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KCNQ2 gene

Known as: HNSPC, POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY Q, MEMBER 2, KCNA11 
 
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Neonatal-onset epilepsies are rare conditions, mostly genetically determined, that can have a benign or severe phenotype.1,2… Expand
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Highly Cited
2010
Highly Cited
2010
In this work, 64 samples of cereals purchased from local markets in the Valencian community (Spain) were investigated for the… Expand
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Highly Cited
2003
Highly Cited
2003
The KCNQ family of voltage-dependent non-inactivating K+ channels is composed of five members, four of which (KCNQ2-5) are… Expand
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Highly Cited
2002
Highly Cited
2002
M‐type K+ currents (IK(M)) play a key role in regulating neuronal excitability. In sympathetic neurons, M‐channels are thought to… Expand
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Highly Cited
2000
Highly Cited
2000
Channels from KCNQ2 and KCNQ3 genes have been suggested to underlie the neuronal M-type K+ current. The M current is modulated by… Expand
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Highly Cited
2000
Highly Cited
2000
Abstract : Benign familial neonatal convulsion (BFNC) is a common idiopathic epilepsy with autosomal dominant inheritance… Expand
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Highly Cited
2000
Highly Cited
2000
Retigabine is a novel anticonvulsant with an unknown mechanism of action. It has recently been reported that retigabine modulates… Expand
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Highly Cited
2000
Highly Cited
2000
KCNQ1‐4 potassium channels were expressed in mammalian Chinese hamster ovary (CHO) cells stably transfected with M1 muscarinic… Expand
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Highly Cited
2000
Highly Cited
2000
Mutations in either KCNQ2 or KCNQ3 underlie benign familial neonatal convulsions (BFNC), an inherited epilepsy. The corresponding… Expand
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Highly Cited
1998
Highly Cited
1998
Epileptic disorders affect about 20-40 million people worldwide, and 40% of these are idiopathic generalized epilepsies (IGEs… Expand
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