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Antiviral Chemistry & Chemotherapy|May 20, 2000
Phosphoramidate derivatives of stavudine as inhibitors of HIV: unnatural amino acids may substitute for alanineC McGuigan, L Bidois, A Hiouni, et al.
Antiviral Research|December 1, 1995
Antiviral activity of selected acyclic nucleoside analogues against human herpesvirus 6D Reymen, L Naesens, J Balzarini, et al.
European Journal of Medicinal Chemistry|January 15, 2011
Synthesis of new C5-(1-substituted-1,2,3-triazol-4 or 5-yl)-2'-deoxyuridines and their antiviral evaluationAurélien Montagu, Vincent Roy, Jan Balzarini, et al.
Bioorganic & Medicinal Chemistry Letters|March 14, 2000
Enhancing the aqueous solubility of d4T-based phosphoramidate prodrugsA Siddiqui, C McGuigan, C Ballatore, et al.
Nucleosides, Nucleotides & Nucleic Acids|October 21, 2003
Bicyclic nucleoside inhibitors of varicella-zoster virus: 5'-chloro and 3'-chloro derivativesG Luoni, C McGuigan, G Andrei, et al.
Antiviral Chemistry & Chemotherapy|January 14, 2005
Non-nucleoside structures retain full anti-HCMV potency of the dideoxy furanopyrimidine familyOlivier Bidet, Christopher McGuigan, Robert Snoeck, et al.
Antimicrobial Agents and Chemotherapy|February 25, 2005
Susceptibilities of several clinical varicella-zoster virus (VZV) isolates and drug-resistant VZV strains to bicyclic furano pyrimidine nucleosidesGraciela Andrei, Rebecca Sienaert, Chris McGuigan, et al.
Molecular Pharmacology|March 25, 2006
Mutations distal to the substrate site can affect varicella zoster virus thymidine kinase activity: implications for drug designKamel El Omari, Sandra Liekens, Louise E Bird, et al.
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