(Q47951370)

7 February 2018

title

Paternal allele of IGF2 gene haplotype CTG is associated with fetal and placental growth in Japanese. (English)

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7 February 2018

author name string

Ken Nagaya

1

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7 February 2018

Yoshio Makita

2

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7 February 2018

Genya Taketazu

3

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7 February 2018

Toshio Okamoto

4

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7 February 2018

Eiki Nakamura

5

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7 February 2018

Tokitsugi Hayashi

6

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7 February 2018

Kenji Fujieda

7

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7 February 2018

language of work or name

English

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publication date

1 August 2009

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7 February 2018

published in

Pediatric Research

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7 February 2018

volume

66

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7 February 2018

page(s)

135-139

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7 February 2018

issue

2

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7 February 2018

https://scigraph.springernature.com/pub.10.1203/pdr.0b013e3181a9e818

exact match

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cites work

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Intrauterine growth retardation and postnatal growth failure associated with deletion of the insulin-like growth factor I gene

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Homozygous deletion of the human insulin receptor gene results in leprechaunism

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

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Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

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Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

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

21 January 2018

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

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Low circulating IGF-II concentrations predict weight gain and obesity in humans

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10.1203/PDR.0B013E3181A9E818

21 January 2018

Identifiers

DOI

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7 February 2018

Dimensions Publication ID

0 references

1 reference

7 February 2018