272 related articles for article (PubMed ID: 23264583)
1. Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation.
Christophersen IE; Olesen MS; Liang B; Andersen MN; Larsen AP; Nielsen JB; Haunsø S; Olesen SP; Tveit A; Svendsen JH; Schmitt N
Eur Heart J; 2013 May; 34(20):1517-25. PubMed ID: 23264583
[TBL] [Abstract][Full Text] [Related]
2. In-silico investigations of the functional impact of KCNA5 mutations on atrial mechanical dynamics.
Ni H; Adeniran I; Zhang H
J Mol Cell Cardiol; 2017 Oct; 111():86-95. PubMed ID: 28803858
[TBL] [Abstract][Full Text] [Related]
3. Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.
Hayashi K; Konno T; Tada H; Tani S; Liu L; Fujino N; Nohara A; Hodatsu A; Tsuda T; Tanaka Y; Kawashiri MA; Ino H; Makita N; Yamagishi M
Circ Arrhythm Electrophysiol; 2015 Oct; 8(5):1095-104. PubMed ID: 26129877
[TBL] [Abstract][Full Text] [Related]
4. [Identification and functional analysis of a KCNA5 mutation responsible for idiopathic atrial fibrillation].
Yang YQ; Lin XP; Li J; Chen YH
Zhonghua Yi Xue Za Zhi; 2010 Apr; 90(16):1100-4. PubMed ID: 20646426
[TBL] [Abstract][Full Text] [Related]
5. A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.
Olesen MS; Refsgaard L; Holst AG; Larsen AP; Grubb S; Haunsø S; Svendsen JH; Olesen SP; Schmitt N; Calloe K
Cardiovasc Res; 2013 Jun; 98(3):488-95. PubMed ID: 23400760
[TBL] [Abstract][Full Text] [Related]
6. Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation.
Nielsen JB; Bentzen BH; Olesen MS; David JP; Olesen SP; Haunsø S; Svendsen JH; Schmitt N
Biomark Med; 2014; 8(4):557-70. PubMed ID: 24796621
[TBL] [Abstract][Full Text] [Related]
7. Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation.
Yang Y; Li J; Lin X; Yang Y; Hong K; Wang L; Liu J; Li L; Yan D; Liang D; Xiao J; Jin H; Wu J; Zhang Y; Chen YH
J Hum Genet; 2009 May; 54(5):277-83. PubMed ID: 19343045
[TBL] [Abstract][Full Text] [Related]
8. In silico assessment of genetic variation in KCNA5 reveals multiple mechanisms of human atrial arrhythmogenesis.
Colman MA; Ni H; Liang B; Schmitt N; Zhang H
PLoS Comput Biol; 2017 Jun; 13(6):e1005587. PubMed ID: 28622331
[TBL] [Abstract][Full Text] [Related]
9. Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation.
Yang T; Yang P; Roden DM; Darbar D
Heart Rhythm; 2010 Sep; 7(9):1246-52. PubMed ID: 20638934
[TBL] [Abstract][Full Text] [Related]
10. IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation.
Steffensen AB; Refsgaard L; Andersen MN; Vallet C; Mujezinovic A; Haunsø S; Svendsen JH; Olesen SP; Olesen MS; Schmitt N
J Cardiovasc Electrophysiol; 2015 Jul; 26(7):715-23. PubMed ID: 25786344
[TBL] [Abstract][Full Text] [Related]
11. High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.
Olesen MS; Yuan L; Liang B; Holst AG; Nielsen N; Nielsen JB; Hedley PL; Christiansen M; Olesen SP; Haunsø S; Schmitt N; Jespersen T; Svendsen JH
Circ Cardiovasc Genet; 2012 Aug; 5(4):450-9. PubMed ID: 22685113
[TBL] [Abstract][Full Text] [Related]
12. Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.
Olson TM; Alekseev AE; Liu XK; Park S; Zingman LV; Bienengraeber M; Sattiraju S; Ballew JD; Jahangir A; Terzic A
Hum Mol Genet; 2006 Jul; 15(14):2185-91. PubMed ID: 16772329
[TBL] [Abstract][Full Text] [Related]
13. Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.
Olesen MS; Bentzen BH; Nielsen JB; Steffensen AB; David JP; Jabbari J; Jensen HK; Haunsø S; Svendsen JH; Schmitt N
BMC Med Genet; 2012 Apr; 13():24. PubMed ID: 22471742
[TBL] [Abstract][Full Text] [Related]
14. Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation.
Ritchie MD; Rowan S; Kucera G; Stubblefield T; Blair M; Carter S; Roden DM; Darbar D
J Am Coll Cardiol; 2012 Sep; 60(13):1173-81. PubMed ID: 22818067
[TBL] [Abstract][Full Text] [Related]
15. [Long term outcome of atrial fibrillation patients with KCNA5 and NPPA mutations post circumferential pulmonary vein ablation].
Zhang RF; Xia YL; Wang CC; Gao LJ; Yin XM; Chang D; Cong PX; Dong YX; Zhang SL; Tu X; Wang Q; Yang YZ
Zhonghua Xin Xue Guan Bing Za Zhi; 2013 May; 41(5):387-9. PubMed ID: 24021120
[TBL] [Abstract][Full Text] [Related]
16. Four and a half LIM protein 1: a partner for KCNA5 in human atrium.
Yang Z; Browning CF; Hallaq H; Yermalitskaya L; Esker J; Hall MR; Link AJ; Ham AJ; McGrath MJ; Mitchell CA; Murray KT
Cardiovasc Res; 2008 Jun; 78(3):449-57. PubMed ID: 18281375
[TBL] [Abstract][Full Text] [Related]
17. Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.
Olesen MS; Andreasen L; Jabbari J; Refsgaard L; Haunsø S; Olesen SP; Nielsen JB; Schmitt N; Svendsen JH
Heart Rhythm; 2014 Feb; 11(2):246-51. PubMed ID: 24144883
[TBL] [Abstract][Full Text] [Related]
18. Interaction of KCNA5, CX43, and CX40 proteins in the atrial muscle of patients with atrial fibrillation.
Wang K; Zhao J; Guo Z
Cell Biol Int; 2022 Nov; 46(11):1834-1840. PubMed ID: 35870168
[TBL] [Abstract][Full Text] [Related]
19. Function of Kv1.5 channels and genetic variations of KCNA5 in patients with idiopathic pulmonary arterial hypertension.
Remillard CV; Tigno DD; Platoshyn O; Burg ED; Brevnova EE; Conger D; Nicholson A; Rana BK; Channick RN; Rubin LJ; O'connor DT; Yuan JX
Am J Physiol Cell Physiol; 2007 May; 292(5):C1837-53. PubMed ID: 17267549
[TBL] [Abstract][Full Text] [Related]
20. Screening of KCNN3 in patients with early-onset lone atrial fibrillation.
Olesen MS; Jabbari J; Holst AG; Nielsen JB; Steinbrüchel DA; Jespersen T; Haunsø S; Svendsen JH
Europace; 2011 Jul; 13(7):963-7. PubMed ID: 21398315
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
