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Titlebook: Concepts, Mechanisms, and New Targets for Chemotherapy; F. M. Muggia Book 1995 Springer Science+Business Media New York 1995 DNA.breast ca

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發(fā)表于 2025-3-25 03:51:31 | 只看該作者
Book 1995. One route that has not beentravelled previously is that of protein kinase C inhibition. Thispathway may be exploited to give potent inhibitors, such as thebryostatins, now in clinical trial. A summary is given of the currentstatus of topoisomerase, focusing on recent clinical advances withcamptoth
22#
發(fā)表于 2025-3-25 10:51:20 | 只看該作者
Ein Aufwachsen mit zahlreichen Anforderungenising preclinical activity has stimulated tremendous excitement about these agents. The remainder of this chapter reviews the mechanism of action, clinical pharmacology, toxicity profiles, and antitumor activities of these drugs used either as single agents or in combination chemotherapy.
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發(fā)表于 2025-3-25 12:45:09 | 只看該作者
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發(fā)表于 2025-3-25 15:53:09 | 只看該作者
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發(fā)表于 2025-3-25 21:20:59 | 只看該作者
0927-3042 rapy usingvarious skin malignancies. In prostate cancer, estramustine phosphatewill likely play an expanding role. Taxanes are restructuringtreatment regimens i978-1-4613-5829-9978-1-4615-2007-8Series ISSN 0927-3042 Series E-ISSN 2509-8497
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發(fā)表于 2025-3-26 03:22:25 | 只看該作者
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發(fā)表于 2025-3-26 08:23:46 | 只看該作者
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發(fā)表于 2025-3-26 12:16:04 | 只看該作者
Die Suche nach der eigenen Identit?tsed following treatment with, more conventional doses of the same agents. Some patients achieve prolonged disease-free survival and are possibly cured. This modality has been associated with substantial morbidity and morality, however, principally due to the relatively prolonged period of pancytopen
29#
發(fā)表于 2025-3-26 12:52:23 | 只看該作者
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發(fā)表于 2025-3-26 19:06:07 | 只看該作者
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