(Q42673049)

English

The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy

scientific article published on January 1998

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

4 November 2017

The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy (English)

1 reference

Europe PubMed Central

4 November 2017

Joerg T. Epplen

8

1 reference

Europe PubMed Central

4 November 2017

author name string

Sander T

1

1 reference

Europe PubMed Central

4 November 2017

Peters C

2

1 reference

Europe PubMed Central

4 November 2017

Janz D

3

1 reference

Europe PubMed Central

4 November 2017

Bianchi A

4

1 reference

Europe PubMed Central

4 November 2017

Bauer G

5

1 reference

Europe PubMed Central

4 November 2017

Wienker TF

6

1 reference

Europe PubMed Central

4 November 2017

Hildmann T

7

1 reference

Europe PubMed Central

4 November 2017

Riess O

9

1 reference

Europe PubMed Central

4 November 2017

publication date

1 January 1998

1 reference

Europe PubMed Central

4 November 2017

Epilepsy Research

1 reference

Europe PubMed Central

4 November 2017

29

1 reference

Europe PubMed Central

4 November 2017

2

1 reference

Europe PubMed Central

4 November 2017

115-122

1 reference

Europe PubMed Central

4 November 2017

The idiopathic generalized epilepsies of adolescence with childhood and juvenile age of onset

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

The genetics of idiopathic generalized epilepsy: implications for the understanding of its aetiology

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Concepts of absence epilepsies: discrete syndromes or biological continuum?

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of convulsive disorders. II. Genetic and electroencephalographic studies in centrencephalic epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic dissection of complex traits

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Targeting epilepsy genes

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Human/mouse homology relationships

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Calcium channels prove to be a real headache

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

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

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Calcium-dependent regulation of genetically determined spike and waves by the reticular thalamic nucleus of rats.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Selective increase in T-type calcium conductance of reticular thalamic neurons in a rat model of absence epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Presynaptic inhibition of elicited neurotransmitter release

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Distinctive pharmacology and kinetics of cloned neuronal Ca2+ channels and their possible counterparts in mammalian CNS neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Basic mechanisms of generalized absence seizures

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping of genes predisposing to idiopathic generalized epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene-targeting studies of mammalian behavior: is it the mutation or the background genotype?

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2897%2900073-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0920-1211(97)00073-9

1 reference

Europe PubMed Central

4 November 2017

1 reference

Europe PubMed Central

4 November 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q42673049&oldid=1965186536"