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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

497 related items for PubMed ID: 2154702

  • 1. Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping.
    Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GA.
    Nature; 1990 Feb 22; 343(6260):774-8. PubMed ID: 2154702
    [Abstract] [Full Text] [Related]

  • 2. Homozygous intragenic deletion in the WT1 gene in a sporadic Wilms' tumour associated with high levels of expression of a truncated transcript.
    Algar EM, Kenney MT, Simms LA, Smith SI, Kida Y, Smith PJ.
    Hum Mutat; 1995 Feb 22; 5(3):221-7. PubMed ID: 7599632
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Intragenic homozygous deletion of the WT1 gene in Wilms' tumor.
    Tadokoro K, Fujii H, Ohshima A, Kakizawa Y, Shimizu K, Sakai A, Sumiyoshi K, Inoue T, Hayashi Y, Yamada M.
    Oncogene; 1992 Jun 22; 7(6):1215-21. PubMed ID: 1350671
    [Abstract] [Full Text] [Related]

  • 5. 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 12; 346(6280):194-7. PubMed ID: 2164159
    [Abstract] [Full Text] [Related]

  • 6. Altered trans-activational properties of a mutated WT1 gene product in a WAGR-associated Wilms' tumor.
    Park S, Tomlinson G, Nisen P, Haber DA.
    Cancer Res; 1993 Oct 15; 53(20):4757-60. PubMed ID: 8402654
    [Abstract] [Full Text] [Related]

  • 7. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour.
    Pelletier J, Bruening W, Li FP, Haber DA, Glaser T, Housman DE.
    Nature; 1991 Oct 03; 353(6343):431-4. PubMed ID: 1654525
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.
    Cooper PR, Smilinich NJ, Day CD, Nowak NJ, Reid LH, Pearsall RS, Reece M, Prawitt D, Landers J, Housman DE, Winterpacht A, Zabel BU, Pelletier J, Weissman BE, Shows TB, Higgins MJ.
    Genomics; 1998 Apr 01; 49(1):38-51. PubMed ID: 9570947
    [Abstract] [Full Text] [Related]

  • 10. Infrequent mutation of the WT1 gene in 77 Wilms' Tumors.
    Gessler M, König A, Arden K, Grundy P, Orkin S, Sallan S, Peters C, Ruyle S, Mandell J, Li F.
    Hum Mutat; 1994 Apr 01; 3(3):212-22. PubMed ID: 8019557
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers.
    Filippova GN, Lindblom A, Meincke LJ, Klenova EM, Neiman PE, Collins SJ, Doggett NA, Lobanenkov VV.
    Genes Chromosomes Cancer; 1998 May 17; 22(1):26-36. PubMed ID: 9591631
    [Abstract] [Full Text] [Related]

  • 13. Identification of the cellular protein encoded by the human Wilms' tumor (WT1) gene.
    Telerman A, Dodemont H, Degraef C, Galand P, Bauwens S, Van Oostveldt P, Amson RB.
    Oncogene; 1992 Dec 17; 7(12):2545-8. PubMed ID: 1334252
    [Abstract] [Full Text] [Related]

  • 14. cDNA sequence, genomic organization, and evolutionary conservation of a novel gene from the WAGR region.
    Schwartz F, Eisenman R, Knoll J, Gessler M, Bruns G.
    Genomics; 1995 Sep 20; 29(2):526-32. PubMed ID: 8666403
    [Abstract] [Full Text] [Related]

  • 15. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus.
    Call KM, Glaser T, Ito CY, Buckler AJ, Pelletier J, Haber DA, Rose EA, Kral A, Yeger H, Lewis WH.
    Cell; 1990 Feb 09; 60(3):509-20. PubMed ID: 2154335
    [Abstract] [Full Text] [Related]

  • 16. Wilms tumour: a developmental anomaly.
    Hastie ND, Bickmore W, Pritchard-Jones K, Porteous DJ, van Heyningen V.
    Princess Takamatsu Symp; 1989 Feb 09; 20():145-50. PubMed ID: 2562179
    [Abstract] [Full Text] [Related]

  • 17. Cloning and characterization of ZNF189, a novel human Krüppel-like zinc finger gene localized to chromosome 9q22-q31.
    Odeberg J, Røsok O, Gudmundsson GH, Ahmadian A, Roshani L, Williams C, Larsson C, Pontén F, Uhlén M, Asheim HC, Lundeberg J.
    Genomics; 1998 Jun 01; 50(2):213-21. PubMed ID: 9653648
    [Abstract] [Full Text] [Related]

  • 18. An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor.
    Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE.
    Cell; 1990 Jun 29; 61(7):1257-69. PubMed ID: 2163761
    [Abstract] [Full Text] [Related]

  • 19. Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome.
    Baird PN, Groves N, Haber DA, Housman DE, Cowell JK.
    Oncogene; 1992 Nov 29; 7(11):2141-9. PubMed ID: 1331933
    [Abstract] [Full Text] [Related]

  • 20. The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.
    Glaser T, Lewis WH, Bruns GA, Watkins PC, Rogler CE, Shows TB, Powers VE, Willard HF, Goguen JM, Simola KO.
    Nature; 1992 Nov 29; 321(6073):882-7. PubMed ID: 3014343
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 25.