[HTML][HTML] Cardiac transmembrane ion channels and action potentials: cellular physiology and arrhythmogenic behavior

V András, J Tomek, N Nagy, L Virág… - Physiological …, 2021 - journals.physiology.org
Cardiac arrhythmias are among the leading causes of mortality. They often arise from
alterations in the electrophysiological properties of cardiac cells and their underlying ionic …

[HTML][HTML] hERG K+ channels: structure, function, and clinical significance

JI Vandenberg, MD Perry, MJ Perrin… - Physiological …, 2012 - journals.physiology.org
The human ether-a-go-go related gene (hERG) encodes the pore-forming subunit of the
rapid component of the delayed rectifier K+ channel, Kv11. 1, which are expressed in the …

Development, calibration, and validation of a novel human ventricular myocyte model in health, disease, and drug block

J Tomek, A Bueno-Orovio, E Passini, X Zhou… - Elife, 2019 - elifesciences.org
Human-based modelling and simulations are becoming ubiquitous in biomedical science
due to their ability to augment experimental and clinical investigations. Cardiac …

The hERG potassium channel and hERG screening for drug-induced torsades de pointes

JC Hancox, MJ McPate, A El Harchi… - Pharmacology & …, 2008 - Elsevier
Drug-induced torsades de pointes (TdP) arrhythmia is a major safety concern in the process
of drug design and development. The incidence of TdP tends to be low, so early pre-clinical …

Potassium dependent structural changes in the selectivity filter of HERG potassium channels

CHY Lau, E Flood, MJ Hunter… - Nature …, 2024 - nature.com
The fine tuning of biological electrical signaling is mediated by variations in the rates of
opening and closing of gates that control ion flux through different ion channels. Human …

Pro-arrhythmic effects of gain-of-function potassium channel mutations in the short QT syndrome

JC Hancox, CY Du, A Butler… - … of the Royal …, 2023 - royalsocietypublishing.org
The congenital short QT syndrome (SQTS) is a rare condition characterized by abbreviated
rate-corrected QT (QTc) intervals on the electrocardiogram and by increased susceptibility to …

An update on the structure of hERG

A Butler, MV Helliwell, Y Zhang, JC Hancox… - Frontiers in …, 2020 - frontiersin.org
The human voltage-sensitive K+ channel hERG plays a fundamental role in cardiac action
potential repolarization, effectively controlling the QT interval of the electrocardiogram …

Murine electrophysiological models of cardiac arrhythmogenesis

CLH Huang - Physiological reviews, 2017 - journals.physiology.org
Cardiac arrhythmias can follow disruption of the normal cellular electrophysiological
processes underlying excitable activity and their tissue propagation as coherent wavefronts …

Stretch-Sensitive KCNQ1Mutation: A Link Between Genetic and Environmental Factors in the Pathogenesis of Atrial Fibrillation?

R Otway, JI Vandenberg, G Guo, A Varghese… - Journal of the American …, 2007 - jacc.org
Objectives: This study sought to evaluate mutations in genes encoding the slow component
of the cardiac delayed rectifier K+ current (I Ks) channel in familial atrial fibrillation (AF) …

Drug binding to the inactivated state is necessary but not sufficient for high-affinity binding to human ether-a-go-go-related gene channels

MJ Perrin, PW Kuchel, TJ Campbell… - Molecular …, 2008 - ASPET
Drug block of the human ether-à-go-go-related gene K+ channel (hERG) is the most
common cause of acquired long QT syndrome, a disorder of cardiac repolarization that may …