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

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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Bibliographic Details
Main Authors: Cinzia Signorini, Silvia Leoncini, Claudio De Felice, Alessandra Pecorelli, Ilaria Meloni, Francesca Ariani, Francesca Mari, Sonia Amabile, Eugenio Paccagnini, Mariangela Gentile, Giuseppe Belmonte, Gloria Zollo, Giuseppe Valacchi, Thierry Durand, Jean-Marie Galano, Lucia Ciccoli, Alessandra Renieri, Joussef Hayek
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:Oxidative Medicine and Cellular Longevity
Online Access:http://dx.doi.org/10.1155/2014/195935

Internet

http://dx.doi.org/10.1155/2014/195935

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