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MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number
scientific journal article
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scholarly article
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stated in
PubMed
PubMed publication ID
17920015
retrieved
24 January 2017
title
MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number
(English)
1 reference
stated in
PubMed
PubMed publication ID
17920015
retrieved
24 January 2017
main subject
Methyl CpG binding protein 2
1 reference
stated in
GOA release 2020-03-11
author
Huda Zoghbi
series ordinal
2
0 references
Christian Rosenmund
series ordinal
3
0 references
author name string
Hsiao-Tuan Chao
series ordinal
1
1 reference
stated in
PubMed
PubMed publication ID
17920015
retrieved
24 January 2017
language of work or name
English
0 references
publication date
4 October 2007
1 reference
stated in
PubMed
PubMed publication ID
17920015
retrieved
24 January 2017
published in
Neuron
1 reference
stated in
PubMed
PubMed publication ID
17920015
retrieved
24 January 2017
volume
56
1 reference
stated in
PubMed
PubMed publication ID
17920015
retrieved
24 January 2017
issue
1
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stated in
PubMed
PubMed publication ID
17920015
retrieved
24 January 2017
page(s)
58–65
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PubMed
PubMed publication ID
17920015
retrieved
24 January 2017
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ImageJ
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Europe PubMed Central
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11 June 2022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2198899/fullTextXML
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inferred from PubMed Central ID database lookup
cites work
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
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PubMed Central
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Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome
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Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome
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19 March 2017
Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome
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Homeostatic plasticity in the developing nervous system
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Identification of MeCP2 mutations in a series of females with autistic disorder
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
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19 March 2017
Short-term synaptic plasticity
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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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PubMed Central
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19 March 2017
Identification of a vesicular glutamate transporter that defines a glutamatergic phenotype in neurons
1 reference
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PubMed Central
reference URL
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19 March 2017
Uptake of glutamate into synaptic vesicles by an inorganic phosphate transporter
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PubMed Central
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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
reference URL
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19 March 2017
Interaction between the C terminus of NMDA receptor subunits and multiple members of the PSD-95 family of membrane-associated guanylate kinases
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PubMed Central
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19 March 2017
Domain interaction between NMDA receptor subunits and the postsynaptic density protein PSD-95
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2198899
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19 March 2017
The rat brain postsynaptic density fraction contains a homolog of the Drosophila discs-large tumor suppressor protein
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PubMed Central
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19 March 2017
Reversal of neurological defects in a mouse model of Rett syndrome
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PubMed Central
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7 April 2017
Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2198899
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7 April 2017
Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?
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PubMed Central
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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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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2198899
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7 April 2017
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
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PubMed Central
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7 April 2017
Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2198899
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29 September 2017
Homeostatic control of neural activity: from phenomenology to molecular design
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PubMed Central
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29 September 2017
Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2198899
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29 September 2017
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males
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PubMed Central
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29 September 2017
Morphological study of neocortical areas in Rett syndrome
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PubMed Central
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29 September 2017
Selective dendritic alterations in the cortex of Rett syndrome
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29 September 2017
SAP90, a rat presynaptic protein related to the product of the Drosophila tumor suppressor gene dlg-A.
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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
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PubMed Central
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29 September 2017
On a unusual brain atrophy syndrome in hyperammonemia in childhood
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PubMed Central
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29 September 2017
Excitatory and inhibitory autaptic currents in isolated hippocampal neurons maintained in cell culture
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2198899
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29 September 2017
Three-dimensional structure of dendritic spines and synapses in rat hippocampus (CA1) at postnatal day 15 and adult ages: implications for the maturation of synaptic physiology and long-term potentiation
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PubMed Central
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2 June 2018
Synaptic vesicles recycling spontaneously and during activity belong to the same vesicle pool
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=2198899
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27 November 2018
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=2198899
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27 November 2018
Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28.
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=2198899
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27 November 2018
MeCP2-dependent transcriptional repression regulates excitatory neurotransmission
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=2198899
retrieved
27 November 2018
Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).
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=2198899
retrieved
27 November 2018
Mild overexpression of MeCP2 causes a progressive neurological disorder 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=2198899
retrieved
27 November 2018
The effects of temperature on vesicular supply and release in autaptic cultures of rat and mouse hippocampal neurons
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2198899
retrieved
27 November 2018
MECP2 is highly mutated in X-linked mental retardation
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=2198899
retrieved
27 November 2018
MECP2 mutation in male patients with non-specific X-linked mental retardation.
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=2198899
retrieved
27 November 2018
Released fraction and total size of a pool of immediately available transmitter quanta at a calyx synapse
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=2198899
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27 November 2018
Heterogeneity in the molecular composition of excitatory postsynaptic sites during development of hippocampal neurons in culture.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2198899
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27 November 2018
The probability of transmitter release at a mammalian central synapse.
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=2198899
retrieved
27 November 2018
Nonuniform probability of glutamate release at a hippocampal synapse
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17920015
retrieved
12 December 2020
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Identifiers
DOI
10.1016/J.NEURON.2007.08.018
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
636158
OpenCitations bibliographic resource ID
636158
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
636158
PMC publication ID
2198899
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
636158
PubMed publication ID
17920015
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
636158
ResearchGate publication ID
5925093
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