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5. Liposomal vincristine preparations which exhibit decreased drug toxicity and increased activity against murine L1210 and P388 tumors. Mayer LD; Bally MB; Loughrey H; Masin D; Cullis PR Cancer Res; 1990 Feb; 50(3):575-9. PubMed ID: 2297698 [TBL] [Abstract][Full Text] [Related]
6. Experimental antitumor activity and toxicity of the selected triazolo- and imidazoacridinones. Kuśnierczyk H; Chołody WM; Paradziej-Lukowicz J; Radzikowski C; Konopa J Arch Immunol Ther Exp (Warsz); 1994; 42(5-6):415-23. PubMed ID: 8572901 [TBL] [Abstract][Full Text] [Related]
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8. Reduced toxicity and enhanced antitumor effects in mice of the ionophoric drug valinomycin when incorporated in liposomes. Daoud SS; Juliano RL Cancer Res; 1986 Nov; 46(11):5518-23. PubMed ID: 3756900 [TBL] [Abstract][Full Text] [Related]
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11. Liposomal vincristine which exhibits increased drug retention and increased circulation longevity cures mice bearing P388 tumors. Boman NL; Masin D; Mayer LD; Cullis PR; Bally MB Cancer Res; 1994 Jun; 54(11):2830-3. PubMed ID: 8187061 [TBL] [Abstract][Full Text] [Related]
12. F 11782, a dual inhibitor of topoisomerases I and II with an original mechanism of action in vitro, and markedly superior in vivo antitumour activity, relative to three other dual topoisomerase inhibitors, intoplicin, aclarubicin and TAS-103. Etiévant C; Kruczynski A; Barret JM; Perrin D; van Hille B; Guminski Y; Hill BT Cancer Chemother Pharmacol; 2000; 46(2):101-13. PubMed ID: 10972479 [TBL] [Abstract][Full Text] [Related]
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14. A fluorine-containing anthracycline (ME2303) as a new antitumor agent against murine and human tumors and their multidrug-resistant sublines. Tsuruo T; Yusa K; Sudo Y; Takamori R; Sugimoto Y Cancer Res; 1989 Oct; 49(20):5537-42. PubMed ID: 2790778 [TBL] [Abstract][Full Text] [Related]
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