Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: MEP1A[original query] |
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Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG. Neuroscience letters 2006 Mar 396 (2): 137-42. Norberg Anna, Forsgren Lars, Holmberg Dan, Holmberg Moni |
MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel disease. Mucosal immunology 2009 May 2 (3): 220-31. Banerjee S, Oneda B, Yap L M, Jewell D P, Matters G L, Fitzpatrick L R, Seibold F, Sterchi E E, Ahmad T, Lottaz D, Bond J |
Association of MEP1A gene variants with insulin metabolism in central European women with polycystic ovary syndrome. Gene 2014 Mar 537 (2): 245-52. Lam Uyen D P, Lerchbaum Elisabeth, Schweighofer Natascha, Trummer Olivia, Eberhard Katharina, Genser Bernd, Pieber Thomas R, Obermayer-Pietsch Barba |
Genetic analysis of atherosclerosis identifies a major susceptibility locus in the major histocompatibility complex of mice. Atherosclerosis 2016 Oct 254 124-132. Grainger Andrew T, Jones Michael B, Li Jing, Chen Mei-Hua, Manichaikul Ani, Shi Weib |
An inflammation-related gene landscape predicts prognosis and response to immunotherapy in virus-associated hepatocellular carcinoma. Frontiers in oncology 2023 3 13 1118152. Gao Ying-Jie, Li Shi-Rong, Huang Yu |
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- Page last updated:Apr 22, 2024
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