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Journal of Medicinal Chemistry|December 8, 2006
2-triazole-substituted adenosines: a new class of selective A3 adenosine receptor agonists, partial agonists, and antagonistsLiesbet Cosyn, Krishnan K Palaniappan, Soo-Kyung Kim, et al.The Journal of Biological Chemistry|June 1, 2006
A missense mutation in the seven-transmembrane domain of the human Ca2+ receptor converts a negative allosteric modulator into a positive allosteric modulatorJianxin Hu, Jiankang Jiang, Stefano Costanzi, et al.AJR. American Journal of Roentgenology|December 21, 2012
The role of sonography in differentiating full versus partial distal biceps tendon tears: correlation with surgical findingsLucas Da Gama Lobo, David P Fessell, Bruce S Miller, et al.Clinical Transplantation|January 29, 2013
Inflammation in the setting of chronic allograft dysfunction post-kidney transplant: phenotype and genotypeAjay K Israni, Robert Leduc, Pamala A Jacobson, et al.Journal of the American Heart Association|December 17, 2025
Sarco/Endoplasmic Reticulum Ca2+ ATPase Activation Shifts Cardiac Fuel Preference Without Impairing Cardiac Function in Obese MiceDeveena R Banerjee, Clinton M Hasenour, Mohsin Rahim, et al.Nature|August 7, 2024
Structure of the human dopamine transporter and mechanisms of inhibitionDushyant Kumar Srivastava, Vikas Navratna, Dilip K Tosh, et al.Journal of Medicinal Chemistry|August 28, 2012
Structural sweet spot for A1 adenosine receptor activation by truncated (N)-methanocarba nucleosides: receptor docking and potent anticonvulsant activityDilip K Tosh, Silvia Paoletta, Francesca Deflorian, et al.Equine Veterinary Journal|May 28, 2019
Clinical efficacy of bronchodilators in equine asthma: Looking for minimal important differenceL Calzetta, R Crupi, P Roncada, et al.Science Signaling|September 21, 2017
TALK-1 channels control β cell endoplasmic reticulum Ca2+ homeostasisNicholas C Vierra, Prasanna K Dadi, Sarah C Milian, et al.Bioorganic & Medicinal Chemistry|January 24, 2004
Structure-activity relationships of thiazole and thiadiazole derivatives as potent and selective human adenosine A3 receptor antagonistsKwan-Young Jung, Soo-Kyung Kim, Zhan-Guo Gao, et al.Pageof 246