(Q29616516)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

30 April 2017

0 references

9

Zoghbi H

1 reference

30 April 2017

6

Noebels J

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

30 April 2017

author name string

Shahbazian M

1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

30 April 2017

Young J

2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

30 April 2017

Yuva-Paylor L

3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

30 April 2017

Spencer C

4

1 reference

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30 April 2017

Antalffy B

5

1 reference

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Armstrong D

7

1 reference

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30 April 2017

Paylor R

8

1 reference

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

30 April 2017

language of work or name

1 reference

30 April 2017

publication date

18 July 2002

1 reference

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30 April 2017

1 reference

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volume

35

1 reference

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page(s)

243-54

1 reference

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issue

2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

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

30 April 2017

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Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

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MECP2 mutations account for most cases of typical forms of Rett syndrome.

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Functional divergence between histone deacetylases in fission yeast by distinct cellular localization and in vivo specificity

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A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients

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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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MECP2 mutation in a boy with language disorder and schizophrenia

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Rett syndrome: characterization of seizures versus non-seizures

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DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1.

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

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Rett variants: a suggested model for inclusion criteria.

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

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MeCP2 mutations in children with and without the phenotype of Rett syndrome

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MECP2 mutation in non-fatal, non-progressive encephalopathy in a male

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The Ski protein family is required for MeCP2-mediated transcriptional repression

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Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

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7 January 2021

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

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Social Dominance in Inbred Mouse Strains

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Methylation-mediated proviral silencing is associated with MeCP2 recruitment and localized histone H3 deacetylation

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A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

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7 January 2021

A new test for aggression in rats without aversive stimulation: Differential effects of d-amphetamine and cocaine

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Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

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DNA methylation specifies chromosomal localization of MeCP2.

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

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7 January 2021

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

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7 January 2021

Altered chromatin structure associated with methylation-induced gene silencing in cancer cells: correlation of accessibility, methylation, MeCP2 binding and acetylation

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MECP2 mutation in male patients with non-specific X-linked mental retardation.

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A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map.

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7 January 2021

Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

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

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Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome

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

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Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

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MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

636199

636199

1 reference

Consolidated OpenCitations Corpus – April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12160743

2 references

30 April 2017

Consolidated OpenCitations Corpus – April 2017