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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Détails bibliographiques
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: Frontiers Media S.A. 2014
Sujets:
Neuroscience
Accès en ligne: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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