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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and MEP1A[original query]
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
The effect of rs2910686 on ERAP2 expression in IBD and epithelial inflammatory response.
Journal of translational medicine 2024 8 22 (1): 750.
Siri Sæterstad, Ann Elisabeth Østvik, Marianne Doré Hansen, Torunn Bruland, Atle van Beelen Granlu
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