Llwytho...

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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Neurophysiol
Prif Awduron: Lo, Fu-Sun, Blue, Mary E., Erzurumlu, Reha S.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Physiological Society 2015
Pynciau:
Mynediad Ar-lein: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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