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CX(3)CR1 ablation ameliorates motor and respiratory dysfunctions and improves survival of a Rett syndrome mouse model

Rett syndrome (RTT) is a neurodevelopmental disorder caused by loss-of-function mutations in the gene encoding MeCP2, an epigenetic modulator that binds the methyl CpG dinucleotide in target genes to regulate transcription. Previously we and others reported a role of microglia in the pathophysiology...

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Detalhes bibliográficos
Publicado no:Brain Behav Immun
Main Authors: Horiuchi, Makoto, Smith, Lucas, Maezawa, Izumi, Jin, Lee-Way
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5531048/
https://ncbi.nlm.nih.gov/pubmed/26883520
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbi.2016.02.014
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