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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Nat Neurosci
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: 2016
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars