(Q28177120)

2

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Nick Adkins

3

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Christopher L Woodcock

4

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Paul A Wade

5

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Jeffrey C Hansen

Journal of Biological Chemistry

6

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language of work or name

English

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publication date

22 August 2003

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published in

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volume

278

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issue

34

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page(s)

32181-8

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cites work

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Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome

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The DNA methyltransferases of mammals

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Methyl CpG-binding proteins and transcriptional repression

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

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Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

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Functional consequences of Rett syndrome mutations on human MeCP2.

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MENT, a heterochromatin protein that mediates higher order chromatin folding, is a new serpin family member

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Cooperative binding of the globular domains of histones H1 and H5 to DNA

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Solution structure of the methyl-CpG binding domain of human MBD1 in complex with methylated DNA

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DNA recognition by the methyl-CpG binding domain of MeCP2.

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Nucleosomes, linker DNA, and linker histone form a unique structural motif that directs the higher-order folding and compaction of chromatin

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DNA methylation specifies chromosomal localization of MeCP2.

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Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

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Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA

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The solution structure of the domain from MeCP2 that binds to methylated DNA

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MeCP2 driven transcriptional repression in vitro: selectivity for methylated DNA, action at a distance and contacts with the basal transcription machinery

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Methyl-CpG-binding protein MeCP2 represses Sp1-activated transcription of the human leukosialin gene when the promoter is methylated

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Identifiers

DOI

10.1074/JBC.M305308200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12788925

1 reference

Consolidated OpenCitations Corpus – April 2017