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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Nat Neurosci
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2016
Pynciau:
Article
Mynediad Ar-lein: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
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