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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Shinichi Tokuda, Connie L. Mahaffey, B. Monks, Christian Faulkner, Morris J. Birnbaum, Steve C. Danzer, Wayne N. Frankel
Fformat: Artigo
Iaith:Saesneg
Cyhoeddwyd: 2010
Mynediad Ar-lein:https://doi.org/10.1093/hmg/ddq544
Tagiau: Ychwanegu Tag
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