Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology (Q35099241)

6 August 2017

title

Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology (English)

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6 August 2017

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Nurit Ballas

1

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6 August 2017

Daniel T Lioy

series ordinal

2

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6 August 2017

Christopher Grunseich

series ordinal

3

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6 August 2017

Gail Mandel

series ordinal

4

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6 August 2017

language of work or name

English

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publication date

22 February 2009

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6 August 2017

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6 August 2017

volume

12

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6 August 2017

issue

3

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6 August 2017

page(s)

311-317

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

6 August 2017

cites work

1 reference

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Mutant SOD1 in cell types other than motor neurons and oligodendrocytes accelerates onset of disease in ALS mice.

9 July 2018

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

9 July 2018

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The story of Rett syndrome: from clinic to neurobiology

9 July 2018

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Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease

9 July 2018

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MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

9 July 2018

1 reference

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Dynamic changes in Histone H3 lysine 9 acetylation localization patterns during neuronal maturation require MeCP2.

9 July 2018

1 reference

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Culturing hippocampal neurons

9 July 2018

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Reversal of neurological defects in a mouse model of Rett syndrome

9 July 2018

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Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

9 July 2018

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Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model

9 July 2018

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Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation

9 July 2018

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Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome

9 July 2018

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Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

9 July 2018

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Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice

9 July 2018

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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

9 July 2018

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Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome

9 July 2018

1 reference

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Hyaluronan accumulates in demyelinated lesions and inhibits oligodendrocyte progenitor maturation.

9 July 2018

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

9 July 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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Human endogenous retrovirus glycoprotein-mediated induction of redox reactants causes oligodendrocyte death and demyelination

9 July 2018

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DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

9 July 2018

1 reference

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Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

9 July 2018

1 reference

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DNA methylation and Rett syndrome

9 July 2018

1 reference

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.

9 July 2018

1 reference

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Regulation of neuronal traits by a novel transcriptional complex

9 July 2018

1 reference

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Glutamate transporters in neurologic disease

9 July 2018

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Control of synapse number by glia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

The co-repressor mSin3A is a functional component of the REST-CoREST repressor complex

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Selective dendritic alterations in the cortex of Rett syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Brain magnetic resonance study of Mecp2 deletion effects on anatomy and metabolism

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Optimization of oligodendrocyte progenitor cell culture method for enhanced survival

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3134296

Trophic interactions between astroglial cells and hippocampal neurons in culture

27 September 2018

1 reference

12 December 2020

Neuropathology of Rett syndrome

1 reference

12 December 2020

Preliminary evidence for neurodegenerative changes in the substantia nigra of Rett syndrome

1 reference

12 December 2020

Cerebral proton magnetic resonance spectroscopy in Rett syndrome

1 reference

12 December 2020

The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA

1 reference

12 December 2020

Neuropathology of Rett syndrome

1 reference

12 December 2020

Extraction, purification and analysis of histones

1 reference

12 December 2020

Identifiers

DOI

10.1038/NN.2275

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6 August 2017

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6 August 2017

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