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Microbiology (Reading, England)|August 10, 2001
Serine/threonine protein kinases PknF and PknG of Mycobacterium tuberculosis: characterization and localizationAnil Koul, Axel Choidas, Anil K Tyagi, et al.
Cancers|September 23, 2022
White Paper: Mimetics of Class 2 Tumor Suppressor Proteins as Novel Drug Candidates for Personalized Cancer TherapyEdgar Dahl, Sophia Villwock, Peter Habenberger, et al.
The Journal of Clinical Investigation|January 5, 2005
Identification of cellular deoxyhypusine synthase as a novel target for antiretroviral therapyIlona Hauber, Dorian Bevec, Jochen Heukeshoven, et al.
Nucleic Acids Research|October 25, 2003
Exploiting features of adenovirus replication to support mammalian kinase productionMatt Cotten, Kerstin Stegmueller, Jan Eickhoff, et al.
Journal of Medicinal Chemistry|June 22, 2018
Discovery of N-[4-(Quinolin-4-yloxy)phenyl]benzenesulfonamides as Novel AXL Kinase InhibitorsIstván Szabadkai, Robert Torka, Rita Garamvölgyi, et al.
Chemmedchem|August 18, 2022
Synthesis, Biological Evaluation, and Binding Mode of a New Class of Oncogenic K-Ras4b InhibitorsStephan Jeuken, Oleksandr Shkura, Marc Röger, et al.
British Journal of Pharmacology|December 17, 2017
Identification of an (-)-englerin A analogue, which antagonizes (-)-englerin A at TRPC1/4/5 channelsHussein N Rubaiy, Tobias Seitz, Sven Hahn, et al.
Journal of Medicinal Chemistry|September 12, 2012
Development of selective, potent RabGGTase inhibitorsE Anouk Stigter, Zhong Guo, Robin S Bon, et al.
European Journal of Medicinal Chemistry|May 4, 2023
A highly selective purine-based inhibitor of CSF1R potently inhibits osteoclast differentiationThomas Ihle Aarhus, Jan Eickhoff, Bert Klebl, et al.
Angewandte Chemie (International Ed. in English)|August 24, 2017
Discovery of a Novel Inhibitor of the Hedgehog Signaling Pathway through Cell-based Compound Discovery and Target PredictionLea Kremer, Carsten Schultz-Fademrecht, Matthias Baumann, et al.
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