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Annals of Neurology|June 1, 1982
Cognition in Parkinson disease: an event-related potential perspectiveE C Hansch, K Syndulko, S N Cohen, et al.Journal of Medicinal Chemistry|May 1, 1986
Inhibition of chicken liver dihydrofolate reductase by 5-(substituted benzyl)-2,4-diaminopyrimidines. A quantitative structure-activity relationship and graphics analysisC D Selassie, Z X Fang, R L Li, et al.Journal of Medicinal Chemistry|March 1, 1986
Thiopurine methyltransferase: structure-activity relationships for benzoic acid inhibitors and thiophenol substratesM M Ames, C D Selassie, L C Woodson, et al.Fundamental and Applied Toxicology : Official Journal of the Society of Toxicology|March 1, 1997
Correlation between hydrophobicity of short-chain aliphatic alcohols and their ability to alter plasma membrane integrityS C McKarns, C Hansch, W S Caldwell, et al.Journal of Medicinal Chemistry|September 1, 1983
Studies of N-hydroxy-N'-aminoguanidine derivatives by nitrogen-15 nuclear magnetic resonance spectroscopy and as ribonucleotide reductase inhibitorsA W Tai, E J Lien, E C Moore, et al.Biochemical Pharmacology|August 1, 1985
Inhibition of ribonucleotide reductase and L1210 cell growth by N-hydroxy-N'-aminoguanidine derivativesJ G Cory, G L Carter, P E Bacon, et al.Anticancer Research|February 19, 2002
Inhibition of tumor cell growth by Schiff bases of hydroxysemicarbazideS Ren, Z A Tokes, C Csipke, et al.Radiology|January 22, 2000
Chronically occluded inferior venae cavae: endovascular treatmentM K Razavi, E C Hansch, S T Kee, et al.Journal of Medicinal Chemistry|April 1, 1979
Quantitative structure-activity relationships in 1-aryl-2-(alkylamino)ethanol antimalarialsK H Kim, C Hansch, J Y Fukunaga, et al.Pharmaceutical Research|August 1, 1991
Quantitative structure-activity relationship (QSAR) analysis of the cytotoxicities of aminohydroxyguanidine derivatives and their antiviral activities in vitroP H Wang, M B Hui, P Nandy, et al.Pageof 19