Showing results (341-350 of 370) with videos related to
Sort By:
Pageof 37
The American Journal of Gastroenterology|November 17, 2023
Ten-Day Vonoprazan-Amoxicillin Dual Therapy vs Standard 14-Day Bismuth-Based Quadruple Therapy for First-Line Helicobacter pylori Eradication: A Multicenter Randomized Clinical TrialTian-Lian Yan, Jing-Hua Wang, Xin-Jue He, et al.Journal of Medicinal Chemistry|April 28, 2006
Orthogonal activation of the reengineered A3 adenosine receptor (neoceptor) using tailored nucleoside agonistsZhan-Guo Gao, Heng T Duong, Tatiana Sonina, et al.Pain|May 6, 2024
Terpenes from Cannabis sativa induce antinociception in a mouse model of chronic neuropathic pain via activation of adenosine A 2A receptorsAbigail M Schwarz, Attila Keresztes, Thai Bui, et al.Journal of Medicinal Chemistry|October 26, 2018
Preclinical Evaluation of the First Adenosine A1 Receptor Partial Agonist Radioligand for Positron Emission Tomography ImagingMin Guo, Zhan-Guo Gao, Ryan Tyler, et al.Journal of Medicinal Chemistry|September 25, 2008
Structure-activity relationships of truncated D- and l-4'-thioadenosine derivatives as species-independent A3 adenosine receptor antagonistsLak Shin Jeong, Shantanu Pal, Seung Ah Choe, et al.Journal of Economic Entomology|May 14, 2005
Laboratory and field evaluations of transgenic soybean exhibiting high-dose expression of a synthetic Bacillus thuringiensis cry1A gene for control of LepidopteraTed C MacRae, Matthew E Baur, David J Boethel, et al.Biorxiv : the Preprint Server for Biology|April 10, 2023
Terpenes from Cannabis sativa Induce Antinociception in Mouse Chronic Neuropathic Pain via Activation of Spinal Cord Adenosine A2A ReceptorsAbigail M Schwarz, Attila Keresztes, Thai Bui, et al.Journal of Medicinal Chemistry|January 6, 2006
Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-uronamides as highly potent and selective agonists at the human A3 adenosine receptorLak Shin Jeong, Hyuk Woo Lee, Kenneth A Jacobson, et al.Journal of Medicinal Chemistry|June 29, 2023
Alicyclic Ring Size Variation of 4-Phenyl-2-naphthoic Acid Derivatives as P2Y14 Receptor AntagonistsZhiwei Wen, Asmita Pramanik, Sarah A Lewicki, et al.Journal of Medicinal Chemistry|August 17, 2022
GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for the A2A Adenosine ReceptorAnna Shiriaeva, Daejin Park, Gyudong Kim, et al.Pageof 37