Associated Papers
Genetic Variants in Potassium Channel Genes and Their Clinical Implications in Kazakhstani Patients with Cardiac Arrhythmias.
Chamoieva A et al.
Journal of Personalized Medicine, 2026
Clinical characteristics and mortality risk factors in pediatric hypertrophic, restrictive, and rapidly progressive hypertrophic cardiomyopathy: a retrospective cohort study with follow-up.
Nawaz A et al.
Frontiers in Cardiovascular Medicine, 2025
Deciphering the pathogenic role of a variant with uncertain significance for short QT and Brugada syndromes using gene-edited human-induced pluripotent stem cell-derived cardiomyocytes and preclinical drug screening.
El-Battrawy I et al.
Clinical and Translational Medicine, 2021
Brugada syndrome: A comprehensive review of pathophysiological mechanisms and risk stratification strategies.
Li KHC et al.
International Journal of Cardiology. Heart & Vasculature, 2020
Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome.
Hosseini SM et al.
Circulation, 2018
Re-evaluating pathogenicity of variants associated with the long QT syndrome.
Kaltman JR et al.
Journal of Cardiovascular Electrophysiology, 2018
Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death.
Oshima Y et al.
Journal of Human Genetics, 2017
Brugada syndrome: a fatal disease with complex genetic etiologies - still a long way to go.
Wu Y et al.
Forensic Sciences Research, 2017
Novel exon 1 protein-coding regions N-terminally extend human KCNE3 and KCNE4.
Abbott GW
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2016
KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channel regulation.
Abbott GW
Gene, 2016
Kcne3 deletion initiates extracardiac arrhythmogenesis in mice.
Hu Z et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2014
Arrhythmogenic KCNE gene variants: current knowledge and future challenges.
Crump SM et al.
Frontiers in Genetics, 2014
KCNE3 T4A as the genetic basis of Brugada-pattern electrocardiogram.
Nakajima T et al.
Circulation Journal : Official Journal of the Japanese Circulation Society, 2012
Deep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitus.
Sand PG et al.
Behavioral and Brain Functions : Bbf, 2011
Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome.
Ohno S et al.
Human Mutation, 2009