Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function-Reference-Cited by-同舟云学术

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Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function

Published:2016-08-23 Issue:10 Volume:468 Page:1663-1671
ISSN:0031-6768
Container-title:Pflügers Archiv - European Journal of Physiology
language:en
Short-container-title:Pflugers Arch - Eur J Physiol

Author:

Biel Stephanie,Aquila Marco,Hertel Brigitte,Berthold Anne,Neumann Thomas,DiFrancesco Dario,Moroni Anna,Thiel Gerhard,Kauferstein Silke

Funder

Fondazione Cariplo

MAECI

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Clinical Biochemistry,Physiology

Link

http://link.springer.com/content/pdf/10.1007/s00424-016-1870-1.pdf

Reference37 articles.

1. Anderson JB, Benson DW (2010) Genetics of sick sinus syndrome. Cardiac Electrophysiol Clinics 2:499–507

2. Antzelevitch C (2005) Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European heart rhythm association. Circulation 111:659–670

3. Altomare C, Terragni B, Brioschi C, Milanesi R, Pagliuca C, Viscomi C, Moroni A, DiFrancesco D (2003) Heteromeric HCN1-HCN4 channels: a comparison with native pacemaker channels from the rabbit sinoatrial node. J Physiol 549:347–359

4. Arbelo E, Brugada J (2014) Risk stratification and treatment of Brugada syndrome. Curr Cardiol Rep 16:508. doi: 10.1007/s11886-014-0508-1

5. Baruscotti M, Bucchi A, Viscomi C, Mandelli G, Consalez G, Gnecchi-Rusconi T, Montano N, Rabello Casali K, Micheloni S, Barbuti A, DiFrancesco D (2011) Deep bradycardia and heart block caused by inducible cardiac-specific knockout of the pacemaker channel gene Hcn4. Proc Natl Acad Sci U S A 108:1705–1710

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1. Pacemaker Channels and the Chronotropic Response in Health and Disease;Circulation Research;2024-05-10

2. Brugada syndrome: variability of clinical and genetic characteristics;Cardiac Arrhythmias;2023-12-08

3. Age-dependent contribution of intrinsic mechanisms to sinoatrial node function in humans;Scientific Reports;2023-11-01

4. Brugada Syndrome: More than a Monogenic Channelopathy;Biomedicines;2023-08-18

5. A195V mutation identified in sudden cardiac death decreases membrane localization and activation current density and abolishes cAMP sensitivity of HCN4 channels;2023-03-16

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