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Brain Research|October 24, 1983
Response of dopaminergic neurons in cat to auditory stimuli presented across the sleep-waking cycleG F Steinfels, J Heym, R E Strecker, et al.The Review of Scientific Instruments|April 1, 2019
On using Rayleigh scattering for in situ spectral calibration of Thomson scattering diagnosticsS A Bozhenkov, S J Heym, M N A Beurskens, et al.Journal of Medicinal Chemistry|October 15, 1993
Synthesis, in vitro binding profile, and autoradiographic analysis of [3H]-cis-3-[(2-methoxybenzyl)amino]-2-phenylpiperidine, a highly potent and selective nonpeptide substance P receptor antagonist radioligandT Rosen, T F Seeger, S McLean, et al.Science (New York, N.Y.)|January 25, 1991
Activity and distribution of binding sites in brain of a nonpeptide substance P (NK1) receptor antagonistS McLean, A H Ganong, T F Seeger, et al.Journal of Medicinal Chemistry|October 1, 1990
Thiazole as a carbonyl bioisostere. A novel class of highly potent and selective 5-HT3 receptor antagonistsT Rosen, A A Nagel, J P Rizzi, et al.Journal of Aquatic Animal Health|October 24, 2020
Reference Intervals for Blood Analytes of Adult Aquarium-Housed Russian Sturgeon Acipenser gueldenstaedtiiStephen E Cassle, Roy P E Yanong, Deborah B Pouder, et al.Proceedings of the National Academy of Sciences of the United States of America|September 17, 1996
CP-154,526: a potent and selective nonpeptide antagonist of corticotropin releasing factor receptorsD W Schulz, R S Mansbach, J Sprouse, et al.The Journal of Pharmacology and Experimental Therapeutics|May 1, 1996
Characterization of CP-122,721; a nonpeptide antagonist of the neurokinin NK1 receptorS McLean, A Ganong, P A Seymour, et al.Pageof 3