(Q28280354)

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Characterization of three episodic ataxia mutations in the human Kv1.1 potassium channel

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Characterization of three episodic ataxia mutations in the human Kv1.1 potassium channel (English)

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P Zerr

1

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J P Adelman

series ordinal

2

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J Maylie

series ordinal

3

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language of work or name

English

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publication date

24 July 1998

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published in

FEBS Letters

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volume

431

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issue

3

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page(s)

461-4

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cites work

A dominantly inherited syndrome with continuous motor neuron discharges.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Familial paroxysmal kinesigenic ataxia and continuous myokymia.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

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

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Three novel KCNA1 mutations in episodic ataxia type I families

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Episodic ataxia type-1 mutations in the hKv1.1 cytoplasmic pore region alter the gating properties of the channel

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Episodic ataxia results from voltage-dependent potassium channels with altered functions

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Shaker potassium channel gating. II: Transitions in the activation pathway

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Two types of inactivation in Shaker K+ channels: effects of alterations in the carboxy-terminal region.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Mutation of conserved negatively charged residues in the S2 and S3 transmembrane segments of a mammalian K+ channel selectively modulates channel gating

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Contribution of the S4 segment to gating charge in the Shaker K+ channel.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Modulation of K+ current by frequency and external [K+]: a tale of two inactivation mechanisms.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

21 January 2018

Episodic ataxia mutations in Kv1.1 alter potassium channel function by dominant negative effects or haploinsufficiency

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stated in

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reference URL

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900814-X

retrieved

7 January 2021

Pore mutations in Shaker K+ channels distinguish between the sites of tetraethylammonium blockade and C-type inactivation

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Crossref

reference URL

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7 January 2021

Identifiers

DOI

10.1016/S0014-5793(98)00814-X

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PubMed publication ID

9714564

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ResearchGate publication ID

13569962

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(Q28280354)

Characterization of three episodic ataxia mutations in the human Kv1.1 potassium channel

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