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Channelopathies: ion channel defects linked to heritable clinical disorders.

Channelopathies: ion channel defects linked to heritable clinical disorders.

http://www.wikidata.org/entity/Q34051594

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Identification of functional voltage-gated Na(+) channels in cultured human pulmonary artery smooth muscle cells High throughput screening technologies for ion channels Genetic neurological channelopathies: molecular genetics and clinical phenotypes.KCNE1 induces fenestration in the Kv7.1/KCNE1 channel complex that allows for highly specific pharmacological targeting Functional ion channels in human pulmonary artery smooth muscle cells: Voltage-dependent cation channels.Mapping convulsants' binding to the GABA-A receptor chloride ionophore: a proposed model for channel binding sites.Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2 Long-term regulation of voltage-gated Ca(2+) channels by gabapentin.

P2860

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P2860

Channelopathies: ion channel defects linked to heritable clinical disorders.

http://www.wikidata.org/entity/Q34051594

description

2000 nî lūn-bûn

@nan

2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2000年の論文

@ja

2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

@wuu

name

Channelopathies: ion channel defects linked to heritable clinical disorders.

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Channelopathies: ion channel defects linked to heritable clinical disorders.

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Channelopathies: ion channel defects linked to heritable clinical disorders.

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type

label

Channelopathies: ion channel defects linked to heritable clinical disorders.

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Channelopathies: ion channel defects linked to heritable clinical disorders.

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Channelopathies: ion channel defects linked to heritable clinical disorders.

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prefLabel

Channelopathies: ion channel defects linked to heritable clinical disorders.

@ast

Channelopathies: ion channel defects linked to heritable clinical disorders.

@en

Channelopathies: ion channel defects linked to heritable clinical disorders.

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Journal of Medical Genetics

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Channelopathies: ion channel defects linked to heritable clinical disorders.

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P2860

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

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

Identification and cloning of putative human neuronal voltage-gated calcium channel gamma-2 and gamma-3 subunits: neurologic implications

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

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

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

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

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

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

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729-740

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scholarly article

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10.1136/JMG.37.10.729

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10

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37

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12309169

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11015449

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1757150

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