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Journal Abstract Search

228 related items for PubMed ID: 8388768

  • 1.
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  • 2. Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11.
    Wadey RB, Pal N, Buckle B, Yeomans E, Pritchard J, Cowell JK.
    Oncogene; 1990 Jun; 5(6):901-7. PubMed ID: 2163053
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  • 4. Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: a preliminary analysis.
    Grundy P, Telzerow P, Moksness J, Breslow NE.
    Med Pediatr Oncol; 1996 Nov; 27(5):429-33. PubMed ID: 8926924
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  • 5. The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor gene.
    Rahman N, Arbour L, Tonin P, Baruchel S, Pritchard-Jones K, Narod SA, Stratton MR.
    Oncogene; 1997 Jun 26; 14(25):3099-102. PubMed ID: 9223674
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  • 7. Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.
    Mannens M, Devilee P, Bliek J, Mandjes I, de Kraker J, Heyting C, Slater RM, Westerveld A.
    Cancer Res; 1990 Jun 01; 50(11):3279-83. PubMed ID: 2159377
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  • 8. Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome.
    Grundy PE, Telzerow PE, Breslow N, Moksness J, Huff V, Paterson MC.
    Cancer Res; 1994 May 01; 54(9):2331-3. PubMed ID: 8162576
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  • 9. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
    Grundy P, Koufos A, Morgan K, Li FP, Meadows AT, Cavenee WK.
    Nature; 1988 Nov 24; 336(6197):374-6. PubMed ID: 2848199
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  • 10. Molecular and cellular biology of Wilms' tumour.
    Maitland NJ, Brown KW, Poirier V, Shaw AP, Williams J.
    Anticancer Res; 1989 Nov 24; 9(5):1417-26. PubMed ID: 2556071
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  • 11.
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  • 12. Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour.
    Grundy RG, Pritchard J, Scambler P, Cowell JK.
    Oncogene; 1998 Jul 23; 17(3):395-400. PubMed ID: 9690521
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  • 13. Loss of heterozygosity at 7p in Wilms' tumour development.
    Powlesland RM, Charles AK, Malik KT, Reynolds PA, Pires S, Boavida M, Brown KW.
    Br J Cancer; 2000 Jan 23; 82(2):323-9. PubMed ID: 10646884
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  • 15. Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours.
    Satoh Y, Nakadate H, Nakagawachi T, Higashimoto K, Joh K, Masaki Z, Uozumi J, Kaneko Y, Mukai T, Soejima H.
    Br J Cancer; 2006 Aug 21; 95(4):541-7. PubMed ID: 16909133
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  • 16. Molecular analysis of E-cadherin and cadherin-11 in Wilms' tumours.
    Schulz S, Becker KF, Braungart E, Reichmuth C, Klamt B, Becker I, Atkinson M, Gessler M, Höfler H.
    J Pathol; 2000 Jun 21; 191(2):162-9. PubMed ID: 10861576
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  • 17.
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  • 18. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour.
    Ogawa O, Eccles MR, Szeto J, McNoe LA, Yun K, Maw MA, Smith PJ, Reeve AE.
    Nature; 1993 Apr 22; 362(6422):749-51. PubMed ID: 8097018
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  • 19. Structural rearrangements of the WT1 gene in Wilms' tumour cells.
    Cowell JK, Wadey RB, Haber DA, Call KM, Housman DE, Pritchard J.
    Oncogene; 1991 Apr 22; 6(4):595-9. PubMed ID: 1851548
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  • 20. [Molecular genetics of Wilms' tumor].
    Papezová M, Mares J, Goetz P.
    Cas Lek Cesk; 2001 Jun 07; 140(11):323-7. PubMed ID: 11431850
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