KCNH2 gene

Known as: POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY H, MEMBER 2, Kv11.1, ETHER-A-GO-GO-RELATED GENE, HUMAN 
 

Topic mentions per year

Topic mentions per year

1995-2017
020406019952017

Papers overview

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Highly Cited
2007
Highly Cited
2007
BACKGROUND The hypothesis that some cases of sudden infant death syndrome (SIDS) could be caused by long-QT syndrome (LQTS) has… (More)
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Highly Cited
2000
Highly Cited
2000
BACKGROUND Long-QT Syndrome (LQTS) is a cardiovascular disorder characterized by prolongation of the QT interval on ECG and… (More)
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Highly Cited
2000
Highly Cited
2000
Mutations in the HERG K(+) channel gene cause inherited long QT syndrome (LQT), a disorder of cardiac repolarization that… (More)
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Highly Cited
1999
Highly Cited
1999
A novel potassium channel gene has been cloned, characterized, and associated with cardiac arrhythmia. The gene encodes MinK… (More)
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Highly Cited
1998
Highly Cited
1998
We have established stably transfected HEK 293 cell lines expressing high levels of functional human ether-a go-go-related gene… (More)
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Highly Cited
1997
Highly Cited
1997
MinK is a widely expressed protein of relative molecular mass approximately 15K that forms potassium channels by aggregation with… (More)
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Highly Cited
1996
Highly Cited
1996
The mechanism of rectification of HERG, the human cardiac delayed rectifier K+ channel, was studied after heterologous expression… (More)
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Highly Cited
1995
Highly Cited
1995
To identify genes involved in cardiac arrhythmia, we investigated patients with long QT syndrome (LQT), an inherited disorder… (More)
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Highly Cited
1995
Highly Cited
1995
Mutations in HERG cause an inherited cardiac arrhythmia, long QT syndrome (LQT). To define the function of HERG, we expressed the… (More)
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Highly Cited
1995
Highly Cited
1995
In contrast to other members of the Eag family of voltage-gated, outwardly rectifying potassium channels, the human eag-related… (More)
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