A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos

retracted scientific article

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos is …
instance of (P31):
scholarly articleQ13442814
retracted paperQ45182324

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P356DOI10.1016/S1097-2765(03)00276-4
P698PubMed publication ID14536082

P50authorHuda ZoghbiQ1633764
Irina StanchevaQ30505459
Richard MeehanQ42846183
P2093author name stringAnne L Collins
Ingatia B Van den Veyver
P2860cites workEarly neurogenesis in Xenopus: the spatio-temporal pattern of proliferation and cell lineages in the embryonic spinal cordQ46228698
Molecular targets of vertebrate segmentation: two mechanisms control segmental expression of Xenopus hairy2 during somite formationQ48333452
The Vi element. A transposon-like repeated DNA sequence interspersed in the vitellogenin locus of Xenopus laevisQ48372410
Intrinsic differences between the superficial and deep layers of the Xenopus ectoderm control primary neuronal differentiationQ48559576
DNA methylation patterns and epigenetic memoryQ22065780
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2Q22337290
The Ski protein family is required for MeCP2-mediated transcriptional repressionQ24291417
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complexQ24324026
Nuclear localization of CBF1 is regulated by interactions with the SMRT corepressor complexQ24550850
A histone deacetylase corepressor complex regulates the Notch signal transduction pathwayQ24598533
Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNAQ28265233
Species-specific organization of CpG island promoters at mammalian homologous genesQ28343947
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndromeQ28504458
MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatinQ28576622
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcriptionQ29547568
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in miceQ29616328
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3Q29616516
Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus EmbryosQ29620084
Functional consequences of Rett syndrome mutations on human MeCP2.Q33826022
Co-localization of Polycomb protein and GAGA factor on regulatory elements responsible for the maintenance of homeotic gene expressionQ33886885
Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlationsQ34141668
Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brainQ34387585
Methyl CpG-binding proteins and transcriptional repressionQ34464674
Neurogenesis in embryos and in adult neural stem cells.Q34516002
Vertebrate hairy and Enhancer of split related proteins: transcriptional repressors regulating cellular differentiation and embryonic patterningQ34526571
DNA methylation in animal developmentQ35043702
In vivo repression of an erythroid-specific gene by distinct corepressor complexesQ39644809
Loss of the maintenance methyltransferase, xDnmt1, induces apoptosis in Xenopus embryosQ39645050
Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulationQ40834659
DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryosQ43887369
P433issue2
P921main subjectRett syndromeQ917357
P304page(s)425-435
P577publication date2003-08-01
P1433published inMolecular CellQ3319468
P1476titleA mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos
P478volume12

Reverse relations

cites work (P2860)
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