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G E Adams

Showing results (151-160 of 163) with videos related to

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International Journal of Radiation Biology|April 1, 1991
Protection of pig epidermis against radiation-induced damage by the infusion of BW12CG J van den Aardweg, J W Hopewell, G E Adams, et al.
International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine|December 1, 1980
Structure-activity relationships in the development of hypoxic cell radiosensitizers. III. Effects of basic substituents in nitroimidazole sidechainsG E Adams, I Ahmed, E D Clarke, et al.
British Journal of Cancer|April 1, 1994
Phosphorus metabolism during growth of lymphoma in mouse liver: a comparison of 31P magnetic resonance spectroscopy in vivo and in vitroC P Thomas, R M Dixon, M Tian, et al.
Journal of Medicinal Chemistry|July 1, 1991
Synthesis of a series of nitrothiophenes with basic or electrophilic substituents and evaluation as radiosensitizers and as bioreductively activated cytotoxinsM D Threadgill, P Webb, P O'Neill, et al.
Anti-Cancer Drug Design|July 1, 1991
Aziridinyl nitropyrroles and nitropyrazoles as hypoxia-selective cytotoxins and radiosensitizersM A Naylor, M A Stephens, I J Stratford, et al.
Journal of Medicinal Chemistry|July 18, 1997
2-Cyclopropylindoloquinones and their analogues as bioreductively activated antitumor agents: structure-activity in vitro and efficacy in vivoM A Naylor, M Jaffar, J Nolan, et al.
British Journal of Cancer|December 1, 1992
Increasing the effect of photodynamic therapy on the RIF-1 murine sarcoma, using the bioreductive drugs RSU1069 and RB6145J C Bremner, G E Adams, J K Pearson, et al.
International Journal of Radiation Oncology, Biology, Physics|January 1, 1996
Fused pyrazine mono-n-oxides as bioreductive drugs. II Cytotoxicity in human cells and oncogenicity in a rodent transformation assayV K Langmuir, K R Laderoute, H L Mendonca, et al.
International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine|February 1, 1979
Structure-activity relationships in the development of hypoxic cell radiosensitizers. II. Cytotoxicity and therapeutic ratioG E Adams, E D Clarke, P Gray, et al.
Journal of Medicinal Chemistry|September 1, 1990
Synthesis and evaluation of alpha-[[(2-haloethyl)amino]methyl]-2- nitro-1H-imidazole-1-ethanols as prodrugs of alpha-[(1-aziridinyl)methyl]-2- nitro-1H-imidazole-1-ethanol (RSU-1069) and its analogues which are radiosensitizers and bioreductively activated cytotoxinsT C Jenkins, M A Naylor, P O'Neill, et al.
Pageof 17

Showing results (151-160 of 163) with videos related to

Sort By:
Pageof 17
International Journal of Radiation Biology|April 1, 1991
Protection of pig epidermis against radiation-induced damage by the infusion of BW12CG J van den Aardweg, J W Hopewell, G E Adams, et al.
International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine|December 1, 1980
Structure-activity relationships in the development of hypoxic cell radiosensitizers. III. Effects of basic substituents in nitroimidazole sidechainsG E Adams, I Ahmed, E D Clarke, et al.
British Journal of Cancer|April 1, 1994
Phosphorus metabolism during growth of lymphoma in mouse liver: a comparison of 31P magnetic resonance spectroscopy in vivo and in vitroC P Thomas, R M Dixon, M Tian, et al.
Journal of Medicinal Chemistry|July 1, 1991
Synthesis of a series of nitrothiophenes with basic or electrophilic substituents and evaluation as radiosensitizers and as bioreductively activated cytotoxinsM D Threadgill, P Webb, P O'Neill, et al.
Anti-Cancer Drug Design|July 1, 1991
Aziridinyl nitropyrroles and nitropyrazoles as hypoxia-selective cytotoxins and radiosensitizersM A Naylor, M A Stephens, I J Stratford, et al.
Journal of Medicinal Chemistry|July 18, 1997
2-Cyclopropylindoloquinones and their analogues as bioreductively activated antitumor agents: structure-activity in vitro and efficacy in vivoM A Naylor, M Jaffar, J Nolan, et al.
British Journal of Cancer|December 1, 1992
Increasing the effect of photodynamic therapy on the RIF-1 murine sarcoma, using the bioreductive drugs RSU1069 and RB6145J C Bremner, G E Adams, J K Pearson, et al.
International Journal of Radiation Oncology, Biology, Physics|January 1, 1996
Fused pyrazine mono-n-oxides as bioreductive drugs. II Cytotoxicity in human cells and oncogenicity in a rodent transformation assayV K Langmuir, K R Laderoute, H L Mendonca, et al.
International Journal of Radiation Biology and Related Studies in Physics, Chemistry, and Medicine|February 1, 1979
Structure-activity relationships in the development of hypoxic cell radiosensitizers. II. Cytotoxicity and therapeutic ratioG E Adams, E D Clarke, P Gray, et al.
Journal of Medicinal Chemistry|September 1, 1990
Synthesis and evaluation of alpha-[[(2-haloethyl)amino]methyl]-2- nitro-1H-imidazole-1-ethanols as prodrugs of alpha-[(1-aziridinyl)methyl]-2- nitro-1H-imidazole-1-ethanol (RSU-1069) and its analogues which are radiosensitizers and bioreductively activated cytotoxinsT C Jenkins, M A Naylor, P O'Neill, et al.
Pageof 17