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Journal Abstract Search

81 related items for PubMed ID: 21567044

  • 1. Multidrug-resistance circumvention and inhibition of [h-3] azidopine photolabeling of p-glycoprotein by new dihydropyridine derivatives displaying a low-affinity for calcium channels.
    Leonce S, Pierre A, Perez V, Guilbaud N, Krausberthier L, Genton A, Lombet A, Peglion J, Atassi G.
    Int J Oncol; 1994 Jun; 4(6):1243-50. PubMed ID: 21567044
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  • 2. [In vitro characterization of S9788, a new modulator of multidrug resistance].
    Pérez V, Pierré A, Léonce S, Anstett M, Prost JF, Atassi G.
    Bull Cancer; 1993 Apr; 80(4):310-25. PubMed ID: 8173185
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  • 5. In vitro cytotoxicity of S16020-2, a new olivacine derivative.
    Léonce S, Perez V, Casabianca-Pignede MR, Anstett M, Bisagni E, Pierré A, Atassi G.
    Invest New Drugs; 1996 Apr; 14(2):169-80. PubMed ID: 8913838
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  • 7. Activities of newly synthesized dihydropyridines in overcoming of vincristine resistance, calcium antagonism, and inhibition of photoaffinity labeling of P-glycoprotein in rodents.
    Kiue A, Sano T, Suzuki K, Inada H, Okumura M, Kikuchi J, Sato S, Kohno K, Kuwano M.
    Cancer Res; 1990 Jan 15; 50(2):310-7. PubMed ID: 1967223
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  • 8. Circumvention of P-glycoprotein-mediated multidrug resistance by S16020-2: kinetics of uptake and efflux in sensitive and resistant cell lines.
    Pierré A, Léonce S, Pérez V, Atassi G.
    Cancer Chemother Pharmacol; 1998 Jan 15; 42(6):454-60. PubMed ID: 9788571
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  • 10. In vitro and in vivo circumvention of multidrug resistance by Servier 9788, a novel triazinoaminopiperidine derivative.
    Pierré A, Dunn TA, Kraus-Berthier L, Léonce S, Saint-Dizier D, Régnier G, Dhainaut A, Berlion M, Bizzari JP, Atassi G.
    Invest New Drugs; 1992 Aug 15; 10(3):137-48. PubMed ID: 1428723
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  • 11. Reversal of multidrug resistance by a novel quinoline derivative, MS-209.
    Sato W, Fukazawa N, Nakanishi O, Baba M, Suzuki T, Yano O, Naito M, Tsuruo T.
    Cancer Chemother Pharmacol; 1995 Aug 15; 35(4):271-7. PubMed ID: 7828268
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  • 12. Potentiation of etoposide and vincristine by two synthetic 1,4-dihydropyridine derivatives in multidrug-resistant and atypical multidrug-resistant human cancer cells.
    Watanabe Y, Takano H, Kiue A, Kohno K, Kuwano M.
    Anticancer Drug Des; 1991 Feb 15; 6(1):47-57. PubMed ID: 2015041
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  • 16. Reversal by two dihydropyridine compounds of resistance to multiple anticancer agents in mouse P388 leukemia in vivo and in vitro.
    Kiue A, Sano T, Naito A, Inada H, Suzuki K, Okumura M, Kikuchi J, Sato S, Takano H, Kohno K.
    Jpn J Cancer Res; 1990 Oct 15; 81(10):1057-64. PubMed ID: 1977728
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  • 17. Correlation between reversing of multidrug resistance and inhibiting of [3H]azidopine photolabeling of P-glycoprotein by newly synthesized dihydropyridine analogues in a human cell line.
    Kamiwatari M, Nagata Y, Kikuchi H, Yoshimura A, Sumizawa T, Shudo N, Sakoda R, Seto K, Akiyama S.
    Cancer Res; 1989 Jun 15; 49(12):3190-5. PubMed ID: 2566378
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  • 18. Potentiation of the vincristine effect on P388 mouse leukemia cells by a newly synthesized dihydropyridine analogue, PAK-200.
    Shudo N, Fujii R, Matsumoto T, Mizoguchi T, Seto K, Sakoda R, Akiyama S.
    Jpn J Cancer Res; 1992 Sep 15; 83(9):1011-7. PubMed ID: 1429198
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  • 19. New triazine derivatives as potent modulators of multidrug resistance.
    Dhainaut A, Régnier G, Atassi G, Pierré A, Léonce S, Kraus-Berthier L, Prost JF.
    J Med Chem; 1992 Jun 26; 35(13):2481-96. PubMed ID: 1352353
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  • 20. Circumvention of vincristine and Adriamycin resistance in vitro and in vivo by calcium influx blockers.
    Tsuruo T, Iida H, Nojiri M, Tsukagoshi S, Sakurai Y.
    Cancer Res; 1983 Jun 26; 43(6):2905-10. PubMed ID: 6850602
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