A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos (Q33973072)

30 July 2017

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

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30 July 2017

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1

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30 July 2017

4

Huda Zoghbi

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Richard Meehan

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Richard R Meehan

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5

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author name string

Anne L Collins

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2

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PubMed ID

14536082

30 July 2017

Ingatia B Van den Veyver

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3

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30 July 2017

1 August 2003

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30 July 2017

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30 July 2017

12

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2

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30 July 2017

425-435

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Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations

30 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

DNA methylation patterns and epigenetic memory

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Intrinsic differences between the superficial and deep layers of the Xenopus ectoderm control primary neuronal differentiation.

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Species-specific organization of CpG island promoters at mammalian homologous genes

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Vertebrate hairy and Enhancer of split related proteins: transcriptional repressors regulating cellular differentiation and embryonic patterning

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Molecular targets of vertebrate segmentation: two mechanisms control segmental expression of Xenopus hairy2 during somite formation.

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus Embryos

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Early neurogenesis in Xenopus: the spatio-temporal pattern of proliferation and cell lineages in the embryonic spinal cord

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

A histone deacetylase corepressor complex regulates the Notch signal transduction pathway

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Neurogenesis in embryos and in adult neural stem cells.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

The Ski protein family is required for MeCP2-mediated transcriptional repression

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

DNA methylation in animal development

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

In vivo repression of an erythroid-specific gene by distinct corepressor complexes

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

The Vi element. A transposon-like repeated DNA sequence interspersed in the vitellogenin locus of Xenopus laevis.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Loss of the maintenance methyltransferase, xDnmt1, induces apoptosis in Xenopus embryos

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryos

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Co-localization of Polycomb protein and GAGA factor on regulatory elements responsible for the maintenance of homeotic gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Methyl CpG-binding proteins and transcriptional repression

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https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Functional consequences of Rett syndrome mutations on human MeCP2.

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

Nuclear localization of CBF1 is regulated by interactions with the SMRT corepressor complex

1 reference

https://api.crossref.org/works/10.1016%2FS1097-2765%2803%2900276-4

7 January 2021

10.1016/S1097-2765(03)00276-4

Identifiers

DOI

1 reference

30 July 2017

1 reference

PubMed ID

14536082