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Journal Abstract Search

439 related items for PubMed ID: 9851976

  • 1. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.
    Thorvaldsen JL, Duran KL, Bartolomei MS.
    Genes Dev; 1998 Dec 01; 12(23):3693-702. PubMed ID: 9851976
    [Abstract] [Full Text] [Related]

  • 2. Developmental profile of H19 differentially methylated domain (DMD) deletion alleles reveals multiple roles of the DMD in regulating allelic expression and DNA methylation at the imprinted H19/Igf2 locus.
    Thorvaldsen JL, Fedoriw AM, Nguyen S, Bartolomei MS.
    Mol Cell Biol; 2006 Feb 01; 26(4):1245-58. PubMed ID: 16449639
    [Abstract] [Full Text] [Related]

  • 3. Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2.
    Braunschweig MH, Owczarek-Lipska M, Stahlberger-Saitbekova N.
    BMC Genet; 2011 May 17; 12():47. PubMed ID: 21575277
    [Abstract] [Full Text] [Related]

  • 4. Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting.
    Thorvaldsen JL, Mann MR, Nwoko O, Duran KL, Bartolomei MS.
    Mol Cell Biol; 2002 Apr 17; 22(8):2450-62. PubMed ID: 11909940
    [Abstract] [Full Text] [Related]

  • 5. Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes.
    Feil R, Walter J, Allen ND, Reik W.
    Development; 1994 Oct 17; 120(10):2933-43. PubMed ID: 7607083
    [Abstract] [Full Text] [Related]

  • 6. Tandem repeat hypothesis in imprinting: deletion of a conserved direct repeat element upstream of H19 has no effect on imprinting in the Igf2-H19 region.
    Lewis A, Mitsuya K, Constancia M, Reik W.
    Mol Cell Biol; 2004 Jul 17; 24(13):5650-6. PubMed ID: 15199123
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Tissue-specific relationship of S-adenosylhomocysteine with allele-specific H19/Igf2 methylation and imprinting in mice with hyperhomocysteinemia.
    Glier MB, Ngai YF, Sulistyoningrum DC, Aleliunas RE, Bottiglieri T, Devlin AM.
    Epigenetics; 2013 Jan 15; 8(1):44-53. PubMed ID: 23221482
    [Abstract] [Full Text] [Related]

  • 10. Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans.
    Forné T, Oswald J, Dean W, Saam JR, Bailleul B, Dandolo L, Tilghman SM, Walter J, Reik W.
    Proc Natl Acad Sci U S A; 1997 Sep 16; 94(19):10243-8. PubMed ID: 9294195
    [Abstract] [Full Text] [Related]

  • 11. Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor.
    Frevel MA, Sowerby SJ, Petersen GB, Reeve AE.
    J Biol Chem; 1999 Oct 08; 274(41):29331-40. PubMed ID: 10506193
    [Abstract] [Full Text] [Related]

  • 12. Mechanisms of Igf2/H19 imprinting: DNA methylation, chromatin and long-distance gene regulation.
    Sasaki H, Ishihara K, Kato R.
    J Biochem; 2000 May 08; 127(5):711-5. PubMed ID: 10788777
    [Abstract] [Full Text] [Related]

  • 13. Developmentally regulated functions of the H19 differentially methylated domain.
    Vernucci M, Cerrato F, Pedone PV, Dandolo L, Bruni CB, Riccio A.
    Hum Mol Genet; 2004 Feb 01; 13(3):353-61. PubMed ID: 14681296
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 5(12):2027-32. PubMed ID: 8968759
    [Abstract] [Full Text] [Related]

  • 15. Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19.
    Hu JF, Vu TH, Hoffman AR.
    J Biol Chem; 1997 Aug 15; 272(33):20715-20. PubMed ID: 9252392
    [Abstract] [Full Text] [Related]

  • 16. Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.
    Constância M, Dean W, Lopes S, Moore T, Kelsey G, Reik W.
    Nat Genet; 2000 Oct 15; 26(2):203-6. PubMed ID: 11017078
    [Abstract] [Full Text] [Related]

  • 17. CTCF binding sites promote transcription initiation and prevent DNA methylation on the maternal allele at the imprinted H19/Igf2 locus.
    Engel N, Thorvaldsen JL, Bartolomei MS.
    Hum Mol Genet; 2006 Oct 01; 15(19):2945-54. PubMed ID: 16928784
    [Abstract] [Full Text] [Related]

  • 18. Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops.
    Murrell A, Heeson S, Reik W.
    Nat Genet; 2004 Aug 01; 36(8):889-93. PubMed ID: 15273689
    [Abstract] [Full Text] [Related]

  • 19. Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting.
    Dao D, Walsh CP, Yuan L, Gorelov D, Feng L, Hensle T, Nisen P, Yamashiro DJ, Bestor TH, Tycko B.
    Hum Mol Genet; 1999 Jul 01; 8(7):1337-52. PubMed ID: 10369881
    [Abstract] [Full Text] [Related]

  • 20. H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19.
    Srivastava M, Hsieh S, Grinberg A, Williams-Simons L, Huang SP, Pfeifer K.
    Genes Dev; 2000 May 15; 14(10):1186-95. PubMed ID: 10817754
    [Abstract] [Full Text] [Related]

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