KCNQ2 gene

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

Papers overview

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2014
2014
KCNQ potassium channels composed of KCNQ2 and KCNQ3 subunits give rise to the M-current, a slow-activating and non-inactivating… (More)
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2008
2008
M-type K(+) channels, consisting of KCNQ1-5 (Kv7.1-7.5) subunits, form a variety of homomeric and heteromeric channels. Whereas… (More)
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2004
2004
M utations in the voltage gated potassium channels KCNQ2 (OMIM 602235) and KCNQ3 (OMIM 602232) are associated with an autosomal… (More)
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2004
2004
The non-inactivating potassium M-current exerts a strong influence on neuronal excitability. The channels responsible for this… (More)
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Highly Cited
2003
Highly Cited
2003
KCNQ2 and KCNQ3 potassium-channel subunits can form both homomeric and heteromeric channels; the latter are thought to constitute… (More)
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Highly Cited
2002
Highly Cited
2002
M-type K(+) currents (I(K(M))) play a key role in regulating neuronal excitability. In sympathetic neurons, M-channels are… (More)
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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… (More)
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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… (More)
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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… (More)
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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… (More)
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