BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

92 related articles for article (PubMed ID: 1478670)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. Isolation and characterization of somatic cell hybrids with breakpoints spanning 17q22-->q24.
    Flejter WL; Watkins M; Abel KJ; Chandrasekharappa SC; Weber BL; Collins FS; Glover TW
    Cytogenet Cell Genet; 1993; 64(3-4):222-3. PubMed ID: 8404043
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Mapping of the gene for human cysteine proteinase inhibitor stefin A, STF1, to chromosome 3cen-q21.
    Hsieh WT; Fong D; Sloane BF; Golembieski W; Smith DI
    Genomics; 1991 Jan; 9(1):207-9. PubMed ID: 2004763
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A somatic cell hybrid map of human chromosome 13.
    Washington SS; Bowcock AM; Gerken S; Matsunami N; Lesh D; Osborne-Lawrence SL; Cowell J; Ledbetter DH; White RL; Chakravarti A
    Genomics; 1993 Dec; 18(3):486-95. PubMed ID: 8307557
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Regional localization of 188 sequence tagged sites on a somatic cell hybrid mapping panel for human chromosome 3.
    Leach RJ; Chinn R; Reus BE; Hayes S; Schantz L; Dubois B; Overhauser J; Ballabio A; Drabkin H; Lewis TB
    Genomics; 1994 Dec; 24(3):549-56. PubMed ID: 7713507
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Definition of a tumor suppressor locus within human chromosome 3p21-p22.
    Killary AM; Wolf ME; Giambernardi TA; Naylor SL
    Proc Natl Acad Sci U S A; 1992 Nov; 89(22):10877-81. PubMed ID: 1438292
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Regional localization of chromosome 3-specific DNA fragments by using a hybrid cell deletion mapping panel.
    Gerber MJ; Drabkin HA; Firnhaber C; Miller YE; Scoggin CH; Smith DI
    Am J Hum Genet; 1988 Oct; 43(4):442-51. PubMed ID: 2902784
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Assignment of the human serotonin 1F receptor gene (HTR1F) to the short arm of chromosome 3 (3p13-p14.1).
    Erdmann J; Shimron-Abarbanell D; Shridhar V; Smith DI; Propping P; Nöthen MM
    Mol Membr Biol; 1997; 14(3):133-5. PubMed ID: 9394293
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation and genetic mapping of four microsatellite repeats from chromosome 3p21 using 40 CEPH pedigrees.
    Kumar-Singh R; Humphries P
    Genomics; 1993 Dec; 18(3):717-9. PubMed ID: 8307583
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Refining a proximal breakpoint cluster at chromosome 3p11.2 in non-papillary renal cell carcinomas.
    Bugert P; Kenck C; Wilhelm M; Kovacs G
    Int J Cancer; 1996 Dec; 68(6):723-6. PubMed ID: 8980173
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A hamster-human subchromosomal hybrid cell panel for chromosome 2.
    Jeggo PA; Hafezparast M; Thompson AF; Kaur GP; Sandhu AK; Athwal RS
    Somat Cell Mol Genet; 1993 Jan; 19(1):39-49. PubMed ID: 8460397
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.