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International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine|October 1, 1983
Radiosensitization in vivo: a study with an homologous series of 2-nitroimidazolesD J Chaplin, P W Sheldon, I J Stratford, et al.BMJ (Clinical Research Ed.)|January 11, 1997
Are short normal children at a disadvantage? The Wessex growth studyA B Downie, J Mulligan, R J Stratford, et al.The British Journal of Radiology|December 21, 2012
Comparison of adaptive radiotherapy techniques for the treatment of bladder cancerG J Webster, J Stratford, J Rodgers, et al.Bioorganic & Medicinal Chemistry Letters|September 30, 2004
Synthesis and enzymatic evaluation of xanthine oxidase-activated prodrugs based on inhibitors of thymidine phosphorylasePhilip Reigan, Abdul Gbaj, Edwin Chinje, et al.Radiation Research|October 1, 1990
Dual-function 2-nitroimidazoles as hypoxic cell radiosensitizers and bioreductive cytotoxins: in vivo evaluation in KHT murine sarcomasS Cole, I J Stratford, G E Adams, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 3, 2005
Tirapazamine administered as a neoadjuvant to radiotherapy reduces metastatic disseminationSarah Jane Lunt, Brian A Telfer, Richard J Fitzmaurice, et al.International Journal of Radiation Oncology, Biology, Physics|January 31, 2004
The bioreductive agent RH1 and gamma-irradiation both cause G2/M cell cycle phase arrest and polyploidy in a p53-mutated human breast cancer cell lineJoo-Young Kim, Chul-Hwan Kim, Ian J Stratford, et al.Anti-Cancer Drug Design|April 15, 2000
A similarity model for the human angiogenic factor, thymidine phosphorylase/platelet derived-endothelial cell growth factorC Cole, D S Marks, M Jaffar, et al.Analytical and Bioanalytical Chemistry|February 20, 2010
Spectrophotometric analysis of nucleic acids: oxygenation-dependent hyperchromism of DNARupak Doshi, Philip J R Day, Paolo Carampin, et al.British Journal of Cancer|June 1, 1993
Differential modulation of doxorubicin toxicity to multidrug and intrinsically drug resistant cell lines by anti-oestrogens and their major metabolitesJ Kirk, S Houlbrook, N S Stuart, et al.Pageof 33