(Q51935592)

17 April 2018

title

The impact of MECP2 mutations in the expression patterns of Rett syndrome patients. (English)

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17 April 2018

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1

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17 April 2018

Manel Esteller

12

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17 April 2018

Miguel Alaminos

Miguel Alaminos

3

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Mario F Fraga

7

Mario F Fraga

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17 April 2018

Santiago Ropero

2

Santiago Ropero

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17 April 2018

Fernando Setien

5

Fernando Setien

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17 April 2018

Michel Herranz

8

Michel Herranz

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17 April 2018

author name string

Judith Armstrong

4

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17 April 2018

Ruben Agrelo

6

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17 April 2018

Sonia Avila

9

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17 April 2018

Mercedes Pineda

10

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17 April 2018

Eugenia Monros

11

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17 April 2018

publication date

11 November 2004

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17 April 2018

published in

Human Genetics

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17 April 2018

volume

116

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17 April 2018

issue

1-2

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17 April 2018

page(s)

91-104

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17 April 2018

Epigenetic lesions causing genetic lesions in human cancer: promoter hypermethylation of DNA repair genes

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Rett syndrome and the MECP2 gene

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

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Functional consequences of Rett syndrome mutations on human MeCP2.

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The affinity of different MBD proteins for a specific methylated locus depends on their intrinsic binding properties

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

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Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

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Rett syndrome in Spain: mutation analysis and clinical correlations

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

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Isolation of a novel oncogene, NET1, from neuroepithelioma cells by expression cDNA cloning

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A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

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Genome-wide analysis of gene expression associated with MYCN in human neuroblastoma.

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Chromatin compaction by human MeCP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation

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12 December 2020

The biological functions of the methyl-CpG-binding protein MeCP2 and its implication in Rett syndrome.

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DNA methylation and Rett syndrome

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

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MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region

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Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome

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Breaking the silence in Rett syndrome

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12 December 2020

Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA

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Significance analysis of microarrays applied to the ionizing radiation response

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Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

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

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Phylogenetic Reconstruction Using an Unsupervised Growing Neural Network That Adopts the Topology of a Phylogenetic Tree

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Missing value estimation methods for DNA microarrays

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12 December 2020

Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes

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12 December 2020

Immortalization of human primary B lymphocytes in vitro with DNA

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Mapping chromosomal proteins in vivo by formaldehyde-crosslinked-chromatin immunoprecipitation

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12 December 2020

10.1007/S00439-004-1200-0

Identifiers

DOI

1 reference

17 April 2018

1 reference

17 April 2018