A carregar...

Single-channel study of the spasmodic mutation α1A52S in recombinant rat glycine receptors

Inherited defects in glycine receptors lead to hyperekplexia, or startle disease. A mutant mouse, spasmodic, that has a startle phenotype, has a point mutation (A52S) in the glycine receptor α1 subunit. This mutation reduces the sensitivity of the receptor to glycine, but the mechanism by which this...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Plested, Andrew J R, Groot-Kormelink, Paul J, Colquhoun, David, Sivilotti, Lucia G
Formato: Artigo
Idioma:Inglês
Publicado em: Blackwell Science Inc 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2075205/
https://ncbi.nlm.nih.gov/pubmed/17331994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2006.126920
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!