S. S. Joyner

发表

High-affinity inhibitors of dihydrofolate reductase: antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular size.

L. Kuyper, D. Baccanari, H. Friedman, 1996, Journal of medicinal chemistry.

High-Affinity Inhibitors of Dihydrofolate Reductase: Antimicrobial and Anticancer Activities of 7,8-Dialkyl-1,3-diaminopyrrolo(3,2-f) quinazolines with Small Molecular Size.

L. Kuyper, D. Baccanari, H. Friedman, 1996 .

5-Ethynyluracil (776C85): protection from 5-fluorouracil-induced neurotoxicity in dogs.

D. Baccanari, S. T. Davis, T. Spector, 1994, Biochemical pharmacology.

Dihydrofolate reductase hysteresis and its effect of inhibitor binding analyses.

D. Baccanari, S. S. Joyner, S. Joyner, 1981, Biochemistry.

5-Ethynyluracil (776C85): effects on the antitumor activity and pharmacokinetics of tegafur, a prodrug of 5-fluorouracil.

D. Baccanari, Y. Rustum, S. T. Davis, 1995, Cancer research.

The anti-human immunodeficiency virus agent 3'-fluorothymidine induces DNA damage and apoptosis in human lymphoblastoid cells

R. Sundseth, J. Moore, S. S. Joyner, 1996, Antimicrobial agents and chemotherapy.

Selective inhibitors of Candida albicans dihydrofolate reductase: activity and selectivity of 5-(arylthio)-2,4-diaminoquinazolines.

L. Kuyper, D. Baccanari, S. K. Rudolph, 1995, Journal of medicinal chemistry.

Inhibition of uridine phosphorylase: synthesis and structure-activity relationships of aryl-substituted 5-benzyluracils and 1-[(2-hydroxyethoxy)methyl]-5-benzyluracils.

D. Baccanari, S. T. Davis, S. S. Joyner, 1995, Journal of medicinal chemistry.

Species-dependent differences in the biochemical effects and metabolism of 5-benzylacyclouridine.

D. Baccanari, S. T. Davis, S. S. Joyner, 1993, Biochemical pharmacology.

Inhibition of Uridine Phosphorylase: Synthesis and Structure-Activity Relationships of Aryl-Substituted 5-Benzyluracils and 1-((2- Hydroxyethoxy)methyl)-5-benzyluracils.

D. Baccanari, S. T. Davis, S. S. Joyner, 1996 .

Inhibition of uridine phosphorylase. Synthesis and structure-activity relationships of aryl-substituted 1-((2-hydroxyethoxy)methyl)-5-(3-phenoxybenzyl)uracil.

D. Baccanari, S. T. Davis, S. S. Joyner, 1997, Journal of medicinal chemistry.

Characterization of an R-plasmid dihydrofolate reductase with a monomeric structure.

D. Baccanari, M. Fling, D. Stone, 1984, The Journal of biological chemistry.

Characterization of Candida albicans dihydrofolate reductase.

D. Baccanari, M. Fling, J. Freisheim, 1989, The Journal of biological chemistry.