Genes Related to Mitochondrial Functions, Protein Degradation, and Chromatin Folding Are Differentially Expressed in Lymphomonocytes of Rett Syndrome Patients

Rett syndrome (RTT) is mainly caused by mutations in the X-linked methyl-CpG binding protein (MeCP2) gene. By binding to methylated promoters on CpG islands, MeCP2 protein is able to modulate several genes and important cellular pathways. Therefore, mutations in MeCP2 can seriously affect the cellul...

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Autori principali: Pecorelli, Alessandra, Leoni, Guido, Cervellati, Franco, Canali, Raffaella, Signorini, Cinzia, Leoncini, Silvia, Cortelazzo, Alessio, De Felice, Claudio, Ciccoli, Lucia, Hayek, Joussef, Valacchi, Giuseppe
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi Publishing Corporation 2013
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3876710/
https://ncbi.nlm.nih.gov/pubmed/24453408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/137629
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