(Q24329192)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Calcium channel beta 4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

3

1 reference

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12 November 2019

Peter F. Hitchcock

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

author name string

Escayg A

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Jones JM

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Meisler MH

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

language of work or name

English

0 references

publication date

1 May 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

volume

50

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

page(s)

14-22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

Assignment of the human gene for the beta subunit of the voltage-dependent calcium channel (CACNLB1) to chromosome 17 using somatic cell hybrids and linkage mapping

12 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Physical linkage of the murine Hox-b cluster and nerve growth factor receptor on yeast artificial chromosomes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

The structures of the human calcium channel alpha 1 subunit (CACNL1A2) and beta subunit (CACNLB3) genes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Genetic mapping of the mouse genes encoding the voltage-sensitive calcium channel subunits

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Close linkage of three neuronal genes on distal mouse Chromosome 15

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Subcellular localization of alpha-tubulin and opsin mRNA in the goldfish retina using digoxigenin-labeled cRNA probes detected by alkaline phosphatase and HRP histochemistry

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Characterization of an L-type calcium channel expressed by human retinal Müller (glial) cells

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Structure and functional expression of alpha 1, alpha 2, and beta subunits of a novel human neuronal calcium channel subtype

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Ca2+ channel regulation by a conserved beta subunit domain

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

The amino terminus of a calcium channel beta subunit sets rates of channel inactivation independently of the subunit's effect on activation.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Auxiliary subunits of voltage-gated ion channels

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Dependence of photoreceptor glutamate release on a dihydropyridine-sensitive calcium channel

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Acceleration of activation and inactivation by the β subunit of the skeletal muscle calcium channel

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Calcium channel β-subunit binds to a conserved motif in the I–II cytoplasmic linker of the α1-subunit

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

A method for constructing radiation hybrid maps of whole genomes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Molecular diversity of Ca2+ channel beta subunits

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Ion channels--basic science and clinical disease

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Beta subunit heterogeneity in N-type Ca2+ channels.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Alternative splicing of the sodium channel SCN8A predicts a truncated two-domain protein in fetal brain and non-neuronal cells.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

The dihydropyridine-sensitive calcium channel subtype in cone photoreceptors

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Genetic mapping of the beta 1- and gamma-subunits of the human skeletal muscle L-type voltage-dependent calcium channel on chromosome 17q and exclusion as candidate genes for malignant hyperthermia susceptibility

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

A calcium channel mutation causing hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Phenotype variation and newcomers in ion channel disorders

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Developmental regulation of voltage-activated Na+ and Ca2+ currents in rat retinal ganglion cells.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Cloning, chromosomal location and functional expression of the human voltage-dependent calcium-channel beta 3 subunit

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

The absence epilepsies.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

The role of GABAB receptor activation in absence seizures of lethargic (lh/lh) mice

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

The roles of the subunits in the function of the calcium channel.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

An STS-based map of the human genome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Dihydropyridine-sensitive calcium current mediates neurotransmitter release from bipolar cells of the goldfish retina

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5311

7 January 2021

Identifiers

DOI

10.1006/GENO.1998.5311

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9628818%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference