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J Balzarini

Showing results (291-300 of 563) with videos related to

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Journal of Medicinal Chemistry|October 1, 1988
Synthesis and anti-HIV activity of different sugar-modified pyrimidine and purine nucleosidesP Herdewijn, J Balzarini, M Baba, et al.
Journal of Medicinal Chemistry|September 1, 1990
Synthesis and biological evaluation of some cyclic phosphoramidate nucleoside derivativesA Kumar, P L Coe, A S Jones, et al.
Antiviral Research|July 21, 2007
Comparative evaluation of the activity of antivirals towards feline immunodeficiency virus in different cell culture systemsF J U M van der Meer, N M P Schuurman, J Balzarini, et al.
Molecular Pharmacology|May 1, 1989
5-Halogeno-3'-fluoro-2',3'-dideoxyuridines as inhibitors of human immunodeficiency virus (HIV): potent and selective anti-HIV activity of 3'-fluoro-2',3'-dideoxy-5-chlorouridineJ Balzarini, A Van Aerschot, R Pauwels, et al.
Journal of Medicinal Chemistry|February 1, 1990
Synthesis and antiviral activity of 3'-heterocyclic substituted 3'-deoxythymidinesP Wigerinck, A Van Aerschot, G Janssen, et al.
The Journal of Infectious Diseases|November 14, 1997
Zidovudine-resistant human immunodeficiency virus type 1 strains subcultured in the presence of both lamivudine and quinoxaline HBY 097 retain marked sensitivity to HBY 097 but not to lamivudineJ Balzarini, H Pelemans, G Riess, et al.
Biochemical Pharmacology|March 27, 1998
Retention of marked sensitivity to (S)-4-isopropoxycarbonyl-6-methoxy-3-(methylthiomethyl)-3,4-di hydroquin oxaline-2(1H)-thione (HBY 097) by an azidothymidine (AZT)-resistant human immunodeficiency virus type 1 (HIV-1) strain subcultured in the combined presence of quinoxaline HBY 097 and 2',3'-dideoxy-3'-thiacytidine (lamivudine)J Balzarini, H Pelemans, G Riess, et al.
Antiviral Research|June 1, 1992
The mannose-specific plant lectins from Cymbidium hybrid and Epipactis helleborine and the (N-acetylglucosamine)n-specific plant lectin from Urtica dioica are potent and selective inhibitors of human immunodeficiency virus and cytomegalovirus replication in vitroJ Balzarini, J Neyts, D Schols, et al.
Journal of Medicinal Chemistry|August 1, 1989
Nucleic acid related compounds. 57. Synthesis, x-ray crystal structure, lipophilic partition properties, and antiretroviral activities of anomeric 3'-azido-2',3'-dideoxy-2,6-diaminopurine ribosidesM J Robins, S G Wood, N K Dalley, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|June 6, 2000
Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14F Damian, N Blaton, L Naesens, et al.
Pageof 57

Showing results (291-300 of 563) with videos related to

Sort By:
Pageof 57
Journal of Medicinal Chemistry|October 1, 1988
Synthesis and anti-HIV activity of different sugar-modified pyrimidine and purine nucleosidesP Herdewijn, J Balzarini, M Baba, et al.
Journal of Medicinal Chemistry|September 1, 1990
Synthesis and biological evaluation of some cyclic phosphoramidate nucleoside derivativesA Kumar, P L Coe, A S Jones, et al.
Antiviral Research|July 21, 2007
Comparative evaluation of the activity of antivirals towards feline immunodeficiency virus in different cell culture systemsF J U M van der Meer, N M P Schuurman, J Balzarini, et al.
Molecular Pharmacology|May 1, 1989
5-Halogeno-3'-fluoro-2',3'-dideoxyuridines as inhibitors of human immunodeficiency virus (HIV): potent and selective anti-HIV activity of 3'-fluoro-2',3'-dideoxy-5-chlorouridineJ Balzarini, A Van Aerschot, R Pauwels, et al.
Journal of Medicinal Chemistry|February 1, 1990
Synthesis and antiviral activity of 3'-heterocyclic substituted 3'-deoxythymidinesP Wigerinck, A Van Aerschot, G Janssen, et al.
The Journal of Infectious Diseases|November 14, 1997
Zidovudine-resistant human immunodeficiency virus type 1 strains subcultured in the presence of both lamivudine and quinoxaline HBY 097 retain marked sensitivity to HBY 097 but not to lamivudineJ Balzarini, H Pelemans, G Riess, et al.
Biochemical Pharmacology|March 27, 1998
Retention of marked sensitivity to (S)-4-isopropoxycarbonyl-6-methoxy-3-(methylthiomethyl)-3,4-di hydroquin oxaline-2(1H)-thione (HBY 097) by an azidothymidine (AZT)-resistant human immunodeficiency virus type 1 (HIV-1) strain subcultured in the combined presence of quinoxaline HBY 097 and 2',3'-dideoxy-3'-thiacytidine (lamivudine)J Balzarini, H Pelemans, G Riess, et al.
Antiviral Research|June 1, 1992
The mannose-specific plant lectins from Cymbidium hybrid and Epipactis helleborine and the (N-acetylglucosamine)n-specific plant lectin from Urtica dioica are potent and selective inhibitors of human immunodeficiency virus and cytomegalovirus replication in vitroJ Balzarini, J Neyts, D Schols, et al.
Journal of Medicinal Chemistry|August 1, 1989
Nucleic acid related compounds. 57. Synthesis, x-ray crystal structure, lipophilic partition properties, and antiretroviral activities of anomeric 3'-azido-2',3'-dideoxy-2,6-diaminopurine ribosidesM J Robins, S G Wood, N K Dalley, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|June 6, 2000
Physicochemical characterization of solid dispersions of the antiviral agent UC-781 with polyethylene glycol 6000 and Gelucire 44/14F Damian, N Blaton, L Naesens, et al.
Pageof 57