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2. A point mutation found in the WT1 gene in a sporadic Wilms' tumor without genitourinary abnormalities is identical with the most frequent point mutation in Denys-Drash syndrome. Akasaka Y; Kikuchi H; Nagai T; Hiraoka N; Kato S; Hata J FEBS Lett; 1993 Feb; 317(1-2):39-43. PubMed ID: 8381368 [TBL] [Abstract][Full Text] [Related]
3. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Pelletier J; Bruening W; Kashtan CE; Mauer SM; Manivel JC; Striegel JE; Houghton DC; Junien C; Habib R; Fouser L Cell; 1991 Oct; 67(2):437-47. PubMed ID: 1655284 [TBL] [Abstract][Full Text] [Related]
5. Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database. Jeanpierre C; Denamur E; Henry I; Cabanis MO; Luce S; Cécille A; Elion J; Peuchmaur M; Loirat C; Niaudet P; Gubler MC; Junien C Am J Hum Genet; 1998 Apr; 62(4):824-33. PubMed ID: 9529364 [TBL] [Abstract][Full Text] [Related]
6. 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; 35(37):12070-6. PubMed ID: 8810912 [TBL] [Abstract][Full Text] [Related]
8. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene. Furtado LV; Pysher T; Opitz J; Lamb R; Comstock J; Batish S; Mauch T; Nelson R; Zhou H Fetal Pediatr Pathol; 2011; 30(4):266-72. PubMed ID: 21434831 [TBL] [Abstract][Full Text] [Related]
9. Regulation of renal EGF receptor expression is normal in Denys-Drash syndrome. Vicanek C; Ferretti E; Goodyer C; Torban E; Moffett P; Pelletier J; Goodyer P Kidney Int; 1997 Sep; 52(3):614-9. PubMed ID: 9291179 [TBL] [Abstract][Full Text] [Related]
10. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X. Heathcott RW; Morison IM; Gubler MC; Corbett R; Reeve AE Hum Mutat; 2002 Apr; 19(4):462. PubMed ID: 11933209 [TBL] [Abstract][Full Text] [Related]
11. Inherited WT1 mutation in Denys-Drash syndrome. Coppes MJ; Liefers GJ; Higuchi M; Zinn AB; Balfe JW; Williams BR Cancer Res; 1992 Nov; 52(21):6125-8. PubMed ID: 1327525 [TBL] [Abstract][Full Text] [Related]
12. 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; 13(2):146-53. PubMed ID: 10094551 [TBL] [Abstract][Full Text] [Related]
14. Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene. Ito S; Takata A; Hataya H; Ikeda M; Kikuchi H; Hata J; Honda M J Pediatr; 2001 Mar; 138(3):425-7. PubMed ID: 11241056 [TBL] [Abstract][Full Text] [Related]
15. [Clinical and pathological features of Denys-Drash syndrome: report of 3 cases]. Wang HY; Sun LZ; Yue ZH; Yang J; Jiang XY; Mo Y Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):855-8. PubMed ID: 23302619 [TBL] [Abstract][Full Text] [Related]
16. Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations. Schumacher V; Schärer K; Wühl E; Altrogge H; Bonzel KE; Guschmann M; Neuhaus TJ; Pollastro RM; Kuwertz-Bröking E; Bulla M; Tondera AM; Mundel P; Helmchen U; Waldherr R; Weirich A; Royer-Pokora B Kidney Int; 1998 Jun; 53(6):1594-600. PubMed ID: 9607189 [TBL] [Abstract][Full Text] [Related]
17. Genotype/phenotype correlations in Wilms' tumor. Huff V Med Pediatr Oncol; 1996 Nov; 27(5):408-14. PubMed ID: 8827067 [TBL] [Abstract][Full Text] [Related]