Role of sodium channels in propagation in heart muscle: how subtle genetic alterations result in major arrhythmic disorders (Q36822944)

16 August 2017

1 reference

title

Role of sodium channels in propagation in heart muscle: how subtle genetic alterations result in major arrhythmic disorders (English)

1 reference

16 August 2017

Cecile Terrenoire

1

1 reference

16 August 2017

Daniel Simhaee

series ordinal

2

1 reference

16 August 2017

Robert S Kass

series ordinal

3

1 reference

16 August 2017

publication date

14 May 2007

1 reference

Journal of Cardiovascular Electrophysiology

16 August 2017

published in

1 reference

16 August 2017

volume

18

1 reference

16 August 2017

issue

8

1 reference

16 August 2017

page(s)

900-905

1 reference

Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

16 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Calcium channel characteristics conferred on the sodium channel by single mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

The Na+ channel inactivation gate is a molecular complex: a novel role of the COOH-terminal domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

External pore residue mediates slow inactivation in mu 1 rat skeletal muscle sodium channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Multiple mechanisms of Na+ channel--linked long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

The congenital long QT syndromes from genotype to phenotype: clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Arrhythmogenic mechanism of an LQT-3 mutation of the human heart Na(+) channel alpha-subunit: A computational analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A de novo missense mutation of human cardiac Na+ channel exhibiting novel molecular mechanisms of long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Genetics of acquired long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Drug-induced long-QT syndrome associated with a subclinical SCN5A mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A novel missense mutation in the SCN5A gene associated with Brugada syndrome bidirectionally affecting blocking actions of antiarrhythmic drugs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Double SCN5A mutation underlying asymptomatic Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Brugada syndrome and fever: genetic and molecular characterization of patients carrying SCN5A mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

High risk for bradyarrhythmic complications in patients with Brugada syndrome caused by SCN5A gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A sodium-channel mutation causes isolated cardiac conduction disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Bradycardias and atrioventricular conduction block

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Specific therapy based on the genotype and cellular mechanism in inherited cardiac arrhythmias. Long QT syndrome and Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Structural parts involved in activation and inactivation of the sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

Linking a genetic defect to its cellular phenotype in a cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2007.00838.X

10.1111/J.1540-8167.2007.00838.X

21 January 2018

Identifiers

DOI

1 reference

16 August 2017

1 reference