Deletion of the K(V)1.1 potassium channel causes epilepsy in mice (Q48472743)

11 February 2018

title

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

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11 February 2018

author name string

Smart SL

1

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11 February 2018

Lopantsev V

2

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11 February 2018

Zhang CL

3

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11 February 2018

Robbins CA

4

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11 February 2018

Wang H

5

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11 February 2018

Chiu SY

6

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11 February 2018

Schwartzkroin PA

7

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11 February 2018

Messing A

8

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11 February 2018

Tempel BL

9

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11 February 2018

language of work or name

English

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publication date

1 April 1998

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11 February 2018

published in

Neuron

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11 February 2018

volume

20

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11 February 2018

issue

4

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11 February 2018

page(s)

809-819

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11 February 2018

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

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

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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

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Evidence for the presence of potassium channels in the paranodal region of acutely demyelinated mammalian single nerve fibres

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Action-potential propagation gated by an axonal I(A)-like K+ conductance in hippocampus

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The role of extracellular potassium in hippocampal epilepsy

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Absence epilepsy in tottering mutant mice is associated with calcium channel defects

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Physiologic and morphologic characteristics of granule cell circuitry in human epileptic hippocampus

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Introduction of a subtle mutation into the Hox-2.6 locus in embryonic stem cells

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Pleiotropic effects of a disrupted K+ channel gene: reduced body weight, impaired motor skill and muscle contraction, but no seizures

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Evidence for the formation of heteromultimeric potassium channels in Xenopus oocytes

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Epileptogenic effect of hypoxia in the immature rodent brain

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Quantal components of unitary EPSCs at the mossy fibre synapse on CA3 pyramidal cells of rat hippocampus

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7 January 2021

Multiple products of the Drosophila Shaker gene may contribute to potassium channel diversity

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Clustering of Shaker-type K+ channels by interaction with a family of membrane-associated guanylate kinases

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Maturation of mammalian myelinated fibers: changes in action-potential characteristics following 4-aminopyridine application

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7 January 2021

Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome

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7 January 2021

Kainic acid induced limbic seizures: metabolic, behavioral, electroencephalographic and neuropathological correlates

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Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor.

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Differential distribution of closely related potassium channels in rat Schwann cells

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Single neurones can initiate synchronized population discharge in the hippocampus

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7 January 2021

Extracellular potassium activity during epileptogenesis

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Targeting epilepsy genes

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Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene from Drosophila

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7 January 2021

Gene targeting in embryonic stem cells

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7 January 2021

Inactivation properties of voltage-gated K+ channels altered by presence of beta-subunit

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7 January 2021

Association and colocalization of K+ channel alpha- and beta-subunit polypeptides in rat brain

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7 January 2021

Heteromultimeric channels formed by rat brain potassium-channel proteins

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7 January 2021

Epileptiform activity in the hippocampus produced by tetraethylammonium

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7 January 2021

Genetic modification of potassium channels in Drosophila Shaker mutants

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7 January 2021

Conditions required for polysynaptic excitation of dentate granule cells by area CA3 pyramidal cells in rat hippocampal slices

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7 January 2021

Cellular electrophysiology of human epilepsy

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7 January 2021

Multiple potassium-channel components are produced by alternative splicing at the Shaker locus in Drosophila

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Presynaptic A-current based on heteromultimeric K+ channels detected in vivo

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7 January 2021

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

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7 January 2021

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

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7 January 2021

The type 1 inositol 1,4,5-trisphosphate receptor gene is altered in the opisthotonos mouse

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7 January 2021

Potassium channels expressed from rat brain cDNA have delayed rectifier properties

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7 January 2021

Abnormal action potentials associated with the Shaker complex locus of Drosophila

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7 January 2021

Sequence of a probable potassium channel component encoded at Shaker locus of Drosophila

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7 January 2021

Cloning of a probable potassium channel gene from mouse brain

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7 January 2021

Models of synchronized hippocampal bursts in the presence of inhibition. II. Ongoing spontaneous population events

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7 January 2021

Potassium-induced spontaneous electrographic seizures in the rat hippocampal slice

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7 January 2021

Immunohistochemical localization of five members of the Kv1 channel subunits: contrasting subcellular locations and neuron-specific co-localizations in rat brain

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7 January 2021

Heteromultimeric K+ channels in terminal and juxtaparanodal regions of neurons

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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

Hypomyelination alters K+ channel expression in mouse mutants shiverer and Trembler

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7 January 2021

Synchronized burst discharge in disinhibited hippocampal slice. I. Initiation in CA2-CA3 region

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7 January 2021

10.1016/S0896-6273(00)81018-1

Identifiers

DOI

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11 February 2018

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11 February 2018