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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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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… Expand
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Highly Cited
2006
Highly Cited
2006
OBJECTIVES The function of Kv4.3 (KCND3) channels, which underlie the transient outward current I(to) in human heart, can be… Expand
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Highly Cited
2005
Highly Cited
2005
OBJECTIVE The voltage-gated K+ channel KCNQ1 associates with the small KCNE1 beta subunit to underlie the IKs repolarizing… Expand
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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… Expand
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Highly Cited
2004
Highly Cited
2004
MinK-related protein (MiRP1 or KCNE2) interacts with the hyperpolarization-activated, cyclic nucleotidegated (HCN) family of… Expand
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Highly Cited
2002
Highly Cited
2002
Although it has been suggested that coexpression of minK related peptide (MiRP1) is required for reconstitution of native rapid… Expand
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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… Expand
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Highly Cited
2001
Highly Cited
2001
Abstract. The KCNQ1 potassium channel α-subunit can associate with various KCNE β-subunits that drastically influence channel… Expand
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Highly Cited
2000
Highly Cited
2000
BackgroundLong-QT Syndrome (LQTS) is a cardiovascular disorder characterized by prolongation of the QT interval on ECG and… Expand
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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… Expand
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