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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Pecorelli, Alessandra, Leoni, Guido, Cervellati, Franco, Canali, Raffaella, Signorini, Cinzia, Leoncini, Silvia, Cortelazzo, Alessio, De Felice, Claudio, Ciccoli, Lucia, Hayek, Joussef, Valacchi, Giuseppe
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2013
Assuntos:
Research Article
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados