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Journal Abstract Search

190 related items for PubMed ID: 8612230

  • 21. Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.
    Okamoto K, Morison IM, Taniguchi T, Reeve AE.
    Proc Natl Acad Sci U S A; 1997 May 13; 94(10):5367-71. PubMed ID: 9144243
    [Abstract] [Full Text] [Related]

  • 22. 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 13; 9(6):409-18. PubMed ID: 11436121
    [Abstract] [Full Text] [Related]

  • 23. 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 Jun 13; 14():1-9. PubMed ID: 19293570
    [Abstract] [Full Text] [Related]

  • 24. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.
    Weksberg R, Shen DR, Fei YL, Song QL, Squire J.
    Nat Genet; 1993 Oct 13; 5(2):143-50. PubMed ID: 8252039
    [Abstract] [Full Text] [Related]

  • 25. Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.
    Poole RL, Leith DJ, Docherty LE, Shmela ME, Gicquel C, Splitt M, Temple IK, Mackay DJ.
    Eur J Hum Genet; 2012 Feb 13; 20(2):240-3. PubMed ID: 21863054
    [Abstract] [Full Text] [Related]

  • 26. 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 13; 8(7):1337-52. PubMed ID: 10369881
    [Abstract] [Full Text] [Related]

  • 27. Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor.
    Taniguchi T, Sullivan MJ, Ogawa O, Reeve AE.
    Proc Natl Acad Sci U S A; 1995 Mar 14; 92(6):2159-63. PubMed ID: 7534414
    [Abstract] [Full Text] [Related]

  • 28. 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
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  • 30. A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues.
    Hu RJ, Lee MP, Johnson LA, Feinberg AP.
    Hum Mol Genet; 1996 Nov 15; 5(11):1743-8. PubMed ID: 8923002
    [Abstract] [Full Text] [Related]

  • 31. Nesidioblastosis and mixed hamartoma of the liver in Beckwith-Wiedemann syndrome: case study including analysis of H19 methylation and insulin-like growth factor 2 genotyping and imprinting.
    Fukuzawa R, Umezawa A, Morikawa Y, Kim KC, Nagai T, Hata J.
    Pediatr Dev Pathol; 2001 Nov 15; 4(4):381-90. PubMed ID: 11441340
    [Abstract] [Full Text] [Related]

  • 32. Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis.
    Bachmann N, Crazzolara R, Bohne F, Kotzot D, Maurer K, Enklaar T, Prawitt D, Bergmann C.
    Pediatr Blood Cancer; 2017 Mar 15; 64(3):. PubMed ID: 27650505
    [Abstract] [Full Text] [Related]

  • 33. 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 15; 37(12):921-6. PubMed ID: 11106355
    [Abstract] [Full Text] [Related]

  • 34. Inactivation of H19, an imprinted and putative tumor repressor gene, is a preneoplastic event during Wilms' tumorigenesis.
    Cui H, Hedborg F, He L, Nordenskjöld A, Sandstedt B, Pfeifer-Ohlsson S, Ohlsson R.
    Cancer Res; 1997 Oct 15; 57(20):4469-73. PubMed ID: 9377554
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  • 36. 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]

  • 37. Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome.
    Abi Habib W, Azzi S, Brioude F, Steunou V, Thibaud N, Das Neves C, Le Jule M, Chantot-Bastaraud S, Keren B, Lyonnet S, Michot C, Rossi M, Pasquier L, Gicquel C, Rossignol S, Le Bouc Y, Netchine I.
    Hum Mol Genet; 2014 Nov 01; 23(21):5763-73. PubMed ID: 24916376
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  • 39. Molecular biology of Beckwith-Wiedemann syndrome.
    Weksberg R, Squire JA.
    Med Pediatr Oncol; 1996 Nov 01; 27(5):462-9. PubMed ID: 8827075
    [Abstract] [Full Text] [Related]

  • 40. 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]

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