(Q33680946)

28 July 2017

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title

Calcium channelopathies in the central nervous system (English)

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28 July 2017

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Jen J

1

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28 July 2017

publication date

1 June 1999

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Current Opinion in Neurobiology

28 July 2017

published in

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28 July 2017

volume

9

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28 July 2017

issue

3

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28 July 2017

page(s)

274-280

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Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system

28 July 2017

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Primary structure and functional expression from complementary DNA of a brain calcium channel

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7 January 2021

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

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7 January 2021

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

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7 January 2021

A gene for familial hemiplegic migraine maps to chromosome 19

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7 January 2021

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p

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7 January 2021

Episodic ataxias as channelopathies

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7 January 2021

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

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7 January 2021

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia

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7 January 2021

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

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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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7 January 2021

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

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7 January 2021

Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene

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7 January 2021

A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia

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7 January 2021

Molecular properties of sodium and calcium channels

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7 January 2021

Subunit interaction sites in voltage-dependent Ca2+ channels: role in channel function.

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7 January 2021

Distinct calcium channels are generated by alternative splicing and are differentially expressed in the mammalian CNS

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7 January 2021

Localization of mRNAs of voltage-dependent Ca2+-channels: four subtypes of α1- and β-subunits in developing and mature rat brain

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7 January 2021

IgG from patients with Lambert-Eaton syndrome blocks voltage-dependent calcium channels

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7 January 2021

Calcium-channel antibodies in the Lambert-Eaton syndrome and other paraneoplastic syndromes

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7 January 2021

Nearby Stop Codons in Exons of the Neurofibromatosis Type 1 Gene Are Disparate Splice Effectors

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7 January 2021

Evidence for a 95 kDa Short Form of the α1ASubunit Associated with the ω-Conotoxin MVIIC Receptor of the P/Q-type Ca2+Channels

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7 January 2021

Protein fate in neurodegenerative proteinopathies: polyglutamine diseases join the (mis)fold

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7 January 2021

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

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7 January 2021

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

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7 January 2021

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

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7 January 2021

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

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7 January 2021

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

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7 January 2021

Purkinje cell loss from alternating sagittal zones in the cerebellum of leaner mutant mice

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7 January 2021

Expression of calcium channel alpha1A mRNA and protein in the leaner mouse (tgla/tgla) cerebellum

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Regional expression and cellular localization of the alpha1 and beta subunit of high voltage-activated calcium channels in rat brain.

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7 January 2021

Altered expression and assembly of N-type calcium channel alpha1B and beta subunits in epileptic lethargic (lh/lh) mouse

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7 January 2021

Binding of the inward rectifier K+ channel Kir 2.3 to PSD-95 is regulated by protein kinase A phosphorylation

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7 January 2021

Physical link and functional coupling of presynaptic calcium channels and the synaptic vesicle docking/fusion machinery

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7 January 2021

Selective failure of brain-derived neurotrophic factor mRNA expression in the cerebellum of stargazer, a mutant mouse with ataxia

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7 January 2021

Cerebellar brain-derived neurotrophic factor-TrkB defect associated with impairment of eyeblink conditioning in Stargazer mutant mice.

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7 January 2021

Ca2+ influx regulates BDNF transcription by a CREB family transcription factor-dependent mechanism

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7 January 2021

Identification of a signaling pathway involved in calcium regulation of BDNF expression

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7 January 2021

A new locus for hemiplegic migraine maps to chromosome 1q31

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7 January 2021

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

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7 January 2021

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

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7 January 2021

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

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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

10.1016/S0959-4388(99)80040-3

Identifiers

DOI

1 reference

28 July 2017

1 reference