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Mechanisms of Functional Hypoconnectivity in the Medial Prefrontal Cortex of Mecp2 Null Mice

Frontal cortical dysfunction is thought to contribute to cognitive and behavioral features of autism spectrum disorders; however, underlying mechanisms are poorly understood. The present study sought to define how loss of Mecp2, the gene mutated in Rett syndrome (RTT), disrupts function in the murin...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Cereb Cortex
Prif Awduron: Sceniak, Michael P., Lang, Min, Enomoto, Addison C., James Howell, C., Hermes, Douglas J., Katz, David M.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2016
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5006177/
https://ncbi.nlm.nih.gov/pubmed/25662825
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhv002
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