Impact of recent molecular studies on evaluation of ventricular arrhythmias (Q33789839)

29 July 2017

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title

Impact of recent molecular studies on evaluation of ventricular arrhythmias (English)

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29 July 2017

Roden DM

1

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29 July 2017

publication date

1 January 2000

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Journal of Interventional Cardiac Electrophysiology

29 July 2017

published in

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29 July 2017

volume

4 Suppl 1

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29 July 2017

page(s)

7-16

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Isoproterenol antagonizes prolongation of refractory period by the class III antiarrhythmic agent E-4031 in guinea pig myocytes. Mechanism of action

29 July 2017

cites work

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12 December 2020

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

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12 December 2020

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

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Sudden cardiac death in heart failure. The role of abnormal repolarization

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Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

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A multivalent PDZ-domain protein assembles signalling complexes in a G-protein-coupled cascade

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ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

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12 December 2020

Class III antiarrhythmic agents have a lot of potential but a long way to go. Reduced effectiveness and dangers of reverse use dependence

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12 December 2020

Separable Kvbeta subunit domains alter expression and gating of potassium channels

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12 December 2020

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

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12 December 2020

Precordial QT interval dispersion as a marker of torsade de pointes. Disparate effects of class Ia antiarrhythmic drugs and amiodarone

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12 December 2020

Ion channels--basic science and clinical disease

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12 December 2020

Abnormal electrical properties of myocytes from chronically infarcted canine heart. Alterations in Vmax and the transient outward current

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12 December 2020

Intracellular calcium handling in isolated ventricular myocytes from patients with terminal heart failure

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12 December 2020

Identification of a gene encoding a hyperpolarization-activated pacemaker channel of brain

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12 December 2020

Characterization of a voltage-gated K+ channel beta subunit expressed in human heart

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12 December 2020

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia

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12 December 2020

Electrophysiological mechanism of the characteristic electrocardiographic morphology of torsade de pointes tachyarrhythmias in the long-QT syndrome: detailed analysis of ventricular tridimensional activation patterns

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12 December 2020

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

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12 December 2020

Sodium channel block with mexiletine is effective in reducing dispersion of repolarization and preventing torsade des pointes in LQT2 and LQT3 models of the long-QT syndrome

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12 December 2020

Cloning and characterization of alpha1H from human heart, a member of the T-type Ca2+ channel gene family

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12 December 2020

A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43

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12 December 2020

Potassium channel down-regulation in heart failure

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12 December 2020

Molecular mechanism for an inherited cardiac arrhythmia

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12 December 2020

Developmental changes in the delayed rectifier K+ channels in mouse heart.

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12 December 2020

Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents

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12 December 2020

A family of hyperpolarization-activated mammalian cation channels

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12 December 2020

The long QT syndrome. A review of recent molecular genetic and physiologic discoveries

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12 December 2020

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

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12 December 2020

Cellular electrophysiology in cardiac hypertrophy and failure

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12 December 2020

Cellular mechanisms of early afterdepolarizations

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12 December 2020

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

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12 December 2020

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

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12 December 2020

Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.

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12 December 2020

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

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12 December 2020

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

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12 December 2020

In vivo and in vitro antiarrhythmic and arrhythmogenic effects of N-acetyl procainamide

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12 December 2020

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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12 December 2020

Reduced inward rectifying and increased E-4031-sensitive K+ current density in arrhythmogenic subendocardial purkinje myocytes from the infarcted heart

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12 December 2020

Frequency-dependent interactions of mexiletine and quinidine on depolarization and repolarization in canine Purkinje fibers

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12 December 2020

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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12 December 2020

Structural and electrophysiological changes in the epicardial border zone of canine myocardial infarcts during infarct healing

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12 December 2020

Role of calcium loading in early afterdepolarizations generated by Cs+ in canine and guinea pig Purkinje fibers

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12 December 2020

Characteristics of the delayed rectifier current (IKr and IKs) in canine ventricular epicardial, midmyocardial, and endocardial myocytes. A weaker IKs contributes to the longer action potential of the M cell

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12 December 2020

Sudden death due to troponin T mutations

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12 December 2020

Genetics, molecular mechanisms and management of long QT syndrome

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12 December 2020

The long QT syndrome: ion channel diseases of the heart

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12 December 2020

A K+ channel splice variant common in human heart lacks a C-terminal domain required for expression of rapidly activating delayed rectifier current

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12 December 2020

A family of sulfonylurea receptors determines the pharmacological properties of ATP-sensitive K+ channels

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12 December 2020

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

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12 December 2020

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

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12 December 2020

The G-protein-gated atrial K+ channel IKACh is a heteromultimer of two inwardly rectifying K(+)-channel proteins

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12 December 2020

Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease

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12 December 2020

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

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12 December 2020

Modification of the frequency- and voltage-dependent effects of quinidine when administered in combination with tocainide in canine Purkinje fibers.

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12 December 2020

Developmental changes in ionic channel activity in the embryonic murine heart

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12 December 2020

The management of hypertrophic cardiomyopathy

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12 December 2020

Bradycardia-dependent triggered activity: relevance to drug-induced multiform ventricular tachycardia.

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12 December 2020

Characteristics of transient outward current in human ventricular myocytes from patients with terminal heart failure

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12 December 2020

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

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12 December 2020

Phenotypic characterization of a novel long-QT syndrome mutation (R1623Q) in the cardiac sodium channel

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12 December 2020

Pharmacological targeting of long QT mutant sodium channels

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12 December 2020

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

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12 December 2020

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

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12 December 2020

Disturbed connexin43 gap junction distribution correlates with the location of reentrant circuits in the epicardial border zone of healing canine infarcts that cause ventricular tachycardia.

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12 December 2020

Molecular basis of the long-QT syndrome associated with deafness

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12 December 2020

Modulation by cAMP of a slowly activating potassium channel expressed in Xenopus oocytes

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12 December 2020

Beta-adrenergic stimulation of calcium channels occurs by potentiation of high-activity gating modes

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12 December 2020

Molecular identification of a hyperpolarization-activated channel in sea urchin sperm

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12 December 2020

Localization of the Kv1.5 K+ channel protein in explanted cardiac tissue

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12 December 2020

Induction of rhythm abnormalities in the fetal rat heart. A tentative mechanism for the embryotoxic effect of the class III antiarrhythmic agent almokalant

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12 December 2020

Developmental changes in transient outward current in mouse ventricle.

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12 December 2020

Primary structure and function of an A kinase anchoring protein associated with calcium channels

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12 December 2020

Sodium channel block produces opposite electrophysiological effects in canine ventricular epicardium and endocardium.

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12 December 2020

Delayed rectifier outward current and repolarization in human atrial myocytes

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12 December 2020

Gap junction protein phenotypes of the human heart and conduction system

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12 December 2020

Identification of a genetic locus for familial atrial fibrillation

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12 December 2020

Rate-dependent prolongation of cardiac action potentials by a methanesulfonanilide class III antiarrhythmic agent. Specific block of rapidly activating delayed rectifier K+ current by dofetilide

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12 December 2020

Evidence for the existence of a cardiac specific isoform of the α1 subunit of the voltage dependent calcium channel

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12 December 2020

QT dispersion: an indication of arrhythmia risk in patients with long QT intervals

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12 December 2020

Action potential prolongation and induction of abnormal automaticity by low quinidine concentrations in canine Purkinje fibers. Relationship to potassium and cycle length.

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12 December 2020

Inner ear defects induced by null mutation of the isk gene

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12 December 2020

Identifiers

DOI

10.1023/A:1009882524965

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Dimensions Publication ID

29 July 2017

1051200667

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