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Journal Abstract Search

187 related items for PubMed ID: 12812984

  • 41. Lack of reciprocal genomic imprinting of sense and antisense RNA of mouse insulin-like growth factor II receptor in the central nervous system.
    Hu JF, Balaguru KA, Ivaturi RD, Oruganti H, Li T, Nguyen BT, Vu TH, Hoffman AR.
    Biochem Biophys Res Commun; 1999 Apr 13; 257(2):604-8. PubMed ID: 10198258
    [Abstract] [Full Text] [Related]

  • 42. Prenatal famine and genetic variation are independently and additively associated with DNA methylation at regulatory loci within IGF2/H19.
    Tobi EW, Slagboom PE, van Dongen J, Kremer D, Stein AD, Putter H, Heijmans BT, Lumey LH.
    PLoS One; 2012 Apr 13; 7(5):e37933. PubMed ID: 22666415
    [Abstract] [Full Text] [Related]

  • 43. Characterization of differentially methylated regions in 3 bovine imprinted genes: a model for studying human germ-cell and embryo development.
    Hansmann T, Heinzmann J, Wrenzycki C, Zechner U, Niemann H, Haaf T.
    Cytogenet Genome Res; 2011 Apr 13; 132(4):239-47. PubMed ID: 21160170
    [Abstract] [Full Text] [Related]

  • 44. Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.
    Sparago A, Cerrato F, Vernucci M, Ferrero GB, Silengo MC, Riccio A.
    Nat Genet; 2004 Sep 13; 36(9):958-60. PubMed ID: 15314640
    [Abstract] [Full Text] [Related]

  • 45. Promoter-restricted histone code, not the differentially methylated DNA regions or antisense transcripts, marks the imprinting status of IGF2R in human and mouse.
    Vu TH, Li T, Hoffman AR.
    Hum Mol Genet; 2004 Oct 01; 13(19):2233-45. PubMed ID: 15294879
    [Abstract] [Full Text] [Related]

  • 46. The prevalence of loss of imprinting of H19 and IGF2 at birth.
    Rancourt RC, Harris HR, Barault L, Michels KB.
    FASEB J; 2013 Aug 01; 27(8):3335-43. PubMed ID: 23620526
    [Abstract] [Full Text] [Related]

  • 47. Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour.
    Steenman MJ, Rainier S, Dobry CJ, Grundy P, Horon IL, Feinberg AP.
    Nat Genet; 1994 Jul 01; 7(3):433-9. PubMed ID: 7920665
    [Abstract] [Full Text] [Related]

  • 48. High incidence of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas. Uncoupling of H19 and IGF2 expression and biallelic hypomethylation of H19.
    Douc-Rasy S, Barrois M, Fogel S, Ahomadegbe JC, Stéhelin D, Coll J, Riou G.
    Oncogene; 1996 Jan 18; 12(2):423-30. PubMed ID: 8570220
    [Abstract] [Full Text] [Related]

  • 49. Loss of genomic imprinting of insulin-like growth factor 2 is strongly associated with cellular proliferation in normal hematopoietic cells.
    Hofmann WK, Takeuchi S, Frantzen MA, Hoelzer D, Koeffler HP.
    Exp Hematol; 2002 Apr 18; 30(4):318-23. PubMed ID: 11937266
    [Abstract] [Full Text] [Related]

  • 50. Hypomethylated and hypermethylated profiles of H19DMR are associated with the aberrant imprinting of IGF2 and H19 in human hepatocellular carcinoma.
    Wu J, Qin Y, Li B, He WZ, Sun ZL.
    Genomics; 2008 May 18; 91(5):443-50. PubMed ID: 18358696
    [Abstract] [Full Text] [Related]

  • 51. IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch.
    Li T, Vu TH, Ulaner GA, Littman E, Ling JQ, Chen HL, Hu JF, Behr B, Giudice L, Hoffman AR.
    Mol Hum Reprod; 2005 Sep 18; 11(9):631-40. PubMed ID: 16219628
    [Abstract] [Full Text] [Related]

  • 52. Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men.
    Boissonnas CC, Abdalaoui HE, Haelewyn V, Fauque P, Dupont JM, Gut I, Vaiman D, Jouannet P, Tost J, Jammes H.
    Eur J Hum Genet; 2010 Jan 18; 18(1):73-80. PubMed ID: 19584898
    [Abstract] [Full Text] [Related]

  • 53. Loss of imprinting and aberrant methylation of IGF2 in placentas from pregnancies complicated with fetal growth restriction.
    Koukoura O, Sifakis S, Soufla G, Zaravinos A, Apostolidou S, Jones A, Widschwendter M, Spandidos DA.
    Int J Mol Med; 2011 Oct 18; 28(4):481-7. PubMed ID: 21805044
    [Abstract] [Full Text] [Related]

  • 54. CTCF maintains differential methylation at the Igf2/H19 locus.
    Schoenherr CJ, Levorse JM, Tilghman SM.
    Nat Genet; 2003 Jan 18; 33(1):66-9. PubMed ID: 12461525
    [Abstract] [Full Text] [Related]

  • 55. Mechanisms of Igf2/H19 imprinting: DNA methylation, chromatin and long-distance gene regulation.
    Sasaki H, Ishihara K, Kato R.
    J Biochem; 2000 May 18; 127(5):711-5. PubMed ID: 10788777
    [Abstract] [Full Text] [Related]

  • 56. Relaxation of IGF2 imprinting in Wilms tumours associated with specific changes in IGF2 methylation.
    Sullivan MJ, Taniguchi T, Jhee A, Kerr N, Reeve AE.
    Oncogene; 1999 Dec 09; 18(52):7527-34. PubMed ID: 10602511
    [Abstract] [Full Text] [Related]

  • 57. Epigenetic regulation of Igf2/H19 imprinting at CTCF insulator binding sites.
    Yang Y, Hu JF, Ulaner GA, Li T, Yao X, Vu TH, Hoffman AR.
    J Cell Biochem; 2003 Dec 01; 90(5):1038-55. PubMed ID: 14624463
    [Abstract] [Full Text] [Related]

  • 58. GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
    Rentería ME, Coolen MW, Statham AL, Choi RS, Qu W, Campbell MJ, Smith S, Henders AK, Montgomery GW, Clark SJ, Martin NG, Medland SE.
    Twin Res Hum Genet; 2013 Aug 01; 16(4):767-81. PubMed ID: 23725790
    [Abstract] [Full Text] [Related]

  • 59. Hypermethylation of the IGF2 differentially methylated region 2 is a specific event in insulinomas leading to loss-of-imprinting and overexpression.
    Dejeux E, Olaso R, Dousset B, Audebourg A, Gut IG, Terris B, Tost J.
    Endocr Relat Cancer; 2009 Sep 01; 16(3):939-52. PubMed ID: 19502451
    [Abstract] [Full Text] [Related]

  • 60. Tissue-, sex-, and age-specific DNA methylation of rat glucocorticoid receptor gene promoter and insulin-like growth factor 2 imprinting control region.
    Agba OB, Lausser L, Huse K, Bergmeier C, Jahn N, Groth M, Bens M, Sahm A, Gall M, Witte OW, Kestler HA, Schwab M, Platzer M.
    Physiol Genomics; 2017 Nov 01; 49(11):690-702. PubMed ID: 28916632
    [Abstract] [Full Text] [Related]

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