(Q36288388)

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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

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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)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

author name string

Minh Vu Chuong Nguyen

1

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Europe PubMed Central

PMC publication ID

13 August 2017

Fang Du

2

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Europe PubMed Central

PMC publication ID

13 August 2017

Christy A Felice

3

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Europe PubMed Central

PMC publication ID

13 August 2017

Xiwei Shan

4

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Europe PubMed Central

PMC publication ID

13 August 2017

Aparna Nigam

5

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Europe PubMed Central

PMC publication ID

13 August 2017

Gail Mandel

6

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Europe PubMed Central

PMC publication ID

13 August 2017

John K Robinson

7

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Europe PubMed Central

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13 August 2017

Nurit Ballas

8

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Europe PubMed Central

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13 August 2017

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publication date

1 July 2012

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Europe PubMed Central

PMC publication ID

13 August 2017

Journal of Neuroscience

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Europe PubMed Central

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13 August 2017

32

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Europe PubMed Central

PMC publication ID

13 August 2017

29

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Europe PubMed Central

PMC publication ID

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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Europe PubMed Central

11 June 2022

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

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

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

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

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

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

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Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

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

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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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