Found 3 results
Filters: Keyword is Rett Syndrome  [Clear All Filters]
2015
Gabel HW, Kinde B, Stroud H, Gilbert CS, Harmin DA, Kastan NR, Hemberg M, Ebert DH, Greenberg ME.  2015.  Disruption of DNA-methylation-dependent long gene repression in Rett syndrome.. Nature. 522(7554):89-93.
2013
Ebert DH, Gabel HW, Robinson ND, Kastan NR, Hu LS, Cohen S, Navarro AJ, Lyst MJ, Ekiert R, Bird AP et al..  2013.  Activity-dependent phosphorylation of MeCP2 threonine 308 regulates interaction with NCoR.. Nature. 499(7458):341-5.
Lyst MJ, Ekiert R, Ebert DH, Merusi C, Nowak J, Selfridge J, Guy J, Kastan NR, Robinson ND, Alves Fde Lima et al..  2013.  Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.. Nat Neurosci. 16(7):898-902.