Calcium channels prove to be a real headache (Q41462629)

1 October 2017

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title

Calcium channels prove to be a real headache (English)

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1 October 2017

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Miller RJ

1

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1 October 2017

1 May 1997

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1 October 2017

Trends in Neurosciences

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1 October 2017

20

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1 October 2017

5

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1 October 2017

189-192

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Presenilins and Alzheimer disease

1 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Ca2+ channels: diversity of form and function

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

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/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

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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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Localization and functional properties of a rat brain alpha 1A calcium channel reflect similarities to neuronal Q- and P-type channels

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Chromosomal localization of the human genes for alpha 1A, alpha 1B, and alpha 1E voltage-dependent Ca2+ channel subunits

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

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/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Distinctive biophysical and pharmacological properties of class A (BI) calcium channel alpha 1 subunits

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Cerebellar cell degeneration in the leaner mutant mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

The modular cerebellum

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Nonselective and G betagamma-insensitive weaver K+ channels

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2896%2901037-5

7 January 2021

10.1016/S0166-2236(96)01037-5

Identifiers

DOI

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1 October 2017

1 reference

PubMed ID

9141192