Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing - sprookjes - yvandenbroek - TriplyDB

Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

http://www.wikidata.org/entity/Q28084651

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Insights into electrosensory organ development, physiology and evolution from a lateral line-enriched transcriptome The Contribution of L-Type Cav1.3 Channels to Retinal Light Responses.ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.LRIT1 Modulates Adaptive Changes in Synaptic Communication of Cone Photoreceptors.Allosteric regulators selectively prevent Ca-feedback of Ca and Na channels

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

http://www.wikidata.org/entity/Q28084651

description

2015 nî lūn-bûn

@nan

2015 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի մայիսին հրատարակված գիտական հոդված

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2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

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name

Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

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type

label

Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

@nl

prefLabel

Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

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Current molecular pharmacology

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Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing

@en

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Five members of a novel Ca(2+)-binding protein (CABP) subfamily with similarity to calmodulin

Ca2+-binding protein-1 facilitates and forms a postsynaptic complex with Cav1.2 (L-type) Ca2+ channels

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness

A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.

Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function.

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene

Molecular mechanism for divergent regulation of Cav1.2 Ca2+ channels by calmodulin and Ca2+-binding protein-1

Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy

Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

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143-148

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scholarly article

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10.2174/1874467208666150507104937

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2

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8

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Mei-Ling Joiner

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2015-05-06T00:00:00Z

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25966695

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4634632

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