BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

874 related articles for article (PubMed ID: 14978789)

  • 21. Localization of tumor suppressor loci on chromosome 9 in primary human renal cell carcinomas.
    Cairns P; Tokino K; Eby Y; Sidransky D
    Cancer Res; 1995 Jan; 55(2):224-7. PubMed ID: 7812948
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of candidate liver tumor suppressor genes from human 11p11.2 by transcription mapping of microcell hybrid cell lines.
    Jahn JE; Ricketts SL; Coleman WB
    Int J Oncol; 2003 Jun; 22(6):1303-10. PubMed ID: 12738998
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of a novel region of homozygous deletion on chromosome 9p in squamous cell carcinoma of the lung: the location of a putative tumor suppressor gene.
    Wiest JS; Franklin WA; Otstot JT; Forbey K; Varella-Garcia M; Rao K; Drabkin H; Gemmill R; Ahrent S; Sidransky D; Saccomanno G; Fountain JW; Anderson MW
    Cancer Res; 1997 Jan; 57(1):1-6. PubMed ID: 8988029
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification of three 11p11.2 candidate liver tumor suppressors through analysis of known human genes.
    Ricketts SL; Carter JC; Coleman WB
    Mol Carcinog; 2003 Feb; 36(2):90-9. PubMed ID: 12557265
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Deletion mapping of chromosome 3p in human uterine cervical cancer.
    Kohno T; Takayama H; Hamaguchi M; Takano H; Yamaguchi N; Tsuda H; Hirohashi S; Vissing H; Shimizu M; Oshimura M
    Oncogene; 1993 Jul; 8(7):1825-32. PubMed ID: 8099726
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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; 22(1):26-36. PubMed ID: 9591631
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Previous loss of chromosome 11 containing a suppressor locus increases radiosensitivity, neoplastic transformation frequency and delayed death in HeLa x fibroblast human hybrid cells.
    Mendonca MS; Howard K; Desmond LA; Derrow CW
    Mutagenesis; 1999 Sep; 14(5):483-90. PubMed ID: 10473652
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genomic organization and mutation analysis of Hel-N1 in lung cancers with chromosome 9p21 deletions.
    Cairns P; Okami K; King P; Bonacum J; Ahrendt S; Wu L; Mao L; Jen J; Sidransky D
    Cancer Res; 1997 Dec; 57(23):5356-9. PubMed ID: 9393760
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mapping of a candidate colorectal cancer tumor-suppressor gene to a 900-kilobase region on the short arm of chromosome 8.
    Flanagan JM; Healey S; Young J; Whitehall V; Trott DA; Newbold RF; Chenevix-Trench G
    Genes Chromosomes Cancer; 2004 Jul; 40(3):247-60. PubMed ID: 15139003
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fine mapping and evaluation of candidate genes for cervical cancer on 11q23.
    Zhang Z; Gerhard DS; Nguyen L; Li J; Traugott A; Huettner PC; Rader JS
    Genes Chromosomes Cancer; 2005 May; 43(1):95-103. PubMed ID: 15672406
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Homozygous deletion at the 9q32-33 candidate tumor suppressor locus in primary human bladder cancer.
    Nishiyama H; Takahashi T; Kakehi Y; Habuchi T; Knowles MA
    Genes Chromosomes Cancer; 1999 Oct; 26(2):171-5. PubMed ID: 10469456
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Localization and characterization of a chromosome 11 tumor suppressor gene using organotypic raft cultures.
    Gioeli D; Conway K; Weissman BE
    Cancer Res; 1997 Mar; 57(6):1157-65. PubMed ID: 9067287
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Understanding the mechanisms of FHIT inactivation in cervical cancer for biomarker development.
    Lea JS; Ashfaq R; Muneer S; Burbee DG; Miller DS; Minna JD; Muller CY
    J Soc Gynecol Investig; 2004 Jul; 11(5):329-37. PubMed ID: 15219888
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Homozygous deletion on the chromosomal region 5q12.3 in human lines of small-cell lung cancers.
    Tamura K; Miwa W; Maruyama T; Sekiya T; Murakami Y
    J Hum Genet; 2002; 47(7):348-54. PubMed ID: 12111368
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular mapping of chromosome 2 deletions in murine radiation-induced AML localizes a putative tumor suppressor gene to a 1.0 cM region homologous to human chromosome segment 11p11-12.
    Silver A; Moody J; Dunford R; Clark D; Ganz S; Bulman R; Bouffler S; Finnon P; Meijne E; Huiskamp R; Cox R
    Genes Chromosomes Cancer; 1999 Feb; 24(2):95-104. PubMed ID: 9885975
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Transcript map and complete genomic sequence for the 310 kb region of minimal allele loss on chromosome segment 11p15.5 in non-small-cell lung cancer.
    Zhao B; Bepler G
    Oncogene; 2001 Dec; 20(56):8154-64. PubMed ID: 11781830
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Suppression of tumorigenicity of rat liver tumor cells by human chromosome 13: evidence against the involvement of pRb and BRCA2.
    Rider MA; Butz GM; Ricketts SL; Newberry ST; Grisham JW; Coleman WB
    Int J Oncol; 2002 Feb; 20(2):235-45. PubMed ID: 11788883
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Fluorescence in situ hybridization deletion mapping at 4p16.3 in bladder cancer cell lines refines the localisation of the critical interval to 30 kb.
    Bell SM; Zuo J; Myers RM; Knowles MA
    Genes Chromosomes Cancer; 1996 Oct; 17(2):108-17. PubMed ID: 8913728
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Homozygous deletion and frequent allelic loss of chromosome 8p22 loci in human prostate cancer.
    Bova GS; Carter BS; Bussemakers MJ; Emi M; Fujiwara Y; Kyprianou N; Jacobs SC; Robinson JC; Epstein JI; Walsh PC
    Cancer Res; 1993 Sep; 53(17):3869-73. PubMed ID: 7689419
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A region on human chromosome 4 (q35.1-->qter) induces senescence in cell hybrids and is involved in cervical carcinogenesis.
    Backsch C; Rudolph B; Kühne-Heid R; Kalscheuer V; Bartsch O; Jansen L; Beer K; Meyer B; Schneider A; Dürst M
    Genes Chromosomes Cancer; 2005 Jul; 43(3):260-72. PubMed ID: 15838843
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 44.