MeCP2 requires interactions with nucleosome linker DNA to read chromatin DNA methylation. [PDF]
Watson JA +9 more
europepmc +1 more source
Dysfunction of a SET3-like complex underlies a family of related neurological disorders. [PDF]
Paton KM +11 more
europepmc +1 more source
MSK1 mediates BDNF-dependent MeCP2-S421 phosphorylation in postnatal striatal development and psychiatric-relevant behaviours. [PDF]
Varela-Andrés N +13 more
europepmc +1 more source
MeCP2 Governs maternal hyperandrogenism-induced cortical defects and behavioral alterations via noncanonical AR-dependent regulation of Mef2c. [PDF]
Wang YM +7 more
europepmc +1 more source
MicroRNA-132 Alleviates Ischemia-Reperfusion-Induced Neuronal Apoptosis by Targeting Mecp2 in Stroke Models. [PDF]
Wang X +7 more
europepmc +1 more source
Mecp2 deficiency induces dysphagia in a preclinical model of Rett syndrome. [PDF]
Oliveira LM +3 more
europepmc +1 more source
MECP2 mutations rewire human ESC fate and bias cortical lineage commitment. [PDF]
Guillon M +13 more
europepmc +1 more source
Mechanistic Links Between DNA Methylation and Protein Translation and Their Impacts on Brain Development. [PDF]
Kadar Shahib A, Rastegar M.
europepmc +1 more source

