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Journal Abstract Search

226 related items for PubMed ID: 25943194

  • 21. Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
    Riccio A, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Ferrero GB, Silengo MC, Russo S, Larizza L, Cerrato F.
    Endocr Dev; 2009; 14():1-9. PubMed ID: 19293570
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. 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 15; 66(3):841-7. PubMed ID: 10712200
    [Abstract] [Full Text] [Related]

  • 24. The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.
    Beygo J, Citro V, Sparago A, De Crescenzo A, Cerrato F, Heitmann M, Rademacher K, Guala A, Enklaar T, Anichini C, Cirillo Silengo M, Graf N, Prawitt D, Cubellis MV, Horsthemke B, Buiting K, Riccio A.
    Hum Mol Genet; 2013 Feb 01; 22(3):544-57. PubMed ID: 23118352
    [Abstract] [Full Text] [Related]

  • 25. 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 01; 6(9):1543-8. PubMed ID: 9285792
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model.
    Freschi A, Del Prete R, Pignata L, Cecere F, Manfrevola F, Mattia M, Cobellis G, Sparago A, Bartolomei MS, Riccio A, Cerrato F.
    Hum Mol Genet; 2021 Jul 28; 30(16):1509-1520. PubMed ID: 34132339
    [Abstract] [Full Text] [Related]

  • 28. Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome.
    Reik W, Brown KW, Slatter RE, Sartori P, Elliott M, Maher ER.
    Hum Mol Genet; 1994 Aug 28; 3(8):1297-301. PubMed ID: 7987305
    [Abstract] [Full Text] [Related]

  • 29. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
    Gaston V, Le Bouc Y, Soupre V, Burglen L, Donadieu J, Oro H, Audry G, Vazquez MP, Gicquel C.
    Eur J Hum Genet; 2001 Jun 28; 9(6):409-18. PubMed ID: 11436121
    [Abstract] [Full Text] [Related]

  • 30. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
    Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MT, Melis D, Manfredini E, Ferrero GB, Pecile V, Larizza L.
    Clin Epigenetics; 2016 Jun 28; 8():23. PubMed ID: 26933465
    [Abstract] [Full Text] [Related]

  • 31. 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 28; 34(5):353-9. PubMed ID: 9152830
    [Abstract] [Full Text] [Related]

  • 32. Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi.
    Paganini L, Carlessi N, Fontana L, Silipigni R, Motta S, Fiori S, Guerneri S, Lalatta F, Cereda A, Sirchia S, Miozzo M, Tabano S.
    Epigenetics; 2015 May 28; 10(7):643-9. PubMed ID: 26061650
    [Abstract] [Full Text] [Related]

  • 33. Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome.
    Kannenberg K, Urban C, Binder G.
    Clin Genet; 2012 Apr 28; 81(4):366-77. PubMed ID: 22248018
    [Abstract] [Full Text] [Related]

  • 34. A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome.
    De Crescenzo A, Coppola F, Falco P, Bernardo I, Ausanio G, Cerrato F, Falco L, Riccio A.
    Eur J Med Genet; 2011 Apr 28; 54(4):e451-4. PubMed ID: 21571108
    [Abstract] [Full Text] [Related]

  • 35. Paternal 132 bp deletion affecting KCNQ1OT1 in 11p15.5 is associated with growth retardation but does not affect imprinting.
    Eggermann T, Kraft F, Lausberg E, Ergezinger K, Kunstmann E.
    J Med Genet; 2021 Mar 28; 58(3):173-176. PubMed ID: 32447323
    [Abstract] [Full Text] [Related]

  • 36. New insights into the pathogenesis of Beckwith-Wiedemann and Silver-Russell syndromes: contribution of small copy number variations to 11p15 imprinting defects.
    Demars J, Rossignol S, Netchine I, Lee KS, Shmela M, Faivre L, Weill J, Odent S, Azzi S, Callier P, Lucas J, Dubourg C, Andrieux J, Le Bouc Y, El-Osta A, Gicquel C.
    Hum Mutat; 2011 Oct 28; 32(10):1171-82. PubMed ID: 21780245
    [Abstract] [Full Text] [Related]

  • 37. Epigenetic anomalies in childhood growth disorders.
    Netchine I, Rossignol S, Azzi S, Le Bouc Y.
    Nestle Nutr Inst Workshop Ser; 2013 Oct 28; 71():65-73. PubMed ID: 23502140
    [Abstract] [Full Text] [Related]

  • 38. Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Calvello M, Tabano S, Colapietro P, Maitz S, Pansa A, Augello C, Lalatta F, Gentilin B, Spreafico F, Calzari L, Perotti D, Larizza L, Russo S, Selicorni A, Sirchia SM, Miozzo M.
    Epigenetics; 2013 Oct 28; 8(10):1053-60. PubMed ID: 23917791
    [Abstract] [Full Text] [Related]

  • 39. Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine.
    Robbins KM, Chen Z, Wells KD, Rivera RM.
    J Biomed Sci; 2012 Nov 15; 19(1):95. PubMed ID: 23153226
    [Abstract] [Full Text] [Related]

  • 40. Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation.
    Bohne F, Langer D, Martiné U, Eider CS, Cencic R, Begemann M, Elbracht M, Bülow L, Eggermann T, Zechner U, Pelletier J, Zabel BU, Enklaar T, Prawitt D.
    Clin Epigenetics; 2016 Nov 15; 8():47. PubMed ID: 27152123
    [Abstract] [Full Text] [Related]

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