(Q40127440)

17 September 2017

A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes (English)

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17 September 2017

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Saenen JB

1

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17 September 2017

Paulussen AD

2

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17 September 2017

Jongbloed RJ

3

1 reference

17 September 2017

Marcelis CL

4

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17 September 2017

Gilissen RA

5

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17 September 2017

Aerssens J

6

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17 September 2017

Snyders DJ

7

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17 September 2017

Raes AL

8

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17 September 2017

language of work or name

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4 May 2007

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Journal of Molecular and Cellular Cardiology

17 September 2017

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17 September 2017

43

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17 September 2017

1

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17 September 2017

63-72

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Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II

17 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management part III

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

The long QT syndromes: genetic basis and clinical implications

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

A structural basis for drug-induced long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Molecular basis of congenital and acquired long QT syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Drug-induced prolongation of the QT interval

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Low penetrance in the long-QT syndrome: clinical impact

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Susceptibility genes and modifiers for cardiac arrhythmias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Cardiac IKr channels minimally comprise hERG 1a and 1b subunits

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Fast inactivation causes rectification of the IKr channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Unique topographical distribution of M cells underlies reentrant mechanism of torsade de pointes in the long-QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Physicochemical features of the HERG channel drug binding site

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

hERG potassium channels and cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Torsade de pointes induced by cisapride/clarithromycin interaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Diagnostic criteria for the long QT syndrome. An update

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Differential effects of amino-terminal distal and proximal domains in the regulation of human erg K(+) channel gating.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Blockade of human cardiac potassium channel human ether-a-go-go-related gene (HERG) by macrolide antibiotics

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Long QT syndrome: diagnosis and management

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Modulation of HERG gating by a charge cluster in the N-terminal proximal domain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

A quantitative analysis of the activation and inactivation kinetics of HERG expressed in Xenopus oocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Defective protein trafficking in hERG-associated hereditary long QT syndrome (LQT2): molecular mechanisms and restoration of intracellular protein processing

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

A computational model of the human left-ventricular epicardial myocyte

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Long QT syndrome: reduced repolarization reserve and the genetic link

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

Low penetrance, subclinical congenital LQTS: concealed LQTS or silent LQTS?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2007.04.012

10.1016/J.YJMCC.2007.04.012

7 January 2021

Identifiers

DOI

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release_2ysgg3zjbfb7hots55nmwfqsza

17 September 2017

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Fatcat

https://api.fatcat.wiki/v0/release/2ysgg3zjbfb7hots55nmwfqsza

mapped directly with Wikidata item

24 November 2022

based on heuristic

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