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The yin and yang of MeCP2 phosphorylation
scholarly article
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
title
The yin and yang of MeCP2 phosphorylation
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
main subject
phosphorylation
0 references
author
Huda Zoghbi
object named as
Huda Y Zoghbi
series ordinal
2
0 references
author name string
Hsiao-Tuan Chao
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
language of work or name
English
0 references
publication date
17 March 2009
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
volume
106
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
issue
12
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
page(s)
4577-4578
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
cites work
Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Disruption of Nectin-like 1 cell adhesion molecule leads to delayed axonal myelination in the CNS.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
MeCP2, a key contributor to neurological disease, activates and represses transcription
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Calcineurin as a multifunctional regulator
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
14 September 2017
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
3 September 2018
Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
3 September 2018
A complete genetic analysis of neuronal Rab3 function.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
3 September 2018
Astrocytes contain a vesicular compartment that is competent for regulated exocytosis of glutamate
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2660756
retrieved
3 September 2018
Identifiers
DOI
10.1073/PNAS.0901518106
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
ADS bibcode
2009PNAS..106.4577C
0 references
PMC publication ID
2660756
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
PubMed publication ID
19293386
1 reference
stated in
Europe PubMed Central
PMC publication ID
2660756
retrieved
18 August 2017
ResearchGate publication ID
24207512
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