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KCNQ5 gene

Known as: KCNQ5, Kv7.5, POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY Q, MEMBER 5 
 
National Institutes of Health

Papers overview

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2017
2017
KCNQ5 is a highly conserved gene encoding an important channel for neuronal function; it is widely expressed in the brain and… Expand
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2011
2011
Little is known about which ion channels determine the resting electrical properties of presynaptic membranes. In recordings made… Expand
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2010
2010
Mutations in KCNQ2 and KCNQ3 voltage-gated potassium channels lead to neonatal epilepsy as a consequence of their key role in… Expand
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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… Expand
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2007
2007
KCNQ, also called Kv7, is a family of voltage-dependent potassium channels with important roles in excitability regulation. Of… Expand
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2005
2005
The KCNQ proteins compose a sub-group of the voltage-activated potassium channel family. The family consists of five members… Expand
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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… Expand
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2002
2002
The novel anti-ischemic compound, BMS-204352 ((3S)-(+)-(5-chloro-2-methoxyphenyl)-1,3-dihydro-3-fluoro-6-(trifluoromethyl)-2H… Expand
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Highly Cited
2000
Highly Cited
2000
KCNQ2 and KCNQ3, both of which are mutated in a type of human neonatal epilepsy, form heteromeric potassium channels that are… Expand
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Highly Cited
2000
Highly Cited
2000
We have isolated KCNQ5, a novel human member of the KCNQ potassium channel gene family that is differentially expressed in… Expand
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