Endoplasmic reticulum retention of KCNQ2 potassium channel mutants following temperature elevation.

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Endoplasmic reticulum retention of KCNQ2 potassium channel mutants following temperature elevation.

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http://www.wikidata.org/entity/Q51074041

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

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Endoplasmic reticulum retentio ...... llowing temperature elevation.

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Endoplasmic reticulum retentio ...... llowing temperature elevation.

@nl

type

Item

label

Endoplasmic reticulum retentio ...... llowing temperature elevation.

@en

Endoplasmic reticulum retentio ...... llowing temperature elevation.

@nl

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Endoplasmic reticulum retentio ...... llowing temperature elevation.

@en

Endoplasmic reticulum retentio ...... llowing temperature elevation.

@nl

P1476

Endoplasmic reticulum retentio ...... llowing temperature elevation.

@en

P2093

Biwen Peng

http://www.w3.org/2001/XMLSchema#string

Fang Yu

http://www.w3.org/2001/XMLSchema#string

Jian Xu

http://www.w3.org/2001/XMLSchema#string

Xiaohua He

http://www.w3.org/2001/XMLSchema#string

Zheman Xiao

http://www.w3.org/2001/XMLSchema#string

P2860

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

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon

Radicals r'aging.

A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly.

Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domains

Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel

Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy

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

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

P304

S243-S253

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P31

scholarly article

P356

10.3233/BME-171647

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-01-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28372301

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P921

endoplasmic reticulum