A mouse model of episodic ataxia type-1 (Q28213245)

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Michael Virk

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Nathan R Rustay

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Chris T Bond

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John P Adelman

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James Maylie

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

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language of work or name

English

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publication date

April 2003

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published in

Nature Neuroscience

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volume

6

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issue

4

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page(s)

378-83

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cites work

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Familial paroxysmal kinesigenic ataxia and continuous myokymia

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

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

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Heteromultimeric K+ channels in terminal and juxtaparanodal regions of neurons

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Deletion of the K(V)1.1 potassium channel causes epilepsy in mice

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Influence of task parameters on rotarod performance and sensitivity to ethanol in mice

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Differential expression of K+ channel mRNAs in the rat brain and down-regulation in the hippocampus following seizures

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Spatial heterogeneity of intracellular Ca2+ signals in axons of basket cells from rat cerebellar slices

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Modulation by K+ channels of action potential-evoked intracellular Ca2+ concentration rises in rat cerebellar basket cell axons

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Beta-adrenergic enhancement of inhibitory synaptic activity in rat cerebellar stellate and Purkinje cells

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Pharmacological evidence for two kinds of GABA receptor on rat hippocampal pyramidal cells studied in vitro

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Giant synaptic potentials in immature rat CA3 hippocampal neurones.

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Excitatory synaptic responses mediated by GABAA receptors in the hippocampus

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Diverse sources of hippocampal unitary inhibitory postsynaptic potentials and the number of synaptic release sites

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Upregulation of the hyperpolarization-activated cation current in rat thalamic relay neurones by acetazolamide

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A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells

21 January 2018

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Inhibitory synaptic currents in rat cerebellar Purkinje cells: modulation by postsynaptic depolarization

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Autosomal dominant episodic ataxia: a heterogeneous syndrome

21 January 2018

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7 January 2021

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

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7 January 2021

Episodic ataxia mutations in Kv1.1 alter potassium channel function by dominant negative effects or haploinsufficiency

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7 January 2021

Expression of Kv1.1, a Shaker-like potassium channel, is temporally regulated in embryonic neurons and glia.

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7 January 2021

Localization of Kv1.1 and Kv1.2, two K channel proteins, to synaptic terminals, somata, and dendrites in the mouse brain

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7 January 2021

Computer model for action potential propagation through branch point in myelinated nerves.

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7 January 2021

Ionic mechanisms of neuronal excitation by inhibitory GABAA receptors

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7 January 2021

Identifiers

DOI

10.1038/NN1025

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12612586

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Consolidated OpenCitations Corpus – April 2017