(Q33894804)

English

Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

29 July 2017

Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome (English)

1 reference

Europe PubMed Central

29 July 2017

0 references

Mireille Claustres

6

object named as

Mireille Claustres

1 reference

Europe PubMed Central

29 July 2017

author name string

Marie-Elisabeth Brun

1

1 reference

Europe PubMed Central

29 July 2017

Erica Lana

2

1 reference

Europe PubMed Central

29 July 2017

Isabelle Rivals

3

1 reference

Europe PubMed Central

29 July 2017

Gérard Lefranc

4

1 reference

Europe PubMed Central

29 July 2017

Pierre Sarda

5

1 reference

Europe PubMed Central

29 July 2017

André Mégarbané

7

1 reference

Europe PubMed Central

29 July 2017

Albertina De Sario

8

1 reference

Europe PubMed Central

29 July 2017

language of work or name

0 references

publication date

29 April 2011

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

6

1 reference

Europe PubMed Central

29 July 2017

e19464

1 reference

Europe PubMed Central

29 July 2017

4

1 reference

Europe PubMed Central

29 July 2017

copyright license

Creative Commons Attribution 4.0 International

29 April 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

DNMT3B interacts with constitutive centromere protein CENP-C to modulate DNA methylation and the histone code at centromeric regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Selective POTE paralogs on chromosome 2 are expressed in human embryonic stem cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Expression of POTE protein in human testis detected by novel monoclonal antibodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

High-resolution profiling of histone methylations in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Mapping of the juxtacentromeric heterochromatin-euchromatin frontier of human chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

POTE paralogs are induced and differentially expressed in many cancers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Frequent DNA hypomethylation of human juxtacentromeric BAGE loci in cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Centromeric chromatin exhibits a histone modification pattern that is distinct from both euchromatin and heterochromatin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Partitioning and plasticity of repressive histone methylation states in mammalian chromatin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

The TPTE gene family: cellular expression, subcellular localization and alternative splicing

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0019464

21 January 2018

Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Comprehensive analysis of CpG islands in human chromosomes 21 and 22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

TPIP: a novel phosphoinositide 3-phosphatase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

The DNA sequence of human chromosome 21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

MethTools--a toolbox to visualize and analyze DNA methylation data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

A sequence assembly and editing program for efficient management of large projects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3084872

5 July 2018

Defective B-cell-negative selection and terminal differentiation in the ICF syndrome.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0019464

21 January 2018

Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0019464

21 January 2018

New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0019464

21 January 2018

BAGE genes generated by juxtacentromeric reshuffling in the Hominidae lineage are under selective pressure.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0019464

21 January 2018

Ezh2 controls B cell development through histone H3 methylation and Igh rearrangement.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0019464

21 January 2018

Duplication and extensive remodeling shaped POTE family genes encoding proteins containing ankyrin repeat and coiled coil domains

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0019464

21 January 2018

Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions

1 reference

https://pubmed.ncbi.nlm.nih.gov/21559330

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/21559330

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21559330

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Roles for Dnmt3b in mammalian development: a mouse model for the ICF syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21559330

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0019464

1 reference

Europe PubMed Central

29 July 2017

2011PLoSO...619464B

0 references

1 reference

Europe PubMed Central

29 July 2017

1 reference

Europe PubMed Central

29 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33894804&oldid=1971256536"