Jay PY - Search Results

1

Mice lacking sister chromatid cohesion protein PDS5B exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome.

Zhang B, Jain S, Song H, Fu M, Heuckeroth RO, Erlich JM, Jay PY, Milbrandt J. Zhang B, et al. Among authors: jay py. Development. 2007 Sep;134(17):3191-201. doi: 10.1242/dev.005884. Epub 2007 Jul 25. Development. 2007. PMID: 17652350

2

Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects.

Jay PY, Bielinska M, Erlich JM, Mannisto S, Pu WT, Heikinheimo M, Wilson DB. Jay PY, et al. Dev Biol. 2007 Jan 15;301(2):602-14. doi: 10.1016/j.ydbio.2006.09.050. Epub 2006 Oct 5. Dev Biol. 2007. PMID: 17069789 Free PMC article.

3

Molecular genetics of congenital diaphragmatic defects.

Bielinska M, Jay PY, Erlich JM, Mannisto S, Urban Z, Heikinheimo M, Wilson DB. Bielinska M, et al. Among authors: jay py. Ann Med. 2007;39(4):261-74. doi: 10.1080/07853890701326883. Ann Med. 2007. PMID: 17558598 Free PMC article. Review.

4

Dosage effects of cohesin regulatory factor PDS5 on mammalian development: implications for cohesinopathies.

Zhang B, Chang J, Fu M, Huang J, Kashyap R, Salavaggione E, Jain S, Kulkarni S, Deardorff MA, Uzielli ML, Dorsett D, Beebe DC, Jay PY, Heuckeroth RO, Krantz I, Milbrandt J. Zhang B, et al. Among authors: jay py. PLoS One. 2009;4(5):e5232. doi: 10.1371/journal.pone.0005232. Epub 2009 May 1. PLoS One. 2009. PMID: 19412548 Free PMC article.

5

Loss of glypican-3 function causes growth factor-dependent defects in cardiac and coronary vascular development.

Ng A, Wong M, Viviano B, Erlich JM, Alba G, Pflederer C, Jay PY, Saunders S. Ng A, et al. Among authors: jay py. Dev Biol. 2009 Nov 1;335(1):208-15. doi: 10.1016/j.ydbio.2009.08.029. Epub 2009 Sep 4. Dev Biol. 2009. PMID: 19733558 Free PMC article.

6

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.

7

Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation.

Winston JB, Schulkey CE, Chen IB, Regmi SD, Efimova M, Erlich JM, Green CA, Aluko A, Jay PY. Winston JB, et al. Among authors: jay py. Circ Cardiovasc Genet. 2012 Jun;5(3):293-300. doi: 10.1161/CIRCGENETICS.111.961136. Epub 2012 Apr 24. Circ Cardiovasc Genet. 2012. PMID: 22534315 Free PMC article.

8

The intracellular domains of Notch1 and Notch2 are functionally equivalent during development and carcinogenesis.

Liu Z, Brunskill E, Varnum-Finney B, Zhang C, Zhang A, Jay PY, Bernstein I, Morimoto M, Kopan R. Liu Z, et al. Among authors: jay py. Development. 2015 Jul 15;142(14):2452-63. doi: 10.1242/dev.125492. Epub 2015 Jun 10. Development. 2015. PMID: 26062937 Free PMC article.

9

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.

10

Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders.

Prendiville T, Jay PY, Pu WT. Prendiville T, et al. Among authors: jay py. Cold Spring Harb Perspect Med. 2014 Oct 1;4(10):a013946. doi: 10.1101/cshperspect.a013946. Cold Spring Harb Perspect Med. 2014. PMID: 25274754 Free PMC article. Review.

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