Astrocytic modulation of excitatory synaptic signaling in a mouse model of Rett syndrome

Studies linking mutations in Methyl CpG Binding Protein 2 (MeCP2) to physiological defects in the neurological disease, Rett syndrome, have focused largely upon neuronal dysfunction despite MeCP2 ubiquitous expression. Here we explore roles for astrocytes in neuronal network function using cortical...

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Detalles Bibliográficos
Autores principales: Rakela, Benjamin, Brehm, Paul, Mandel, Gail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771668/
https://www.ncbi.nlm.nih.gov/pubmed/29313799
http://dx.doi.org/10.7554/eLife.31629

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771668/
https://www.ncbi.nlm.nih.gov/pubmed/29313799
http://dx.doi.org/10.7554/eLife.31629

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