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Advances in Pharmacology (San Diego, Calif.)|May 19, 2011
The structure of the adenosine receptors: implications for drug discoveryJ Robert Lane, Veli-Pekka Jaakola, Adriaan P Ijzerman
Journal of Medicinal Chemistry|March 30, 2010
Hybrid ortho/allosteric ligands for the adenosine A(1) receptorRajeshwar Narlawar, J Robert Lane, Munikumar Doddareddy, et al.
Biochemical Pharmacology|July 6, 2010
Characterization of [3H]LUF5834: A novel non-ribose high-affinity agonist radioligand for the adenosine A1 receptorJ Robert Lane, Elisabeth Klaasse, Judy Lin, et al.
The Journal of Biological Chemistry|February 12, 2010
Ligand binding and subtype selectivity of the human A(2A) adenosine receptor: identification and characterization of essential amino acid residuesVeli-Pekka Jaakola, J Robert Lane, Judy Y Lin, et al.
Trends in Biochemical Sciences|May 19, 2019
Drug-Target Association Kinetics in Drug DiscoveryAdriaan P IJzerman, Dong Guo
Methods in Molecular Biology (Clifton, N.J.)|December 1, 2017
Molecular Basis of Ligand Dissociation from G Protein-Coupled Receptors and Predicting Residence TimeDong Guo, Adriaan P IJzerman
Molecular Pharmacology|December 23, 2011
A novel nonribose agonist, LUF5834, engages residues that are distinct from those of adenosine-like ligands to activate the adenosine A(2a) receptorJ Robert Lane, Carmen Klein Herenbrink, Gerard J P van Westen, et al.
Trends in Pharmacological Sciences|August 30, 2005
Techniques: how to boost GPCR mutagenesis studies using yeastMargot W Beukers, Adriaan P Ijzerman
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