J. M. Woods

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

D. M. Ryan, P. Colman, J. Varghese, 1993, Nature.

The synthesis and antiviral activity of 4-fluoro-1-beta-D-ribofuranosyl-1H-pyrazole-3-carboxamide.

C. J. Ashton, M. Hann, J. M. Woods, 1999, Nucleosides & nucleotides.

4-Guanidino-2,4-dideoxy-2,3-dehydro-N-acetylneuraminic acid is a highly effective inhibitor both of the sialidase (neuraminidase) and of growth of a wide range of influenza A and B viruses in vitro

D. M. Ryan, J. Ticehurst, R. Bethell, 1993, Antimicrobial Agents and Chemotherapy.

Synthesis and Biological Evaluation of Carbocyclic Analogues of Ribavirin

J. M. Woods, C. Penn, R. Storer, 1991 .

Synthesis and Biological Activity of Carbocyclic Clitocine

J. M. Woods, C. Penn, R. Storer, 1991 .

Penicillinase synthesis in Staphylococcus aureus: the effect of inducer and of the cellular location of the genetic determinants on the amount of enzyme formed.

J. M. Woods, K. Dyke, E. Asheshov, 1970, Genetical research.