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Biorxiv : the Preprint Server for Biology|September 15, 2025
Translational reading frame determines the pathogenicity of C-terminal frameshift deletions in MeCP2: an alternative therapeutic approachJacky Guy, Elena Hein, Bea Alexander-Howden, et al.Epigenetics & Chromatin|November 28, 2013
Identical sets of methylated and nonmethylated genes in Ciona intestinalis sperm and muscle cellsMiho M Suzuki, Akiko Yoshinari, Madoka Obara, et al.Epigenetics & Chromatin|August 30, 2014
DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distributionCongdi Song, Yana Feodorova, Jacky Guy, et al.Human Molecular Genetics|December 10, 2015
The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndromeKyla Brown, Jim Selfridge, Sabine Lagger, et al.Nature|October 12, 2017
Radically truncated MeCP2 rescues Rett syndrome-like neurological defectsRebekah Tillotson, Jim Selfridge, Martha V Koerner, et al.Brain : a Journal of Neurology|April 25, 2012
Morphological and functional reversal of phenotypes in a mouse model of Rett syndromeLianne Robinson, Jacky Guy, Leanne McKay, et al.Science (New York, N.Y.)|July 20, 2002
Enhanced CpG mutability and tumorigenesis in MBD4-deficient miceCatherine B Millar, Jacky Guy, Owen J Sansom, et al.Human Molecular Genetics|July 9, 2005
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndromeUlrike A Nuber, Skirmantas Kriaucionis, Tim C Roloff, et al.Nature Communications|April 17, 2026
MeCP2 requires interactions with nucleosome linker DNA to read chromatin DNA methylationJames A Watson, Beatrice K Alexander-Howden, Theo S Hall, et al.Nanoscale|July 17, 2018
High affinity single-chain variable fragments are specific and versatile targeting motifs for extracellular vesiclesAndrea Longatti, Christina Schindler, Andie Collinson, et al.Pageof 10