Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor (Q34572727)

3 August 2017

title

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

1 reference

3 August 2017

1 reference

4

Reeve AE

1 reference

3 August 2017

Taniguchi T

1

1 reference

3 August 2017

Sullivan MJ

series ordinal

2

1 reference

3 August 2017

Ogawa O

series ordinal

3

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 March 1995

1 reference

Proceedings of the National Academy of Sciences of the United States of America

3 August 2017

published in

1 reference

3 August 2017

volume

92

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3 August 2017

issue

6

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3 August 2017

page(s)

2159-2163

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Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation

3 August 2017

cites work

1 reference

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DNA methylation: a phoenix rises

7 July 2018

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Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching

7 July 2018

1 reference

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Evolutionary conservation of possible functional domains of the human and murine XIST genes

7 July 2018

1 reference

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Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome

7 July 2018

1 reference

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Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism

7 July 2018

1 reference

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

7 July 2018

1 reference

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Role for DNA methylation in genomic imprinting

7 July 2018

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New insights reveal complex mechanisms involved in genomic imprinting.

7 July 2018

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Overlapping patterns of IGF2 and H19 expression during human development: biallelic IGF2 expression correlates with a lack of H19 expression

7 July 2018

1 reference

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Parental imprinting of autosomal mammalian genes

7 July 2018

1 reference

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Genomic imprinting: control of gene expression by epigenetic inheritance

7 July 2018

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Isolation of a transforming sequence from a human bladder carcinoma cell line

7 July 2018

1 reference

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Isolation of the human insulin-like growth factor genes: insulin-like growth factor II and insulin genes are contiguous

7 July 2018

1 reference

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DNA methylation and gene activity

7 July 2018

1 reference

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Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues.

7 July 2018

1 reference

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Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors

7 July 2018

1 reference

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The short arm of chromosome 11 is a "hot spot" for hypermethylation in human neoplasia

7 July 2018

1 reference

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Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

7 July 2018

1 reference

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Parental imprinting of the mouse insulin-like growth factor II gene.

7 July 2018

1 reference

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Preferential loss of maternal alleles in sporadic Wilms' tumour.

7 July 2018

1 reference

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The product of the H19 gene may function as an RNA

7 July 2018

1 reference

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Polymerase chain reaction (PCR) for detection of APal polymorphism at the insulin like growth factor II gene (IGF2)

7 July 2018

1 reference

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Methylation, mutation and cancer

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42443

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

7 July 2018

1 reference

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Monoallelic expression of the human H19 gene

7 July 2018

1 reference

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Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42443

Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42443

The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA

7 July 2018

1 reference

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Relaxation of imprinted genes in human cancer.

7 July 2018

1 reference

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Sequence of a cDNA clone encoding human preproinsulin-like growth factor II.

27 October 2018

1 reference

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Epigenetic lesions at the H19 locus in Wilms' tumour patients

27 October 2018

1 reference

12 December 2020

Expression of insulin-like growth factor-II transcripts in Wilms' tumour

1 reference

12 December 2020

Reduced genomic 5-methylcytosine content in human colonic neoplasia

1 reference

12 December 2020

Maternal allele loss in Wilms' tumour

1 reference

12 December 2020

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1 reference

12 December 2020

The expression of the H‐19 and IGF‐2 genes during human embryogenesis and placental development

1 reference

12 December 2020

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

12 December 2020

Parental genomic imprinting of the human IGF2 gene

1 reference

12 December 2020

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

1 reference

12 December 2020

Parental imprinting of an Igf-2 transgene

1 reference

12 December 2020

Tumour-suppressor activity of H19 RNA

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.92.6.2159

1 reference

release_c47l4e4qsvgcjfh7oo643jw3bu

3 August 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/c47l4e4qsvgcjfh7oo643jw3bu

24 November 2022

mapped directly with Wikidata item

PMC publication ID

42443

1 reference

3 August 2017

1 reference