Yang P - Search Results

1

Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndrome.

Yang T, Chung SK, Zhang W, Mullins JG, McCulley CH, Crawford J, MacCormick J, Eddy CA, Shelling AN, French JK, Yang P, Skinner JR, Roden DM, Rees MI. Yang T, et al. Among authors: yang p. Circ Arrhythm Electrophysiol. 2009 Aug;2(4):417-26. doi: 10.1161/CIRCEP.109.850149. Epub 2009 May 22. Circ Arrhythm Electrophysiol. 2009. PMID: 19808498 Free PMC article.

2

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.

Yang P, Kanki H, Drolet B, Yang T, Wei J, Viswanathan PC, Hohnloser SH, Shimizu W, Schwartz PJ, Stanton M, Murray KT, Norris K, George AL Jr, Roden DM. Yang P, et al. Among authors: yang t. Circulation. 2002 Apr 23;105(16):1943-8. doi: 10.1161/01.cir.0000014448.19052.4c. Circulation. 2002. PMID: 11997281

3

Polymorphisms in beta-adrenergic receptor genes in the acquired long QT syndrome.

Kanki H, Yang P, Xie HG, Kim RB, George AL Jr, Roden DM. Kanki H, et al. Among authors: yang p. J Cardiovasc Electrophysiol. 2002 Mar;13(3):252-6. doi: 10.1046/j.1540-8167.2002.00252.x. J Cardiovasc Electrophysiol. 2002. PMID: 11942593

4

Cardiac-enriched LIM domain protein fhl2 is required to generate I(Ks) in a heterologous system.

Kupershmidt S, Yang IC, Sutherland M, Wells KS, Yang T, Yang P, Balser JR, Roden DM. Kupershmidt S, et al. Among authors: yang t, yang p, yang ic. Cardiovasc Res. 2002 Oct;56(1):93-103. doi: 10.1016/s0008-6363(02)00498-4. Cardiovasc Res. 2002. PMID: 12237170

5

Polymorphism screening in the cardiac K+ channel gene KCNA5.

Simard C, Drolet B, Yang P, Kim RB, Roden DM. Simard C, et al. Among authors: yang p. Clin Pharmacol Ther. 2005 Mar;77(3):138-44. doi: 10.1016/j.clpt.2004.10.008. Clin Pharmacol Ther. 2005. PMID: 15735608

6

KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.

Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL Jr, Schwartz PJ. Crotti L, et al. Among authors: yang p. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052

7

Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation.

Yang T, Yang P, Roden DM, Darbar D. Yang T, et al. Among authors: yang p. Heart Rhythm. 2010 Sep;7(9):1246-52. doi: 10.1016/j.hrthm.2010.05.032. Epub 2010 Jun 1. Heart Rhythm. 2010. PMID: 20638934 Free PMC article.

8

Informatic and functional approaches to identifying a regulatory region for the cardiac sodium channel.

Atack TC, Stroud DM, Watanabe H, Yang T, Hall L, Hipkens SB, Lowe JS, Leake B, Magnuson MA, Yang P, Roden DM. Atack TC, et al. Among authors: yang t, yang p. Circ Res. 2011 Jun 24;109(1):38-46. doi: 10.1161/CIRCRESAHA.110.235630. Epub 2011 May 12. Circ Res. 2011. PMID: 21566215 Free PMC article.

9

Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.

Johnson WH Jr, Yang P, Yang T, Lau YR, Mostella BA, Wolff DJ, Roden DM, Benson DW. Johnson WH Jr, et al. Among authors: yang t, yang p. Pediatr Res. 2003 May;53(5):744-8. doi: 10.1203/01.PDR.0000059750.17002.B6. Epub 2003 Mar 5. Pediatr Res. 2003. PMID: 12621127

10

Cloning and initial characterization of the human cardiac sodium channel (SCN5A) promoter.

Yang P, Kupershmidt S, Roden DM. Yang P, et al. Cardiovasc Res. 2004 Jan 1;61(1):56-65. doi: 10.1016/j.cardiores.2003.09.030. Cardiovasc Res. 2004. PMID: 14732202

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