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KCNE3 gene

Known as: POTASSIUM CHANNEL, VOLTAGE-GATED, ISK-RELATED SUBFAMILY, MEMBER 3, MINK-RELATED PEPTIDE 2, MiRP2 
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
The KCNE3 β-subunit constitutively opens outwardly rectifying KCNQ1 (Kv7.1) K+ channels by abolishing their voltage-dependent… Expand
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Highly Cited
2008
Highly Cited
2008
Background— The Brugada syndrome, an inherited syndrome associated with a high incidence of sudden cardiac arrest, has been… Expand
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Highly Cited
2007
Highly Cited
2007
KCNQ1 is a voltage-dependent K+ channel whose gating properties are dramatically altered by association with auxiliary KCNE… 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
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
Highly Cited
2001
Highly Cited
2001
KvLQT1 is a Shaker-like voltage-gated potassium channel that when complexed with minK (KCNE1) produces the slowly activating… Expand
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
Mutations in all four known KCNQ potassium channel α-subunit genes lead to human diseases. KCNQ1 (KvLQT1) interacts with the… 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