Beta-Actin Deficiency with Oxidative Posttranslational Modifications in Rett Syndrome Erythrocytes: Insights into an Altered Cytoskeletal Organization

Beta-actin, a critical player in cellular functions ranging from cell motility and the maintenance of cell shape to transcription regulation, was evaluated in the erythrocyte membranes from patients with typical Rett syndrome (RTT) and methyl CpG binding protein 2 (MECP2) gene mutations. RTT, affect...

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Detalhes bibliográficos
Main Authors: Cortelazzo, Alessio, De Felice, Claudio, Pecorelli, Alessandra, Belmonte, Giuseppe, Signorini, Cinzia, Leoncini, Silvia, Zollo, Gloria, Capone, Antonietta, Giovampaola, Cinzia Della, Sticozzi, Claudia, Valacchi, Giuseppe, Ciccoli, Lucia, Guerranti, Roberto, Hayek, Joussef
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3966888/
https://ncbi.nlm.nih.gov/pubmed/24671107
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0093181
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