1991
DOI: 10.1016/0092-8674(91)90256-x
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Genomic imprinting and the strange case of the insulin-like growth factor II receptor

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Cited by 462 publications
(230 citation statements)
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“…Apparently, the IGF-2r functions to degrade IGF-2 (37). Hence, there is a biochemical tug of war between IGF-2 (promoting growth) and IGF-2r (restricting growth by degrading IGF-2) in mice (23). IGF-2 and IGF-2r are also imprinted in humans, although paternal imprinting of IGF-2r is not absolute (38).…”
Section: Genomic Imprinting and Growth Factorsmentioning
confidence: 99%
“…Apparently, the IGF-2r functions to degrade IGF-2 (37). Hence, there is a biochemical tug of war between IGF-2 (promoting growth) and IGF-2r (restricting growth by degrading IGF-2) in mice (23). IGF-2 and IGF-2r are also imprinted in humans, although paternal imprinting of IGF-2r is not absolute (38).…”
Section: Genomic Imprinting and Growth Factorsmentioning
confidence: 99%
“…The presence, in opposite parental sexes, of this unusual property in two genetically unlinked but functionally coupled genes may be related to opposing e ects of Igf2 and Igf2r expression on fetal growth (Haig and Graham, 1991). It is known that the mitogenic actions of IGF-II are transmitted by the type I IGF receptor (Kiess et al, 1987;Ellis et al, 1996), which binds both IGF-I and IGF-II and acts as a ligand-activated tyrosine kinase.…”
Section: Introductionmentioning
confidence: 99%
“…The phenomenon of genomic imprinting allows gene expression to be dependent on the parent's sex. Haig (1992) realized that ␣ = 0.5 then defines the constrained mother's interests, and ␣ = 0 those of the unconstrained father; this has some remarkable implications (Haig & Graham 1991;Haig & Westoby 1991). For example, in eutherian mammals the paternal genome appears to be particularly active in the development of the extraembryonic membranes, possibly at the expense of the mother.…”
Section: (Ii) Interbrood Competitionmentioning
confidence: 99%