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MeCP2-Mediated Transcription Repression in the Basolateral Amygdala May Underlie Heightened Anxiety in a Mouse Model of Rett Syndrome

Rett syndrome (RTT) is an X-linked neurodevelopmental disorder that results from loss of function mutations in the methyl-CpG binding protein 2 (MECP2) gene. Using viral-mediated basolateral amygdala (BLA)-specific deletion of Mecp2 in mice, we show that intact Mecp2 function is required for normal...

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Detalhes bibliográficos
Main Authors: Adachi, Megumi, Autry, Anita E., Covington, Herb E., Monteggia, Lisa M.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3005250/
https://ncbi.nlm.nih.gov/pubmed/19339616
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4225-08.2009
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