Redox Imbalance and Morphological Changes in Skin Fibroblasts in Typical Rett Syndrome

Evidence of oxidative stress has been reported in the blood of patients with Rett syndrome (RTT), a neurodevelopmental disorder mainly caused by mutations in the gene encoding the Methyl-CpG-binding protein 2. Little is known regarding the redox status in RTT cellular systems and its relationship wi...

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Autors principals: Signorini, Cinzia, Leoncini, Silvia, De Felice, Claudio, Pecorelli, Alessandra, Meloni, Ilaria, Ariani, Francesca, Mari, Francesca, Amabile, Sonia, Paccagnini, Eugenio, Gentile, Mariangela, Belmonte, Giuseppe, Zollo, Gloria, Valacchi, Giuseppe, Durand, Thierry, Galano, Jean-Marie, Ciccoli, Lucia, Renieri, Alessandra, Hayek, Joussef
Format: Artigo
Idioma:Inglês
Publicat: Hindawi Publishing Corporation 2014
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4060159/
https://ncbi.nlm.nih.gov/pubmed/24987493
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/195935
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