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A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease.
Assimes TL, Knowles JW, Priest JR, Basu A, Borchert A, Volcik KA, Grove ML, Tabor HK, Southwick A, Tabibiazar R, Sidney S, Boerwinkle E, Go AS, Iribarren C, Hlatky MA, Fortmann SP, Myers RM, Kuhn H, Risch N, Quertermous T. Assimes TL, et al. Among authors: myers rm. Atherosclerosis. 2008 May;198(1):136-44. doi: 10.1016/j.atherosclerosis.2007.09.003. Epub 2007 Oct 23. Atherosclerosis. 2008. PMID: 17959182 Free PMC article.
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.
Assimes TL, Knowles JW, Basu A, Iribarren C, Southwick A, Tang H, Absher D, Li J, Fair JM, Rubin GD, Sidney S, Fortmann SP, Go AS, Hlatky MA, Myers RM, Risch N, Quertermous T. Assimes TL, et al. Among authors: myers rm. Hum Mol Genet. 2008 Aug 1;17(15):2320-8. doi: 10.1093/hmg/ddn132. Epub 2008 Apr 28. Hum Mol Genet. 2008. PMID: 18443000 Free PMC article.
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.
McGowan KA, Li JZ, Park CY, Beaudry V, Tabor HK, Sabnis AJ, Zhang W, Fuchs H, de Angelis MH, Myers RM, Attardi LD, Barsh GS. McGowan KA, et al. Among authors: myers rm. Nat Genet. 2008 Aug;40(8):963-70. doi: 10.1038/ng.188. Epub 2008 Jul 20. Nat Genet. 2008. PMID: 18641651 Free PMC article.
526 results