Vascular Dysfunction in a Mouse Model of Rett Syndrome and Effects of Curcumin Treatment

Mutations in the coding sequence of the X-linked gene MeCP2 (Methyl CpG–binding protein) are present in around 80% of patients with Rett Syndrome, a common cause of intellectual disability in female and to date without any effective pharmacological treatment. A relevant, and so far unexplored featur...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Panighini, Anna, Duranti, Emiliano, Santini, Ferruccio, Maffei, Margherita, Pizzorusso, Tommaso, Funel, Niccola, Taddei, Stefano, Bernardini, Nunzia, Ippolito, Chiara, Virdis, Agostino, Costa, Mario
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Public Library of Science 2013
विषय:
Research Article
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3660336/
https://ncbi.nlm.nih.gov/pubmed/23705018
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0064863
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