(Q44771531)

6 December 2017

Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels (English)

1 reference

6 December 2017

5

1 reference

6 December 2017

2

Michael J Ackerman

1 reference

6 December 2017

Blake D Anson

1

1 reference

6 December 2017

David J Tester

3

1 reference

6 December 2017

Melissa L Will

4

1 reference

6 December 2017

Corey L Anderson

6

1 reference

6 December 2017

Craig T January

7

1 reference

6 December 2017

language of work or name

1 reference

19 February 2004

1 reference

American Journal of Physiology Heart and Circulatory Physiology

6 December 2017

1 reference

6 December 2017

286

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6 December 2017

6

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6 December 2017

H2434-41

1 reference

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

6 December 2017

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

A structural basis for drug-induced long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Functional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH2 (HERG).

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Interaction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à-go-go-Related Gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

The antihistamine fexofenadine does not affect I(Kr) currents in a case report of drug-induced cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

The inward rectification mechanism of the HERG cardiac potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Regulation of deactivation by an amino terminal domain in human ether-à-go-go-related gene potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

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/10.1152%2FAJPHEART.00891.2003

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00891.2003

10.1152/AJPHEART.00891.2003

21 January 2018

Identifiers

DOI

1 reference

6 December 2017

1 reference