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Biochemical Pharmacology|March 29, 2020
Rational development of a high-affinity secretin receptor antagonistMaoqing Dong, Kaleeckal G Harikumar, Sweta R Raval, et al.Science (New York, N.Y.)|February 19, 2021
Structure and dynamics of the CGRP receptor in apo and peptide-bound formsTracy M Josephs, Matthew J Belousoff, Yi-Lynn Liang, et al.European Journal of Pharmacology|April 14, 2018
Vascular and molecular pharmacology of the metabolically stable CGRP analogue, SAXMajid Sheykhzade, Bahareh Abdolalizadeh, Cassandra Koole, et al.Bioinformatics (Oxford, England)|September 11, 2019
Automatic local resolution-based sharpening of cryo-EM mapsErney Ramírez-Aportela, Jose Luis Vilas, Alisa Glukhova, et al.Proceedings of the National Academy of Sciences of the United States of America|November 20, 2025
Structural basis of modified ligand selectivity from N-terminal PAC1R alternative splicingJessica J Lu, Giuseppe Deganutti, Miaomiao Li, et al.Biochemical Pharmacology|February 19, 2018
Extracellular loops 2 and 3 of the calcitonin receptor selectively modify agonist binding and efficacyEmma Dal Maso, Yue Zhu, Vi Pham, et al.Neuropharmacology|October 26, 2018
Drug-receptor kinetics and sigma-1 receptor affinity differentiate clinically evaluated histamine H3 receptor antagonistsDarren M Riddy, Anna E Cook, David M Shackleford, et al.Science Signaling|November 15, 2022
M1 muscarinic receptor activation reduces the molecular pathology and slows the progression of prion-mediated neurodegenerative diseaseLouis Dwomoh, Mario Rossi, Miriam Scarpa, et al.ACS Chemical Neuroscience|December 15, 2018
6-Phenylpyrimidin-4-ones as Positive Allosteric Modulators at the M1 mAChR: The Determinants of Allosteric ActivityManuela Jörg, Emma T van der Westhuizen, Elham Khajehali, et al.Journal of the American Chemical Society|August 17, 2019
O-GlcNAc Engineering of GPCR Peptide-Agonists Improves Their Stability and in Vivo ActivityPaul M Levine, Aaron T Balana, Emmanuel Sturchler, et al.Pageof 52