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Kv1.1 Potassium Channel

Known as: Kv1.1 Potassium Channel [Chemical/Ingredient], Potassium Channel, Kv1.1, KCNA1 Potassium Channel 
A delayed rectifier subtype of shaker potassium channels that is commonly mutated in human episodic ATAXIA and MYOKYMIA.
National Institutes of Health

Papers overview

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2012
2012
Two voltage‐dependent potassium channels, Kv1.1 (KCNA1) and Kv1.2 (KCNA2), are found to co‐localize at the juxtaparanodal region… Expand
Highly Cited
2007
Highly Cited
2007
Purpose: Mice lacking the Kv1.1 potassium channel α subunit encoded by the Kcna1 gene develop recurrent behavioral seizures early… Expand
Highly Cited
2004
Highly Cited
2004
Nucleus magnocellularis (NM) is a division of the avian cochlear nucleus that extracts the timing of auditory signals. We… Expand
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2003
2003
Summary:  Purpose: To investigate further the membrane properties and postsynaptic potentials of the CA3 pyramidal cells in mice… Expand
2002
2002
Episodic ataxia type 1 (EA1) is an autosomal dominant neurological disorder affecting both central and peripheral nerve function… Expand
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2001
2001
OBJECTIVE It is a matter of dispute whether etomidate exhibits an epileptogenic action. It is also disputed whether frequently… Expand
Highly Cited
2000
Highly Cited
2000
Episodic ataxia type 1 (EA1) is an autosomal dominant central nervous system potassium channelopathy characterized by brief… Expand
Review
1999
Review
1999
Potassium channels play a critical role in limiting neuronal excitability. Mutations in certain voltage-gated potassium channels… Expand
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Highly Cited
1999
Highly Cited
1999
The regulation by protein kinase C (PKC) of recombinant voltage-gated potassium (K) channels in frog oocytes was studied. Phorbol… Expand
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Highly Cited
1998
Highly Cited
1998
Episodic ataxia (EA) is a rare inherited neurological disorder due to mutation in the voltage‐dependent Kv1.1 potassium channel… Expand