These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

339 related articles for article (PubMed ID: 2163761)

  • 21. Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours.
    Little MH; Dunn R; Byrne JA; Seawright A; Smith PJ; Pritchard-Jones K; van Heyningen V; Hastie ND
    Oncogene; 1992 Apr; 7(4):635-41. PubMed ID: 1314367
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Alternative splicing and genomic structure of the Wilms tumor gene WT1.
    Haber DA; Sohn RL; Buckler AJ; Pelletier J; Call KM; Housman DE
    Proc Natl Acad Sci U S A; 1991 Nov; 88(21):9618-22. PubMed ID: 1658787
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Preferential loss of maternal alleles in sporadic Wilms' tumour.
    Pal N; Wadey RB; Buckle B; Yeomans E; Pritchard J; Cowell JK
    Oncogene; 1990 Nov; 5(11):1665-8. PubMed ID: 1980007
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
    Davis LM; Stallard R; Thomas GH; Couillin P; Junien C; Nowak NJ; Shows TB
    Science; 1988 Aug; 241(4867):840-2. PubMed ID: 2841760
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. The candidate Wilms' tumour gene is involved in genitourinary development.
    Pritchard-Jones K; Fleming S; Davidson D; Bickmore W; Porteous D; Gosden C; Bard J; Buckler A; Pelletier J; Housman D
    Nature; 1990 Jul; 346(6280):194-7. PubMed ID: 2164159
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genomic imprinting at the WT1 gene involves a novel coding transcript (AWT1) that shows deregulation in Wilms' tumours.
    Dallosso AR; Hancock AL; Brown KW; Williams AC; Jackson S; Malik K
    Hum Mol Genet; 2004 Feb; 13(4):405-15. PubMed ID: 14681303
    [TBL] [Abstract][Full Text] [Related]  

  • 33. RNA polymerase chain reaction detects different levels of four alternatively spliced WT1 transcripts in Wilms' tumors.
    Brenner B; Wildhardt G; Schneider S; Royer-Pokora B
    Oncogene; 1992 Jul; 7(7):1431-3. PubMed ID: 1320246
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Wilms' tumors and malformation complexes].
    Hata J; Fukuzawa R; Takata A; Kikuchi H
    Nihon Rinsho; 2000 Jul; 58(7):1419-25. PubMed ID: 10921316
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization.
    Altura RA; Valentine M; Li H; Boyett JM; Shearer P; Grundy P; Shapiro DN; Look AT
    Cancer Res; 1996 Aug; 56(16):3837-41. PubMed ID: 8706032
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.
    Fearon ER; Vogelstein B; Feinberg AP
    Nature; 1984 May 10-16; 309(5964):176-8. PubMed ID: 6325939
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The role of Wilms' tumor genes.
    Hirose M
    J Med Invest; 1999 Aug; 46(3-4):130-40. PubMed ID: 10687307
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Aniridia, Wilms' tumor and human chromosome 11.
    Bickmore WA; Hastie ND
    Ophthalmic Paediatr Genet; 1989 Dec; 10(4):229-48. PubMed ID: 2560823
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus.
    Boehm T; Lavenir I; Forster A; Wadey RB; Cowell JK; Harbott J; Lampert F; Waters J; Sherrington P; Couillin P
    Oncogene; 1988 Dec; 3(6):691-5. PubMed ID: 2577871
    [TBL] [Abstract][Full Text] [Related]  

  • 40. RNA editing in the Wilms' tumor susceptibility gene, WT1.
    Sharma PM; Bowman M; Madden SL; Rauscher FJ; Sukumar S
    Genes Dev; 1994 Mar; 8(6):720-31. PubMed ID: 7926762
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.