(Q34175373)

31 July 2017

1 reference

title

Molecular and cellular mechanisms of cardiac arrhythmias (English)

1 reference

31 July 2017

Keating MT

1

1 reference

PubMed ID

11239413

31 July 2017

Sanguinetti MC

series ordinal

2

1 reference

PubMed ID

11239413

31 July 2017

language of work or name

English

0 references

publication date

1 February 2001

1 reference

31 July 2017

1 reference

31 July 2017

104

1 reference

31 July 2017

569-580

1 reference

31 July 2017

4

1 reference

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

31 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Molecular mechanism for an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Blocker protection in the pore of a voltage-gated K+ channel and its structural implications

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Molecular determinants of dofetilide block of HERG K+ channels.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Homozygous premature truncation of the HERG protein : the human HERG knockout.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Sudden death risk in overt coronary heart disease: the Framingham Study

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

The human delta1261 mutation of the HERG potassium channel results in a truncated protein that contains a subunit interaction domain and decreases the channel expression

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

A new form of long QT syndrome associated with syndactyly

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Ventricular fibrillation without apparent heart disease: description of six cases

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

A minK-HERG complex regulates the cardiac potassium current I(Kr)

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

A structural basis for drug-induced long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Trapping of a methanesulfonanilide by closure of the HERG potassium channel activation gate.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Update on MADIT: the Multicenter Automatic Defibrillator Implantation Trial. The long QT interval syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Mechanisms and management of proarrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Diagnostic criteria for the long QT syndrome. An update

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

The inward rectification mechanism of the HERG cardiac potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Fast inactivation causes rectification of the IKr channel

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Molecular basis of the long-QT syndrome associated with deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

MinK potassium channels are heteromultimeric complexes.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Cloning of a membrane protein that induces a slow voltage-gated potassium current

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

HERG, a human inward rectifier in the voltage-gated potassium channel family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Subunit composition of minK potassium channels.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Functional effects of mutations in KvLQT1 that cause long QT syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

A family of potassium channel genes related to eag in Drosophila and mammals

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Circadian variation in the incidence of sudden cardiac death in the Framingham Heart Study population

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900243-4

7 January 2021

10.1016/S0092-8674(01)00243-4

Identifiers

DOI

1 reference

31 July 2017

1 reference

PubMed ID

11239413