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Molecules (Basel, Switzerland)|March 6, 2021
MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in MiceJean A Boutin, Magali Jullian, Lukasz Frankiewicz, et al.
International Journal of Molecular Sciences|July 6, 2018
Hamster Melatonin Receptors: Cloning and Binding Characterization of MT₁ and Attempt to Clone MT₂Célia Gautier, Emilie Dufour, Clémence Dupré, et al.
Journal of Medicinal Chemistry|July 9, 2016
Molecular Dynamics Simulations and Kinetic Measurements to Estimate and Predict Protein-Ligand Residence TimesLuca Mollica, Isabelle Theret, Mathias Antoine, et al.
Molecular & Cellular Proteomics : MCP|May 2, 2008
A generic approach for the purification of signaling complexes that specifically interact with the carboxyl-terminal domain of G protein-coupled receptorsPascal Maurice, Avais M Daulat, Cédric Broussard, et al.
Bioorganic & Medicinal Chemistry|May 7, 2010
Design, synthesis and pharmacological evaluation of novel naphthalenic derivatives as selective MT(1) melatoninergic ligandsChristophe Mésangeau, Basile Pérès, Carole Descamps-François, et al.
Canadian Journal of Physiology and Pharmacology|March 29, 2000
Food intake regulation in rodents: Y5 or Y1 NPY receptors or both?J Duhault, M Boulanger, S Chamorro, et al.
British Journal of Pharmacology|October 10, 2009
The end of a myth: cloning and characterization of the ovine melatonin MT(2) receptorF Cogé, S P Guenin, I Fery, et al.
Molecules (Basel, Switzerland)|February 2, 2017
Role of Quinone Reductase 2 in the Antimalarial Properties of Indolone-Type DerivativesLaure-Estelle Cassagnes, Nambinina Rakotoarivelo, Serena Sirigu, et al.
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