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Potassium Voltage-Gated Channel Subfamily KQT Member 1

Known as: KvLQT1, Voltage-Gated Potassium Channel Subunit Kv7.1, IKs Producing Slow Voltage-Gated Potassium Channel Subunit Alpha KvLQT1 
Potassium voltage-gated channel subfamily KQT member 1 (676 aa, ~75 kDa) is encoded by the human KCNQ1 gene. This protein is involved in cardiac… 
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
Long QT syndrome (LQTS) is a heritable disease associated with ECG QT interval prolongation, ventricular tachycardia, and sudden… 
Highly Cited
2000
Highly Cited
2000
BackgroundLong-QT Syndrome (LQTS) is a cardiovascular disorder characterized by prolongation of the QT interval on ECG and… 
Highly Cited
2000
Highly Cited
2000
Ion Channel Mutations and Drug‐Induced TdP. The aim of this study was to test the hypothesis that some cases of drug‐induced… 
Highly Cited
2000
Highly Cited
2000
The KvLQT1 gene encodes a voltage-gated potassium channel. Mutations in KvLQT1 underlie the dominantly transmitted Ward-Romano… 
Highly Cited
2000
Highly Cited
2000
KvLQT1 is a voltage-gated potassium channel expressed in cardiac cells that is critical for myocardial repolarization. When… 
Highly Cited
1998
Highly Cited
1998
1 The time course and voltage dependence of inactivation of KvLQT1 channels expressed in Xenopus oocytes were studied using two… 
Highly Cited
1998
Highly Cited
1997
Highly Cited
1997
The Jervell and Lange-Nielsen (JLN) syndrome (MIM 220400) is an inherited autosomal recessive disease characterized by a… 
Highly Cited
1997
Highly Cited
1997
The clinical features of long QT syndrome result from episodic life-threatening cardiac arrhythmias, specifically the polymorphic… 
Highly Cited
1996
Highly Cited
1996
The slowly activating delayed-rectifier K+ current, I(Ks), modulates the repolarization of cardiac action potentials. The…