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Anticancer Research|February 1, 2000
Microbial conversion of methyl- and methoxy- substituted derivatives of 5H-indolo[2,3-b]quinoline as a method of developing novel cytotoxic agentsJ Osiadacz, L Kaczmarek, A Opolski, et al.Bioconjugate Chemistry|July 21, 1998
Liposomal formulations of synthetic MUC1 peptides: effects of encapsulation versus surface display of peptides on immune responsesH H Guan, W Budzynski, R R Koganty, et al.Bioorganic & Medicinal Chemistry|January 13, 2000
Synthesis, and cytotoxic activity of some novel indolo[2,3-b]quinoline derivatives: DNA topoisomerase II inhibitorsL Kaczmarek, W Peczyńska-Czoch, J Osiadacz, et al.Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|February 24, 2001
Antitumor effect of electrochemical therapy on transplantable mouse cancersM Wójcicki, M Droździk, S Olewniczak, et al.Oncology Reports|October 18, 2001
Chemoimmunotherapy of cancer: potentiated effectiveness of granulocyte-macrophage colony-stimulating factor and ifosfamide derivative CBM-4AM Indrová, J Bubeník, J Símová, et al.Journal of Medicinal Chemistry|September 10, 1999
8,11-dihydroxy-6-[(aminoalkyl)amino]-7H-benzo[e]perimidin-7-ones with activity in multidrug-resistant cell lines: synthesis and antitumor evaluationB Stefańska, M Dzieduszycka, M M Bontemps-Gracz, et al.Pageof 11