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British Journal of Pharmacology|April 24, 2023
Targeting G protein-coupled receptors for heart failure treatmentBui San Thai, Ling Yeong Chia, Anh T N Nguyen, et al.Proceedings of the National Academy of Sciences of the United States of America|November 13, 2025
Dissociation kinetics of G proteins from G protein-coupled receptors and effects of allosteric modulationJinan Wang, Anh T N Nguyen, Victor A Adediwura, et al.Clinical Science (London, England : 1979)|December 2, 2022
Translating atherosclerosis research from bench to bedside: navigating the barriers for effective preclinical drug discoveryLauren T May, Belinda A Bartolo, David G Harrison, et al.Journal of Medicinal Chemistry|December 14, 2016
Novel Irreversible Agonists Acting at the A1 Adenosine ReceptorManuela Jörg, Alisa Glukhova, Alaa Abdul-Ridha, et al.British Journal of Pharmacology|May 10, 2023
The application of artificial intelligence to accelerate G protein-coupled receptor drug discoveryAnh T N Nguyen, Diep T N Nguyen, Huan Yee Koh, et al.Journal of Medicinal Chemistry|February 16, 2018
A Structure-Activity Relationship Study of Bitopic N6-Substituted Adenosine Derivatives as Biased Adenosine A1 Receptor AgonistsLuigi Aurelio, Jo-Anne Baltos, Leigh Ford, et al.Molecular Pharmacology|September 30, 2016
Extracellular Loop 2 of the Adenosine A1 Receptor Has a Key Role in Orthosteric Ligand Affinity and Agonist EfficacyAnh T N Nguyen, Jo-Anne Baltos, Trayder Thomas, et al.ACS Pharmacology & Translational Science|March 29, 2020
Dominant Negative G Proteins Enhance Formation and Purification of Agonist-GPCR-G Protein Complexes for Structure DeterminationYi-Lynn Liang, Peishen Zhao, Christopher Draper-Joyce, et al.Frontiers in Pharmacology|March 29, 2021
Pharmacological Insights Into Safety and Efficacy Determinants for the Development of Adenosine Receptor Biased Agonists in the Treatment of Heart FailurePatricia Rueda, Jon Merlin, Stefano Chimenti, et al.Nature Communications|August 18, 2025
Molecular basis of ligand binding and receptor activation at the human A3 adenosine receptorLiudi Zhang, Jesse I Mobbs, Felix M Bennetts, et al.Pageof 7