BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 23494989)

  • 21. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare.
    Royer-Pokora B; Ragg S; Heckl-Ostreicher B; Held M; Loos U; Call K; Glaser T; Housman D; Saunders G; Zabel B
    Genes Chromosomes Cancer; 1991 Mar; 3(2):89-100. PubMed ID: 1648959
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Homozygous inactivation of WT1 in a Wilms' tumor associated with the WAGR syndrome.
    Gessler M; König A; Moore J; Qualman S; Arden K; Cavenee W; Bruns G
    Genes Chromosomes Cancer; 1993 Jul; 7(3):131-6. PubMed ID: 7687865
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
    Crolla JA; Cawdery JE; Oley CA; Young ID; Gray J; Fantes J; van Heyningen V
    J Med Genet; 1997 Mar; 34(3):207-12. PubMed ID: 9132491
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The distal region of 11p13 and associated genetic diseases.
    Mannens M; Hoovers JM; Bleeker-Wagemakers EM; Redeker E; Bliek J; Overbeeke-Melkert M; Saunders G; Williams B; van Heyningen V; Junien C
    Genomics; 1991 Oct; 11(2):284-93. PubMed ID: 1769647
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Aniridia, gonadoblastoma, Wilms' tumor and deletion 11p13.
    Stefan H; Semecký V
    Acta Medica (Hradec Kralove); 1998; 41(1):29-33. PubMed ID: 9588071
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Two neonates with congenital aniridia: the necessity of genetic investigation].
    van Os E; Niemarkt HJ; Verreussel MJ; Cruysberg JR; Bok LA; Spruijt L
    Ned Tijdschr Geneeskd; 2008 Mar; 152(10):569-73. PubMed ID: 18402324
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers.
    Valind A; Wessman S; Pal N; Karlsson J; Jonson T; Sandstedt B; Gisselsson D
    Pediatr Blood Cancer; 2018 Nov; 65(11):e27301. PubMed ID: 29968962
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial predisposition to Wilms tumor does not segregate with the WT1 gene.
    Schwartz CE; Haber DA; Stanton VP; Strong LC; Skolnick MH; Housman DE
    Genomics; 1991 Aug; 10(4):927-30. PubMed ID: 1655633
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Paternally inherited WT1 mutation plus uniparental disomy of 11p may be an essential mechanism for development of WT1-mutated familial Wilms tumor.
    Sato Y; Haruta M; Kaneko Y; Nakasato Y; Kurosawa H; Yoshihara S
    Pediatr Blood Cancer; 2019 Jan; 66(1):e27442. PubMed ID: 30221469
    [No Abstract]   [Full Text] [Related]  

  • 30. A mouse model of the aniridia-Wilms tumor deletion syndrome.
    Glaser T; Lane J; Housman D
    Science; 1990 Nov; 250(4982):823-7. PubMed ID: 2173141
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Molecular genetic study of the PAX6 gene in aniridia patients].
    Wolf M; Zabel B; Lorenz B; Blankenagel A; Ghorbani MB; Schwenn O; Wildhardt G
    Ophthalmologe; 1998 Dec; 95(12):828-30. PubMed ID: 10025146
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel WT1 gene mutation associated with wilms' tumor and congenital male genitourinary malformation.
    Sakamoto J; Takata A; Fukuzawa R; Kikuchi H; Sugiyama M; Kanamori Y; Hashizume K; Hata JI
    Pediatr Res; 2001 Sep; 50(3):337-44. PubMed ID: 11518820
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Mutations/deletions of the WT1 gene, loss of heterozygosity on chromosome arms 11p and 11q, chromosome ploidy and histology in Wilms' tumors in Japan.
    Nakadate H; Yokomori K; Watanabe N; Tsuchiya T; Namiki T; Kobayshi H; Suita S; Tsunematsu Y; Horikoshi Y; Hatae Y; Endo M; Komada Y; Eguchi H; Toyoda Y; Kikuta A; Kobayashi R; Kaneko Y
    Int J Cancer; 2001 Nov; 94(3):396-400. PubMed ID: 11745420
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Inactivation of the remaining allele of the WT1 gene in a Wilms' tumour from a WAGR patient.
    Brown KW; Watson JE; Poirier V; Mott MG; Berry PJ; Maitland NJ
    Oncogene; 1992 Apr; 7(4):763-8. PubMed ID: 1314370
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A rare case of an isolated PAX6 mutation, aniridia, and Wilms tumor.
    Lind KT; Cost NG; Zegar K; Kuldanek SA; Enzenauer RW; Schneider KW
    Ophthalmic Genet; 2021 Apr; 42(2):216-217. PubMed ID: 33300417
    [No Abstract]   [Full Text] [Related]  

  • 37. A nude mouse Wilms' tumor line (KCMC-WT-1) derived from an aniridia patient with monoalleleic partial deletion of chromosome 11p.
    Nagashima Y; Nishihira H; Miyagi Y; Tanaka Y; Sasaki Y; Nishi T; Imaizumi K; Aoki I; Misugi K
    Cancer; 1996 Feb; 77(4):799-804. PubMed ID: 8616775
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identical genetic changes in different histologic components of Wilms' tumors.
    Zhuang Z; Merino MJ; Vortmeyer AO; Bryant B; Lash AE; Wang C; Deavers MT; Shelton WF; Kapur S; Chandra RS
    J Natl Cancer Inst; 1997 Aug; 89(15):1148-52. PubMed ID: 9262253
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant.
    Falcone MP; Pritchard-Jones K; Brok J; Mifsud W; Williams RD; Nakata K; Tugnait S; Al-Saadi R; Side L; Anderson J; Duncan C; Marks SD; Bockenhauer D; Chowdhury T
    Pediatr Nephrol; 2022 Apr; 37(4):821-832. PubMed ID: 34608521
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.
    Reeve AE; Sih SA; Raizis AM; Feinberg AP
    Mol Cell Biol; 1989 Apr; 9(4):1799-803. PubMed ID: 2542777
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.