Methyl-CpG binding protein 2 regulates microglia and macrophage gene expression in response to inflammatory stimuli

Mutations in MECP2, encoding the epigenetic regulator methyl-CpG-binding protein 2, are the predominant cause of Rett syndrome, a disease characterized by both neurological symptoms and systemic abnormalities. Microglial dysfunction is thought to contribute to disease pathogenesis, and here we found...

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Detaylı Bibliyografya
Yayımlandı:Immunity
Asıl Yazarlar: Cronk, James C., Derecki, Noël C., Ji, Emily, Xu, Yang, Lampano, Aaron E., Smirnov, Igor, Baker, Wendy, Norris, Geoffrey T., Marin, Ioana, Coddington, Nathan, Wolf, Yochai, Turner, Stephen D., Aderem, Alan, Klibanov, Alexander L., Harris, Tajie H., Jung, Steffen, Litvak, Vladimir, Kipnis, Jonathan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2015
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4407145/
https://ncbi.nlm.nih.gov/pubmed/25902482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.immuni.2015.03.013
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