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Comprehensive mutation scanning of KCNQ1 in 111 Han Chinese patients with lone atrial fibrillation.

Chen LY, Goh JM, Wong RC, Hsu LF, Foo D, Benditt DG, Ling LH, Heng CK.

Heart Asia. 2010 Nov 8;2(1):126-8. doi: 10.1136/ha.2010.002832.


Cardiac Delayed Rectifier Potassium Channels in Health and Disease.

Chen L, Sampson KJ, Kass RS.

Card Electrophysiol Clin. 2016 Jun;8(2):307-22. doi: 10.1016/j.ccep.2016.01.004. Review.


Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation.

Hoffmann S, Clauss S, Berger IM, Weiß B, Montalbano A, Röth R, Bucher M, Klier I, Wakili R, Seitz H, Schulze-Bahr E, Katus HA, Flachsbart F, Nebel A, Guenther SP, Bagaev E, Rottbauer W, Kääb S, Just S, Rappold GA.

Basic Res Cardiol. 2016 May;111(3):36. doi: 10.1007/s00395-016-0557-2.


Next-Generation Sequencing in the Genetics of Human Atrial Fibrillation.

Hsieh CS, Chuang EY, Juang JM, Hwang JJ, Tseng CD, Chiang FT, Lai LP, Lin JL, Tsai CT.

Acta Cardiol Sin. 2013 Jul;29(4):317-22. Review.


Atrial Fibrillation Genetics: Is There a Practical Clinical Value Now or in the Future?

Hucker WJ, Saini H, Lubitz SA, Ellinor PT.

Can J Cardiol. 2016 Nov;32(11):1300-1305. doi: 10.1016/j.cjca.2016.02.032. Review.


Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.

Wang ZC, Ji WH, Ruan CW, Liu XY, Qiu XB, Yuan F, Li RG, Xu YJ, Liu X, Huang RT, Xue S, Yang YQ.

Int J Med Sci. 2016 Jan 23;13(1):60-7. doi: 10.7150/ijms.13264.


Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice.

Mahida S.

Arrhythm Electrophysiol Rev. 2014 Aug;3(2):69-75. doi: 10.15420/aer.2014.3.2.69.


Unnatural amino acid photo-crosslinking of the IKs channel complex demonstrates a KCNE1:KCNQ1 stoichiometry of up to 4:4.

Murray CI, Westhoff M, Eldstrom J, Thompson E, Emes R, Fedida D.

Elife. 2016 Jan 23;5. pii: e11815. doi: 10.7554/eLife.11815.


Voltage-Dependent Gating: Novel Insights from KCNQ1 Channels.

Cui J.

Biophys J. 2016 Jan 5;110(1):14-25. doi: 10.1016/j.bpj.2015.11.023. Review.


Conformational changes of an ion-channel during gating and emerging electrophysiologic properties: Application of a computational approach to cardiac Kv7.1.

Nekouzadeh A, Rudy Y.

Prog Biophys Mol Biol. 2016 Jan;120(1-3):18-27. doi: 10.1016/j.pbiomolbio.2015.12.014.


Gene-guided therapy for catheter-ablation of atrial fibrillation: are we there yet?

Huang H, Darbar D.

J Interv Card Electrophysiol. 2016 Jan;45(1):3-5. doi: 10.1007/s10840-015-0086-1. No abstract available.


Screen-based identification and validation of four new ion channels as regulators of renal ciliogenesis.

Slaats GG, Wheway G, Foletto V, Szymanska K, van Balkom BW, Logister I, Den Ouden K, Keijzer-Veen MG, Lilien MR, Knoers NV, Johnson CA, Giles RH.

J Cell Sci. 2015 Dec 15;128(24):4550-9. doi: 10.1242/jcs.176065.


Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2.

Wu ZJ, Huang Y, Fu YC, Zhao XJ, Zhu C, Zhang Y, Xu B, Zhu QL, Li Y.

J Geriatr Cardiol. 2015 Jul;12(4):394-401. doi: 10.11909/j.issn.1671-5411.2015.04.002.


KCNA5 gene polymorphism associate with idiopathic atrial fibrillation.

Tian L, Liu G, Wang L, Zheng M, Li Y.

Int J Clin Exp Med. 2015 Jun 15;8(6):9890-6.


Neuronal and Cardiovascular Potassium Channels as Therapeutic Drug Targets: Promise and Pitfalls.

Humphries ES, Dart C.

J Biomol Screen. 2015 Oct;20(9):1055-73. doi: 10.1177/1087057115601677. Review.


Ion Channels in the Heart.

Bartos DC, Grandi E, Ripplinger CM.

Compr Physiol. 2015 Jul 1;5(3):1423-64. doi: 10.1002/cphy.c140069. Review.


Paternal allelic mutation at the Kcnq1 locus reduces pancreatic β-cell mass by epigenetic modification of Cdkn1c.

Asahara S, Etoh H, Inoue H, Teruyama K, Shibutani Y, Ihara Y, Kawada Y, Bartolome A, Hashimoto N, Matsuda T, Koyanagi-Kimura M, Kanno A, Hirota Y, Hosooka T, Nagashima K, Nishimura W, Inoue H, Matsumoto M, Higgins MJ, Yasuda K, Inagaki N, Seino S, Kasuga M, Kido Y.

Proc Natl Acad Sci U S A. 2015 Jul 7;112(27):8332-7. doi: 10.1073/pnas.1422104112.


Your Father and Grandfather's Atrial Fibrillation: A Review of the Genetics of the Most Common Pathologic Cardiac Dysrhythmia.

Palatinus JA, Das S.

Curr Genomics. 2015 Apr;16(2):75-81. doi: 10.2174/1389202916666150108222031.


The Genetic Basis of Coronary Artery Disease and Atrial Fibrillation: A Search for Disease Mechanisms and Therapeutic Targets.

Neelankavil J, Rau CD, Wang Y.

J Cardiothorac Vasc Anesth. 2015 Oct;29(5):1328-32. doi: 10.1053/j.jvca.2015.01.031. Review. No abstract available.

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