Action potential broadening in a presynaptic channelopathy. - Test2 - elhamkhani - TriplyDB

Action potential broadening in a presynaptic channelopathy.

Action potential broadening in a presynaptic channelopathy.

http://www.wikidata.org/entity/Q37072556

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Dynamic Control of Neurotransmitter Release by Presynaptic Potential Mutations underlying Episodic Ataxia type-1 antagonize Kv1.1 RNA editing A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia Kv1.1 channelopathy abolishes presynaptic spike width modulation by subthreshold somatic depolarization.Resistance to action potential depression of a rat axon terminal in vivo.Alteration of Neuronal Excitability and Short-Term Synaptic Plasticity in the Prefrontal Cortex of a Mouse Model of Mental Illness.Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior.Genetic perturbations suggest a role of the resting potential in regulating the expression of the ion channels of the KCNA and HCN families in octopus cells of the ventral cochlear nucleus.Purkinje Cell Signaling Deficits in Animal Models of Ataxia.Sodium Channel-Dependent and -Independent Mechanisms Underlying Axonal Afterdepolarization at Mouse Hippocampal Mossy Fibers

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Action potential broadening in a presynaptic channelopathy.

http://www.wikidata.org/entity/Q37072556

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article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 06 July 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Action potential broadening in a presynaptic channelopathy.

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Action potential broadening in a presynaptic channelopathy.

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type

label

Action potential broadening in a presynaptic channelopathy.

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Action potential broadening in a presynaptic channelopathy.

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prefLabel

Action potential broadening in a presynaptic channelopathy.

@en

Action potential broadening in a presynaptic channelopathy.

@nl

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Nature Communications

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Action potential broadening in a presynaptic channelopathy.

@en

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Rahima Begum

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

Yamina Bakiri

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P2860

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

Episodic ataxia type-1 mutations in the hKv1.1 cytoplasmic pore region alter the gating properties of the channel

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

Episodic ataxia type 1 mutations in the human Kv1.1 potassium channel alter hKvbeta 1-induced N-type inactivation

A mouse model of episodic ataxia type-1

Identification of two new KCNA1 mutations in episodic ataxia/myokymia families

Variable K(+) channel subunit dysfunction in inherited mutations of KCNA1

Heteromultimeric K+ channels in terminal and juxtaparanodal regions of neurons

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12102

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scholarly article

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10.1038/NCOMMS12102

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7

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Dimitri Kullmann

Kirill Volynski

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2016-07-06T00:00:00Z

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27381274

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4935806

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