Gap junctions in cardiovascular disease

HJ Jongsma, R Wilders - Circulation research, 2000 - Am Heart Assoc
… M, Groenewegen WA, Allessie MA, Jongsma HJ. Altered pattern of connexin40 distribution
in … AJ, van Veen TAA, Allessie MA, Jongsma HJ. Gap junctional remodeling in relation to …

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II

SG Priori, J Barhanin, RNW Hauer, W Haverkamp… - Circulation, 1999 - Am Heart Assoc
Genetic approaches have succeeded in defining the molecular basis of an increasing array
of heart diseases, such as hypertrophic cardiomyopathy and the long-QT syndromes, …

Connexins in mammalian heart function

DB Gros, HJ Jongsma - Bioessays, 1996 - Wiley Online Library
In heart, the propagation of electrical activity is mediated by intercellular channels, referred
to as junctional channels, aggregated into gap junctions and localised between myocytes. …

Reverse structural and gap-junctional remodeling after prolonged atrial fibrillation in the goat

J Ausma, HMW van der Velden, MH Lenders… - Circulation, 2003 - Am Heart Assoc
Background— Prolonged atrial fibrillation (AF) results in electrical, structural, and gap-junctional
remodeling. We examined the reversibility of the changes in (ultra)structure and gap …

Gap junctional remodeling in relation to stabilization of atrial fibrillation in the goat

HMW van der Velden, J Ausma, MB Rook… - Cardiovascular …, 2000 - academic.oup.com
Objective: It has been postulated that high atrial rate induced changes at the level of the gap
junctions (‘gap junctional remodeling’, ie changes in distribution, intercellular orientation …

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

WA Groenewegen, M Firouzi, CR Bezzina… - Circulation …, 2003 - Am Heart Assoc
Atrial standstill (AS) is a rare arrhythmia that occasionally appears to be genetically determined.
This study investigates the genetic background of this arrhythmogenic disorder in a …

Slow conduction and enhanced anisotropy increase the propensity for ventricular tachyarrhythmias in adult mice with induced deletion of connexin43

HVM van Rijen, D Eckardt, J Degen, M Theis, T Ott… - Circulation, 2004 - Am Heart Assoc
Background— Connexin 43 (Cx43) is a major determinant of conduction in the ventricular
working myocardium of mammals. We investigated the effect of decreased Cx43 expression …

Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in …

CR Bezzina, MB Rook, WA Groenewegen… - Circulation …, 2003 - Am Heart Assoc
Cardiac conduction defects associate with mutations in SCN5A, the gene encoding the cardiac
Na + channel. In the present study, we characterized a family in which the proband was …

Differences in gap junction channels between cardiac myocytes, fibroblasts, and heterologous pairs

MB Rook, AC Van Ginneken… - … of Physiology-Cell …, 1992 - journals.physiology.org
Cultures of neonatal rat heart cells contain predominantly myocytes and fibroblastic cells.
Most abundant are groups of synchronously contracting myocytes, which are electrically well …

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome

MB Rook, C Bezzina Alshinawi… - Cardiovascular …, 1999 - academic.oup.com
Background: Primary dysrhythmias other than those associated with the long QT syndrome,
are increasingly recognized. One of these are represented by patients with a history of …