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Journal of Computer-Aided Molecular Design|December 7, 2007
An eleven amino acid residue deletion expands the substrate specificity of acetyl xylan esterase II (AXE II) from Penicillium purpurogenumMarcela Colombres, José A Garate, Carlos F Lagos, et al.
Infection and Drug Resistance|August 16, 2019
Fluorescence enzymatic assay for bacterial polyphosphate kinase 1 (PPK1) as a platform for screening antivirulence moleculesFrancisca Campos, Javiera A Álvarez, Javiera Ortiz-Severín, et al.
Journal of Cellular Physiology|July 15, 2009
Calpain inhibitors prevent p38 MAPK activation and germ cell apoptosis after heat stress in pubertal rat testesCarlos Lizama, Carlos F Lagos, Raúl Lagos-Cabré, et al.
Antioxidants (Basel, Switzerland)|July 29, 2025
Influence of an Antioxidant Nanomaterial on Oral Tablet Formulation: Flow Properties and Critical Quality AttributesAndrea C Ortiz, Javiera Carrasco-Rojas, Sofía Peñaloza, et al.
Chromatographia|April 1, 2014
LC-MS/MS Method for the Simultaneous Determination of Free Urinary SteroidsFidel Allende, Sandra Solari, Carmen Campino, et al.
Molecular Biology of the Cell|March 6, 2015
Basolateral sorting of chloride channel 2 is mediated by interactions between a dileucine motif and the clathrin adaptor AP-1Erwin de la Fuente-Ortega, Diego Gravotta, Andres Perez Bay, et al.
Pharmaceuticals (Basel, Switzerland)|July 2, 2021
Novel N-Arylsulfonylindoles Targeted as Ligands of the 5-HT6 Receptor. Insights on the Influence of C-5 Substitution on Ligand AffinityLoreto Arrieta-Rodríguez, Daniela Espinoza-Rosales, Gonzalo Vera, et al.
Molecules (Basel, Switzerland)|March 10, 2017
2D-QSAR and 3D-QSAR/CoMSIA Studies on a Series of (R)-2-((2-(1H-Indol-2-yl)ethyl)amino)-1-Phenylethan-1-ol with Human β₃-Adrenergic ActivityGastón Apablaza, Luisa Montoya, Cesar Morales-Verdejo, et al.
Molecules (Basel, Switzerland)|August 19, 2016
Extended N-Arylsulfonylindoles as 5-HT₆ Receptor Antagonists: Design, Synthesis & Biological EvaluationGonzalo Vera, Carlos F Lagos, Sebastián Almendras, et al.
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