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Journal of Receptor and Signal Transduction Research|September 1, 1996
Comparison of indolidan analog binding sites of drug antibody and sarcoplasmic reticulum with inhibition of cyclic AMP phosphodiesteraseT Ashikaga, D W Robertson, R J Sportsman, et al.Journal of Medicinal Chemistry|January 1, 1988
Molecular structure of fluoxetine hydrochloride, a highly selective serotonin-uptake inhibitorD W Robertson, N D Jones, J K Swartzendruber, et al.Life Sciences|January 1, 1988
LY227942, an inhibitor of serotonin and norepinephrine uptake: biochemical pharmacology of a potential antidepressant drugD T Wong, D W Robertson, F P Bymaster, et al.Epilepsia|January 1, 1988
Pharmacological effects of enantiomers of 4-amino-N-(alpha-methylbenzyl)benzamide, a chemically novel anticonvulsantJ D Leander, D W Robertson, C R Clark, et al.Breast Cancer Research and Treatment|January 1, 1986
Nitrosourea and nitrosocarbamate derivatives of the antiestrogen tamoxifen as potential estrogen receptor-mediated cytotoxic agents in human breast cancer cellsL L Wei, B S Katzenellenbogen, D W Robertson, et al.Critical Reviews in Biomedical Engineering|January 1, 1992
High-performance computing, high-speed networks, and configurable computing environments: progress toward fully distributed computingW E Johnston, V L Jacobson, S C Loken, et al.Journal of Neurochemistry|February 1, 1996
Antagonism of serotonin 5-HT1A receptors potentiates the increases in extracellular monoamines induced by duloxetine in rat hypothalamusE A Engleman, D W Robertson, D C Thompson, et al.The Journal of Pharmacology and Experimental Therapeutics|November 1, 1986
Molecular basis for the in vitro and in vivo cardiotonic activities of AR-L100J S Hayes, V L Wyss, H C Wilson, et al.Journal of Medicinal Chemistry|December 1, 1990
Synthesis and biochemical evaluation of tritium-labeled 1-methyl-N-(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)-1H-indazole-3-carboxa mide, a useful radioligand for 5HT3 receptorsD W Robertson, W Bloomquist, M L Cohen, et al.Journal of Medicinal Chemistry|January 24, 1992
Zatosetron, a potent, selective, and long-acting 5HT3 receptor antagonist: synthesis and structure-activity relationshipsD W Robertson, W B Lacefield, W Bloomquist, et al.Pageof 9