Martha V. Koerner
Edinburgh, SCT, United Kingdom
Last Updated: 09/26/2026
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Found 8 publications
Neuronal non-CG methylation is an essential target for MeCP2 function.
Journal: Molecular cell
Published: July 03, 2020
Toxicity of overexpressed MeCP2 is independent of HDAC3 activity.
Journal: Genes & development
Published: September 03, 2018
A mutation-led search for novel functional domains in MeCP2.
Journal: Human molecular genetics
Published: March 07, 2018
Affinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2.
Journal: Cell reports
Published: December 13, 2017
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
Journal: Nature
Published: March 29, 2017
The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome.
Journal: Human molecular genetics
Published: August 24, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026