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NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.
Schwerd T, Bryant RV, Pandey S, Capitani M, Meran L, Cazier JB, Jung J, Mondal K, Parkes M, Mathew CG, Fiedler K, McCarthy DJ; WGS500 Consortium; Oxford IBD cohort study investigators; COLORS in IBD group investigators; UK IBD Genetics Consortium; Sullivan PB, Rodrigues A, Travis SPL, Moore C, Sambrook J, Ouwehand WH, Roberts DJ, Danesh J; INTERVAL Study; Russell RK, Wilson DC, Kelsen JR, Cornall R, Denson LA, Kugathasan S, Knaus UG, Serra EG, Anderson CA, Duerr RH, McGovern DP, Cho J, Powrie F, Li VS, Muise AM, Uhlig HH. Schwerd T, et al. Among authors: mathew cg. Mucosal Immunol. 2018 Mar;11(2):562-574. doi: 10.1038/mi.2017.74. Epub 2017 Nov 1. Mucosal Immunol. 2018. PMID: 29091079 Free PMC article.
A MseI polymorphism in exon 48 of the dystrophin gene.
Yau SC, Roberts RG, Bentley DR, Mathew CG, Bobrow M. Yau SC, et al. Among authors: mathew cg. Nucleic Acids Res. 1991 Oct 25;19(20):5803. doi: 10.1093/nar/19.20.5803-a. Nucleic Acids Res. 1991. PMID: 1682892 Free PMC article.
Association of DLG5 R30Q variant with inflammatory bowel disease.
Daly MJ, Pearce AV, Farwell L, Fisher SA, Latiano A, Prescott NJ, Forbes A, Mansfield J, Sanderson J, Langelier D, Cohen A, Bitton A, Wild G, Lewis CM, Annese V, Mathew CG, Rioux JD. Daly MJ, et al. Among authors: mathew cg. Eur J Hum Genet. 2005 Jul;13(7):835-9. doi: 10.1038/sj.ejhg.5201403. Eur J Hum Genet. 2005. PMID: 15841097
329 results