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Sandrine Ruchaud

Showing results (41-50 of 65) with videos related to

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Molecules (Basel, Switzerland)|January 6, 2019
The Anti-<i>Candida albicans</i> Agent 4-AN Inhibits Multiple Protein KinasesMaciej Masłyk, Monika Janeczko, Aleksandra Martyna, et al.
European Journal of Medicinal Chemistry|May 23, 2026
Identification of novel CLK1 inhibitors by computational fragment-based ligand design, co-crystallization, chemical synthesis and structure activity relationshipsStéphane Bourg, Matthieu Place, Chloé Copin, et al.
European Journal of Medicinal Chemistry|May 21, 2018
Structure-based design of novel quinoxaline-2-carboxylic acids and analogues as Pim-1 inhibitorsBruno Oyallon, Marie Brachet-Botineau, Cédric Logé, et al.
The Journal of Cell Biology|October 22, 2008
Deconstructing Survivin: comprehensive genetic analysis of Survivin function by conditional knockout in a vertebrate cell lineZuojun Yue, Ana Carvalho, Zhenjie Xu, et al.
Marine Drugs|February 6, 2019
Neurymenolide A, a Novel Mitotic Spindle Poison from the New Caledonian Rhodophyta <i>Phacelocarpus neurymenioides</i>Sofia-Eléna Motuhi, Omid Feizbakhsh, Béatrice Foll-Josselin, et al.
European Journal of Medicinal Chemistry|July 14, 2020
Discovery of simplified benzazole fragments derived from the marine benzosceptrin B as necroptosis inhibitors involving the receptor interacting protein Kinase-1Mohamed Benchekroun, Ludmila Ermolenko, Minh Quan Tran, et al.
European Journal of Medicinal Chemistry|October 20, 2015
Development of new highly potent imidazo[1,2-b]pyridazines targeting Toxoplasma gondii calcium-dependent protein kinase 1Espérance Moine, Isabelle Dimier-Poisson, Cécile Enguehard-Gueiffier, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 12, 2008
A promoter-hijack strategy for conditional shutdown of multiply spliced essential cell cycle genesKumiko Samejima, Hiromi Ogawa, Carol A Cooke, et al.
European Journal of Medicinal Chemistry|February 8, 2019
New pyrido[3,4-g]quinazoline derivatives as CLK1 and DYRK1A inhibitors: synthesis, biological evaluation and binding mode analysisHelmi Tazarki, Wael Zeinyeh, Yannick J Esvan, et al.
Molecules (Basel, Switzerland)|July 18, 2015
Synthetic Development of New 3-(4-Arylmethylamino)butyl-5-arylidene-rhodanines under Microwave Irradiation and Their Effects on Tumor Cell Lines and against Protein KinasesCamille Déliko Dago, Christelle N'ta Ambeu, Wacothon-Karime Coulibaly, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Molecules (Basel, Switzerland)|January 6, 2019
The Anti-<i>Candida albicans</i> Agent 4-AN Inhibits Multiple Protein KinasesMaciej Masłyk, Monika Janeczko, Aleksandra Martyna, et al.
European Journal of Medicinal Chemistry|May 23, 2026
Identification of novel CLK1 inhibitors by computational fragment-based ligand design, co-crystallization, chemical synthesis and structure activity relationshipsStéphane Bourg, Matthieu Place, Chloé Copin, et al.
European Journal of Medicinal Chemistry|May 21, 2018
Structure-based design of novel quinoxaline-2-carboxylic acids and analogues as Pim-1 inhibitorsBruno Oyallon, Marie Brachet-Botineau, Cédric Logé, et al.
The Journal of Cell Biology|October 22, 2008
Deconstructing Survivin: comprehensive genetic analysis of Survivin function by conditional knockout in a vertebrate cell lineZuojun Yue, Ana Carvalho, Zhenjie Xu, et al.
Marine Drugs|February 6, 2019
Neurymenolide A, a Novel Mitotic Spindle Poison from the New Caledonian Rhodophyta <i>Phacelocarpus neurymenioides</i>Sofia-Eléna Motuhi, Omid Feizbakhsh, Béatrice Foll-Josselin, et al.
European Journal of Medicinal Chemistry|July 14, 2020
Discovery of simplified benzazole fragments derived from the marine benzosceptrin B as necroptosis inhibitors involving the receptor interacting protein Kinase-1Mohamed Benchekroun, Ludmila Ermolenko, Minh Quan Tran, et al.
European Journal of Medicinal Chemistry|October 20, 2015
Development of new highly potent imidazo[1,2-b]pyridazines targeting Toxoplasma gondii calcium-dependent protein kinase 1Espérance Moine, Isabelle Dimier-Poisson, Cécile Enguehard-Gueiffier, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 12, 2008
A promoter-hijack strategy for conditional shutdown of multiply spliced essential cell cycle genesKumiko Samejima, Hiromi Ogawa, Carol A Cooke, et al.
European Journal of Medicinal Chemistry|February 8, 2019
New pyrido[3,4-g]quinazoline derivatives as CLK1 and DYRK1A inhibitors: synthesis, biological evaluation and binding mode analysisHelmi Tazarki, Wael Zeinyeh, Yannick J Esvan, et al.
Molecules (Basel, Switzerland)|July 18, 2015
Synthetic Development of New 3-(4-Arylmethylamino)butyl-5-arylidene-rhodanines under Microwave Irradiation and Their Effects on Tumor Cell Lines and against Protein KinasesCamille Déliko Dago, Christelle N'ta Ambeu, Wacothon-Karime Coulibaly, et al.
Pageof 7