H19 and Igf2--enhancing the confusion? (Q35031144)

5 August 2017

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title

H19 and Igf2--enhancing the confusion? (English)

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5 August 2017

Katharine L Arney

1

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5 August 2017

1 January 2003

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5 August 2017

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5 August 2017

19

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5 August 2017

17-23

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5 August 2017

1

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

5 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Elucidation of the minimal sequence required to imprint H19 transgenes.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

An enhancer deletion affects both H19 and Igf2 expression

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

A silencer element identified in Drosophila is required for imprinting of H19 reporter transgenes in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Height depends on month of birth.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Regulatory mechanisms at the mouse Igf2/H19 locus.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Appropriate expression of the mouse H19 gene utilises three or more distinct enhancer regions spread over more than 130 kb.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Deletion of a nuclease-sensitive region between the Igf2 and H19 genes leads to Igf2 misregulation and increased adiposity

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Placental-specific IGF-II is a major modulator of placental and fetal growth.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

An intragenic methylated region in the imprinted Igf2 gene augments transcription.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Deletion of a direct repeat element has no effect on Igf2 and H19 imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

An upstream repressor element plays a role in Igf2 imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Igf2 imprinting does not require its own DNA methylation or H19 RNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

Enhancer competition between H19 and Igf2 does not mediate their imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2802%2900004-5

7 January 2021

10.1016/S0168-9525(02)00004-5

Identifiers

DOI

1 reference

5 August 2017

1 reference

PubMed ID

12493244