S C Cavalcanti - JoVE Visualize

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Nucleosides, Nucleotides & Nucleic Acids|April 25, 2000

Synthesis and antiviral activities of enantiomeric 1-[2-(hydroxymethyl) cyclopropyl] methyl nucleosidesC Pierra, S Olgen, S C Cavalcanti, et al.

BMC Pharmacology|September 28, 2001

Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extractF G de Miranda, J C Vilar, I A Alves, et al.

Nucleosides & Nucleotides|January 5, 2000

Synthesis of 2',3'-dideoxy-2'-fluoro-L-threo-pentofuranosyl nucleosides as potential antiviral agentsS C Cavalcanti, Y Xiang, M G Newton, et al.

Antimicrobial Agents and Chemotherapy|June 20, 2000

In vitro selection of mutations in the human immunodeficiency virus type 1 reverse transcriptase that decrease susceptibility to (-)-beta-D-dioxolane-guanosine and suppress resistance to 3'-azido-3'-deoxythymidineH Z Bazmi, J L Hammond, S C Cavalcanti, et al.

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Showing results (1-10 of 4) with videos related to

Sort By:

Pageof 1

Nucleosides, Nucleotides & Nucleic Acids|April 25, 2000

Synthesis and antiviral activities of enantiomeric 1-[2-(hydroxymethyl) cyclopropyl] methyl nucleosidesC Pierra, S Olgen, S C Cavalcanti, et al.

BMC Pharmacology|September 28, 2001

Antinociceptive and antiedematogenic properties and acute toxicity of Tabebuia avellanedae Lor. ex Griseb. inner bark aqueous extractF G de Miranda, J C Vilar, I A Alves, et al.

Nucleosides & Nucleotides|January 5, 2000

Synthesis of 2',3'-dideoxy-2'-fluoro-L-threo-pentofuranosyl nucleosides as potential antiviral agentsS C Cavalcanti, Y Xiang, M G Newton, et al.

Antimicrobial Agents and Chemotherapy|June 20, 2000

In vitro selection of mutations in the human immunodeficiency virus type 1 reverse transcriptase that decrease susceptibility to (-)-beta-D-dioxolane-guanosine and suppress resistance to 3'-azido-3'-deoxythymidineH Z Bazmi, J L Hammond, S C Cavalcanti, et al.

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