KCNE2 gene

Known as: KCNE2, MIRP1, POTASSIUM CHANNEL, VOLTAGE-GATED, ISK-RELATED SUBFAMILY, MEMBER 2 
 
National Institutes of Health

Papers overview

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2008
2008
The KCNE2 gene encodes a single transmembrane domain protein that modulates a variety of K+ channel functions in various tissues… (More)
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2008
2008
Mutations in human KCNE2, which encodes the MiRP1 potassium channel ancillary subunit, associate with long QT syndrome (LQTS), a… (More)
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Highly Cited
2006
Highly Cited
2006
Genes in the KCNE family encode single transmembrane domain ancillary subunits that co-assemble with voltage-gated potassium (Kv… (More)
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Highly Cited
2004
Highly Cited
2004
Atrial fibrillation (AF) is the most common cardiac arrhythmia encountered in clinical practice. We first reported an S140G… (More)
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2003
2003
The HCN4 gene encodes a hyperpolarization-activated cation current contributing to the slow components of the pacemaking currents… (More)
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2001
2001
The cardiac delayed rectifier potassium current mediates repolarization of the action potential and underlies the QT interval of… (More)
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2001
2001
Mutations in the cyclic nucleotide binding domain (CNBD) of the human ether-a-go-go-related gene (HERG) K+ channel are associated… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND & AIMS Gastric H+ secretion via the H+/K+-adenosine triphosphatase is coupled to the uptake of K+. However, the… (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 HERG and KCNQ1 (or KVLQT1) genes cause the life-threatening Long QT syndrome. These genes encode K(+) channel pore… (More)
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