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Nature|November 18, 2021
Structure, function and pharmacology of human itch GPCRsCan Cao, Hye Jin Kang, Isha Singh, et al.Nature|September 28, 2022
Bespoke library docking for 5-HT2A receptor agonists with antidepressant activityAnat Levit Kaplan, Danielle N Confair, Kuglae Kim, et al.Nature Chemical Biology|July 12, 2011
A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cellsMasoud Vedadi, Dalia Barsyte-Lovejoy, Feng Liu, et al.Nature Structural & Molecular Biology|February 17, 2015
Structural basis for bifunctional peptide recognition at human δ-opioid receptorGustavo Fenalti, Nadia A Zatsepin, Cecilia Betti, et al.Pharmacological Reviews|December 28, 2020
International Union of Basic and Clinical Pharmacology. CX. Classification of Receptors for 5-hydroxytryptamine; Pharmacology and FunctionNicholas M Barnes, Gerard P Ahern, Carine Becamel, et al.Nature Reviews. Drug Discovery|February 24, 2018
Unexplored therapeutic opportunities in the human genomeTudor I Oprea, Cristian G Bologa, Søren Brunak, et al.Nature Reviews. Drug Discovery|March 24, 2018
Unexplored therapeutic opportunities in the human genomeTudor I Oprea, Cristian G Bologa, Søren Brunak, et al.Biorxiv : the Preprint Server for Biology|June 12, 2025
De novo design of miniprotein agonists and antagonists targeting G protein-coupled receptorsEdin Muratspahić, David Feldman, David E Kim, et al.Elife|April 21, 2018
Donated chemical probes for open scienceSusanne Müller, Suzanne Ackloo, Cheryl H Arrowsmith, et al.Nature|May 21, 2026
De novo design of miniproteins targeting GPCRsEdin Muratspahić, David Feldman, David E Kim, et al.Pageof 44