Retraction Notice to: A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos (A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos (2003) 12(2) (425–435), (S1097276503002764), (10.1016/S1097-2765(03)00276-4));A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by Notch in Xenopus embryos

Molecular Cell

Volumn 12, Issue 2, 2003, Pages 425-435

  Stancheva, Irina ^a   Collins, Anne L ^b   Van Den Veyver, Ingatia B ^b   Zoghbi, Huda ^b,c   Meehan, Richard R ^a  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b Dept of Molec and Human Genetics ^*  (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA BINDING PROTEIN; DNA BINDING PROTEIN MECP2; MUTANT PROTEIN; NOTCH RECEPTOR; REPRESSOR PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL DIFFERENTIATION; CONTROLLED STUDY; DNA METHYLATION; EMBRYO; GENE ACTIVATION; GENE CONTROL; GENE EXPRESSION REGULATION; GENE MUTATION; GENE SILENCING; NERVE CELL; NERVOUS SYSTEM DEVELOPMENT; NEUROECTODERM; NONHUMAN; PROMOTER REGION; PROTEIN BINDING; PROTEIN PROTEIN INTERACTION; REPRESSOR GENE; RETT SYNDROME; SILENCER GENE; XENOPUS LAEVIS;

ANIMALIA; XENOPUS LAEVIS;

EID: 0043178993     PISSN: 10972765     EISSN: 10974164     Source Type: Journal    
DOI: 10.1016/j.molcel.2019.02.022     Document Type: Erratum

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