MeCP2 heterochromatin organization is modulated by arginine methylation and serine phosphorylation.
MeCP2
Rett syndrome
arginine (di)methylation
heterochromatin organization
protein arginine methyltransferases
Journal
Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250
Informations de publication
Date de publication:
2022
2022
Historique:
received:
11
05
2022
accepted:
19
08
2022
entrez:
29
9
2022
pubmed:
30
9
2022
medline:
30
9
2022
Statut:
epublish
Résumé
Rett syndrome is a human intellectual disability disorder that is associated with mutations in the X-linked
Identifiants
pubmed: 36172281
doi: 10.3389/fcell.2022.941493
pii: 941493
pmc: PMC9510713
doi:
Types de publication
Journal Article
Langues
eng
Pagination
941493Informations de copyright
Copyright © 2022 Schmidt, Frei, Poetsch, Chittka, Zhang, Aßmann, Lehmkuhl, Bauer, Nuber and Cardoso.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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