Matthew J. Lyst
Hugh Robson Building, George Square
Edinburgh, SCT EH89XF, United Kingdom
Edinburgh, SCT EH89XF, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Dysfunction of a SET3-like complex underlies a family of related neurological disorders.
Journal: Nature communications
Published: July 23, 2025
A screen for MeCP2-TBL1 interaction inhibitors using a luminescence-based assay.
Journal: Scientific reports
Published: November 16, 2022
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
Affinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2.
Journal: Cell reports
Published: December 13, 2017
Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: March 29, 2017
Sequence-specific DNA binding by AT-hook motifs in MeCP2.
Journal: FEBS letters
Published: June 24, 2016
Rett syndrome: a complex disorder with simple roots.
Journal: Nature reviews. Genetics
Published: March 04, 2015
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.
Journal: Nature neuroscience
Published: February 15, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026