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J Atwell

Showing results (141-150 of 158) with videos related to

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Bioorganic & Medicinal Chemistry|June 29, 2010
Hypoxic selectivity and solubility--investigating the properties of A-ring substituted nitro seco-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-ones (nitroCBIs) as hypoxia-activated prodrugs for antitumor therapyMoana Tercel, Shangjin Yang, Graham J Atwell, et al.
Bioorganic & Medicinal Chemistry|June 1, 1995
Synthesis, DNA interactions and biological activity of DNA minor groove targeted polybenzamide-linked nitrogen mustardsG J Atwell, B M Yaghi, P R Turner, et al.
Journal of Proteome Research|November 26, 2013
Manipulating root water supply elicits major shifts in the shoot proteomeMehdi Mirzaei, Neda Soltani, Elham Sarhadi, et al.
Proteomics|April 13, 2013
The influence of signals from chilled roots on the proteome of shoot tissues in rice seedlingsKarlie A Neilson, Andrew P Scafaro, Joel M Chick, et al.
Journal of Experimental Botany|June 21, 2021
Comparisons of photosynthetic and anatomical traits between wild and domesticated cottonZhangying Lei, Fang Liu, Ian J Wright, et al.
Cancer Chemotherapy and Pharmacology|May 18, 2010
Reductive metabolism of the dinitrobenzamide mustard anticancer prodrug PR-104 in miceYongchuan Gu, Christopher P Guise, Kashyap Patel, et al.
Journal of Medicinal Chemistry|May 28, 2004
Aziridinyldinitrobenzamides: synthesis and structure-activity relationships for activation by E. coli nitroreductaseNuala A Helsby, Graham J Atwell, Shangjin Yang, et al.
Angewandte Chemie (International Ed. in English)|March 4, 2011
Selective treatment of hypoxic tumor cells in vivo: phosphate pre-prodrugs of nitro analogues of the duocarmycinsMoana Tercel, Graham J Atwell, Shangjin Yang, et al.
Journal of Medicinal Chemistry|November 3, 2009
Hypoxia-activated prodrugs: substituent effects on the properties of nitro seco-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (nitroCBI) prodrugs of DNA minor groove alkylating agentsMoana Tercel, Graham J Atwell, Shangjin Yang, et al.
Bioorganic & Medicinal Chemistry|January 14, 2014
Morpholylureas are a new class of potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase (AKR1C3)Jack U Flanagan, Graham J Atwell, Daniel M Heinrich, et al.
Pageof 16

Showing results (141-150 of 158) with videos related to

Sort By:
Pageof 16
Bioorganic & Medicinal Chemistry|June 29, 2010
Hypoxic selectivity and solubility--investigating the properties of A-ring substituted nitro seco-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-ones (nitroCBIs) as hypoxia-activated prodrugs for antitumor therapyMoana Tercel, Shangjin Yang, Graham J Atwell, et al.
Bioorganic & Medicinal Chemistry|June 1, 1995
Synthesis, DNA interactions and biological activity of DNA minor groove targeted polybenzamide-linked nitrogen mustardsG J Atwell, B M Yaghi, P R Turner, et al.
Journal of Proteome Research|November 26, 2013
Manipulating root water supply elicits major shifts in the shoot proteomeMehdi Mirzaei, Neda Soltani, Elham Sarhadi, et al.
Proteomics|April 13, 2013
The influence of signals from chilled roots on the proteome of shoot tissues in rice seedlingsKarlie A Neilson, Andrew P Scafaro, Joel M Chick, et al.
Journal of Experimental Botany|June 21, 2021
Comparisons of photosynthetic and anatomical traits between wild and domesticated cottonZhangying Lei, Fang Liu, Ian J Wright, et al.
Cancer Chemotherapy and Pharmacology|May 18, 2010
Reductive metabolism of the dinitrobenzamide mustard anticancer prodrug PR-104 in miceYongchuan Gu, Christopher P Guise, Kashyap Patel, et al.
Journal of Medicinal Chemistry|May 28, 2004
Aziridinyldinitrobenzamides: synthesis and structure-activity relationships for activation by E. coli nitroreductaseNuala A Helsby, Graham J Atwell, Shangjin Yang, et al.
Angewandte Chemie (International Ed. in English)|March 4, 2011
Selective treatment of hypoxic tumor cells in vivo: phosphate pre-prodrugs of nitro analogues of the duocarmycinsMoana Tercel, Graham J Atwell, Shangjin Yang, et al.
Journal of Medicinal Chemistry|November 3, 2009
Hypoxia-activated prodrugs: substituent effects on the properties of nitro seco-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (nitroCBI) prodrugs of DNA minor groove alkylating agentsMoana Tercel, Graham J Atwell, Shangjin Yang, et al.
Bioorganic & Medicinal Chemistry|January 14, 2014
Morpholylureas are a new class of potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase (AKR1C3)Jack U Flanagan, Graham J Atwell, Daniel M Heinrich, et al.
Pageof 16