Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows (Q34278418)

1 August 2017

title

Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows (English)

1 reference

1 August 2017

Hélène Cheval

1

1 reference

ORCID Public Data File 2021

author name string

Jacky Guy

2

1 reference

1 August 2017

Cara Merusi

3

1 reference

1 August 2017

Dina De Sousa

4

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1 August 2017

Jim Selfridge

5

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1 August 2017

Adrian Bird

6

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1 August 2017

publication date

31 May 2012

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1 August 2017

published in

Human Molecular Genetics

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1 August 2017

volume

21

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1 August 2017

issue

17

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1 August 2017

page(s)

3806-3814

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describes a project that uses

1 August 2017

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3412380/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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6 July 2018

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Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.

6 July 2018

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Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome

6 July 2018

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Paradoxical role of an Egr transcription factor family member, Egr2/Krox20, in learning and memory

6 July 2018

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A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

6 July 2018

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MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions

6 July 2018

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Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain

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Efficient recombination in diverse tissues by a tamoxifen-inducible form of Cre: a tool for temporally regulated gene activation/inactivation in the mouse

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

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

6 July 2018

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

6 July 2018

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6 July 2018

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Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study

6 July 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDS208

Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic mice

21 January 2018

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Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDS208

An altered neonatal behavioral phenotype in Mecp2 mutant mice.

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDS208

Two affected boys in a Rett syndrome family: clinical and molecular findings

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/22653753

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Neuropathology of Rett syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22653753

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDS208

1 reference

1 August 2017

1 reference

1 August 2017

1 reference