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Pharmaceuticals (Basel, Switzerland)|October 23, 2021
Discovery of a Novel Class of Norovirus Inhibitors with High Barrier of ResistanceJana Van Dycke, Michela Puxeddu, Giuseppe La Regina, et al.The Journal of Antimicrobial Chemotherapy|April 27, 2012
Ivermectin is a potent inhibitor of flavivirus replication specifically targeting NS3 helicase activity: new prospects for an old drugEloise Mastrangelo, Margherita Pezzullo, Tine De Burghgraeve, et al.Journal of Molecular Biology|April 28, 2009
Structural basis for bivalent Smac-mimetics recognition in the IAP protein familyFederica Cossu, Mario Milani, Eloise Mastrangelo, et al.Journal of Virology|November 17, 2017
Identification of a Small Molecule That Compromises the Structural Integrity of Viroplasms and Rotavirus Double-Layered ParticlesCatherine Eichwald, Giuditta De Lorenzo, Elisabeth M Schraner, et al.Plos Neglected Tropical Diseases|April 1, 2020
Comprehensive response to Usutu virus following first isolation in blood donors in the Friuli Venezia Giulia region of Italy: Development of recombinant NS1-based serology and sensitivity to antiviral drugsIlaria Caracciolo, Erick Mora-Cardenas, Chiara Aloise, et al.Scientific Reports|September 3, 2024
Acid-sensing ion channel 3 is a new potential therapeutic target for the control of glioblastoma cancer stem cells growthAndrea Balboni, Camilla D'Angelo, Nicoletta Collura, et al.Antiviral Research|March 9, 2019
Broad spectrum anti-flavivirus pyridobenzothiazolones leading to less infective virionsRolando Cannalire, Delia Tarantino, Geraldine Piorkowski, et al.Journal of Molecular Biology|July 31, 2007
Crystal structure and activity of Kunjin virus NS3 helicase; protease and helicase domain assembly in the full length NS3 proteinEloise Mastrangelo, Mario Milani, Michela Bollati, et al.Frontiers in Cellular and Infection Microbiology|December 10, 2024
The antipsychotic drug lurasidone inhibits coronaviruses by affecting multiple targetsSara Baroni, Tea Carletti, Manuela Donalisio, et al.Bioorganic & Medicinal Chemistry|October 6, 2012
Homo- and heterodimeric Smac mimetics/IAP inhibitors as in vivo-active pro-apoptotic agents. Part I: SynthesisLeonardo Manzoni, Laura Belvisi, Aldo Bianchi, et al.Pageof 8