Results 211 to 220 of about 27,643 (268)

MeCP2 requires interactions with nucleosome linker DNA to read chromatin DNA methylation. [PDF]

open access: yesNat Commun
Watson JA   +9 more
europepmc   +1 more source

Dysfunction of a SET3-like complex underlies a family of related neurological disorders. [PDF]

open access: yesNat Commun
Paton KM   +11 more
europepmc   +1 more source

MSK1 mediates BDNF-dependent MeCP2-S421 phosphorylation in postnatal striatal development and psychiatric-relevant behaviours. [PDF]

open access: yesMol Psychiatry
Varela-Andrés N   +13 more
europepmc   +1 more source

Mecp2 deficiency induces dysphagia in a preclinical model of Rett syndrome. [PDF]

open access: yesProc Natl Acad Sci U S A
Oliveira LM   +3 more
europepmc   +1 more source

MECP2 mutations rewire human ESC fate and bias cortical lineage commitment. [PDF]

open access: yesStem Cell Reports
Guillon M   +13 more
europepmc   +1 more source

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