KCNQ1 gene

Known as: Jervell and Lange-Nielsen syndrome 1, LQT1, Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 1 Gene 
This gene is involved in both potassium transport and cardiac repolarization.
National Institutes of Health

Papers overview

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Highly Cited
2008
Highly Cited
2008
We conducted a genome-wide association study using 207,097 SNP markers in Japanese individuals with type 2 diabetes and unrelated… (More)
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Highly Cited
2008
Highly Cited
2008
We carried out a multistage genome-wide association study of type 2 diabetes mellitus in Japanese individuals, with a total of 1… (More)
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Highly Cited
2008
Highly Cited
2008
AbstractAccording to recent genome-wide association studies, a number of single nucleotide polymorphisms (SNPs) are reported to… (More)
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Highly Cited
2008
Highly Cited
2008
KCNE1 is a single-span membrane protein that modulates the voltage-gated potassium channel KCNQ1 (K V7.1) by slowing activation… (More)
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Highly Cited
2007
Highly Cited
2007
BACKGROUND Type-1 long-QT syndrome (LQTS) is caused by loss-of-function mutations in the KCNQ1-encoded I(Ks) cardiac potassium… (More)
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Highly Cited
2005
Highly Cited
2005
OBJECTIVE We describe a genetic basis for atrial fibrillation and short QT syndrome in utero. Heterologous expression of the… (More)
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Highly Cited
2005
Highly Cited
2005
The QT interval (QT) reflects cardiac ventricular repolarization and varies according to various known factors such as heart rate… (More)
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Highly Cited
2003
Highly Cited
2003
Administration of specific drugs may occasionally induce acquired long QT syndrome (aLQTS), a disorder that predisposes to… (More)
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Highly Cited
2002
Highly Cited
2002
KCNE4 is a membrane protein belonging to a family of single transmembrane domain proteins known to have dramatic effect on the… (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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