(Q38853829)

7 September 2017

1 reference

title

MECP2, a multi-talented modulator of chromatin architecture (English)

1 reference

7 September 2017

Salvatore Fioriniello

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Giuseppe Pepe

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

author name string

Floriana Della Ragione

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Marcella Vacca

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Maurizio D'Esposito

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

publication date

12 June 2016

1 reference

Briefings in functional genomics

7 September 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

volume

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

page(s)

420-431

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

Methyl-CpG-binding domain proteins: readers of the epigenome

8 June 2020

cites work

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DNA methylation landscapes: provocative insights from epigenomics

21 January 2018

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Multivalent engagement of chromatin modifications by linked binding modules

21 January 2018

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DNA methylation 40 years later: Its role in human health and disease

21 January 2018

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Structure and function of eukaryotic DNA methyltransferases

21 January 2018

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Genome-wide profiling of DNA methylation in human cancer cells

21 January 2018

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Reconfiguration of nucleosome-depleted regions at distal regulatory elements accompanies DNA methylation of enhancers and insulators in cancer

21 January 2018

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Targeted and genome-scale strategies reveal gene-body methylation signatures in human cells

21 January 2018

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Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

21 January 2018

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DNA methylation and control of gene expression in vertebrate development

21 January 2018

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Gene number, noise reduction and biological complexity

21 January 2018

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Identification and characterization of a family of mammalian methyl-CpG binding proteins

21 January 2018

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The methyl-CpG binding domain and the evolving role of DNA methylation in animals

21 January 2018

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A Drosophila MBD family member is a transcriptional corepressor associated with specific genes

21 January 2018

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Methyl-CpG binding domain 1 (MBD1) interacts with the Suv39h1-HP1 heterochromatic complex for DNA methylation-based transcriptional repression

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

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

21 January 2018

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Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.

21 January 2018

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Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.

21 January 2018

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A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

21 January 2018

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Rett syndrome: revised diagnostic criteria and nomenclature

21 January 2018

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The story of Rett syndrome: from clinic to neurobiology

21 January 2018

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Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain

21 January 2018

1 reference

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Functional consequences of Rett syndrome mutations on human MeCP2.

21 January 2018

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https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

The MECP2 duplication syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

DNA binding selectivity of MeCP2 due to a requirement for A/T sequences adjacent to methyl-CpG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

An AT-hook domain in MeCP2 determines the clinical course of Rett syndrome and related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

X inactivation and reactivation in X-linked diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Differential distribution of the MeCP2 splice variants in the postnatal mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

The major form of MeCP2 has a novel N-terminus generated by alternative splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Intrinsic disorder and autonomous domain function in the multifunctional nuclear protein, MeCP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Direct homo- and hetero-interactions of MeCP2 and MBD2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

21 January 2018

1 reference

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MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions

21 January 2018

1 reference

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Experimental models of Rett syndrome based on Mecp2 dysfunction.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Molecular biology. MeCP2 repression goes nonglobal.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

MeCP2, a key contributor to neurological disease, activates and represses transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Cell-type-specific repression by methyl-CpG-binding protein 2 is biased toward long genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Analysis of neonatal brain lacking ATRX or MeCP2 reveals changes in nucleosome density, CTCF binding and chromatin looping

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

MeCP2 interacts with HP1 and modulates its heterochromatin association during myogenic differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

L1 retrotransposition in neurons is modulated by MeCP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

RNA truncation by premature polyadenylation attenuates human mobile element activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

ATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Methyl CpG-binding proteins and transcriptional repression

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

ATRX in chromatin assembly and genome architecture during development and disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Syndromal mental retardation due to mutations in a regulator of gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Testing for association between MeCP2 and the brahma-associated SWI/SNF chromatin-remodeling complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Self-interaction of heterochromatin protein 1 is required for direct binding to histone methyltransferase, SUV39H1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Methyl CpG-binding proteins induce large-scale chromatin reorganization during terminal differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Multiple modes of interaction between the methylated DNA binding protein MeCP2 and chromatin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Global epigenomic reconfiguration during mammalian brain development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Reading the unique DNA methylation landscape of the brain: Non-CpG methylation, hydroxymethylation, and MeCP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Distribution, recognition and regulation of non-CpG methylation in the adult mammalian brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

MeCP2 binds to 5hmC enriched within active genes and accessible chromatin in the nervous system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Disruption of DNA-methylation-dependent long gene repression in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

The MBD protein family-reading an epigenetic mark?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Chromatin compaction by human MeCP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

MeCP2 binds cooperatively to its substrate and competes with histone H1 for chromatin binding sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Higher order structure in a short repeat length chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Neuronal nuclei and glial nuclei from mammalian cerebral cortex. Nucleosome repeat lengths, DNA contents and H1 contents.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Integrative analysis of the cancer transcriptome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Reversible disruption of pericentric heterochromatin and centromere function by inhibiting deacetylases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

A functional enhancer suppresses silencing of a transgene and prevents its localization close to centrometric heterochromatin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Dynamic repositioning of genes in the nucleus of lymphocytes preparing for cell division

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Position-effect variegation and the new biology of heterochromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Heterochromatin maintenance and establishment: lessons from the mouse pericentromere

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Mouse centric and pericentric satellite repeats form distinct functional heterochromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

A high-resolution imaging approach to investigate chromatin architecture in complex tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

DNA methylation specifies chromosomal localization of MeCP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

MeCP2 Rett mutations affect large scale chromatin organization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Targeted manipulation of heterochromatin rescues MeCP2 Rett mutants and re-establishes higher order chromatin organization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

SUMOylation of MeCP2 is essential for transcriptional repression and hippocampal synapse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Impaired in vivo binding of MeCP2 to chromatin in the absence of its DNA methyl-binding domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

Gene repositioning within the cell nucleus is not random and is determined by its genomic neighborhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELW023

21 January 2018

Identifiers

DOI

10.1093/BFGP/ELW023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27296483%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

1 reference