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ACS Medicinal Chemistry Letters|October 24, 2017
Discovery of a Tetrahydrobenzisoxazole Series of γ-Secretase ModulatorsZhiqiang Zhao, Dmitri A Pissarnitski, Xianhai Huang, et al.
Environmental Entomology|August 14, 2022
Effects of Temperature and Wildflower Strips on Survival and Macronutrient Stores of the Alfalfa Leafcutting Bee (Hymenoptera: Megachilidae) Under Extended Cold StorageMia G Park, Casey M Delphia, Cassandra Prince, et al.
Molecular Pharmacology|February 1, 1997
Dual agonistic and antagonistic property of nonpeptide angiotensin AT1 ligands: susceptibility to receptor mutationsS Perlman, C M Costa-Neto, A A Miyakawa, et al.
The Journal of Experimental Biology|June 2, 2025
Hypoxia extends lifespan but does not alter telomere length or oxidative stress in a solitary bee (Megachile rotundata)Andre Szejner-Sigal, Britt J Heidinger, Aurelia C Kucera, et al.
Veterinary Pathology|May 20, 2008
Experimental transmission of chronic wasting disease (CWD) of elk (Cervus elaphus nelsoni), white-tailed deer (Odocoileus virginianus), and mule deer (Odocoileus hemionus hemionus) to white-tailed deer by intracerebral routeA N Hamir, J A Richt, J M Miller, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Himbacine-derived thrombin receptor antagonists: c7-spirocyclic analogues of vorapaxarMariappan V Chelliah, Keith Eagen, Zhuyan Guo, et al.
The Journal of Infectious Diseases|November 7, 2022
Characterization of Classical Sheep Scrapie in White-tailed Deer after Experimental Oronasal ExposureJustin J Greenlee, S Jo Moore, Eric D Cassmann, et al.
Bioorganic & Medicinal Chemistry Letters|January 20, 2007
3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonistsLisa S Silverman, John P Caldwell, William J Greenlee, et al.
Journal of Medicinal Chemistry|April 7, 2023
Identification of a Selective SCoR2 Inhibitor That Protects Against Acute Kidney InjuryHua-Lin Zhou, Alfred Hausladen, Puneet Anand, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1992
In vivo pharmacology of L-158,809, a new highly potent and selective nonpeptide angiotensin II receptor antagonistP K Siegl, R S Chang, N B Mantlo, et al.
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