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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Bibliografiska uppgifter
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Academic Press 2014
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Article
Länkar: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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