Loss of methylation at chromosome 11p15.5 is common in human adult tumors (Q77996281)

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10 December 2019

title

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

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10 December 2019

11

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10 December 2019

author name string

Rosaria A M Scelfo

1

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10 December 2019

Christine Schwienbacher

2

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10 December 2019

Angelo Veronese

3

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10 December 2019

Laura Gramantieri

4

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10 December 2019

Luigi Bolondi

5

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10 December 2019

Patrizia Querzoli

6

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10 December 2019

Italo Nenci

7

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10 December 2019

George A Calin

8

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10 December 2019

Adriano Angioni

9

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10 December 2019

Giuseppe Barbanti-Brodano

10

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10 December 2019

language of work or name

English

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publication date

1 April 2002

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10 December 2019

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10 December 2019

volume

21

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10 December 2019

page(s)

2564-2572

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10 December 2019

issue

16

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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

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7 January 2021

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

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

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7 January 2021

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

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

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7 January 2021

The CpG dinucleotide and human genetic disease

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Role of DNA methylation in the regulation of transcription

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7 January 2021

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

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7 January 2021

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

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7 January 2021

Tumour-suppressor activity of H19 RNA

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7 January 2021

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

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7 January 2021

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

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7 January 2021

Epigenetic lesions at the H19 locus in Wilms' tumour patients

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7 January 2021

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

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7 January 2021

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

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7 January 2021

DNA methylation in health and disease

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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.

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7 January 2021

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

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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

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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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021