.; Norgard, M.V.; Pasare, C. 2018: MyD88 Signaling in T Cells Is Critical for Effector CD4 T Cell Differentiation following a Transitional T Follicular Helper Cell Stage. Infection and Immunity 86(5)

Hoff, S.; Oyoshi, M.K.; Hornick, J.L.; Geha, R.S. 2018: MyD88 signaling in T regulatory cells by endogenous ligands dampens skin inflammation in filaggrin deficient mice. Clinical Immunology 195: 88-92

Treon, S.P.; Gustine, J.; Xu, L.; Manning, R.J.; Tsakmaklis, N.; Demos, M.; Meid, K.; Guerrera, M.L.; Munshi, M.; Chan, G.; Chen, J.; Kofides, A.; Patterson, C.J.; Yang, G.; Liu, X.; Severns, P.; Dubeau, T.; Hunter, Z.R.; Castillo, J.J. 2018: MYD88 wild-type Waldenstrom Macroglobulinaemia: differential diagnosis, risk of histological transformation, and overall survival. British Journal of Haematology 180(3): 374-380

Berki, B. 2017: My daughter's death shows why toxic air is a public health issue. Journal of Family Health 27(3): 8-10

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Cadre, B.; Al Oraimi, M.; Grinholtz-Haddad, J.; Benkhatar, H. 2019: "My Dog Deafened Me!": Case Report of Capnocytophaga canimorsus Infection and Literature Review. Laryngoscope 129(1): E41-E43

Menchetti, L.; Calipari, S.; Guelfi, G.; Catanzaro, A.; Diverio, S. 2018: My Dog Is not my Cat: Owner Perception of the Personalities of Dogs and Cats Living in the Same Household. Animals: An Open Access Journal from Mdpi 8(6)

Nakatsuka, A.S.; Beaver, H.A.; Lee, A.G. 2018: Mydriasis due to Opcon-A: An indication to avoid pharmacologic testing for anisocoria. Canadian Journal of Ophthalmology. Journal Canadien d'Ophtalmologie 53(1): E6-E7

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Hu, B.; McCollum, M.; Ravi, V.; Arpag, S.; Moiseev, D.; Castoro, R.; Mobley, B.; Burnette, B.; Siskind, C.; Day, J.; Yawn, R.; Feely, S.; Li, Y.; Yan, Q.; Shy, M.; Li, J. 2018: Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination. Annals of Neurology 83(4): 756-770

Lancaster, E.; Li, J.; Hanania, T.; Liem, R.; Scheideler, M.A.; Scherer, S.S. 2018: Myelinated axons fail to develop properly in a genetically authentic mouse model of Charcot-Marie-Tooth disease type 2E. Experimental Neurology 308: 13-25

Tricaud, N. 2017: Myelinating Schwann Cell Polarity and Mechanically-Driven Myelin Sheath Elongation. Frontiers in Cellular Neuroscience 11: 414

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Almeida, R.G.; Pan, S.; Cole, K.L.H.; Williamson, J.M.; Early, J.J.; Czopka, T.; Klingseisen, A.; Chan, J.R.; Lyons, D.A. 2018: Myelination of Neuronal Cell Bodies when Myelin Supply Exceeds Axonal Demand. Current Biology: Cb 28(8): 1296-1305.E5

Collins, L.N.; Hill, D.L.; Brunjes, P.C. 2018: Myelination of the developing lateral olfactory tract and anterior commissure. Journal of Comparative Neurology 526(11): 1843-1858

Gu, L.; Wu, D.; Tang, X.; Qi, X.; Li, X.; Bai, F.; Chen, X.; Ren, Q.; Zhang, Z. 2018: Myelin changes at the early stage of 5XFAD mice. Brain Research Bulletin 137: 285-293

García-Mateo, N.; Pascua-Maestro, R.; Pérez-Castellanos, A.; Lillo, C.ón.; Sanchez, D.; Ganfornina, M.D. 2018: Myelin extracellular leaflet compaction requires apolipoprotein D membrane management to optimize lysosomal-dependent recycling and glycocalyx removal. Glia 66(3): 670-687

