MeCP2 is critical for maintaining mature neuronal networks and global brain anatomy during late stages of postnatal brain development and in the mature adult brain (Q36288388)

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English	MeCP2 is critical for maintaining mature neuronal networks and global brain anatomy during late stages of postnatal brain development and in the mature adult brain	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

13 August 2017

MeCP2 is critical for maintaining mature neuronal networks and global brain anatomy during late stages of postnatal brain development and in the mature adult brain (English)

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Europe PubMed Central

PMC publication ID

13 August 2017

author name string

Minh Vu Chuong Nguyen

1

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13 August 2017

Fang Du

2

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13 August 2017

Christy A Felice

3

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Europe PubMed Central

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13 August 2017

Xiwei Shan

4

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13 August 2017

Aparna Nigam

5

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13 August 2017

Gail Mandel

6

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13 August 2017

John K Robinson

7

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13 August 2017

Nurit Ballas

8

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13 August 2017

language of work or name

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publication date

1 July 2012

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13 August 2017

Journal of Neuroscience

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13 August 2017

32

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13 August 2017

29

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Europe PubMed Central

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13 August 2017

10021-10034

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Europe PubMed Central

PMC publication ID

13 August 2017

describes a project that uses

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3461266/fullTextXML

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Wild-type microglia arrest pathology in a mouse model of Rett syndrome

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A role for glia in the progression of Rett's syndrome

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30 September 2017

Experience-dependent retinogeniculate synapse remodeling is abnormal in MeCP2-deficient mice

1 reference

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Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

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30 September 2017

Genome-wide analysis reveals methyl-CpG-binding protein 2-dependent regulation of microRNAs in a mouse model of Rett syndrome

1 reference

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Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome

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Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate

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Look who is weaving the neural web: glial control of synapse formation

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Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions

1 reference

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

1 reference

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Expression of GABA(B) receptors is altered in brains of subjects with autism

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Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches

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30 September 2017

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

1 reference

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30 September 2017

The regulation of dendritic arbor development and plasticity by glutamatergic synaptic input: a review of the synaptotrophic hypothesis

1 reference

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30 September 2017

Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.

1 reference

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30 September 2017

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

1 reference

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Reversal of neurological defects in a mouse model of Rett syndrome

1 reference

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Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

1 reference

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AMPA receptors regulate experience-dependent dendritic arbor growth in vivo

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

1 reference

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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

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

1 reference

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Dendritic organization in the neurons of the visual and motor cortices of the cat

1 reference

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Selective regulation of neurite extension and synapse formation by the beta but not the alpha isoform of CaMKII

1 reference

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Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461266

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

1 reference

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Regulation of neuronal traits by a novel transcriptional complex

1 reference

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

1 reference

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

1 reference

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Selective dendritic alterations in the cortex of Rett syndrome

1 reference

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Adult neural function requires MeCP2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461266

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

1 reference

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22 September 2018

Identifiers

10.1523/JNEUROSCI.1316-12.2012

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

ResearchGate publication ID

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