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Enhancement of postsynaptic GABA(A) and extrasynaptic NMDA receptor-mediated responses in the barrel cortex of Mecp2-null mice

Rett syndrome (RTT) is a neurodevelopmental disorder that results from mutations in the X-linked gene for methyl-CpG-binding protein 2 (MECP2). The underlying cellular mechanism for the sensory deficits in patients with RTT is largely unknown. This study used the Bird mouse model of RTT to investiga...

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Detalhes bibliográficos
Publicado no:J Neurophysiol
Main Authors: Lo, Fu-Sun, Blue, Mary E., Erzurumlu, Reha S.
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4808090/
https://ncbi.nlm.nih.gov/pubmed/26683074
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/jn.00944.2015
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