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A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing
scientific journal article
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scholarly article
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stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
title
A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing
(English)
1 reference
stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
main subject
brain
0 references
author
Peter L. Jones
series ordinal
4
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author name string
Steven W. Long
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
Jenny Y. Y. Ooi
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
Peter M. Yau
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
publication date
1 October 2011
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stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
published in
Bioscience Reports
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stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
volume
31
1 reference
stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
issue
5
1 reference
stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
page(s)
333–343
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stated in
PubMed
PubMed ID
21070191
retrieved
31 January 2017
cites work
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MeCP2, a key contributor to neurological disease, activates and represses transcription
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19 March 2017
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes
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PubMed Central
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19 March 2017
Phosphorylation of methyl-CpG binding protein 2 (MeCP2) regulates the intracellular localization during neuronal cell differentiation
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Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing
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MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions
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PubMed Central
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19 March 2017
Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice
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PubMed Central
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19 March 2017
Identification of MeCP2 mutations in a series of females with autistic disorder
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Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
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19 March 2017
The Ski protein family is required for MeCP2-mediated transcriptional repression
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PubMed Central
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19 March 2017
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
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19 March 2017
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
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PubMed Central
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Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
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Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome
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The human U4/U6 snRNP contains 60 and 90kD proteins that are structurally homologous to the yeast splicing factors Prp4p and Prp3p
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19 March 2017
MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
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PubMed Central
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19 March 2017
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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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?
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7 April 2017
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
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Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.
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29 September 2017
Recent advances in MeCP2 structure and function
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29 September 2017
Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology
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PubMed Central
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29 September 2017
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
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29 September 2017
Formation of a Tap/NXF1 homotypic complex is mediated through the amino-terminal domain of Tap and enhances interaction with nucleoporins
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29 September 2017
MeCP2 interacts with HP1 and modulates its heterochromatin association during myogenic differentiation
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PubMed Central
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29 September 2017
Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.
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29 September 2017
MeCP2 dysfunction in humans and mice
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29 September 2017
ATPase/helicase activities of p68 RNA helicase are required for pre-mRNA splicing but not for assembly of the spliceosome
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29 September 2017
MeCP2 behaves as an elongated monomer that does not stably associate with the Sin3a chromatin remodeling complex
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29 September 2017
The RNA binding protein YB-1 binds A/C-rich exon enhancers and stimulates splicing of the CD44 alternative exon v4.
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29 September 2017
Up-regulation of a novel mRNA (NY-CO-1) involved in the methyl 4-methoxy-3-(3-methyl-2-butenoyl) benzoate (VT1)-induced proliferation arrest of a non-small-cell lung carcinoma cell line (NSCLC-N6).
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29 September 2017
Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein
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29 September 2017
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
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29 September 2017
On a unusual brain atrophy syndrome in hyperammonemia in childhood
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29 September 2017
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome
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3 June 2018
MECP2 mutation analysis in patients with mental retardation.
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Crossref
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21 January 2018
Identifiers
DOI
10.1042/BSR20100124
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
456646
OpenCitations bibliographic resource ID
456646
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
456646
PMCID
3148018
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
456646
PubMed ID
21070191
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
456646
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