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European Journal of Medicinal Chemistry|May 24, 2016
Straightforward synthesis of 2,4,6-trisubstituted 1,3,5-triazine compounds targeting cysteine cathepsins K and SElżbieta Plebanek, Florian Chevrier, Vincent Roy, et al.Talanta|August 28, 2019
Monitoring of phosphorylation using immobilized kinases by on-line enzyme bioreactors hyphenated with High-Resolution Mass SpectrometryJustine Ferey, David Da Silva, Cyril Colas, et al.Biochemical and Biophysical Research Communications|March 18, 2015
Active site labeling of cysteine cathepsins by a straightforward diazomethylketone probe derived from the N-terminus of human cystatin CThibaut Garenne, Ahlame Saidi, Brendan F Gilmore, et al.Neurotoxicity Research|April 28, 2010
Neuroprotective effects of PACAP against ethanol-induced toxicity in the developing rat cerebellumBéatrice Botia, Valérie Jolivel, Delphine Burel, et al.ACS Infectious Diseases|May 17, 2025
LAVR-289, an Acyclo-Nucleoside Phosphonate, Has Broad-Spectrum Activity against HerpesvirusesSandrine Kappler-Gratias, Charlotte Quentin-Froignant, Elie Marcheteau, et al.Analytica Chimica Acta|January 8, 2019
Monitoring of successive phosphorylations of thymidine using free and immobilized human nucleoside/nucleotide kinases by Flow Injection Analysis with High-Resolution Mass SpectrometryJustine Ferey, David Da Silva, Cyril Colas, et al.Bioorganic & Medicinal Chemistry|July 28, 2018
Selective inhibition of human cathepsin S by 2,4,6-trisubstituted 1,3,5-triazine analogsZahira Tber, Mylène Wartenberg, Jean-Eddy Jacques, et al.Nucleosides, Nucleotides & Nucleic Acids|May 31, 2011
Synthesis and anti-HIV evaluation of 3'-triazolo nucleosidesVincent Roy, Aleksandr Obikhod, Hong-Wang Zhang, et al.Molecular Neurobiology|October 27, 2015
Selenoprotein T Deficiency Leads to Neurodevelopmental Abnormalities and Hyperactive Behavior in MiceMatthieu T Castex, Arnaud Arabo, Magalie Bénard, et al.International Journal of Pharmaceutics|September 12, 2024
Lyotropic liquid crystal emulsions of LAVR-289: Influence of internal mesophase structure on cytotoxicity and in-vitro antiviral activityMathias Brouillard, Thomas Mathieu, Samuel Guillot, et al.Pageof 11