Disruption of Src Is Associated with Phenotypes Related to Williams-Beuren Syndrome and Altered Cellular Localization of TFII-I1,2

Src is a nonreceptor protein tyrosine kinase that is expressed widely throughout the central nervous system and is involved in diverse biological functions. Mice homozygous for a spontaneous mutation in Src (Src (thl/thl)) exhibited hypersociability and hyperactivity along with impairments in visuos...

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Detalhes bibliográficos
Publicado no:eNeuro
Main Authors: Sinai, Laleh, Ivakine, Evgueni A., Lam, Emily, Deurloo, Marielle, Dida, Joana, Zirngibl, Ralph A.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2015
Assuntos:
New Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4596087/
https://ncbi.nlm.nih.gov/pubmed/26464974
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/ENEURO.0016-14.2015
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