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Heterogeneity of genetic modifiers ensures normal cardiac development.
Winston JB, Erlich JM, Green CA, Aluko A, Kaiser KA, Takematsu M, Barlow RS, Sureka AO, LaPage MJ, Janss LL, Jay PY. Winston JB, et al. Among authors: jay py. Circulation. 2010 Mar 23;121(11):1313-21. doi: 10.1161/CIRCULATIONAHA.109.887687. Epub 2010 Mar 8. Circulation. 2010. PMID: 20212279 Free PMC article.
The Complex Genetic Basis of Congenital Heart Defects.
Akhirome E, Walton NA, Nogee JM, Jay PY. Akhirome E, et al. Among authors: jay py. Circ J. 2017 Apr 25;81(5):629-634. doi: 10.1253/circj.CJ-16-1343. Epub 2017 Apr 1. Circ J. 2017. PMID: 28381817 Free PMC article. Review.
Function follows form: cardiac conduction system defects in Nkx2-5 mutation.
Jay PY, Harris BS, Buerger A, Rozhitskaya O, Maguire CT, Barbosky LA, McCusty E, Berul CI, O'brien TX, Gourdie RG, Izumo S. Jay PY, et al. Anat Rec A Discov Mol Cell Evol Biol. 2004 Oct;280(2):966-72. doi: 10.1002/ar.a.20102. Anat Rec A Discov Mol Cell Evol Biol. 2004. PMID: 15368343 Free article. Review.
Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.
Jay PY, Harris BS, Maguire CT, Buerger A, Wakimoto H, Tanaka M, Kupershmidt S, Roden DM, Schultheiss TM, O'Brien TX, Gourdie RG, Berul CI, Izumo S. Jay PY, et al. J Clin Invest. 2004 Apr;113(8):1130-7. doi: 10.1172/JCI19846. J Clin Invest. 2004. PMID: 15085192 Free PMC article.
66 results