MeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?

Although Rett syndrome (RTT) represents one of the most frequent forms of severe intellectual disability in females worldwide, we still have an inadequate knowledge of the many roles played by MeCP2 (whose mutations are responsible for most cases of RTT) and their relevance for RTT pathobiology. Sev...

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Detalles Bibliográficos
Autores principales: Bellini, Elisa, Pavesi, Giulio, Barbiero, Isabella, Bergo, Anna, Chandola, Chetan, Nawaz, Mohammad S., Rusconi, Laura, Stefanelli, Gilda, Strollo, Marta, Valente, Maria M., Kilstrup-Nielsen, Charlotte, Landsberger, Nicoletta
Formato: Artigo
Lenguaje:Inglês
Publicado: Frontiers Media S.A. 2014
Materias:
Neuroscience
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4131190/
https://ncbi.nlm.nih.gov/pubmed/25165434
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2014.00236
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