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187 related items for PubMed ID: 12812984

  • 1. Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions.
    Sandovici I, Leppert M, Hawk PR, Suarez A, Linares Y, Sapienza C.
    Hum Mol Genet; 2003 Jul 01; 12(13):1569-78. PubMed ID: 12812984
    [Abstract] [Full Text] [Related]

  • 2. Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
    Vu TH, Li T, Nguyen D, Nguyen BT, Yao XM, Hu JF, Hoffman AR.
    Genomics; 2000 Mar 01; 64(2):132-43. PubMed ID: 10729220
    [Abstract] [Full Text] [Related]

  • 3. Quantitative allele-specific expression and DNA methylation analysis of H19, IGF2 and IGF2R in the human placenta across gestation reveals H19 imprinting plasticity.
    Buckberry S, Bianco-Miotto T, Hiendleder S, Roberts CT.
    PLoS One; 2012 Mar 01; 7(12):e51210. PubMed ID: 23227253
    [Abstract] [Full Text] [Related]

  • 4. Conservation of IGF2-H19 and IGF2R imprinting in sheep: effects of somatic cell nuclear transfer.
    Young LE, Schnieke AE, McCreath KJ, Wieckowski S, Konfortova G, Fernandes K, Ptak G, Kind AJ, Wilmut I, Loi P, Feil R.
    Mech Dev; 2003 Dec 01; 120(12):1433-42. PubMed ID: 14654216
    [Abstract] [Full Text] [Related]

  • 5. Interindividual variability and parent of origin DNA methylation differences at specific human Alu elements.
    Sandovici I, Kassovska-Bratinova S, Loredo-Osti JC, Leppert M, Suarez A, Stewart R, Bautista FD, Schiraldi M, Sapienza C.
    Hum Mol Genet; 2005 Aug 01; 14(15):2135-43. PubMed ID: 15972727
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region.
    Tost J, Jammes H, Dupont JM, Buffat C, Robert B, Mignot TM, Mondon F, Carbonne B, Siméoni U, Grangé G, Kerjean A, Ferré F, Gut IG, Vaiman D.
    Nucleic Acids Res; 2006 May 25; 34(19):5438-48. PubMed ID: 17012269
    [Abstract] [Full Text] [Related]

  • 8. Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locus.
    Heijmans BT, Kremer D, Tobi EW, Boomsma DI, Slagboom PE.
    Hum Mol Genet; 2007 Mar 01; 16(5):547-54. PubMed ID: 17339271
    [Abstract] [Full Text] [Related]

  • 9. Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site.
    Cui H, Niemitz EL, Ravenel JD, Onyango P, Brandenburg SA, Lobanenkov VV, Feinberg AP.
    Cancer Res; 2001 Jul 01; 61(13):4947-50. PubMed ID: 11431321
    [Abstract] [Full Text] [Related]

  • 10. Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: relation to expression and imprinting.
    Weber M, Milligan L, Delalbre A, Antoine E, Brunel C, Cathala G, Forné T.
    Mech Dev; 2001 Mar 01; 101(1-2):133-41. PubMed ID: 11231066
    [Abstract] [Full Text] [Related]

  • 11. Disrupted imprinting status at the H19 differentially methylated region is associated with the resorbed embryo phenotype in rats.
    Pathak S, Saxena M, D'Souza R, Balasinor NH.
    Reprod Fertil Dev; 2010 Mar 01; 22(6):939-48. PubMed ID: 20591328
    [Abstract] [Full Text] [Related]

  • 12. Disruption of imprinting in cloned mouse fetuses from embryonic stem cells.
    Ogawa H, Ono Y, Shimozawa N, Sotomaru Y, Katsuzawa Y, Hiura H, Ito M, Kono T.
    Reproduction; 2003 Oct 01; 126(4):549-57. PubMed ID: 14525537
    [Abstract] [Full Text] [Related]

  • 13. Methylation status of putative differentially methylated regions of porcine IGF2 and H19.
    Han DW, Im YB, Do JT, Gupta MK, Uhm SJ, Kim JH, Schöler HR, Lee HT.
    Mol Reprod Dev; 2008 May 01; 75(5):777-84. PubMed ID: 18247333
    [Abstract] [Full Text] [Related]

  • 14. Epigenetic specificity of loss of imprinting of the IGF2 gene in Wilms tumors.
    Bjornsson HT, Brown LJ, Fallin MD, Rongione MA, Bibikova M, Wickham E, Fan JB, Feinberg AP.
    J Natl Cancer Inst; 2007 Aug 15; 99(16):1270-3. PubMed ID: 17686827
    [Abstract] [Full Text] [Related]

  • 15. Loss of imprinting of IGF2 correlates with hypermethylation of the H19 differentially methylated region in hepatoblastoma.
    Honda S, Arai Y, Haruta M, Sasaki F, Ohira M, Yamaoka H, Horie H, Nakagawara A, Hiyama E, Todo S, Kaneko Y.
    Br J Cancer; 2008 Dec 02; 99(11):1891-9. PubMed ID: 19034281
    [Abstract] [Full Text] [Related]

  • 16. Cross-species clues of an epigenetic imprinting regulatory code for the IGF2R gene.
    Vu TH, Jirtle RL, Hoffman AR.
    Cytogenet Genome Res; 2006 Dec 02; 113(1-4):202-8. PubMed ID: 16575181
    [Abstract] [Full Text] [Related]

  • 17. Hypomethylation of the IGF2 DMR in colorectal tumors, detected by bisulfite pyrosequencing, is associated with poor prognosis.
    Baba Y, Nosho K, Shima K, Huttenhower C, Tanaka N, Hazra A, Giovannucci EL, Fuchs CS, Ogino S.
    Gastroenterology; 2010 Dec 02; 139(6):1855-64. PubMed ID: 20682317
    [Abstract] [Full Text] [Related]

  • 18. Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus.
    Waterland RA, Lin JR, Smith CA, Jirtle RL.
    Hum Mol Genet; 2006 Mar 01; 15(5):705-16. PubMed ID: 16421170
    [Abstract] [Full Text] [Related]

  • 19. Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology.
    Turan N, Katari S, Gerson LF, Chalian R, Foster MW, Gaughan JP, Coutifaris C, Sapienza C.
    PLoS Genet; 2010 Jul 22; 6(7):e1001033. PubMed ID: 20661447
    [Abstract] [Full Text] [Related]

  • 20. Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19.
    Takada S, Paulsen M, Tevendale M, Tsai CE, Kelsey G, Cattanach BM, Ferguson-Smith AC.
    Hum Mol Genet; 2002 Jan 01; 11(1):77-86. PubMed ID: 11773001
    [Abstract] [Full Text] [Related]

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