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Chemical Communications (Cambridge, England)|January 6, 2004
Demystifying the three dimensional structure of G protein-coupled receptors (GPCRs) with the aid of molecular modelingStefano Moro, Francesca Deflorian, Giampiero Spalluto, et al.
European Journal of Medicinal Chemistry|December 3, 2019
Conjugable A3 adenosine receptor antagonists for the development of functionalized ligands and their use in fluorescent probesStephanie Federico, Enrico Margiotta, Stefano Moro, et al.
Cells|May 16, 2020
Allosteric Antagonism of the A2A Adenosine Receptor by a Series of Bitopic LigandsZhan-Guo Gao, Kiran S Toti, Ryan Campbell, et al.
Obesity Research|September 1, 2005
Diet induction of monocyte chemoattractant protein-1 and its impact on obesityAiru Chen, Sheena Mumick, Chunsheng Zhang, et al.
Biochemical Pharmacology|March 8, 2003
Tumor necrosis factor alpha-induced apoptosis in astrocytes is prevented by the activation of P2Y6, but not P2Y4 nucleotide receptorsSeong G Kim, Kelly A Soltysiak, Zhan-Guo Gao, et al.
Experimental Eye Research|May 11, 2007
Barrier qualities of the mouse eye to topically applied drugsZhao Wang, Chi Wai Do, Marcel Y Avila, et al.
Journal of Medicinal Chemistry|March 18, 2005
(N)-methanocarba 2,N6-disubstituted adenine nucleosides as highly potent and selective A3 adenosine receptor agonistsSusanna Tchilibon, Bhalchandra V Joshi, Soo-Kyung Kim, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 4, 2004
Induction of novel agonist selectivity for the ADP-activated P2Y1 receptor versus the ADP-activated P2Y12 and P2Y13 receptors by conformational constraint of an ADP analogMariya Chhatriwala, R Gnana Ravi, Roshni I Patel, et al.
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