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FEMS Microbiology Letters|March 1, 1997
Synthesis and antifungal activity of two novel spermidine analoguesC A Mackintosh, L A Slater, C A McClintock, et al.Cancer Chemotherapy and Pharmacology|January 1, 1986
CB 1954 revisited. II. Toxicity and antitumour activityP Workman, J E Morgan, K Talbot, et al.Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|January 1, 1991
The combination of multiple doses of etanidazole and pimonidazole in 48 patients: a toxicity and pharmacokinetic studyN M Bleehen, T S Maughan, P Workman, et al.British Journal of Cancer|August 1, 1995
The novel fluorinated 2-nitroimidazole hypoxia probe SR-4554: reductive metabolism and semiquantitative localisation in human ovarian cancer multicellular spheroids as measured by electron energy loss spectroscopic analysisE O Aboagye, A D Lewis, A Johnson, et al.British Journal of Cancer|September 1, 1992
Tumour concentrations of flavone acetic acid (FAA) in human melanoma: comparison with mouse dataT S Maughan, R Ward, I Dennis, et al.Phytochemistry|January 8, 2000
Specificities of the enzymes of N-alkyltropane biosynthesis in Brugmansia and DaturaH D Boswell, B Dräger, W R McLauchlan, et al.The Biochemical Journal|January 15, 1995
Escherichia coli dihydrodipicolinate synthase: characterization of the imine intermediate and the product of bromopyruvate treatment by electrospray mass spectrometryE B Borthwick, S J Connell, D W Tudor, et al.Journal of Chromatography. B, Biomedical Applications|October 6, 1995
Development and validation of a solid-phase extraction and high-performance liquid chromatographic assay for a novel fluorinated 2-nitroimidazole hypoxia probe (SR-4554) in Balb/c mouse plasmaE O Aboagye, M A Graham, A D Lewis, et al.Molecular Pharmacology|October 20, 2000
Establishment of an isogenic human colon tumor model for NQO1 gene expression: application to investigate the role of DT-diaphorase in bioreductive drug activation in vitro and in vivoS Y Sharp, L R Kelland, M R Valenti, et al.Biochemical Pharmacology|October 23, 1998
Reduction of the indoloquinone anticancer drug EO9 by purified DT-diaphorase: a detailed kinetic study and analysis of metabolitesS M Bailey, A D Lewis, R J Knox, et al.Pageof 25