Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor. (Q47924478)

6 February 2018

title

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

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6 February 2018

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Frevel MA

1

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6 February 2018

Sowerby SJ

series ordinal

2

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6 February 2018

Petersen GB

series ordinal

3

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6 February 2018

Reeve AE

series ordinal

4

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6 February 2018

language of work or name

English

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publication date

1 October 1999

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6 February 2018

Journal of Biological Chemistry

published in

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6 February 2018

volume

274

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6 February 2018

issue

41

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6 February 2018

page(s)

29331-29340

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6 February 2018

Parental imprinting of the mouse H19 gene

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Monoallelic expression of the human H19 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Parental imprinting of the human H19 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

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

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Relaxation of imprinted genes in human cancer.

21 January 2018

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Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Disruption of imprinting caused by deletion of the H19 gene region in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Imprinting and the initiation of gene silencing in the germ line.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

A potential imprint control element: identification of a conserved 42 bp sequence upstream of H19.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

High sensitivity mapping of methylated cytosines

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

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

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Somatic overgrowth associated with overexpression of insulin-like growth factor II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Developmental differences in methylation of human Alu repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.41.29331

21 January 2018

Identifiers

DOI

10.1074/JBC.274.41.29331

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6 February 2018

PubMed ID

10506193

1 reference

6 February 2018