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Showing results (31-40 of 37) with videos related to

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Journal of Medicinal Chemistry|March 31, 2011
Design and synthesis of novel N-hydroxy-dihydronaphthyridinones as potent and orally bioavailable HIV-1 integrase inhibitorsTed W Johnson, Steven P Tanis, Scott L Butler, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 29, 1999
Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypesD A Matthews, P S Dragovich, S E Webber, et al.
Journal of Medicinal Chemistry|July 21, 1998
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. Michael acceptor structure-activity studiesP S Dragovich, S E Webber, R E Babine, et al.
Journal of Medicinal Chemistry|July 21, 1998
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 2. Peptide structure-activity studiesP S Dragovich, S E Webber, R E Babine, et al.
Biochemistry|December 8, 1998
Interaction of a novel GDP exchange inhibitor with the Ras proteinA K Ganguly, Y S Wang, B N Pramanik, et al.
Canadian Journal of Surgery. Journal Canadien De Chirurgie|April 30, 2022
Canadian Surgery Forum 2018: St. John's, NL Sept. 13-15, 2018S Jayaraman, L Lee, J Mata, et al.
Canadian Journal of Surgery. Journal Canadien De Chirurgie|April 30, 2022
Canadian Surgery Forum: Abstracts of presentations to the Annual Meetings of the Canadian Association of Bariatric Physicians and Surgeons, Canadian Association of General Surgeons, Canadian Association of Thoracic Surgeons, Canadian Hepato-Pancreato-Biliary Society, Canadian Society of Surgical Oncology, Canadian Society of Colon and Rectal Surgeons, London, Ont. Sept. 15-18, 2011J C Chiu, X Shi, S Karmali, et al.
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Showing results (31-40 of 37) with videos related to

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Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Journal of Medicinal Chemistry|March 31, 2011
Design and synthesis of novel N-hydroxy-dihydronaphthyridinones as potent and orally bioavailable HIV-1 integrase inhibitorsTed W Johnson, Steven P Tanis, Scott L Butler, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 29, 1999
Structure-assisted design of mechanism-based irreversible inhibitors of human rhinovirus 3C protease with potent antiviral activity against multiple rhinovirus serotypesD A Matthews, P S Dragovich, S E Webber, et al.
Journal of Medicinal Chemistry|July 21, 1998
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. Michael acceptor structure-activity studiesP S Dragovich, S E Webber, R E Babine, et al.
Journal of Medicinal Chemistry|July 21, 1998
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 2. Peptide structure-activity studiesP S Dragovich, S E Webber, R E Babine, et al.
Biochemistry|December 8, 1998
Interaction of a novel GDP exchange inhibitor with the Ras proteinA K Ganguly, Y S Wang, B N Pramanik, et al.
Canadian Journal of Surgery. Journal Canadien De Chirurgie|April 30, 2022
Canadian Surgery Forum 2018: St. John's, NL Sept. 13-15, 2018S Jayaraman, L Lee, J Mata, et al.
Canadian Journal of Surgery. Journal Canadien De Chirurgie|April 30, 2022
Canadian Surgery Forum: Abstracts of presentations to the Annual Meetings of the Canadian Association of Bariatric Physicians and Surgeons, Canadian Association of General Surgeons, Canadian Association of Thoracic Surgeons, Canadian Hepato-Pancreato-Biliary Society, Canadian Society of Surgical Oncology, Canadian Society of Colon and Rectal Surgeons, London, Ont. Sept. 15-18, 2011J C Chiu, X Shi, S Karmali, et al.
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