D. E. Slade

发表

Antiviral activity of the dihydropyrone PNU-140690, a new nonpeptidic human immunodeficiency virus protease inhibitor

D. Ho, M. Markowitz, H. Mo, 1997, Antimicrobial agents and chemotherapy.

Structure-based design of HIV protease inhibitors: sulfonamide-containing 5,6-dihydro-4-hydroxy-2-pyrones as non-peptidic inhibitors.

W. Howe, K. Watenpaugh, F. Schwende, 1996, Journal of medicinal chemistry.

A chimeric virus created by DNA shuffling of the capsid genes of different subtypes of porcine circovirus type 2 (PCV2) in the backbone of the non-pathogenic PCV1 induces protective immunity against the predominant PCV2b and the emerging PCV2d in pigs.

T. Opriessnig, C. Xiao, Shannon R. Matzinger, 2016, Virology.

CD163 Expression Confers Susceptibility to Porcine Reproductive and Respiratory Syndrome Viruses

J. Calvert, S. Welch, R. Jolie, 2007, Journal of Virology.

(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes

K. Rank, L. Kopta, R. Olmsted, 1996, Journal of virology.

A drug resistance mutation in the inhibitor binding pocket of human immunodeficiency virus type 1 reverse transcriptase impairs DNA synthesis and RNA degradation.

D. B. Evans, K. Rank, L. Kopta, 1996, Biochemistry.

Generation and characterization of monoclonal antibodies reactive with the 49-kDa proteinase of tobacco etch virus.

R. Johnston, W. Dougherty, D. E. Slade, 1989, Virology.

Radiosensitization of mammalian cells by iodoacetamide and related compounds.

D. E. Slade, D. K. Myers, 1967, Radiation research.