(Q35682326)

9 August 2017

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title

In vivo analysis of voltage-dependent calcium channels (English)

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9 August 2017

Ling Liu

1

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9 August 2017

Theresa A Zwingman

series ordinal

2

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9 August 2017

Colin F Fletcher

series ordinal

3

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9 August 2017

publication date

1 December 2003

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Journal of Bioenergetics and Biomembranes

9 August 2017

published in

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9 August 2017

volume

35

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9 August 2017

issue

6

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9 August 2017

page(s)

671-685

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Nomenclature of voltage-gated calcium channels.

9 August 2017

cites work

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12 December 2020

Neurotransmitter release from tottering mice nerve terminals with reduced expression of mutated P- and Q-type Ca2+-channels

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12 December 2020

Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p

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12 December 2020

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit

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12 December 2020

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

12 December 2020

Functional embryonic cardiomyocytes after disruption of the L-type alpha1C (Cav1.2) calcium channel gene in the mouse.

1 reference

12 December 2020

Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F

1 reference

12 December 2020

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

1 reference

12 December 2020

The genetic basis of migraine: how much do we know?

1 reference

12 December 2020

Suppression of inflammatory and neuropathic pain symptoms in mice lacking the N-type Ca2+ channel

1 reference

12 December 2020

Familial Episodic Ataxias and Related Ion Channel Disorders

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12 December 2020

Relations between cortical and thalamic cellular events during transition from sleep patterns to paroxysmal activity.

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12 December 2020

Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel

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12 December 2020

Ca(v)2.3 (alpha1E) Ca2+ channel participates in the control of sperm function

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12 December 2020

Models of the normal and abnormal rod system

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12 December 2020

Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6)

1 reference

12 December 2020

Analysis of Ca2+ Currents in Spermatocytes from Mice Lacking Cav2.3 (α1E) Ca2+ Channel

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12 December 2020

On the action of the anti-absence drug ethosuximide in the rat and cat thalamus.

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

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12 December 2020

Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy

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12 December 2020

Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a

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12 December 2020

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2

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12 December 2020

A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

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12 December 2020

The observation of rolling mouse Nagoya (rol), a new neurological mutant, and its maintenance (author's transl)

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12 December 2020

Functional disorders of the sympathetic nervous system in mice lacking the alpha 1B subunit (Cav 2.2) of N-type calcium channels

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12 December 2020

Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering

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12 December 2020

Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer

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12 December 2020

Channelopathies: ion channel defects linked to heritable clinical disorders

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12 December 2020

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p

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12 December 2020

Sisters homozygous for the spinocerebellar ataxia type 6 (SCA6)/CACNA1A gene associated with different clinical phenotypes

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12 December 2020

Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13

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12 December 2020

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine

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12 December 2020

Selective peptide antagonist of the class E calcium channel from the venom of the tarantula Hysterocrates gigas

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12 December 2020

Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function

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12 December 2020

Intracellular recordings in thalamic neurones during spontaneous spike and wave discharges in rats with absence epilepsy

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12 December 2020

Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2.

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12 December 2020

Cortical spreading depression and migraine: new insights from imaging?

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12 December 2020

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia

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12 December 2020

Differential nociceptive responses in mice lacking the alpha(1B) subunit of N-type Ca(2+) channels

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12 December 2020

The status of voltage-dependent calcium channels in alpha 1E knock-out mice

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12 December 2020

The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells

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12 December 2020

Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha1A subunit of P/Q type calcium channels

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12 December 2020

Calcium channelopathies in the central nervous system

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12 December 2020

Genetic heterogeneity in Italian families with familial hemiplegic migraine

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12 December 2020

Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations

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12 December 2020

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

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12 December 2020

Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia

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12 December 2020

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family

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12 December 2020

Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A gene

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12 December 2020

Mice lacking Ca(v)2.3 (alpha1E) calcium channel exhibit hyperglycemia

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12 December 2020

A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cM region on chromosome 19p

1 reference

12 December 2020

Increased expression of alpha 1A Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6.

1 reference

12 December 2020

Neurobiology of migraine.

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12 December 2020

Direct alteration of the P/Q-type Ca2+ channel property by polyglutamine expansion in spinocerebellar ataxia 6.