Wang, S.-S.; Zhang, Z.; Zhu, T.-B.; Chu, S.-F.; He, W.-B.; Chen, N.-H. 2018: Myelin injury in the central nervous system and Alzheimer's disease. Brain Research Bulletin 140: 162-168

Bellesi, M.; Haswell, J.D.; de Vivo, L.; Marshall, W.; Roseboom, P.H.; Tononi, G.; Cirelli, C. 2018: Myelin modifications after chronic sleep loss in adolescent mice. Sleep 41(5)

Duignan, S.; Wright, S.; Rossor, T.; Cazabon, J.; Gilmour, K.; Ciccarelli, O.; Wassmer, E.; Lim, M.; Hemingway, C.; Hacohen, Y. 2018: Myelin oligodendrocyte glycoprotein and aquaporin-4 antibodies are highly specific in children with acquired demyelinating syndromes. Developmental Medicine and Child Neurology 60(9): 958-962

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Chen, J.J.; Flanagan, E.P.; Jitprapaikulsan, J.; López-Chiriboga, A.S.S.; Fryer, J.P.; Leavitt, J.A.; Weinshenker, B.G.; McKeon, A.; Tillema, J.-M.; Lennon, V.A.; Tobin, W.O.; Keegan, B.M.; Lucchinetti, C.F.; Kantarci, O.H.; McClelland, C.M.; Lee, M.S.; Bennett, J.L.; Pelak, V.S.; Chen, Y.; VanStavern, G.; Adesina, O.-O.O.; Eggenberger, E.R.; Acierno, M.D.; Wingerchuk, D.M.; Brazis, P.W.; Sagen, J.; Pittock, S.J. 2018: Myelin Oligodendrocyte Glycoprotein Antibody-Positive Optic Neuritis: Clinical Characteristics, Radiologic Clues, and Outcome. American Journal of Ophthalmology 195: 8-15

Kon, T.; Hikichi, H.; Ueno, T.; Suzuki, C.; Nunomura, J.; Kaneko, K.; Takahashi, T.; Nakashima, I.; Tomiyama, M. 2018: Myelin Oligodendrocyte Glycoprotein-IgG-positive Recurrent Bilateral Optic Papillitis with Serous Retinal Detachment. Internal Medicine 57(22): 3307-3312

Trinh, Q.D.; Pham, N.T.K.; Takada, K.; Komine-Aizawa, S.; Hayakawa, S. 2018: Myelin Oligodendrocyte Glycoprotein-Independent Rubella Infection of Keratinocytes and Resistance of First-Trimester Trophoblast Cells to Rubella Virus in Vitro. Viruses 10(1)

Lotan, I.; Brody, J.; Hellmann, M.Andrew.; Bialer, O.; Ganelin-Cohen, E.; Michaeli, N.; Marignier, R.; Stiebel-Kalish, H. 2018: Myelin oligodendrocyte glycoprotein-positive optic neuritis masquerading as pseudotumor cerebri at presentation. Journal of Neurology 265(9): 1985-1988

Monje, M. 2018: Myelin Plasticity and Nervous System Function. Annual Review of Neuroscience 41: 61-76

Gonsalvez, D.G.; Yoo, S.; Craig, G.A.; Wood, R.J.; Fletcher, J.L.; Murray, S.S.; Xiao, J. 2018: Myelin Protein Zero180-199 Peptide Induced Experimental Autoimmune Neuritis in C57BL/6 Mice. Methods in Molecular Biology 1791: 243-250

King, E.M.; Sabatier, M.J.; Hoque, M.; Kesar, T.M.; Backus, D.; Borich, M.R. 2018: Myelin status is associated with change in functional mobility following slope walking in people with multiple sclerosis. Multiple Sclerosis Journal-Experimental Translational and Clinical 4(2): 2055217318773540

