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Nature Communications|May 16, 2026
Dysfunction of a SET3-like complex underlies a family of related neurological disordersKatie M Paton, Beatrice Alexander-Howden, Jenna I Hare, et al.Nature|April 16, 2010
CpG islands influence chromatin structure via the CpG-binding protein Cfp1John P Thomson, Peter J Skene, Jim Selfridge, et al.Nature Neuroscience|June 18, 2013
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressorMatthew J Lyst, Robert Ekiert, Daniel H Ebert, et al.Human Molecular Genetics|February 8, 2017
Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypesPaul D Ross, Jacky Guy, Jim Selfridge, et al.Neuroscience Research|October 18, 2015
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndromeAlessio Cortelazzo, Claudio De Felice, Roberto Guerranti, et al.Nature Communications|August 19, 2020
Identifying proteins bound to native mitotic ESC chromosomes reveals chromatin repressors are important for compactionDounia Djeghloul, Bhavik Patel, Holger Kramer, et al.Neurobiology of Disease|April 29, 2014
Oxidative brain damage in Mecp2-mutant murine models of Rett syndromeClaudio De Felice, Floriana Della Ragione, Cinzia Signorini, et al.Disease Models & Mechanisms|November 2, 2012
Preclinical research in Rett syndrome: setting the foundation for translational successDavid M Katz, Joanne E Berger-Sweeney, James H Eubanks, et al.Pageof 3