Vincent GM - Search Results

1

Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.

Zhang X, Chen S, Zhang L, Liu M, Redfearn S, Bryant RM, Oberti C, Vincent GM, Wang QK. Zhang X, et al. Among authors: vincent gm. BMC Med Genet. 2008 Sep 23;9:87. doi: 10.1186/1471-2350-9-87. BMC Med Genet. 2008. PMID: 18808722 Free PMC article.

2

KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.

Chen S, Zhang L, Bryant RM, Vincent GM, Flippin M, Lee JC, Brown E, Zimmerman F, Rozich R, Szafranski P, Oberti C, Sterba R, Marangi D, Tchou PJ, Chung MK, Wang Q. Chen S, et al. Among authors: vincent gm. Clin Genet. 2003 Apr;63(4):273-82. doi: 10.1034/j.1399-0004.2003.00048.x. Clin Genet. 2003. PMID: 12702160 Free PMC article.

3

The role of genotyping in diagnosing cardiac channelopathies : progress to date.

Vincent GM, Zhang L. Vincent GM, et al. Mol Diagn. 2005;9(3):105-18. doi: 10.2165/00066982-200509030-00001. Mol Diagn. 2005. PMID: 16271012 Review.

4

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

Wang Q, Shen J, Li Z, Timothy K, Vincent GM, Priori SG, Schwartz PJ, Keating MT. Wang Q, et al. Among authors: vincent gm. Hum Mol Genet. 1995 Sep;4(9):1603-7. doi: 10.1093/hmg/4.9.1603. Hum Mol Genet. 1995. PMID: 8541846

5

Nonsense-mediated mRNA decay caused by a frameshift mutation in a large kindred of type 2 long QT syndrome.

Zarraga IG, Zhang L, Stump MR, Gong Q, Vincent GM, Zhou Z. Zarraga IG, et al. Among authors: vincent gm. Heart Rhythm. 2011 Aug;8(8):1200-6. doi: 10.1016/j.hrthm.2011.03.039. Epub 2011 Mar 15. Heart Rhythm. 2011. PMID: 21419236 Free PMC article.

6

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.

Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT. Wang Q, et al. Among authors: vincent gm. Nat Genet. 1996 Jan;12(1):17-23. doi: 10.1038/ng0196-17. Nat Genet. 1996. PMID: 8528244

7

The inherited long QT syndrome: from ion channel to bedside.

Vincent GM, Timothy K, Fox J, Zhang L. Vincent GM, et al. Cardiol Rev. 1999 Jan-Feb;7(1):44-55. Cardiol Rev. 1999. PMID: 10348966 Review.

8

Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndrome.

Gong Q, Zhang L, Vincent GM, Horne BD, Zhou Z. Gong Q, et al. Among authors: vincent gm. Circulation. 2007 Jul 3;116(1):17-24. doi: 10.1161/CIRCULATIONAHA.107.708818. Epub 2007 Jun 18. Circulation. 2007. PMID: 17576861 Free PMC article.

9

A splice site mutation in hERG leads to cryptic splicing in human long QT syndrome.

Gong Q, Zhang L, Moss AJ, Vincent GM, Ackerman MJ, Robinson JC, Jones MA, Tester DJ, Zhou Z. Gong Q, et al. Among authors: vincent gm. J Mol Cell Cardiol. 2008 Mar;44(3):502-9. doi: 10.1016/j.yjmcc.2008.01.002. Epub 2008 Jan 17. J Mol Cell Cardiol. 2008. PMID: 18272172 Free PMC article.

10

Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.

Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, Medina A, Zhang L, Wang Z. Moss AJ, et al. Among authors: vincent gm. Circulation. 2002 Feb 19;105(7):794-9. doi: 10.1161/hc0702.105124. Circulation. 2002. PMID: 11854117

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