Chd7 Cooperates with Sox10 and Regulates the Onset of CNS Myelination and Remyelination

Mutations in CHD7, encoding ATP-dependent chromodomain-helicase-DNA-binding protein 7, in CHARGE syndrome leads to multiple congenital anomalies including craniofacial malformations, neurological dysfunction and growth delay. Currently, mechanisms underlying the CNS phenotypes remain poorly understo...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Nat Neurosci
Autori principali: He, Danyang, Marie, Corentine, Zhao, Chuntao, Kim, Bongwoo, Wang, Jincheng, Deng, Yaqi, Clavairoly, Adrien, Frah, Magali, Wang, Haibo, He, Xuelian, Hmidan, Hatem, Jones, Blaise V., Witte, David, Zalc, Bernard, Zhou, Xin, Choo, Daniel I., Martin, Donna M., Parras, Carlos, Lu, Q. Richard
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2016
Soggetti:
Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4846514/
https://ncbi.nlm.nih.gov/pubmed/26928066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nn.4258
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi