(Q24312199)

chemical synaptic transmission

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

potassium

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author name string

D L Browne

1

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S T Gancher

2

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J G Nutt

3

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E R Brunt

4

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E A Smith

5

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P Kramer

6

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M Litt

https://scigraph.springernature.com/pub.10.1038/ng1094-136

7

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language of work or name

English

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publication date

October 1994

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published in

Nature Genetics

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volume

8

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page(s)

136-40

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issue

2

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exact match

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cites work

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

20 April 2017

1 reference

Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel

20 April 2017

1 reference

Inactivation properties of voltage-gated K+ channels altered by presence of beta-subunit

20 April 2017

1 reference

Familial intermittent ataxia with possible X-linked recessive inheritance. Two patients with abnormal pyruvate metabolism and a response to acetazolamide

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Familial paroxysmal kinesigenic ataxia and continuous myokymia.

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Autosomal dominant episodic ataxia: a heterogeneous syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Contractures, continuous muscle discharges, and titubation

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Hereditary myokymia and periodic ataxia

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

A family of three mouse potassium channel genes with intronless coding regions

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Human potassium channel genes: Molecular cloning and functional expression

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Members of the RCK potassium channel family are differentially expressed in the rat nervous system.

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Antibodies specific for distinct Kv subunits unveil a heterooligomeric basis for subtypes of alpha-dendrotoxin-sensitive K+ channels in bovine brain.

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Scanning detection of mutations in human ornithine transcarbamoylase by chemical mismatch cleavage

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021

Molecular biology of voltage-dependent potassium channels

1 reference

https://api.crossref.org/works/10.1038%2FNG1094-136

7 January 2021