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Journal Abstract Search

95 related items for PubMed ID: 6848172

  • 1. Cytocidal action of the quinone group and its relationship to antitumor activity.
    Begleiter A.
    Cancer Res; 1983 Feb; 43(2):481-4. PubMed ID: 6848172
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  • 3. Characterization of L5178Y murine lymphoblasts resistant to quinone antitumor agents.
    Begleiter A, Leith MK, McClarty G, Beenken S, Goldenberg GJ, Wright JA.
    Cancer Res; 1988 Apr 01; 48(7):1727-35. PubMed ID: 3127038
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  • 4. Activity of quinone alkylating agents in quinone-resistant cells.
    Begleiter A, Leith MK.
    Cancer Res; 1990 May 15; 50(10):2872-6. PubMed ID: 1692249
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  • 5. Studies on the mechanism of action of quinone antitumor agents.
    Begleiter A.
    Biochem Pharmacol; 1985 Aug 01; 34(15):2629-36. PubMed ID: 4015705
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  • 6. The contribution of alkylation to the activity of quinone antitumor agents.
    Begleiter A.
    Can J Physiol Pharmacol; 1986 May 01; 64(5):581-5. PubMed ID: 3730943
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  • 7. The effect of functional groups on reduction and activation of quinone bioreductive agents by DT-diaphorase.
    Fourie J, Oleschuk CJ, Guziec F, Guziec L, Fiterman DJ, Monterrosa C, Begleiter A.
    Cancer Chemother Pharmacol; 2002 Feb 01; 49(2):101-10. PubMed ID: 11862423
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  • 11. Structure-activity study with bioreductive benzoquinone alkylating agents: effects on DT-diaphorase-mediated DNA crosslink and strand break formation in relation to mechanisms of cytotoxicity.
    Fourie J, Guziec F, Guziec L, Monterrosa C, Fiterman DJ, Begleiter A.
    Cancer Chemother Pharmacol; 2004 Mar 01; 53(3):191-203. PubMed ID: 14614574
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  • 12. Increased sensitivity of quinone resistant cells to mitomycin C.
    Begleiter A, Robotham E, Lacey G, Leith MK.
    Cancer Lett; 1989 Jun 01; 45(3):173-6. PubMed ID: 2471583
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  • 13. Increased expression of cytosolic glutathione S-transferases in drug-resistant L5178Y murine lymphoblasts: chemical selectivity and molecular mechanisms.
    Stelmack GL, Goldenberg GJ.
    Cancer Res; 1993 Aug 01; 53(15):3530-5. PubMed ID: 8101761
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  • 14. Characterization of the DNA-DNA cross-linking activity of 3'-(3-cyano-4-morpholinyl)-3'-deaminoadriamycin.
    Jesson MI, Johnston JB, Robotham E, Begleiter A.
    Cancer Res; 1989 Dec 15; 49(24 Pt 1):7031-6. PubMed ID: 2531036
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  • 15. Metabolic activation of PCBs to quinones: reactivity toward nitrogen and sulfur nucleophiles and influence of superoxide dismutase.
    Amaro AR, Oakley GG, Bauer U, Spielmann HP, Robertson LW.
    Chem Res Toxicol; 1996 Dec 15; 9(3):623-9. PubMed ID: 8728508
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  • 16. The role of NAD(P)H:quinone oxidoreductase in quinone-mediated p21 induction in human colon carcinoma cells.
    Qiu XB, Cadenas E.
    Arch Biochem Biophys; 1997 Oct 15; 346(2):241-51. PubMed ID: 9343371
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  • 17. Preclinical screening for drugs effective against 5-fluorouracil-resistant cells with a murine L5178Y cell line in vitro.
    Hill BT.
    J Natl Cancer Inst; 1983 Aug 15; 71(2):335-40. PubMed ID: 6576190
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  • 18. Effect of hydroxyurea treatment on lysosomal membrane stability and enzyme latency in L5178Y cells in culture.
    Przybyszewski WM, Czartoryska B, Malec J.
    Neoplasma; 1986 Aug 15; 33(1):27-31. PubMed ID: 3960209
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  • 19. Cytotoxicity and DNA cross-linking activity of 4-sulfidocyclophosphamides in mouse leukemia cells in vitro.
    Erickson LC, Ramonas LM, Zaharko DS, Kohn KW.
    Cancer Res; 1980 Nov 15; 40(11):4216-20. PubMed ID: 7471062
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  • 20. Data mining the NCI cancer cell line compound GI(50) values: identifying quinone subtypes effective against melanoma and leukemia cell classes.
    Marx KA, O'Neil P, Hoffman P, Ujwal ML.
    J Chem Inf Comput Sci; 2003 Nov 15; 43(5):1652-67. PubMed ID: 14502500
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