(Q24312207)

potassium ion transmembrane transporter activity

GOA release 2020-03-11

1 reference

A dominantly inherited syndrome with continuous motor neuron discharges.

GOA release 2020-03-11

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1 reference

M Pessia

3

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author name string

J P Adelman

series ordinal

1

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C T Bond

series ordinal

2

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J Maylie

series ordinal

4

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language of work or name

English

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publication date

December 1995

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published in

Neuron

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volume

15

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page(s)

1449-54

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issue

6

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cites work

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Autosomal dominant episodic ataxia: a heterogeneous syndrome

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Calcium-activated potassium channels expressed from cloned complementary DNAs

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

The S4-S5 loop contributes to the ion-selective pore of potassium channels

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Deletion analysis of K+ channel assembly.

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

The internal quaternary ammonium receptor site of Shaker potassium channels

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Truncated K+ channel DNA sequences specifically suppress lymphocyte K+ channel gene expression

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Familial periodic ataxia responsive to acetazolamide.

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Putative receptor for the cytoplasmic inactivation gate in the Shaker K+ channel

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Evidence that the S6 segment of the Shaker voltage-gated K+ channel comprises part of the pore

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Familial paroxysmal kinesigenic ataxia and continuous myokymia.

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Identification of two new KCNA1 mutations in episodic ataxia/myokymia families

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

The syndrome of continuous muscle fiber activity. Evidence to suggest proximal neurogenic causation

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021

Acetazolamide-responsive episodic ataxia syndrome

1 reference

https://api.crossref.org/works/10.1016%2F0896-6273%2895%2990022-5

7 January 2021