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Uwe Grether

Showing results (81-90 of 95) with videos related to

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Journal of Medicinal Chemistry|January 19, 2024
Development of Potent and Selective Monoacylglycerol Lipase Inhibitors. SARs, Structural Analysis, and Biological CharacterizationStefania Butini, Uwe Grether, Kwang-Mook Jung, et al.
Journal of the American Chemical Society|March 10, 2025
Highly Specific Miniaturized Fluorescent Monoacylglycerol Lipase Probes Enable Translational ResearchAxel Hentsch, Mónica Guberman, Silke Radetzki, et al.
Chemical Science|March 20, 2026
Single-position ligand modifications tune CB<sub>2</sub>R activity by targeting the toggle switchRudolf L Z Ganzoni, Miroslav Kosar, Yongqi Han, et al.
Molecular & Cellular Proteomics : MCP|April 5, 2025
CellEKT: A Robust Chemical Proteomics Workflow to Profile Cellular Target Engagement of Kinase InhibitorsJoel Rüegger, Berend Gagestein, Antonius P A Janssen, et al.
Journal of Medicinal Chemistry|March 18, 2025
Discovery of a Potent SARM1 Base-Exchange Inhibitor with In Vivo EfficacyMaude Giroud, Bernd Kuhn, Sandra Steiner, et al.
European Journal of Medicinal Chemistry|January 10, 2025
Radiosynthesis and evaluation of novel <sup>18</sup>F labeled PET ligands for imaging monoacylglycerol lipaseYinlong Li, Wakana Mori, Ahmad Chaudhary, et al.
Frontiers in Pharmacology|July 29, 2024
RG7774 (Vicasinabin), an orally bioavailable cannabinoid receptor 2 (CB2R) agonist, decreases retinal vascular permeability, leukocyte adhesion, and ocular inflammation in animal modelsUwe Grether, Richard H Foxton, Sabine Gruener, et al.
Nature Communications|January 4, 2017
Cannabinoid CB<sub>2</sub> receptor ligand profiling reveals biased signalling and off-target activityMarjolein Soethoudt, Uwe Grether, Jürgen Fingerle, et al.
Nature Neuroscience|May 21, 2026
Foamy microglia link oxylipins to disease progression in multiple sclerosisDaan van der Vliet, Xinyu Di, Tatiana M Shamorkina, et al.
Journal of Medicinal Chemistry|October 3, 2024
Structure-Guided Discovery of <i>cis</i>-Hexahydro-pyrido-oxazinones as Reversible, Drug-like Monoacylglycerol Lipase InhibitorsBernd Kuhn, Martin Ritter, Benoit Hornsperger, et al.
Pageof 10

Showing results (81-90 of 95) with videos related to

Sort By:
Pageof 10
Journal of Medicinal Chemistry|January 19, 2024
Development of Potent and Selective Monoacylglycerol Lipase Inhibitors. SARs, Structural Analysis, and Biological CharacterizationStefania Butini, Uwe Grether, Kwang-Mook Jung, et al.
Journal of the American Chemical Society|March 10, 2025
Highly Specific Miniaturized Fluorescent Monoacylglycerol Lipase Probes Enable Translational ResearchAxel Hentsch, Mónica Guberman, Silke Radetzki, et al.
Chemical Science|March 20, 2026
Single-position ligand modifications tune CB<sub>2</sub>R activity by targeting the toggle switchRudolf L Z Ganzoni, Miroslav Kosar, Yongqi Han, et al.
Molecular & Cellular Proteomics : MCP|April 5, 2025
CellEKT: A Robust Chemical Proteomics Workflow to Profile Cellular Target Engagement of Kinase InhibitorsJoel Rüegger, Berend Gagestein, Antonius P A Janssen, et al.
Journal of Medicinal Chemistry|March 18, 2025
Discovery of a Potent SARM1 Base-Exchange Inhibitor with In Vivo EfficacyMaude Giroud, Bernd Kuhn, Sandra Steiner, et al.
European Journal of Medicinal Chemistry|January 10, 2025
Radiosynthesis and evaluation of novel <sup>18</sup>F labeled PET ligands for imaging monoacylglycerol lipaseYinlong Li, Wakana Mori, Ahmad Chaudhary, et al.
Frontiers in Pharmacology|July 29, 2024
RG7774 (Vicasinabin), an orally bioavailable cannabinoid receptor 2 (CB2R) agonist, decreases retinal vascular permeability, leukocyte adhesion, and ocular inflammation in animal modelsUwe Grether, Richard H Foxton, Sabine Gruener, et al.
Nature Communications|January 4, 2017
Cannabinoid CB<sub>2</sub> receptor ligand profiling reveals biased signalling and off-target activityMarjolein Soethoudt, Uwe Grether, Jürgen Fingerle, et al.
Nature Neuroscience|May 21, 2026
Foamy microglia link oxylipins to disease progression in multiple sclerosisDaan van der Vliet, Xinyu Di, Tatiana M Shamorkina, et al.
Journal of Medicinal Chemistry|October 3, 2024
Structure-Guided Discovery of <i>cis</i>-Hexahydro-pyrido-oxazinones as Reversible, Drug-like Monoacylglycerol Lipase InhibitorsBernd Kuhn, Martin Ritter, Benoit Hornsperger, et al.
Pageof 10