Wang Q - Search Results

1

Risk stratification in Brugada syndrome.

Glatter KA, Chiamvimonvat N, Viitasalo M, Wang Q, Tuteja D. Glatter KA, et al. Among authors: wang q. Lancet. 2005 Aug 13-19;366(9485):530-1. doi: 10.1016/S0140-6736(05)67078-X. Lancet. 2005. PMID: 16099276 Free PMC article. No abstract available.

2

Effectiveness of sotalol treatment in symptomatic Brugada syndrome.

Glatter KA, Wang Q, Keating M, Chen S, Chiamvimonvat N, Scheinman MM. Glatter KA, et al. Among authors: wang q. Am J Cardiol. 2004 May 15;93(10):1320-2. doi: 10.1016/j.amjcard.2004.02.023. Am J Cardiol. 2004. PMID: 15135718

3

Mechanisms by which SCN5A mutation N1325S causes cardiac arrhythmias and sudden death in vivo.

Tian XL, Yong SL, Wan X, Wu L, Chung MK, Tchou PJ, Rosenbaum DS, Van Wagoner DR, Kirsch GE, Wang Q. Tian XL, et al. Among authors: wang q. Cardiovasc Res. 2004 Feb 1;61(2):256-67. doi: 10.1016/j.cardiores.2003.11.007. Cardiovasc Res. 2004. PMID: 14736542 Free PMC article.

4

ST-segment elevation myocardial infarction in China from 2001 to 2011 (the China PEACE-Retrospective Acute Myocardial Infarction Study): a retrospective analysis of hospital data.

Li J, Li X, Wang Q, Hu S, Wang Y, Masoudi FA, Spertus JA, Krumholz HM, Jiang L; China PEACE Collaborative Group. Li J, et al. Among authors: wang y, wang q. Lancet. 2015 Jan 31;385(9966):441-51. doi: 10.1016/S0140-6736(14)60921-1. Epub 2014 Jun 23. Lancet. 2015. PMID: 24969506 Free PMC article.

5

Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.

Oberti C, Wang L, Li L, Dong J, Rao S, Du W, Wang Q. Oberti C, et al. Among authors: wang l, wang q. Circulation. 2004 Dec 21;110(25):3753-9. doi: 10.1161/01.CIR.0000150333.87176.C7. Epub 2004 Dec 13. Circulation. 2004. PMID: 15596564 Free PMC article.

6

Functional analysis of TBX5 missense mutations associated with Holt-Oram syndrome.

Fan C, Liu M, Wang Q. Fan C, et al. Among authors: wang q. J Biol Chem. 2003 Mar 7;278(10):8780-5. doi: 10.1074/jbc.M208120200. Epub 2002 Dec 23. J Biol Chem. 2003. PMID: 12499378 Free PMC article.

7

Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome.

Tian XL, Kadaba R, You SA, Liu M, Timur AA, Yang L, Chen Q, Szafranski P, Rao S, Wu L, Housman DE, DiCorleto PE, Driscoll DJ, Borrow J, Wang Q. Tian XL, et al. Among authors: wang q. Nature. 2004 Feb 12;427(6975):640-5. doi: 10.1038/nature02320. Nature. 2004. PMID: 14961121 Free PMC article.

8

LQT4 gene: the "missing" ankyrin.

Yong S, Tian X, Wang Q. Yong S, et al. Among authors: wang q. Mol Interv. 2003 May;3(3):131-6. doi: 10.1124/mi.3.3.131. Mol Interv. 2003. PMID: 14993420 Free PMC article. Review.

9

Activated regulatory T-cells attenuate myocardial ischaemia/reperfusion injury through a CD39-dependent mechanism.

Xia N, Jiao J, Tang TT, Lv BJ, Lu YZ, Wang KJ, Zhu ZF, Mao XB, Nie SF, Wang Q, Tu X, Xiao H, Liao YH, Shi GP, Cheng X. Xia N, et al. Among authors: wang kj, wang q. Clin Sci (Lond). 2015 May 1;128(10):679-93. doi: 10.1042/CS20140672. Clin Sci (Lond). 2015. PMID: 25558978

10

Identification and molecular characterization of a de novo supernumerary ring chromosome 18 in a patient with Klippel-Trenaunay syndrome.

Timur AA, Sadgephour A, Graf M, Schwartz S, Libby ED, Driscoll DJ, Wang Q. Timur AA, et al. Among authors: wang q. Ann Hum Genet. 2004 Jul;68(Pt 4):353-61. doi: 10.1046/j.1529-8817.2004.00095.x. Ann Hum Genet. 2004. PMID: 15225160

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