Lana-Peixoto, M.A.; Pedrosa, D.; Talim, Nália.; Amaral, J.M.S.S.; Lacerda, Pâmela.E.; Kleinpaul, R. 2018: Myelitis and cauda equina involvement following dengue fever. A case report and review of the literature. Multiple Sclerosis and Related Disorders 20: 48-50

Marques, I.ês.B.; Marto, N.ál.; Raimundo, A.; Gil-Gouveia, R. 2018: Myelitis and Polyradiculoneuropathy with Severe Pain: Unusual Neurological Manifestations as Presenting Symptoms of Brucellosis. Neurologist 23(4): 131-134

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Jaulent, P.; Pegat, A.; Grosset-Janin, C.; Durand-Dubief, F.; Vukusic, S.; Marignier, R. 2018: "Myelitis migrans": A rare cause of treatable myelitis. Revue Neurologique (Paris) 174(10): 745-747

Machiels, J.D.; Cobussen, M.; Bosboom, R.W.; van Os, N.J.H.; Hageman, A.T.M.; Hassing, R. 2018: Myelitis transversa caused by neuroschistosomiasis. Nederlands Tijdschrift Voor Geneeskunde 162

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Takamiya, S.; Seki, T.; Ikeda, T.; Shinada, S-Ichiro.; Hamauchi, S.; Terasaka, S.; Houkin, K. 2018: Myelocystocele Mimicking Myelomeningocele: A Case Report and Review of the Literature. World Neurosurgery 119: 172-175

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Schuler, E.; Frank, F.; Hildebrandt, B.; Betz, B.; Strupp, C.; Rudelius, M.; Aul, C.; Schroeder, T.; Gattermann, N.; Haas, R.; Germing, U. 2018: Myelodysplastic syndromes without peripheral monocytosis but with evidence of marrow monocytosis share clinical and molecular characteristics with CMML. Leukemia Research 65: 1-4

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Drevon, L.; Marceau, A.; Maarek, O.; Cuccuini, W.; Clappier, E.; Eclache, V.; Cluzeau, T.; Richez, V.; Berkaoui, Iès.; Dimicoli-Salazar, S.; Bidet, A.; Vial, J-Philippe.; Park, S.; Vieira Dos Santos, C.; Kaphan, Eéonore.; Berthon, Céline.; Stamatoullas, A.; Delhommeau, Fçois.; Abermil, N.; Braun, T.; Sapena, R.; Lusina, D.; Renneville, A.; Adès, L.; Raynaud, S.; Fenaux, P. 2018: Myelodysplastic syndrome (MDS) with isolated trisomy 8: a type of MDS frequently associated with myeloproliferative features? A report by the Groupe Francophone des Myélodysplasies. British Journal of Haematology 182(6): 843-850

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Jiang, Y.; Wang, Y.; Ma, P.; An, D.; Zhao, J.; Liang, S.; Ye, Y.; Lu, Y.; Zhang, P.; Liu, X.; Han, H.; Qin, H. 2019: Myeloid-specific targeting of Notch ameliorates murine renal fibrosis via reduced infiltration and activation of bone marrow-derived macrophage. Protein and Cell 10(3): 196-210

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Gralewski, J.H.; Post, G.R.; van Rhee, F.; Yuan, Y. 2018: Myeloid transformation of plasma cell myeloma: molecular evidence of clonal evolution revealed by next generation sequencing. Diagnostic Pathology 13(1): 15

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Pravalika, K.; Sarmah, D.; Kaur, H.; Wanve, M.; Saraf, J.; Kalia, K.; Borah, A.; Yavagal, D.R.; Dave, K.R.; Bhattacharya, P. 2018: Myeloperoxidase and Neurological Disorder: a Crosstalk. Acs Chemical Neuroscience 9(3): 421-430

Roumeguère, T.; Van Antwerpen, P.; Vanhamme, L.; Delporte, C.; Rousseau, A.; Wespes, E.; Vanhaeverbeek, M.; Boudjeltia, K.Z. 2018: Myeloperoxidase and Prostate volume: a preliminary study. Progres en Urologie: Journal de l'Association Francaise d'Urologie et de la Societe Francaise d'Urologie 28(10): 482-487

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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