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Journal Abstract Search

427 related items for PubMed ID: 8174107

  • 1. Mutations of the p53 tumor suppressor gene occur infrequently in Wilms' tumor.
    Malkin D, Sexsmith E, Yeger H, Williams BR, Coppes MJ.
    Cancer Res; 1994 Apr 15; 54(8):2077-9. PubMed ID: 8174107
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  • 11. Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour.
    Park S, Bernard A, Bove KE, Sens DA, Hazen-Martin DJ, Garvin AJ, Haber DA.
    Nat Genet; 1993 Dec 15; 5(4):363-7. PubMed ID: 8298644
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  • 12. Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1.
    Borel F, Barilla KC, Hamilton TB, Iskandar M, Romaniuk PJ.
    Biochemistry; 1996 Sep 17; 35(37):12070-6. PubMed ID: 8810912
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  • 13. Genotype/phenotype correlations in Wilms' tumor.
    Huff V.
    Med Pediatr Oncol; 1996 Nov 17; 27(5):408-14. PubMed ID: 8827067
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  • 14. Nephroblastoma (Wilms' tumor): a model system of aberrant renal development.
    Re GG, Hazen-Martin DJ, Sens DA, Garvin AJ.
    Semin Diagn Pathol; 1994 May 17; 11(2):126-35. PubMed ID: 7809506
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  • 15. The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor.
    Barbosa AS, Hadjiathanasiou CG, Theodoridis C, Papathanasiou A, Tar A, Merksz M, Györvári B, Sultan C, Dumas R, Jaubert F, Niaudet P, Moreira-Filho CA, Cotinot C, Fellous M.
    Hum Mutat; 1999 May 17; 13(2):146-53. PubMed ID: 10094551
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  • 16. WT1: a novel tumor suppressor gene inactivated in Wilms' tumor.
    Haber DA, Buckler AJ.
    New Biol; 1992 Feb 17; 4(2):97-106. PubMed ID: 1313285
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  • 17. A point mutation within exon 5 of the WT1 gene of a sporadic unilateral Wilms' tumor alters gene function.
    Guan LS, Liu JJ, Xu YH, Wang ZY.
    Cancer Res; 1998 Sep 15; 58(18):4180-4. PubMed ID: 9751632
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  • 18. Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein beta1 gene CTNNB1 for patients with Wilms tumors: results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology.
    Royer-Pokora B, Weirich A, Schumacher V, Uschkereit C, Beier M, Leuschner I, Graf N, Autschbach F, Schneider D, von Harrach M.
    Cancer; 2008 Sep 01; 113(5):1080-9. PubMed ID: 18618575
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  • 20. Exclusion of the Wilms tumour gene (WT1) promoter as a site of frequent mutation in Wilms tumour.
    Grubb GR, Yun K, Reeve AE, Eccles MR.
    Oncogene; 1995 Apr 20; 10(8):1677-81. PubMed ID: 7731725
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