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Complexities of Rett syndrome and MeCP2
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scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
review article
1 reference
stated in
Europe PubMed Central
title
Complexities of Rett syndrome and MeCP2
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
main subject
Rett syndrome
0 references
author
Rodney Samaco
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
Jeffrey L. Neul
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
Jeffrey L. Neul
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2
object named as
Jeffrey L Neul
1 reference
stated in
Europe PubMed Central
PubMed ID
21632916
retrieved
6 August 2017
language of work or name
English
0 references
publication date
1 June 2011
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
published in
Journal of Neuroscience
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
volume
31
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
issue
22
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
page(s)
7951-7959
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
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MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons
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MeCP2 deficiency disrupts axonal guidance, fasciculation, and targeting by altering Semaphorin 3F function.
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8 July 2018
Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions
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Recent advances in MeCP2 structure and function
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8 July 2018
Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology
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Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.
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8 July 2018
Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations
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8 July 2018
Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice
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8 July 2018
MECP2 genomic structure and function: insights from ENCODE
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8 July 2018
Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.
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8 July 2018
Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches
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8 July 2018
A set of differentially expressed miRNAs, including miR-30a-5p, act as post-transcriptional inhibitors of BDNF in prefrontal cortex
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8 July 2018
MeCP2, a key contributor to neurological disease, activates and represses transcription
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8 July 2018
Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.
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8 July 2018
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
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8 July 2018
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
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8 July 2018
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes
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8 July 2018
Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA
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8 July 2018
The story of Rett syndrome: from clinic to neurobiology
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8 July 2018
Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice
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8 July 2018
Brain-derived neurotrophic factor expression and respiratory function improve after ampakine treatment in a mouse model of Rett syndrome.
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8 July 2018
The roles of binding site arrangement and combinatorial targeting in microRNA repression of gene expression
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8 July 2018
Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets
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8 July 2018
Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons
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8 July 2018
Reversal of neurological defects in a mouse model of Rett syndrome
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8 July 2018
Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation
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8 July 2018
Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome
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8 July 2018
Rett syndrome in Australia: a review of the epidemiology.
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8 July 2018
Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice
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8 July 2018
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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8 July 2018
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome
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8 July 2018
Rett syndrome: of girls and mice--lessons for regression in autism
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8 July 2018
X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.
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8 July 2018
Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice
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PubMed Central
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8 July 2018
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
1 reference
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PubMed Central
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8 July 2018
X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome
1 reference
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PubMed Central
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8 July 2018
Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation 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=3127460
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8 July 2018
Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain
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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=3127460
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8 July 2018
Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations
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PubMed Central
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8 July 2018
Corepressor-dependent silencing of chromosomal regions encoding neuronal genes
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127460
retrieved
8 July 2018
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=3127460
retrieved
8 July 2018
Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal 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=3127460
retrieved
8 July 2018
Methyl-CpG-binding protein 2 represses LINE-1 expression and retrotransposition but not Alu 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=3127460
retrieved
8 July 2018
Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.
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=3127460
retrieved
8 July 2018
Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry
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=3127460
retrieved
8 July 2018
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=3127460
retrieved
8 July 2018
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=3127460
retrieved
8 July 2018
Dendritic anomalies in disorders associated with 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=3127460
retrieved
8 July 2018
Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions
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=3127460
retrieved
8 July 2018
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=3127460
retrieved
8 July 2018
Rett syndrome: randomized controlled trial of L-carnitine
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=3127460
retrieved
8 July 2018
The preserved speech variant: a subgroup of the Rett complex: a clinical report of 30 cases
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=3127460
retrieved
8 July 2018
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=3127460
retrieved
8 July 2018
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=3127460
retrieved
8 July 2018
MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
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=3127460
retrieved
8 July 2018
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, 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=3127460
retrieved
8 July 2018
Neuroanatomy of Rett syndrome: a volumetric imaging study
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=3127460
retrieved
8 July 2018
Dissection of the methyl-CpG binding domain from the chromosomal protein 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=3127460
retrieved
8 July 2018
Rett syndrome: controlled study of an oral opiate antagonist, naltrexone.
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=3127460
retrieved
8 July 2018
Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.
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=3127460
retrieved
8 July 2018
Molecular properties of somatostatin receptors.
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=3127460
retrieved
8 July 2018
On a unusual brain atrophy syndrome in hyperammonemia in childhood
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=3127460
retrieved
8 July 2018
Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.
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=3127460
retrieved
8 July 2018
Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA
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=3127460
retrieved
8 July 2018
Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA
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=3127460
retrieved
8 July 2018
Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
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=3127460
retrieved
27 September 2018
Early developmental regression in autism spectrum disorder: evidence from an international multiplex sample.
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=3127460
retrieved
27 September 2018
Brief report: childhood disintegrative disorder: a brief examination of eight case studies.
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=3127460
retrieved
27 September 2018
Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation.
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=3127460
retrieved
27 September 2018
Differential distribution of the MeCP2 splice variants in the postnatal mouse brain
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=3127460
retrieved
27 September 2018
The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.
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=3127460
retrieved
27 September 2018
Rett syndrome: long-term clinical follow-up experiences over four decades.
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=3127460
retrieved
27 September 2018
REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis.
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=3127460
retrieved
27 September 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=3127460
retrieved
27 September 2018
A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression
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=3127460
retrieved
27 September 2018
The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.
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=3127460
retrieved
27 September 2018
Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.
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=3127460
retrieved
27 September 2018
Neuropathology of Rett syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21632916
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Rett syndrome: an overlooked diagnosis in women with stereotypic hand movements, psychomotor retardation, Parkinsonism, and dystonia?
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21632916
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Neuropathology of Rett syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21632916
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Rett syndrome: analysis of deaths in the British survey
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21632916
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Neuropathology of Rett syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21632916
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1523/JNEUROSCI.0169-11.2011
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
PMCID
3127460
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
PubMed ID
21632916
1 reference
stated in
Europe PubMed Central
PMCID
3127460
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21632916%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 February 2020
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