Article

Mecp2 Deficiency Alters M1/M2 Gene Expresion in Bone Marrow-Derived Macrophages Upon Stimulation

2020-08-18

Abstract excerpt

<h4>ABSTRACT</h4> Rett Syndrome (RTT) is a neurodevelopmental disorder mostly caused by mutations in the X-linked gene, MeCP2, which encodes for methyl-CpG binding protein 2 (MeCP2). MeCP2 is member of a family of methyl binding proteins that control the expression of several genes according to the genomic context. Emerging evidence suggests that immune dysfunctions would actively contribute to the pathogenesis o...

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Literature Corpus work: 64df8da7-9740-5fab-b3e0-3c194e5e1493
DOI: 10.1101/2020.08.18.256313

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