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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...
Autores principales: | 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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060159/ https://www.ncbi.nlm.nih.gov/pubmed/24987493 http://dx.doi.org/10.1155/2014/195935 |
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