Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels (Q44771531)

6 December 2017

title

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

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6 December 2017

5

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6 December 2017

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Michael J Ackerman

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6 December 2017

Blake D Anson

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6 December 2017

David J Tester

3

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6 December 2017

Melissa L Will

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Corey L Anderson

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6 December 2017

Craig T January

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6 December 2017

language of work or name

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19 February 2004

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American Journal of Physiology Heart and Circulatory Physiology

6 December 2017

published in

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6 December 2017

volume

286

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6 December 2017

issue

6

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6 December 2017

page(s)

H2434-41

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Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome

6 December 2017

cites work

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

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

21 January 2018

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

21 January 2018

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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

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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

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A structural basis for drug-induced long QT syndrome

21 January 2018

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

21 January 2018

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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

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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

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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

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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

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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

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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

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

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

21 January 2018

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The inward rectification mechanism of the HERG cardiac potassium channel

21 January 2018

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

21 January 2018

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Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia

21 January 2018

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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

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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

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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

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

21 January 2018

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Properties of HERG Channels Stably Expressed in HEK 293 Cells Studied at Physiological Temperature

21 January 2018

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10.1152/AJPHEART.00891.2003

21 January 2018

Identifiers

DOI

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6 December 2017

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