1 reference

12 December 2020

Altered pain responses in mice lacking alpha 1E subunit of the voltage-dependent Ca2+ channel.

1 reference

12 December 2020

Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia

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12 December 2020

Structure and function of neuronal Ca2+ channels and their role in neurotransmitter release

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12 December 2020

A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia

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12 December 2020

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission

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12 December 2020

Characterization of ethosuximide reduction of low-threshold calcium current in thalamic neurons

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12 December 2020

Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels

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12 December 2020

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

1 reference

12 December 2020

Mutations in the CACNA1F and NYX genes in British CSNBX families

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12 December 2020

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine

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12 December 2020

The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes.

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12 December 2020

Molecular basis of the diversity of calcium channels in cardiovascular tissues

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12 December 2020

Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner

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12 December 2020

Mechanisms of migraine aura revealed by functional MRI in human visual cortex

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12 December 2020

Frequency of spinocerebellar ataxia mutations in the Kinki district of Japan.

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12 December 2020

Missense CACNA1A mutation causing episodic ataxia type 2

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12 December 2020

Association between the alpha(1a) calcium channel gene CACNA1A and idiopathic generalized epilepsy

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12 December 2020

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2

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12 December 2020

A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness

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12 December 2020

Whole-cell and single-channel analysis of P-type calcium currents in cerebellar Purkinje cells of leaner mutant mice

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12 December 2020

A Ca(2+)-dependent transgenic model of cardiac hypertrophy: A role for protein kinase Calpha

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12 December 2020

Requirement for the L-type Ca(2+) channel alpha(1D) subunit in postnatal pancreatic beta cell generation

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12 December 2020

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

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12 December 2020

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

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12 December 2020

Antisense oligonucleotides against alpha1E reduce R-type calcium currents in cerebellar granule cells.

1 reference

12 December 2020

A novel insertion mutation of acetazolamide-responsive episodic ataxia in a Japanese family

1 reference

12 December 2020

Altered nociceptive response in mice deficient in the alpha(1B) subunit of the voltage-dependent calcium channel

1 reference

12 December 2020

Molecular basis of R-type calcium channels in central amygdala neurons of the mouse

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12 December 2020

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity

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12 December 2020

Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina

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12 December 2020

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

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12 December 2020

The diversity of calcium channels and their regulation in epithelial cells.

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12 December 2020

Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalami

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12 December 2020

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine

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12 December 2020

Genetic analysis of voltage-dependent calcium channels.

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12 December 2020

Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol))

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12 December 2020

Calcium channels and channelopathies of the central nervous system

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12 December 2020

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons

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12 December 2020

Spinocerebellar ataxia type 6: channelopathy or glutamine repeat disorder?

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12 December 2020

Analysis of voltage-gated and synaptic conductances contributing to network excitability defects in the mutant mouse tottering

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12 December 2020

Spinocerebellar ataxia type 6 and episodic ataxia type 2 in a Korean family

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12 December 2020

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

1 reference

12 December 2020

Cardiac-specific overexpression of the alpha(1) subunit of the L-type voltage-dependent Ca(2+) channel in transgenic mice. Loss of isoproterenol-induced contraction

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12 December 2020

alpha(1E) subunits form the pore of three cerebellar R-type calcium channels with different pharmacological and permeation properties

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12 December 2020

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

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12 December 2020

Molecular diversity of voltage-dependent Ca2+ channels

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12 December 2020

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics

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12 December 2020

Intact LTP and fear memory but impaired spatial memory in mice lacking Ca(v)2.3 (alpha(IE)) channel

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12 December 2020

Molecular biology of calcium channels

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12 December 2020

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

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12 December 2020

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

1 reference

12 December 2020

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

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12 December 2020

Spike-wave complexes and fast components of cortically generated seizures. I. Role of neocortex and thalamus

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12 December 2020

Progressive ataxia due to a missense mutation in a calcium-channel gene

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12 December 2020

Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p

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12 December 2020

10.1023/B:JOBB.0000008031.12485.EE

Identifiers

DOI

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Dimensions Publication ID

9 August 2017

1012602636

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