(Q39990060)

16 September 2017

title

Altered KCNQ3 potassium channel function caused by the W309R pore-helix mutation found in human epilepsy (English)

1 reference

16 September 2017

Akira Uehara

1

1 reference

16 September 2017

Yuki Nakamura

2

1 reference

16 September 2017

Takao Shioya

3

1 reference

16 September 2017

Shinichi Hirose

4

1 reference

16 September 2017

Midori Yasukochi

5

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16 September 2017

Kiyoko Uehara

6

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16 September 2017

language of work or name

1 reference

1 March 2008

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16 September 2017

number of pages

9

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Journal of Membrane Biology

inferred from page(s)

published in

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16 September 2017

volume

222

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16 September 2017

issue

2

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16 September 2017

page(s)

55-63

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Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsions

16 September 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00232-008-9097-5

A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions

21 January 2018

1 reference

12 December 2020

Two types of K(+) channel subunit, Erg1 and KCNQ2/3, contribute to the M-like current in a mammalian neuronal cell

1 reference

12 December 2020

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy

1 reference

12 December 2020

The new voltage gated potassium channel KCNQ5 and neonatal convulsions

1 reference

12 December 2020

Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity

1 reference

12 December 2020

Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)

1 reference

12 December 2020

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

1 reference

12 December 2020

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum

1 reference

12 December 2020

Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy

1 reference

12 December 2020

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1 reference

12 December 2020

Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone

1 reference

12 December 2020

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

1 reference

12 December 2020

Molecular variants of KCNQ channels expressed in murine portal vein myocytes: a role in delayed rectifier current

1 reference

12 December 2020

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

12 December 2020

A structural requirement for processing the cardiac K+ channel KCNQ1.

1 reference

12 December 2020

KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents

1 reference

12 December 2020

A potassium channel mutation in neonatal human epilepsy

1 reference

12 December 2020

10.1007/S00232-008-9097-5

Identifiers

DOI

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16 September 2017

1 reference