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 *

183 related articles for article (PubMed ID: 8682500)

  • 1. Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation.
    Weterman MA; Wilbrink M; Dijkhuizen T; van den Berg E; Geurts van Kessel A
    Hum Genet; 1996 Jul; 98(1):16-21. PubMed ID: 8682500
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.
    Weterman MA; Wilbrink M; Janssen I; Janssen HA; van den Berg E; Fisher SE; Craig I; Geurts van Kessel A
    Cytogenet Cell Genet; 1996; 75(1):2-6. PubMed ID: 8995477
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2.
    Suijkerbuijk RF; Meloni AM; Sinke RJ; de Leeuw B; Wilbrink M; Janssen HA; Geraghty MT; Monaco AP; Sandberg AA; Geurts van Kessel A
    Cancer Genet Cytogenet; 1993 Dec; 71(2):164-9. PubMed ID: 8281521
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case.
    Shipley JM; Birdsall S; Clark J; Crew J; Gill S; Linehan M; Gnarra J; Fisher S; Craig IW; Cooper CS
    Cytogenet Cell Genet; 1995; 71(3):280-4. PubMed ID: 7587394
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma.
    Wilke CM; Guo SW; Hall BK; Boldog F; Gemmill RM; Chandrasekharappa SC; Barcroft CL; Drabkin HA; Glover TW
    Genomics; 1994 Jul; 22(2):319-26. PubMed ID: 7806217
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints.
    Sinke RJ; de Leeuw B; Janssen HA; Weghuis DO; Suijkerbuijk RF; Meloni AM; Gilgenkrantz S; Berger W; Ropers HH; Sandberg AA
    Hum Genet; 1993 Oct; 92(3):305-8. PubMed ID: 8406438
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Defining the position of the breakpoint of the constitutional t(3;6) occurring in a family with renal cell carcinoma.
    van den Berg A; van der Veen AY; Hulsbeek MM; Kovacs G; Gemmill RM; Drabkin HA; Buys CH
    Genes Chromosomes Cancer; 1995 Mar; 12(3):224-8. PubMed ID: 7536463
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mapping of 29 YAC clones and identification of 3 YACs spanning the translocation t(3;8)(p14.2;q24.1) breakpoint at 8q24.1 in hereditary renal cell carcinoma.
    Shi G; Cannizzaro LA
    Cytogenet Cell Genet; 1996; 75(2-3):180-5. PubMed ID: 9040788
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular cytogenetics of t(X;1)(p11.2;q21) with complex rearrangements in a renal cell carcinoma.
    Zattara-Cannoni H; Daniel L; Roll P; Coulange C; Vagner-Capodano A
    Cancer Genet Cytogenet; 2000 Nov; 123(1):61-4. PubMed ID: 11120337
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detailed mapping around the breakpoint of (3;8) translocation in familial renal cell carcinoma and FRA3B.
    Yamakawa K; Takahashi E; Murata M; Okui K; Yokoyama S; Nakamura Y
    Genomics; 1992 Oct; 14(2):412-6. PubMed ID: 1427857
    [TBL] [Abstract][Full Text] [Related]  

  • 11. FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure.
    Riva P; Magnani I; Fuhrmann Conti AM; Gelli D; Sala C; Toniolo D; Larizza L
    Clin Genet; 1996 Oct; 50(4):267-9. PubMed ID: 9001815
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fine mapping of the human renal oncocytoma-associated translocation (5;11)(q35;q13) breakpoint.
    Sinke RJ; Dijkhuizen T; Janssen B; Olde Weghuis D; Merkx G; van den Berg E; Schuuring E; Meloni AM; de Jong B; Geurts van Kessel A
    Cancer Genet Cytogenet; 1997 Jul; 96(2):95-101. PubMed ID: 9216713
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B.
    Boldog FL; Waggoner B; Glover TW; Chumakov I; Le Paslier D; Cohen D; Gemmill RM; Drabkin HA
    Genes Chromosomes Cancer; 1994 Dec; 11(4):216-21. PubMed ID: 7533524
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene.
    Sidhar SK; Clark J; Gill S; Hamoudi R; Crew AJ; Gwilliam R; Ross M; Linehan WM; Birdsall S; Shipley J; Cooper CS
    Hum Mol Genet; 1996 Sep; 5(9):1333-8. PubMed ID: 8872474
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Renal cell carcinoma with translocation (X;1). Further evidence for a cytogenetically defined subtype.
    Tonk V; Wilson KS; Timmons CF; Schneider NR; Tomlinson GE
    Cancer Genet Cytogenet; 1995 May; 81(1):72-5. PubMed ID: 7773963
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
    Laureys G; Speleman F; Versteeg R; van der Drift P; Chan A; Leroy J; Francke U; Opdenakker G; Van Roy N
    Oncogene; 1995 Mar; 10(6):1087-93. PubMed ID: 7700633
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detailed genetic and physical map of the 3p chromosome region surrounding the familial renal cell carcinoma chromosome translocation, t(3;8)(p14.2;q24.1).
    LaForgia S; Lasota J; Latif F; Boghosian-Sell L; Kastury K; Ohta M; Druck T; Atchison L; Cannizzaro LA; Barnea G
    Cancer Res; 1993 Jul; 53(13):3118-24. PubMed ID: 8319219
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG
    Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Delineation of the breakpoint at 18q21.1 in a cell line (Karpas1106) derived from mediastinal B-cell lymphoma by fluorescence in situ hybridization with multiple YAC clones.
    Tamura A; Akagi T; Nakazawa N; Kashima K; Nakamura S; Karpas A; Silverman GA; Morishima Y; Taniwaki M; Seto M
    Int J Cancer; 1998 Sep; 78(1):100-5. PubMed ID: 9724100
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Translocation (X;1)(p11.2;q21) in a papillary renal cell carcinoma in a 14-year-old girl.
    Kardaś I; Denis A; Babińska M; Gronwald J; Podolski J; Zajaczek S; Kram A; Lubiński J; Limon J
    Cancer Genet Cytogenet; 1998 Mar; 101(2):159-61. PubMed ID: 9494621
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.