FAQ

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

Topic mentions per year

Topic mentions per year

1994-2006
01219942006

Related topics

Related topics

9 relations
In BloodKCNA1 geneProcess of secretionagonists
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Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Kv1.1 Potassium Channel
physiological aspects
In Blood
chemical synthesis
standards characteristics
Process of secretion

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Ion channels and epilepsy
Ion channels play a central role in the generation and control of neuronal excitability. Genetic defects in ion channels are… (More)
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2006
2006
Epilepsy and other neurological disorders Ion channels and epilepsy
Ion channels play a central role in the generation and control of neuronal excitability. Genetic defects in ion channels are… (More)
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2001
2001
[Epileptic seizures from etomidate? The human Kv1.1 potassium channel in humans].
OBJECTIVE It is a matter of dispute whether etomidate exhibits an epileptogenic action. It is also disputed whether frequently… (More)
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2000
2000
Identification of a novel missense mutation L329I in the episodic ataxia type 1 gene KCNA1--a challenging problem.
 
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Review
1999
Review
1999
Developmental seizure susceptibility of kv1.1 potassium channel knockout mice.
Potassium channels play a critical role in limiting neuronal excitability. Mutations in certain voltage-gated potassium channels… (More)
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1994
1994
A gene for episodic ataxia/myokymia maps to chromosome 12p13.
Episodic ataxia (EA) is a rare, familial disorder producing attacks of generalized ataxia, with normal or near-normal… (More)
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