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Journal Abstract Search

137 related items for PubMed ID: 9428426

  • 1. Roles of the imprinted gene Igf2 and paternal duplication of distal chromosome 7 in the perinatal abnormalities of androgenetic mouse chimeras.
    McLaughlin KJ, Kochanowski H, Solter D, Schwarzkopf G, Szabó PE, Mann JR.
    Development; 1997 Dec; 124(23):4897-904. PubMed ID: 9428426
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  • 3. Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting.
    Mann JR, Gadi I, Harbison ML, Abbondanzo SJ, Stewart CL.
    Cell; 1990 Jul 27; 62(2):251-60. PubMed ID: 2372828
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  • 4. Embryological and molecular investigations of parental imprinting on mouse chromosome 7.
    Ferguson-Smith AC, Cattanach BM, Barton SC, Beechey CV, Surani MA.
    Nature; 1991 Jun 20; 351(6328):667-70. PubMed ID: 2052093
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  • 6. Mouse embryos with paternal duplication of an imprinted chromosome 7 region die at midgestation and lack placental spongiotrophoblast.
    McLaughlin KJ, Szabó P, Haegel H, Mann JR.
    Development; 1996 Jan 20; 122(1):265-70. PubMed ID: 8565838
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  • 7. Imprinting of the mouse Igf2r gene depends on an intronic CpG island.
    Wutz A, Barlow DP.
    Mol Cell Endocrinol; 1998 May 25; 140(1-2):9-14. PubMed ID: 9722161
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  • 8. Establishment of mouse androgenetic embryonic stem cells by double sperm injection and differentiation into beating embryoid body.
    Lei L, Hu L, Li T, Shen X, Liang X, Chen Y, Feng X, Yang Z, Shan Z.
    Zygote; 2019 Dec 25; 27(6):405-412. PubMed ID: 31544724
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  • 9. Development to term of mouse androgenetic aggregation chimeras.
    Mann JR, Stewart CL.
    Development; 1991 Dec 25; 113(4):1325-33. PubMed ID: 1811946
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  • 10. Disruption of mesodermal enhancers for Igf2 in the minute mutant.
    Davies K, Bowden L, Smith P, Dean W, Hill D, Furuumi H, Sasaki H, Cattanach B, Reik W.
    Development; 2002 Apr 25; 129(7):1657-68. PubMed ID: 11923202
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  • 11. Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome.
    Caspary T, Cleary MA, Perlman EJ, Zhang P, Elledge SJ, Tilghman SM.
    Genes Dev; 1999 Dec 01; 13(23):3115-24. PubMed ID: 10601037
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  • 15. Epigenotype switching of imprintable loci in embryonic germ cells.
    Tada T, Tada M, Hilton K, Barton SC, Sado T, Takagi N, Surani MA.
    Dev Genes Evol; 1998 Feb 01; 207(8):551-61. PubMed ID: 9510550
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  • 16. Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in mice.
    Freschi A, Hur SK, Valente FM, Ideraabdullah FY, Sparago A, Gentile MT, Oneglia A, Di Nucci D, Colucci-D'Amato L, Thorvaldsen JL, Bartolomei MS, Riccio A, Cerrato F.
    PLoS Genet; 2018 Feb 01; 14(2):e1007243. PubMed ID: 29470501
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  • 17. Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes.
    Dean W, Bowden L, Aitchison A, Klose J, Moore T, Meneses JJ, Reik W, Feil R.
    Development; 1998 Jun 01; 125(12):2273-82. PubMed ID: 9584126
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  • 19. Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element.
    Ripoche MA, Kress C, Poirier F, Dandolo L.
    Genes Dev; 1997 Jun 15; 11(12):1596-604. PubMed ID: 9203585
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  • 20. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.
    Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W.
    Hum Mol Genet; 1996 Dec 15; 5(12):2027-32. PubMed ID: 8968759
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