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Parental antagonism, relatedness asymmetries, and genomic imprinting

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title

Parental antagonism, relatedness asymmetries, and genomic imprinting (English)

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author name string

D Haig

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1

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language of work or name

English

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publication date

22 November 1997

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published in

Proceedings of the Royal Society B

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PubMed

volume

264

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page(s)

1657-62

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issue

1388

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cites work

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Genomic imprinting in mammalian development: a parental tug-of-war

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Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r)

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The evolution of genomic imprinting.

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28 September 2017

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

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Parental imprinting of autosomal mammalian genes

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Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality

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Genomic imprinting of Mash2, a mouse gene required for trophoblast development

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Evolutionary theory of parent-offspring conflict

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Cytoplasmic inheritance and intragenomic conflict

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Genomic imprinting and the strange case of the insulin-like growth factor II receptor

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

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Molecular evolution of imprinted genes: no evidence for antagonistic coevolution.

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Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

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Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds.

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A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

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Parent-Specific Gene Expression and the Triploid Endosperm

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Crossref

reference URL

https://api.crossref.org/works/10.1098%2FRSPB.1997.0230

retrieved

7 January 2021

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Identifiers

DOI

10.1098/RSPB.1997.0230

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ResearchGate publication ID

13826228

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(Q24673085)

Parental antagonism, relatedness asymmetries, and genomic imprinting

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