(Q52087714)

21 April 2018

title

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. (English)

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21 April 2018

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neurological disorder

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8

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Jeffrey L. Noebels

object named as

Jeffrey L Noebels

6

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author name string

Ann L Collins

1

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21 April 2018

Jonathan M Levenson

2

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21 April 2018

Alexander P Vilaythong

3

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21 April 2018

Ronald Richman

4

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21 April 2018

Dawna L Armstrong

5

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J David Sweatt

7

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publication date

6 September 2004

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21 April 2018

published in

Human Molecular Genetics

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21 April 2018

volume

13

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21 April 2018

page(s)

2679-2689

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21 April 2018

issue

21

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21 April 2018

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

cites work

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https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

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

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

Precipitous release of methyl-CpG binding protein 2 and histone deacetylase 1 from the methylated human multidrug resistance gene (MDR1) on activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH282

21 January 2018

Identifiers

DOI

10.1093/HMG/DDH282

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21 April 2018

PubMed ID

15351775

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21 April 2018