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1 1200 mg or chemotherapy (physician's choice: vinflunine 320 mg/m(2), paclitaxel 175 mg/m(2), or 75 mg
3 at the mitotic IC(50) value was highest for vinflunine (4.2 +/- 0.2 microM), intermediate for vinore
6 -generation Vinca alkaloids, vinorelbine and vinflunine, affect microtubule dynamics very differently
7 Thus the unique constellation of effects of vinflunine and vinorelbine on dynamic instability and tr
10 latively less powerful inhibitory effects of vinflunine and vinorelbine on microtubule dynamics bette
14 axation times for polymer redistribution for vinflunine consistent with induction of the shortest spi
16 ntation velocity to compare vinorelbine- and vinflunine-induced self-association of porcine brain tub
19 entirely consistent with our hypothesis that vinflunine is likely to result in reduced clinical neuro
20 eservoir(s) may be partially responsible for vinflunine's high efficacy and minimal side effects.
22 shortening in vitro, whereas vinorelbine and vinflunine suppress the rate and extent of microtubule g
23 or inhibition of HeLa cell proliferation for vinflunine, vinorelbine, and vinblastine were 18, 1.25,
24 ng immune cells [IC2/3]), chemotherapy type (vinflunine vs taxanes), liver metastases (yes vs no), an
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