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Biochemical Pharmacology|April 20, 2020
Structural and kinetic evidence of aging after organophosphate inhibition of human Cathepsin AKayla D Bouknight, Kayla M Jurkouich, Jaimee R Compton, et al.
The Biochemical Journal|July 18, 2014
Conserved structure and domain organization among bacterial Slc26 transportersEmma L R Compton, Kimberly Page, Heather E Findlay, et al.
Plos One|March 17, 2016
Complete Reversible Refolding of a G-Protein Coupled Receptor on a Solid SupportNatalie Di Bartolo, Emma L R Compton, Tony Warne, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1993
Cannabinoid structure-activity relationships: correlation of receptor binding and in vivo activitiesD R Compton, K C Rice, B R De Costa, et al.
Antiviral Research|February 12, 2019
Proteolytic cleavage of host proteins by the Group IV viral proteases of Venezuelan equine encephalitis virus and Zika virusElaine M Morazzani, Jaimee R Compton, Dagmar H Leary, et al.
CNS Drug Reviews|July 13, 2006
Pharmacological profile of the selective FAAH inhibitor KDS-4103 (URB597)Daniele Piomelli, Giorgio Tarzia, Andrea Duranti, et al.
Journal of Medicinal Chemistry|November 14, 1997
Synthesis and pharmacological comparison of dimethylheptyl and pentyl analogs of anandamideH H Seltzman, D N Fleming, B F Thomas, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 7, 2007
The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3'-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in miceRoberto Russo, Jesse Loverme, Giovanna La Rana, et al.
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