(Q77996281)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11971191%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

title

Loss of methylation at chromosome 11p15.5 is common in human adult tumors (English)

1 reference

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10 December 2019

11

1 reference

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10 December 2019

author name string

Rosaria A M Scelfo

1

1 reference

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10 December 2019

Christine Schwienbacher

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11971191%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

Angelo Veronese

3

1 reference

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10 December 2019

Laura Gramantieri

4

1 reference

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10 December 2019

Luigi Bolondi

5

1 reference

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10 December 2019

Patrizia Querzoli

6

1 reference

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10 December 2019

Italo Nenci

7

1 reference

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10 December 2019

George A Calin

8

1 reference

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10 December 2019

Adriano Angioni

9

1 reference

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10 December 2019

Giuseppe Barbanti-Brodano

10

1 reference

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10 December 2019

language of work or name

English

0 references

publication date

1 April 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11971191%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

1 reference

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10 December 2019

volume

21

1 reference

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10 December 2019

issue

16

1 reference

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10 December 2019

page(s)

2564-2572

1 reference

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https://scigraph.springernature.com/pub.10.1038/sj.onc.1205336

10 December 2019

exact match

0 references

cites work

Alterations in DNA Methylation: A Fundamental Aspect of Neoplasia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

The CpG dinucleotide and human genetic disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Role of DNA methylation in the regulation of transcription

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Tumour-suppressor activity of H19 RNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Loss of constitutional heterozygosity on chromosome 11p in human ovarian cancer. Positive correlation with grade of differentiation.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Delineation of the centromeric and telomeric chromosome segment 11p15.5 lung cancer suppressor regions LOH11A and LOH11B.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

DNA methylation in health and disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Exon structure and promoter identification of STIM1 (alias GOK), a human gene causing growth arrest of the human tumor cell lines G401 and RD.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Location of enhancers is essential for the imprinting of H19 and Igf2 genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1205336

7 January 2021