(Q33251357)

24 July 2017

title

Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients (English)

1 reference

24 July 2017

0 references

Janine M LaSalle

4

0 references

author name string

Ivan J Delgado

1

1 reference

24 July 2017

Dong Sun Kim

2

1 reference

24 July 2017

Karen N Thatcher

3

1 reference

24 July 2017

Ignatia B Van den Veyver

5

1 reference

24 July 2017

publication date

21 July 2006

1 reference

24 July 2017

1 reference

24 July 2017

volume

7

1 reference

24 July 2017

page(s)

61

1 reference

Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism

24 July 2017

cites work

1 reference

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Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

14 July 2018

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Lipin, a lipodystrophy and obesity gene

14 July 2018

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Characterization of the Bex gene family in humans, mice, and rats

14 July 2018

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Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Rett syndrome: clinical review and genetic update

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Bioconductor: open software development for computational biology and bioinformatics

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

The major form of MeCP2 has a novel N-terminus generated by alternative splicing

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Human proteoglycan testican‐1 inhibits the lysosomal cysteine protease cathepsin L

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Exploration, normalization, and summaries of high density oligonucleotide array probe level data

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Mutations and polymorphisms in the human methyl CpG-binding protein MECP2

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Testican-1 inhibits attachment of Neuro-2a cells

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Methyl-CpG-binding protein, MeCP2, is a target molecule for maintenance DNA methyltransferase, Dnmt1

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Genetic basis of Rett syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

14 July 2018

Testican in human blood.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Distribution of testican expression in human brain

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Methyl-CpG-binding protein 2 mutations in Rett syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Expression of the proteoglycan SPOCK during mouse embryo development

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Rett syndrome, classical and atypical: genealogical support for common origin

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Structure and cellular distribution of mouse brain testican. Association with the postsynaptic area of hippocampus pyramidal cells

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Testican, a multidomain testicular proteoglycan resembling modulators of cell social behaviour

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients

14 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

Is Rett syndrome a loss-of-imprinting disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

Molecular biology. MeCP2 repression goes nonglobal

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 but not intron 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

Balanced X chromosome inactivation patterns in the Rett syndrome brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-61

21 January 2018

Review of Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569822

Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16859563

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Rett syndrome: epidemiology and geographical variability

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16859563

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-7-61

1 reference

Dimensions Publication ID

24 July 2017

0 references

1 reference

24 July 2017

1 reference