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Science Translational Medicine|January 1, 2025
Lipidomic profiling of mouse brain and human neuron cultures reveals a role for Mboat7 in mTOR-dependent neuronal migrationIsaac Tang, Ashna Nisal, Alex Reed, et al.The Journal of Biological Chemistry|December 13, 2006
Closing the gate to the active site: effect of the inhibitor methoxyarachidonyl fluorophosphonate on the conformation and membrane binding of fatty acid amide hydrolaseGiampiero Mei, Almerinda Di Venere, Valeria Gasperi, et al.Nature Chemical Biology|May 17, 2011
Click-generated triazole ureas as ultrapotent in vivo-active serine hydrolase inhibitorsAlexander Adibekian, Brent R Martin, Chu Wang, et al.Biochemistry|November 15, 2011
Phosphatidylinositol 3,4,5-trisphosphate activity probes for the labeling and proteomic characterization of protein binding partnersMeng M Rowland, Heidi E Bostic, Denghuang Gong, et al.Chemistry & Biology|August 28, 2010
The glycerophospho metabolome and its influence on amino acid homeostasis revealed by brain metabolomics of GDE1(-/-) miceFlorian Kopp, Toru Komatsu, Daniel K Nomura, et al.Neuropharmacology|October 20, 2019
The novel MAGL inhibitor MJN110 enhances responding to reward-predictive incentive cues by activation of CB1 receptorsMalte Feja, Martin P K Leigh, Ajay N Baindur, et al.The Journal of Pharmacology and Experimental Therapeutics|March 13, 2015
Selective monoacylglycerol lipase inhibitors: antinociceptive versus cannabimimetic effects in miceBogna Ignatowska-Jankowska, Jenny L Wilkerson, Mohammed Mustafa, et al.The Journal of Biological Chemistry|October 18, 2007
Autosomal ichthyosis with hypotrichosis syndrome displays low matriptase proteolytic activity and is phenocopied in ST14 hypomorphic miceKarin List, Brooke Currie, Tiffany C Scharschmidt, et al.RSC Medicinal Chemistry|December 18, 2024
Exploiting the DCAF16-SPIN4 interaction to identify DCAF16 ligands for PROTAC developmentIsabella A Riha, Miguel A Campos, Xiaokang Jin, et al.Journal of the American Chemical Society|September 9, 2011
Potent and selective inhibitors of glutathione S-transferase omega 1 that impair cancer drug resistanceKatsunori Tsuboi, Daniel A Bachovchin, Anna E Speers, et al.Pageof 56