A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice

In a phenotype-driven mutagenesis screen, a novel, dominant mouse mutation, Nmf350, caused low seizure threshold, sporadic tonic–clonic seizures, brain enlargement and ectopic neurons in the dentate hilus and molecular layer of the hippocampus. Genetic mapping implicated Akt3, one of four candidates...

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Main Authors: Tokuda, Satoko, Mahaffey, Connie L., Monks, Bobby, Faulkner, Christian R., Birnbaum, Morris J., Danzer, Steve C., Frankel, Wayne N.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3033189/
https://ncbi.nlm.nih.gov/pubmed/21159799
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq544
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https://ncbi.nlm.nih.gov/pmc/articles/PMC3033189/
https://ncbi.nlm.nih.gov/pubmed/21159799
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq544