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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Autors principals:	Elisa eBellini, Giulio ePavesi, Isabella eBarbiero, Anna eBergo, Chetan eChandola, Mohammad Sarfaraz eNawaz, Laura eRusconi, Gilda eStefanelli, Marta eStrollo, Maria Maddalena eValente, Charlotte eKilstrup-Nielsen, Nicoletta eLandsberger
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2014-08-01
Col·lecció:	Frontiers in Cellular Neuroscience
Matèries:	Chromatin Neurons Phosphorylation Rett Syndrome MeCP2 synaptic plasticity
Accés en línia:	http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00236/full
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