Suppr超能文献

Does Atrial Fibrillation Follow Function? Ion Channel Mutations and Lone Atrial Fibrillation.

作者信息

Clauss Sebastian, Ellinor Patrick T

机构信息

From the Cardiovascular Research Center, Massachusetts General Hospital, Charlestown, MA (S.C., P.T.E.); Department of Medicine I, Klinikum Grosshadern, University of Munich (LMU), Munich, Germany (S.C.); DZHK (German Centre for Cardiovascular Research), Partner site Munich, Germany (S.C.); and Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA (P.T.E.).

出版信息

Circ Arrhythm Electrophysiol. 2015 Oct;8(5):1005-6. doi: 10.1161/CIRCEP.115.003330.

Abstract
摘要

相似文献

1
Does Atrial Fibrillation Follow Function? Ion Channel Mutations and Lone Atrial Fibrillation.
Circ Arrhythm Electrophysiol. 2015 Oct;8(5):1005-6. doi: 10.1161/CIRCEP.115.003330.
2
IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation.
J Cardiovasc Electrophysiol. 2015 Jul;26(7):715-23. doi: 10.1111/jce.12666. Epub 2015 May 4.
3
Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation.
Eur Heart J. 2013 May;34(20):1517-25. doi: 10.1093/eurheartj/ehs442. Epub 2012 Dec 21.
4
Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.
Circ Arrhythm Electrophysiol. 2015 Oct;8(5):1095-104. doi: 10.1161/CIRCEP.114.002519. Epub 2015 Jun 30.
6
A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.
Cardiovasc Res. 2013 Jun 1;98(3):488-95. doi: 10.1093/cvr/cvt028. Epub 2013 Feb 11.
7
Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.
Cardiovasc Res. 2011 Mar 1;89(4):786-93. doi: 10.1093/cvr/cvq348. Epub 2010 Nov 4.
8
Potassium channel gene mutations rarely cause atrial fibrillation.
BMC Med Genet. 2006 Aug 3;7:70. doi: 10.1186/1471-2350-7-70.
9
The genetics of atrial fibrillation.
Curr Opin Cardiol. 2010 May;25(3):186-91. doi: 10.1097/HCO.0b013e3283385734.
10
The genetics of atrial fibrillation.
Curr Opin Cardiol. 2017 Jan;32(1):10-16. doi: 10.1097/HCO.0000000000000356.

本文引用的文献

1
Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.
Circ Arrhythm Electrophysiol. 2015 Oct;8(5):1095-104. doi: 10.1161/CIRCEP.114.002519. Epub 2015 Jun 30.
2
Genetics of atrial fibrillation: from families to genomes.
J Hum Genet. 2016 Jan;61(1):61-70. doi: 10.1038/jhg.2015.44. Epub 2015 May 21.
6
Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation.
Heart Rhythm. 2014 Jan;11(1):46-52. doi: 10.1016/j.hrthm.2013.10.025. Epub 2013 Oct 10.
7
Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation.
Eur Heart J. 2013 May;34(20):1517-25. doi: 10.1093/eurheartj/ehs442. Epub 2012 Dec 21.
8
High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.
Circ Cardiovasc Genet. 2012 Aug 1;5(4):450-9. doi: 10.1161/CIRCGENETICS.111.962597. Epub 2012 Jun 8.
9
Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro.
Circulation. 2011 Aug 30;124(9):1001-11. doi: 10.1161/CIRCULATIONAHA.110.987248. Epub 2011 Aug 8.
10
Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation.
Heart Rhythm. 2010 Sep;7(9):1246-52. doi: 10.1016/j.hrthm.2010.05.032. Epub 2010 Jun 1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验