(Q41533301)

2 October 2017

1 reference

title

Potassium channelopathies (English)

1 reference

2 October 2017

Sanguinetti MC

1

1 reference

PubMed ID

9225302

2 October 2017

Spector PS

series ordinal

2

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2 October 2017

1 June 1997

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2 October 2017

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2 October 2017

36

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2 October 2017

755-762

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2 October 2017

6

1 reference

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

2 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Familial periodic cerebellar ataxia: a problem of cerebellar intracellular pH homeostasis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Members of the RCK potassium channel family are differentially expressed in the rat nervous system.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Missense mutation in the pore region of HERG causes familial long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Inhibition of IKs in guinea pig cardiac myocytes and guinea pig IsK channels by the chromanol 293B.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Heterologous multimeric assembly is essential for K+ channel activity of neuronal and cardiac G-protein-activated inward rectifiers.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Tonic/clonic seizures in a mouse mutant carrying the weaver gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

The electrophysiological mechanism of ventricular arrhythmias in the long QT syndrome. Tridimensional mapping of activation and recovery patterns

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Neuronal differentiation rescued by implantation of Weaver granule cell precursors into wild-type cerebellar cortex.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Male-sterile phenotype of the neurological mouse mutant weaver.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Mutations in the K+ channel signature sequence

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Early afterdepolarizations: mechanism of induction and block. A role for L-type Ca2+ current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Molecular cloning of a mouse G-protein-activated K+ channel (mGIRK1) and distinct distributions of three GIRK (GIRK1, 2 and 3) mRNAs in mouse brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Functional analysis of the weaver mutant GIRK2 K+ channel and rescue of weaver granule cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Heteromultimerization of G-protein-gated inwardly rectifying K+ channel proteins GIRK1 and GIRK2 and their altered expression in weaver brain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Increased proteolytic activity of the granule neurons may contribute to neuronal death in the weaver mouse cerebellum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Nonselective and G betagamma-insensitive weaver K+ channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Weaver Mutant Mouse Cerebellum: Defective Neuronal Migration Secondary to Abnormality of Bergmann Glia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

The mouse neurological mutant weaver maps within the region of chromosome 16 that is homologous to human chromosome 21

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

KVLQT1 mutations in three families with familial or sporadic long QT syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Conductance and kinetics of delayed rectifier potassium channels in nodal cells of the rabbit heart.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Functional effects of the mouse weaver mutation on G protein-gated inwardly rectifying K+ channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

The inward rectification mechanism of the HERG cardiac potassium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Fast inactivation causes rectification of the IKr channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Cellular electrophysiology of WAY-123,398, a new class III antiarrhythmic agent: specificity of IK block and lack of reverse use dependence in cat ventricular myocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

The weaver mutation of GIRK2 results in a loss of inwardly rectifying K+ current in cerebellar granule cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Cloning of a membrane protein that induces a slow voltage-gated potassium current

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

Hereditary myokymia and periodic ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

A family of potassium channel genes related to eag in Drosophila and mammals

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3908%2897%2900029-4

10.1016/S0028-3908(97)00029-4

7 January 2021

Identifiers

DOI

1 reference

2 October 2017

1 reference

PubMed ID

9225302