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Calcium channels prove to be a real headache
scientific article published on May 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
review article
1 reference
stated in
Europe PubMed Central
title
Calcium channels prove to be a real headache
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
main subject
headache
1 reference
based on heuristic
inferred from title
author name string
Miller RJ
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
publication date
1 May 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
published in
Trends in Neurosciences
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
volume
20
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
page(s)
189-192
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
cites work
Presenilins and Alzheimer disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
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7 January 2021
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Identification of two new KCNA1 mutations in episodic ataxia/myokymia families
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
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7 January 2021
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inferred from DOI database lookup
Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
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7 January 2021
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inferred from DOI database lookup
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
retrieved
7 January 2021
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inferred from DOI database lookup
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
retrieved
7 January 2021
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Ca2+ channels: diversity of form and function
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
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7 January 2021
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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
retrieved
7 January 2021
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Absence epilepsy in tottering mutant mice is associated with calcium channel defects
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
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7 January 2021
based on heuristic
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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
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7 January 2021
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Primary structure and functional expression from complementary DNA of a brain calcium channel
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
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7 January 2021
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inferred from DOI database lookup
Localization and functional properties of a rat brain alpha 1A calcium channel reflect similarities to neuronal Q- and P-type channels
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5
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7 January 2021
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Chromosomal localization of the human genes for alpha 1A, alpha 1B, and alpha 1E voltage-dependent Ca2+ channel subunits
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
1 reference
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Crossref
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7 January 2021
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Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.
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SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat
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Distinctive biophysical and pharmacological properties of class A (BI) calcium channel alpha 1 subunits
1 reference
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Crossref
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7 January 2021
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Cerebellar cell degeneration in the leaner mutant mouse.
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7 January 2021
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The modular cerebellum
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Nonselective and G betagamma-insensitive weaver K+ channels
1 reference
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Crossref
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7 January 2021
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Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Calcium-channel antibodies in the Lambert-Eaton syndrome and other paraneoplastic syndromes
1 reference
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Crossref
reference URL
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7 January 2021
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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
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Crossref
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PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein
1 reference
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7 January 2021
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Identifiers
DOI
10.1016/S0166-2236(96)01037-5
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
PubMed ID
9141192
1 reference
stated in
Europe PubMed Central
PubMed ID
9141192
retrieved
1 October 2017
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