KCNQ4 gene

Known as: POTASSIUM CHANNEL, VOLTAGE-GATED, KQT-LIKE SUBFAMILY, MEMBER 4, potassium voltage-gated channel subfamily Q member 4, POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY Q, MEMBER 4 
 
National Institutes of Health

Papers overview

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Review
2009
Review
2009
Hearing impairment is the most common sensory disorder, present in 1 of every 500 newborns. With 46 genes implicated in… (More)
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Highly Cited
2006
Highly Cited
2006
KCNQ4 is an M-type K+ channel expressed in sensory hair cells of the inner ear and in the central auditory pathway. KCNQ4… (More)
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2006
2006
Age-related hearing impairment (ARHI) is the most common sensory impairment among the elderly. It is a complex disorder… (More)
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Highly Cited
2005
Highly Cited
2005
Calmodulin modulation of ion channels has emerged as a prominent theme in biology. The sensitivity of KCNQ1-5 K+ channels to… (More)
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2005
2005
Human KCNQ4 mutations known as DFNA2 cause non-syndromic, autosomal-dominant, progressive high-frequency hearing loss in which… (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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2001
2001
Activation of potassium channels generally reduces cellular excitability, making potassium channel openers potential drug… (More)
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Highly Cited
2001
Highly Cited
2001
Human cloned KCNQ4 channels were stably expressed in HEK-293 cells and characterized with respect to function and pharmacology… (More)
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Highly Cited
2000
Highly Cited
2000
Mutations in the potassium channel gene KCNQ4 underlie DFNA2, an autosomal dominant form of progressive hearing loss in humans… (More)
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Highly Cited
1999
Highly Cited
1999
Potassium channels regulate electrical signaling and the ionic composition of biological fluids. Mutations in the three known… (More)
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