(Q28595000)

1 February 2017

title

Inducible polymorphic ventricular tachyarrhythmias in a transgenic mouse model with a long Q-T phenotype (English)

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Potassium voltage-gated channel, subfamily H (eag-related), member 2

1 February 2017

0 references

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GOA release 2020-03-11

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A. Jeron

1

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1 February 2017

G. F. Mitchell

2

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1 February 2017

J. Zhou

3

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1 February 2017

M. Murata

4

1 reference

1 February 2017

B. London

5

1 reference

1 February 2017

P. Buckett

6

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1 February 2017

S. D. Wiviott

7

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1 February 2017

G. Koren

8

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1 February 2017

publication date

1 June 2000

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American Journal of Physiology Heart and Circulatory Physiology

1 February 2017

published in

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1 February 2017

volume

278

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1 February 2017

issue

6

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1 February 2017

page(s)

H1891–1898

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Inhibition of cardiac delayed rectifier K+ current by overexpression of the long-QT syndrome HERG G628S mutation in transgenic mice.

1 February 2017

cites work

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

Assembly of mammalian voltage-gated potassium channels: evidence for an important role of the first transmembrane segment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

Functional knockout of the transient outward current, long-QT syndrome, and cardiac remodeling in mice expressing a dominant-negative Kv4 alpha subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

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.2000.278.6.H1891

A cellular model for long QT syndrome. Trapping of heteromultimeric complexes consisting of truncated Kv1.1 potassium channel polypeptides and native Kv1.4 and Kv1.5 channels in the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

Replacement by homologous recombination of the minK gene with lacZ reveals restriction of minK expression to the mouse cardiac conduction system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

Long QT and ventricular arrhythmias in transgenic mice expressing the N terminus and first transmembrane segment of a voltage-gated potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

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.2000.278.6.H1891

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

Electrical turbulence in three-dimensional heart muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.2000.278.6.H1891

10.1152/AJPHEART.2000.278.6.H1891

21 January 2018

Identifiers

DOI

0 references

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