Inhibition of cardiac Kv4.3 (Ito) channel isoforms by class I antiarrhythmic drugs lidocaine and mexiletine-Reference-Cited by-同舟云学术

Inhibition of cardiac Kv4.3 (Ito) channel isoforms by class I antiarrhythmic drugs lidocaine and mexiletine

Published:2020-08 Issue: Volume:880 Page:173159
ISSN:0014-2999
Container-title:European Journal of Pharmacology
language:en
Short-container-title:European Journal of Pharmacology

Author:

Rahm Ann-Kathrin,Müller Mara Elena,Gramlich Dominik,Lugenbiel Patrick,Uludag Ecem,Rivinius Rasmus,Ullrich Nina D.,Schmack Bastian,Ruhparwar Arjang,Heimberger Tanja,Weis Tanja,Karck Matthias,Katus Hugo A.,Thomas Dierk

Funder

Faculty of Medicine, University of Heidelberg, Germany

German Cardiac Society

Elisabeth und Rudolf-Hirsch Stiftung für Medizinische Forschung

Ernst und Berta Grimmke-Stiftung

German Heart Foundation

German Foundation of Heart Research

Joachim Siebeneicher Foundation

Deutsche Forschungsgemeinschaft

Ministry of Science, Research and the Arts Baden-Wuerttemberg

Cardiology Career Program of the Department of Cardiology, University of Heidelberg

Publisher

Elsevier BV

Subject

Pharmacology

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4. Antiarrhythmic drugs–clinical use and clinical decision making: a consensus document from the European Heart Rhythm Association (EHRA) and European Society of Cardiology (ESC) Working Group on Cardiovascular Pharmacology, endorsed by the Heart Rhythm Society (HRS), Asia-Pacific Heart Rhythm Society (APHRS) and International Society of Cardiovascular Pharmacotherapy (ISCP)

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2. Differential Effects of the Betablockers Carvedilol, Metoprolol and Bisoprolol on Cardiac Kv4.3 (Ito) Channel Isoforms;International Journal of Molecular Sciences;2023-09-08

3. Recognition and release of uridine and hCNT3: From multivariate interactions to molecular design;International Journal of Biological Macromolecules;2022-12

4. Electrical Ventricular Remodeling in Dilated Cardiomyopathy;Cells;2021-10-15

5. Effects of Antiarrhythmic Drugs on hERG Gating in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes From a Patient With Short QT Syndrome Type 1;Frontiers in Pharmacology;2021-05-07