Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome

Rett syndrome (RTT) is a rare neurodevelopmental disorder affecting almost exclusively females, caused in the overwhelming majority of the cases by loss-of-function mutations in the gene encoding methyl-CpG binding protein 2 (MECP2). High circulating levels of oxidative stress (OS) markers in patien...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: De Felice, Claudio, Della Ragione, Floriana, Signorini, Cinzia, Leoncini, Silvia, Pecorelli, Alessandra, Ciccoli, Lucia, Scalabrì, Francesco, Marracino, Federico, Madonna, Michele, Belmonte, Giuseppe, Ricceri, Laura, De Filippis, Bianca, Laviola, Giovanni, Valacchi, Giuseppe, Durand, Thierry, Galano, Jean-Marie, Oger, Camille, Guy, Alexandre, Bultel-Poncé, Valérie, Guy, Jacky, Filosa, Stefania, Hayek, Joussef, D'Esposito, Maurizio
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Academic Press 2014
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4076513/
https://ncbi.nlm.nih.gov/pubmed/24769161
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2014.04.006
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