The connexin46 mutant, Cx46T19M, causes loss of gap junction function and alters hemi-channel gating - Wikidata - awgldk - TriplyDB

The connexin46 mutant, Cx46T19M, causes loss of gap junction function and alters hemi-channel gating

The connexin46 mutant, Cx46T19M, causes loss of gap junction function and alters hemi-channel gating

http://www.wikidata.org/entity/Q34990414

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Focus on lens connexins.Identification of a novel GJA3 mutation in a large Chinese family with congenital cataract using targeted exome sequencing.Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families.

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P2860

The connexin46 mutant, Cx46T19M, causes loss of gap junction function and alters hemi-channel gating

http://www.wikidata.org/entity/Q34990414

description

2014 nî lūn-bûn

@nan

2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@ast

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@en

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@nl

type

label

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@ast

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@en

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@nl

prefLabel

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@ast

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@en

The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@nl

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Journal of Membrane Biology

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The connexin46 mutant, Cx46T19 ...... and alters hemi-channel gating

@en

P2093

Jun-Jie Tong

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

Lisa Ebihara

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

Matthew Kobeszko

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Peter J Minogue

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

Viviana M Berthoud

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

P2860

Disruption of alpha3 connexin gene leads to proteolysis and cataractogenesis in mice

A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract

Structure of the connexin 26 gap junction channel at 3.5 A resolution

Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations

Disruption of Gja8 (alpha8 connexin) in mice leads to microphthalmia associated with retardation of lens growth and lens fiber maturation

Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture.

Xenopus connexin38 forms hemi-gap-junctional channels in the nonjunctional plasma membrane of Xenopus oocytes.

Biophysical properties of gap junction channels formed by mouse connexin40 in induced pairs of transfected human HeLa cells

The first extracellular loop domain is a major determinant of charge selectivity in connexin46 channels.

Exchange of gating properties between rat cx46 and chicken cx45.6.

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s00232-014-9752-y

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145-155

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