BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 8406484)

  • 1. Determination of the specificity of aphidicolin-induced breakage of the human 3p14.2 fragile site.
    Wang ND; Testa JR; Smith DI
    Genomics; 1993 Aug; 17(2):341-7. PubMed ID: 8406484
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3.
    Paradee W; Mullins C; He Z; Glover T; Wilke C; Opalka B; Schutte J; Smith DI
    Genomics; 1995 May; 27(2):358-61. PubMed ID: 7558007
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.
    Paradee W; Wilke CM; Wang L; Shridhar R; Mullins CM; Hoge A; Glover TW; Smith DI
    Genomics; 1996 Jul; 35(1):87-93. PubMed ID: 8661108
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions.
    Wang L; Paradee W; Mullins C; Shridhar R; Rosati R; Wilke CM; Glover TW; Smith DI
    Genomics; 1997 May; 41(3):485-8. PubMed ID: 9169152
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors.
    Corbin S; Neilly ME; Espinosa R; Davis EM; McKeithan TW; Le Beau MM
    Cancer Res; 2002 Jun; 62(12):3477-84. PubMed ID: 12067991
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FHIT gene.
    Zimonjic DB; Druck T; Ohta M; Kastury K; Croce CM; Popescu NC; Huebner K
    Cancer Res; 1997 Mar; 57(6):1166-70. PubMed ID: 9067288
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequent breakpoints in the region surrounding FRA3B in sporadic renal cell carcinomas.
    Shridhar V; Wang L; Rosati R; Paradee W; Shridhar R; Mullins C; Sakr W; Grignon D; Miller OJ; Sun QC; Petros J; Smith DI
    Oncogene; 1997 Mar; 14(11):1269-77. PubMed ID: 9178887
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosome breakage and recombination at fragile sites.
    Glover TW; Stein CK
    Am J Hum Genet; 1988 Sep; 43(3):265-73. PubMed ID: 3137811
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes.
    Glover TW; Coyle-Morris JF; Li FP; Brown RS; Berger CS; Gemmill RM; Hecht F
    Cancer Genet Cytogenet; 1988 Mar; 31(1):69-73. PubMed ID: 3125959
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14.
    Tajara EH; Berger CS; Hecht BK; Gemmill RM; Sandberg AA; Hecht F
    Cancer Genet Cytogenet; 1988 Mar; 31(1):75-82. PubMed ID: 3125960
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Localization of three novel hybrid breakpoints and refinement of 18 marker assignments in the human 3cen-p21.1 region.
    Wang ND; Testa JR; Smith DI
    Genomics; 1992 Dec; 14(4):891-6. PubMed ID: 1478670
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations.
    Krummel KA; Roberts LR; Kawakami M; Glover TW; Smith DI
    Genomics; 2000 Oct; 69(1):37-46. PubMed ID: 11013073
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3.
    Haas M; Aburatani H; Stanton VP; Bhatt M; Housman D; Ward DC
    Genomics; 1993 Apr; 16(1):90-6. PubMed ID: 8486389
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Chromosomal fragile site FRA16D and DNA instability in cancer.
    Mangelsdorf M; Ried K; Woollatt E; Dayan S; Eyre H; Finnis M; Hobson L; Nancarrow J; Venter D; Baker E; Richards RI
    Cancer Res; 2000 Mar; 60(6):1683-9. PubMed ID: 10749140
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites.
    Rassool FV; McKeithan TW; Neilly ME; van Melle E; Espinosa R; Le Beau MM
    Proc Natl Acad Sci U S A; 1991 Aug; 88(15):6657-61. PubMed ID: 1862089
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site region.
    Glover TW; Hoge AW; Miller DE; Ascara-Wilke JE; Adam AN; Dagenais SL; Wilke CM; Dierick HA; Beer DG
    Cancer Res; 1998 Aug; 58(15):3409-14. PubMed ID: 9699673
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.
    Rassool FV; Le Beau MM; Shen ML; Neilly ME; Espinosa R; Ong ST; Boldog F; Drabkin H; McCarroll R; McKeithan TW
    Genomics; 1996 Jul; 35(1):109-17. PubMed ID: 8661111
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FHIT gene and the FRA3B region are not involved in the genetics of renal cell carcinomas.
    Bugert P; Wilhelm M; Kovacs G
    Genes Chromosomes Cancer; 1997 Sep; 20(1):9-15. PubMed ID: 9290948
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.