| scholarly article | Q13442814 |
| P2093 | author name string | Takeda Y | |
| Iwasa Y | |||
| Mochizuki A | |||
| P2860 | cites work | Transition from haploidy to diploidy | Q44989990 |
| Mosaic and polymorphic imprinting of the WT1 gene in humans | Q48084685 | ||
| Genomic imprinting--defusing the ovarian time bomb | Q49110236 | ||
| Parental methylation patterns of a transgenic locus in adult somatic tissues are imprinted during gametogenesis | Q49161161 | ||
| Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain. | Q52204453 | ||
| Continual change in mate preferences. | Q52877077 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Embryological and molecular investigations of parental imprinting on mouse chromosome 7. | Q55052972 | ||
| The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans | Q58061470 | ||
| Tumour-suppressor activity of H19 RNA | Q59071440 | ||
| Action at a distance | Q60074124 | ||
| Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis | Q68244654 | ||
| Inherited type of allelic methylation variations in a mouse chromosome region where an integrated transgene shows methylation imprinting | Q68315933 | ||
| Human insulin-like growth factor type I and type II receptors are not imprinted | Q72250045 | ||
| Parental imprinting of the mouse H19 gene | Q22122365 | ||
| Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region | Q28208127 | ||
| Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region | Q28242397 | ||
| The genetical evolution of social behaviour. II | Q28256861 | ||
| Genomic imprinting in mammalian development: a parental tug-of-war | Q28278146 | ||
| Role for DNA methylation in genomic imprinting | Q29618669 | ||
| Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r) | Q29619910 | ||
| Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. | Q34314269 | ||
| Identification of a novel paternally expressed gene in the Prader-Willi syndrome region | Q34318139 | ||
| Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes | Q35889365 | ||
| Genomic imprinting and the strange case of the insulin-like growth factor II receptor | Q37165552 | ||
| Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse | Q38291049 | ||
| Imprinting the genome: imprinted genes, imprinting genes, and a hypothesis for their interaction | Q40722195 | ||
| DNA methylation and genomic imprinting in mammals. | Q40868394 | ||
| Genetic conflict and evolution of mammalian X-chromosome inactivation | Q40948391 | ||
| Genetic conflict in early development: parental imprinting in normal and abnormal growth | Q41670910 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1283-1295 | |
| P577 | publication date | 1996-11-01 | |
| P1433 | published in | Genetics | Q3100575 |
| P1476 | title | The evolution of genomic imprinting | |
| P478 | volume | 144 |
| Q34615913 | Evolutionary genetic models of the ovarian time bomb hypothesis for the evolution of genomic imprinting |
| Q74602226 | Genetic conflicts in genomic imprinting |
| Q34602685 | Genetic conflicts, multiple paternity and the evolution of genomic imprinting. |
| Q35105543 | Genomic imprinting of Grb10: coadaptation or conflict? |
| Q35212932 | Genomic imprinting, sibling solidairity and the logic of collective action |
| Q34340465 | How demography, life history, and kinship shape the evolution of genomic imprinting |
| Q52734843 | Intragenomic conflict over queen determination favours genomic imprinting in eusocial Hymenoptera. |
| Q51528127 | Male genotype influences female reproductive investment in Drosophila melanogaster. |
| Q42567325 | Molecular evolution of an imprinted gene: repeatability of patterns of evolution within the mammalian insulin-like growth factor type II receptor |
| Q55711459 | Molecular evolution of imprinted genes: no evidence for antagonistic coevolution. |
| Q24673085 | Parental antagonism, relatedness asymmetries, and genomic imprinting |
| Q78288697 | Parental modifiers, antisense transcripts and loss of imprinting |
| Q34569498 | Polyandry, life-history trade-offs and the evolution of imprinting at Mendelian loci |
| Q34608309 | Population models of genomic imprinting. I. Differential viability in the sexes and the analogy with genetic dominance |
| Q37306572 | Possible diversifying selection in the imprinted gene, MEDEA, in Arabidopsis |
| Q24604714 | The archaeological record speaks: bridging anthropology and linguistics |
| Q34643086 | The effect of genetic conflict on genomic imprinting and modification of expression at a sex-linked locus |
| Q34613193 | The evolution of X-linked genomic imprinting |
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