Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome (Q28592236)

GOA release 2020-03-11

Histone deacetylase 1

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GOA release 2020-03-11

Shin-ichi Horike

1

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author name string

Shutao Cai

2

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31 January 2017

Masaru Miyano

3

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31 January 2017

Jan-Fang Cheng

4

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31 January 2017

Terumi Kohwi-Shigematsu

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

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31 January 2017

language of work or name

English

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publication date

1 January 2005

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31 January 2017

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31 January 2017

37

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31 January 2017

1

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31 January 2017

31–40

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31 January 2017

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

21 April 2017

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Methyl-CpG-binding protein, MeCP2, is a target molecule for maintenance DNA methyltransferase, Dnmt1

21 April 2017

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

21 April 2017

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Rett syndrome and MeCP2: linking epigenetics and neuronal function

21 April 2017

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Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

21 April 2017

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

21 April 2017

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Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

21 April 2017

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A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids

21 April 2017

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Translating the Histone Code

21 April 2017

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Capturing chromosome conformation

21 April 2017

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Looping and interaction between hypersensitive sites in the active beta-globin locus

21 April 2017

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Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

21 April 2017

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DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

21 April 2017

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Genome imprinting regulated by the mouse Polycomb group protein Eed

21 April 2017

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Tissue-specific nuclear architecture and gene expression regulated by SATB1

21 April 2017

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A tissue-specific MAR/SAR DNA-binding protein with unusual binding site recognition

21 April 2017

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SATB1 targets chromatin remodelling to regulate genes over long distances

21 April 2017

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Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

21 April 2017

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

21 April 2017

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Chromatin modification and epigenetic reprogramming in mammalian development

21 April 2017

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

21 April 2017

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

21 April 2017

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The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation

21 April 2017

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DNA methylation and Rett syndrome

21 January 2018

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Rett syndrome: a surprising result of mutation in MECP2.

21 January 2018

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

21 January 2018

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Parental imprinting and human disease

21 January 2018

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Methylation-dependent silencing at the H19 imprinting control region by MeCP2

21 January 2018

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MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

21 January 2018

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Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6.

21 January 2018

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Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6

21 January 2018

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Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines

21 January 2018

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Bone histomorphometry in three females with Rett syndrome

21 January 2018

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Dlx5, the mouse homologue of the human-imprinted DLX5 gene, is biallelically expressed in the mouse brain.

21 January 2018

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Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.

21 January 2018

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Looping versus linking: toward a model for long-distance gene activation

21 January 2018

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Long-range chromatin regulatory interactions in vivo

21 January 2018

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Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops

21 January 2018

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Chicken MAR-binding protein ARBP is homologous to rat methyl-CpG-binding protein MeCP2

21 January 2018

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A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q

21 January 2018

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LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

21 January 2018

1 reference

Identification of base-unpairing region-binding proteins and characterization of their in vivo binding sequences.

21 January 2018

1 reference

7 January 2021

Asb4, Ata3, and Dcn are novel imprinted genes identified by high-throughput screening using RIKEN cDNA microarray

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7 January 2021

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

1 reference

7 January 2021

Long-range intrachromosomal interactions in the T helper type 2 cytokine locus

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7 January 2021

Identifiers

DOI

10.1038/NG1491

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Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1632193

1021284694

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1632193

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference