Association of a common KCNE1 variant with heart failure.
作者信息
George Alfred L
出版信息
Heart Rhythm. 2010 Mar;7(3):368-9. doi: 10.1016/j.hrthm.2009.12.014. Epub 2009 Dec 24.
Abstract
摘要
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本文引用的文献
1
S38G single-nucleotide polymorphism at the KCNE1 locus is associated with heart failure.S38G 单核苷酸多态性位于 KCNE1 基因座与心力衰竭相关。
Heart Rhythm. 2010 Mar;7(3):363-7. doi: 10.1016/j.hrthm.2009.11.032. Epub 2009 Dec 2.
2
Genomics of heart failure.心力衰竭的基因组学。
Heart Fail Clin. 2010 Jan;6(1):115-24. doi: 10.1016/j.hfc.2009.08.002.
3
Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes.
BMC Evol Biol. 2009 Aug 6;9:188. doi: 10.1186/1471-2148-9-188.
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Genome-wide association studies of coronary artery disease and heart failure: where are we going?冠状动脉疾病和心力衰竭的全基因组关联研究：我们将何去何从？
Pharmacogenomics. 2009 Feb;10(2):213-23. doi: 10.2217/14622416.10.2.213.
5
A GRK5 polymorphism that inhibits beta-adrenergic receptor signaling is protective in heart failure.一种抑制β-肾上腺素能受体信号传导的GRK5基因多态性在心力衰竭中具有保护作用。
Nat Med. 2008 May;14(5):510-7. doi: 10.1038/nm1750. Epub 2008 Apr 20.
6
MinK gene polymorphism in the pathogenesis of lone atrial fibrillation.MinK基因多态性在孤立性心房颤动发病机制中的作用
Kardiol Pol. 2006 Nov;64(11):1205-11; discussion 1212-3.
7
Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation.分析minK基因和内皮型一氧化氮合酶基因作为非瓣膜性心房颤动易感性的候选基因座。
Eur Heart J. 2006 Jul;27(14):1712-8. doi: 10.1093/eurheartj/ehl087. Epub 2006 Jun 7.
8
Incidence and epidemiology of heart failure.心力衰竭的发病率与流行病学
Heart Fail Rev. 2000 Jun;5(2):167-73. doi: 10.1023/A:1009884820941.
9
Atrial fibrillation-associated minK38G/S polymorphism modulates delayed rectifier current and membrane localization.心房颤动相关的minK38G/S多态性调节延迟整流电流和膜定位。
Cardiovasc Res. 2005 Aug 15;67(3):520-8. doi: 10.1016/j.cardiores.2005.03.007. Epub 2005 Apr 12.
10
Genetic causes of human heart failure.人类心力衰竭的遗传原因。
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