Recent developments in the design of antiviral agents von Saunders, John, Cameron, Janet M.

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Rational design of potent sialidase-based inhibitors of influenza virus replication von von Itzstein, Mark, Wu, Wen-Yang, Kok, Gaik B, Pegg, Michael S, Dyason, Jeffrey C, Jin, Betty, Phan, Tho Van, Smythe, Mark L, White, Hume F, Oliver, Stuart W, Colman, Peter M, Varghese, Joseph N, Ryan, D. Michael, Woods, Jacqueline M, Bethell, Richard C, Hotham, Vanessa J, Cameron, Janet M, Penn, Charles R

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The intracellular phosphorylation of (−)-2′-deoxy-3′-thiacytidine (3TC) and the incorporation of 3TC 5′-monophosphate into DNA by HIV-1 reverse transcriptase and human DNA polymera... von Gray, Norman M., Marr, Clara L.P., Penn, Charles R., Cameron, Janet M., Bethell, Richard C.

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Cellular metabolism of (−) enantiomeric 2′-deoxy-3′-thiacytidine von Cammack, Nicholas, Rouse, Philippa, Marr, Clara L.P., Reid, Paula J., Boehme, Richard E., Coates, Jonathan A.V., Penn, Charles R., Cameron, Janet M.

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Ribonucleotide Reductase Encoded by Herpes Simplex Virus Is a Determinant of the Pathogenicity of the Virus in Mice and a Valid Antiviral Target von Cameron, Janet M, McDougall, Iris, Marsden, Howard S, Preston, Valerie G, Ryan, D. Michael, Subak-Sharpe, John H

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A novel class of 1,3-oxathiolane nucleoside analogues having potent anti-HIV activity von Belleau, Bernard, Brasili, Livio, Chan, Laval, DiMarco, Marika P., Zacharie, Boulos, Nguyen-Ba, Nghe, Jenkinson, Helen J., Coates, Jonathan A.V., Cameron, Janet M.

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A consensus sequence for substrate hydrolysis by rhino virus 3C proteinase von Long, Audrey C., Orr, David C., Cameron, Janet M., Dunn, Ben M., Kay, John

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DNA chain termination activity and inhibition of human immunodeficiency virus reverse transcriptase by carbocyclic 2',3'-didehydro-2',3'-dideoxyguanosine triphosphate von ORR, DC, FIGUEIREDO, HT, MO, CL, PENN, CR, CAMERON, JM

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Hydrolysis of a Series of Synthetic Peptide Substrates by the Human Rhinovirus 14 3C Proteinase, Cloned and Expressed in Escherichia coli von Orr, David C, Long, Audrey C, Kay, John, Dunn, Ben M, Cameron, Janet M

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Synthesis and enzymatic resolution of carbocyclic 2'-ara-fluoro-guanosine: a potent new anti-herpetic agent von BORTHWICK, A. D, BUTT, S, MARR, C. L. P, SHILL, M. D, BIGGADIKE, K, EXALL, A. M, ROBERTS, S. M, YOUDS, P. M, KIRK, B. E, BOOTH, B. R, CAMERON, J. M, COX, S. W

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Antiviral optically pure dioxolane purine nucleosides analogues von Siddiqui, M.Arshad, Brown, William L., Nguyen-Ba, Nghe, Dixit, Dilip M., Mansour, Tarek S., Hooker, Elizabeth, Viner, K.Claire, Cameron, Janet M.

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Carbovir: the (—) enantiomer is a potent and selective antiviral agent against human immunodeficiency virus in vitro von Coates, Jonathan A.V., Inggall, Helen J., Pearson, Bridget A., Penn, Charles R., Storer, Richard, Williamson, Christopher, Cameron, Janet M.

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Antiviral combinations von CAMERON, JANET M

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Discovery and Analysis of a Series of C2-Symmetric HIV-1 Proteinase Inhibitors Derived from Penicillin von Gray, N.M., Cameron, J.M., Cammack, N., Cobley, K.N., Holmes, D.S., Humber, D.C., Orr, D.C., Penn, C.R., Potter, R., Madar, S., Weingarten, G.G., Bethell, R.C.

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ANTIVIRAL COMBINATION, PHARMACEUTICAL COMPOSITION CONTAINING THEREOF AND ITS USE von CAMERON JANET M, CAMMACK NICHOLAS

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Antiviral combinations von CAMERON, JANET M, CAMMACK, NICHOLAS

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ANTIVIRAL COMBINATIONS von CAMERON JANET M, CAMMACK NICHOLAS

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ANTIVIRAL COMPOUNDS von CAMMACK, NICHOLAS, CAMERON, JANET M

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Comparison of the Immediate Early Polypeptides of Human Cytomegalovirus Isolates von Cameron, Janet M, Preston, Chris M

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Nuclear transfer studies of amoeba proteus after the inhibition of cell division by injection of non-homologous cytoplasm von Cameron, Janet M., Hawkins, Shirley E.

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