J. M. Cameron

Rational design of potent sialidase-based inhibitors of influenza virus replication

Mark von Itzstein, Wen‐Yang Wu, Gaik B. Kok et al. · Nature · 1993 · 1.8K citations

Rational Design, Medicine, Antiviral Therapy +6

High-level resistance to (-) enantiomeric 2'-deoxy-3'-thiacytidine in vitro is due to one amino acid substitution in the catalytic site of human immunodeficiency virus type 1 reverse transcriptase

Charles A. Boucher, N. Cammack, P Schipper et al. · Antimicrobial Agents and Chemotherapy · 1993 · 319 citations · Full text

The separated enantiomers of 2'-deoxy-3'-thiacytidine (BCH 189) both inhibit human immunodeficiency virus replication in vitro

Jonathon Alexis Coates, N. Cammack, H J Jenkinson et al. · Antimicrobial Agents and Chemotherapy · 1992 · 288 citations · Full text

Bioorganic Chemistry, Immunology, Molecular Biology +18

(-)-2'-deoxy-3'-thiacytidine is a potent, highly selective inhibitor of human immunodeficiency virus type 1 and type 2 replication in vitro

Jonathon Alexis Coates, N. Cammack, H J Jenkinson et al. · Antimicrobial Agents and Chemotherapy · 1992 · 240 citations · Full text

Immunology, Pharmacotherapy, Antiviral Drug +16

Construction and characterization of a herpes simplex virus type 1 mutant unable to transinduce immediate-early gene expression

C I, Thomas McKee, Jane Ryan et al. · Journal of Virology · 1989 · 230 citations · Full text

Mutant In1814, Viral Replication, Low Multiplicity +14