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526 related items for PubMed ID: 9285792

  • 1. Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.
    Joyce JA, Lam WK, Catchpoole DJ, Jenks P, Reik W, Maher ER, Schofield PN.
    Hum Mol Genet; 1997 Sep; 6(9):1543-8. PubMed ID: 9285792
    [Abstract] [Full Text] [Related]

  • 2. Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.
    Squire JA, Li M, Perlikowski S, Fei YL, Bayani J, Zhang ZM, Weksberg R.
    Genomics; 2000 May 01; 65(3):234-42. PubMed ID: 10857747
    [Abstract] [Full Text] [Related]

  • 3. Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
    Sperandeo MP, Ungaro P, Vernucci M, Pedone PV, Cerrato F, Perone L, Casola S, Cubellis MV, Bruni CB, Andria G, Sebastio G, Riccio A.
    Am J Hum Genet; 2000 Mar 01; 66(3):841-7. PubMed ID: 10712200
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Engel JR, Smallwood A, Harper A, Higgins MJ, Oshimura M, Reik W, Schofield PN, Maher ER.
    J Med Genet; 2000 Dec 01; 37(12):921-6. PubMed ID: 11106355
    [Abstract] [Full Text] [Related]

  • 6. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
    Catchpoole D, Lam WW, Valler D, Temple IK, Joyce JA, Reik W, Schofield PN, Maher ER.
    J Med Genet; 1997 May 01; 34(5):353-9. PubMed ID: 9152830
    [Abstract] [Full Text] [Related]

  • 7. Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.
    Reik W, Brown KW, Schneid H, Le Bouc Y, Bickmore W, Maher ER.
    Hum Mol Genet; 1995 Dec 01; 4(12):2379-85. PubMed ID: 8634713
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 36(9):958-60. PubMed ID: 15314640
    [Abstract] [Full Text] [Related]

  • 9. Maintenance of normal imprinting of H19 and IGF2 genes in neuroblastoma.
    Wada M, Seeger RC, Mizoguchi H, Koeffler HP.
    Cancer Res; 1995 Aug 01; 55(15):3386-8. PubMed ID: 7614476
    [Abstract] [Full Text] [Related]

  • 10. Role of genomic imprinting in Wilms' tumour and overgrowth disorders.
    Reeve AE.
    Med Pediatr Oncol; 1996 Nov 01; 27(5):470-5. PubMed ID: 8827076
    [Abstract] [Full Text] [Related]

  • 11. A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
    Jurkiewicz D, Kugaudo M, Skórka A, Śmigiel R, Smyk M, Ciara E, Chrzanowska K, Krajewska-Walasek M.
    Am J Med Genet A; 2017 Jan 01; 173(1):72-78. PubMed ID: 27612309
    [Abstract] [Full Text] [Related]

  • 12. Rapid detection of methylation change at H19 in human imprinting disorders using methylation-sensitive high-resolution melting.
    Wojdacz TK, Dobrovic A, Algar EM.
    Hum Mutat; 2008 Oct 01; 29(10):1255-60. PubMed ID: 18473334
    [Abstract] [Full Text] [Related]

  • 13. Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.
    Cerrato F, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Rinaldi MM, Boccuto L, Neri G, Magnani C, D'Angelo P, Collini P, Perotti D, Sebastio G, Maher ER, Riccio A.
    Hum Mol Genet; 2008 May 15; 17(10):1427-35. PubMed ID: 18245780
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site.
    Ulaner GA, Vu TH, Li T, Hu JF, Yao XM, Yang Y, Gorlick R, Meyers P, Healey J, Ladanyi M, Hoffman AR.
    Hum Mol Genet; 2003 Mar 01; 12(5):535-49. PubMed ID: 12588801
    [Abstract] [Full Text] [Related]

  • 16. Somatic overgrowth associated with overexpression of insulin-like growth factor II.
    Morison IM, Becroft DM, Taniguchi T, Woods CG, Reeve AE.
    Nat Med; 1996 Mar 01; 2(3):311-6. PubMed ID: 8612230
    [Abstract] [Full Text] [Related]

  • 17. Loss of imprinting mutations define both distinct and overlapping roles for misexpression of IGF2 and of H19 lncRNA.
    Park KS, Mitra A, Rahat B, Kim K, Pfeifer K.
    Nucleic Acids Res; 2017 Dec 15; 45(22):12766-12779. PubMed ID: 29244185
    [Abstract] [Full Text] [Related]

  • 18. Genomic imprinting of IGF2 and H19 in human meningiomas.
    Müller S, Zirkel D, Westphal M, Zumkeller W.
    Eur J Cancer; 2000 Mar 15; 36(5):651-5. PubMed ID: 10738131
    [Abstract] [Full Text] [Related]

  • 19. Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations.
    Li M, Squire J, Shuman C, Fei YL, Atkin J, Pauli R, Smith A, Nishikawa J, Chitayat D, Weksberg R.
    Genomics; 2001 Jun 15; 74(3):370-6. PubMed ID: 11414765
    [Abstract] [Full Text] [Related]

  • 20. A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.
    Higashimoto K, Jozaki K, Kosho T, Matsubara K, Fuke T, Yamada D, Yatsuki H, Maeda T, Ohtsuka Y, Nishioka K, Joh K, Koseki H, Ogata T, Soejima H.
    Clin Genet; 2014 Dec 15; 86(6):539-44. PubMed ID: 24299031
    [Abstract] [Full Text] [Related]

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