Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour (Q40441171)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15798773%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

title

Epigenetic alteration at the DLK1-GTL2 imprinted domain in human neoplasia: analysis of neuroblastoma, phaeochromocytoma and Wilms' tumour (English)

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10 January 2020

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8

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10 January 2020

Eamonn R Maher

9

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10 January 2020

author name string

D Astuti

1

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10 January 2020

F Latif

2

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10 January 2020

K Wagner

3

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10 January 2020

D Gentle

4

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10 January 2020

W N Cooper

5

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10 January 2020

D Catchpoole

6

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10 January 2020

R Grundy

7

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10 January 2020

language of work or name

English

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publication date

1 April 2005

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British Journal of Cancer

10 January 2020

published in

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10 January 2020

volume

92

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10 January 2020

issue

8

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10 January 2020

page(s)

1574-1580

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A Pituitary-Derived MEG3 Isoform Functions as a Growth Suppressor in Tumor Cells

10 January 2020

cites work

1 reference

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The callipyge locus: evidence for the trans interaction of reciprocally imprinted genes

22 September 2017

1 reference

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High delta-like 1 expression in a subset of neuroblastoma cell lines corresponds to a differentiated chromaffin cell type

22 September 2017

1 reference

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Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

22 September 2017

1 reference

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Identification of the single base change causing the callipyge muscle hypertrophy phenotype, the only known example of polar overdominance in mammals.

22 September 2017

1 reference

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DNA methylation and genomic imprinting: insights from cancer into epigenetic mechanisms

22 September 2017

1 reference

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Insights from gene arrays on the development and growth regulation of uterine leiomyomata

22 September 2017

1 reference

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Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Genomic imprinting: parental influence on the genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

SAGE analysis of neuroblastoma reveals a high expression of the human homologue of the Drosophila Delta gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

The Dlk1 and Gtl2 genes are linked and reciprocally imprinted

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Epigenetic gene silencing in cancer

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

dlk modulates mitogen-activated protein kinase signaling to allow or prevent differentiation

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Imprinting status of DLK1 gene in brain tumors and lymphomas

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362015

Tumour-suppressor activity of H19 RNA

20 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.BJC.6602478

Paternal UPD14 is responsible for a distinctive malformation complex

21 January 2018

1 reference

12 December 2020

Epigenetic detection of human chromosome 14 uniparental disomy

1 reference

12 December 2020

The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status

1 reference

12 December 2020

Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site

1 reference

12 December 2020

Identification of myelodysplastic syndrome-specific genes by DNA microarray analysis with purified hematopoietic stem cell fraction

1 reference

12 December 2020

Identifiers

DOI

10.1038/SJ.BJC.6602478

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15798773%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

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10 January 2020

PubMed publication ID

15798773

1 reference