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Structure (London, England : 1993)|April 16, 2020
Dual Specificity PDZ- and 14-3-3-Binding Motifs: A Structural and Interactomics StudyGergo Gogl, Pau Jane, Célia Caillet-Saguy, et al.Human Molecular Genetics|August 23, 2008
Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPARBarbara Royer-Zemmour, Magali Ponsole-Lenfant, Hyam Gara, et al.Journal of Medicinal Chemistry|September 10, 2019
Structure-Reactivity Relationships on Substrates and Inhibitors of the Lysine Deacylase Sirtuin 2 from Schistosoma mansoni (SmSirt2)Daria Monaldi, Dante Rotili, Julien Lancelot, et al.Journal of Chemical Information and Modeling|September 23, 2014
Discovery of inhibitors of Schistosoma mansoni HDAC8 by combining homology modeling, virtual screening, and in vitro validationSrinivasaraghavan Kannan, Jelena Melesina, Alexander-Thomas Hauser, et al.Journal of Structural Biology|March 23, 2011
Robots, pipelines, polyproteins: enabling multiprotein expression in prokaryotic and eukaryotic cellsLakshmi Sumitra Vijayachandran, Cristina Viola, Frederic Garzoni, et al.European Journal of Medicinal Chemistry|June 5, 2020
Design, synthesis, and biological evaluation of dual targeting inhibitors of histone deacetylase 6/8 and bromodomain BRPF1Ehab Ghazy, Patrik Zeyen, Daniel Herp, et al.Methods in Molecular Biology (Clifton, N.J.)|July 4, 2019
High-Throughput Production of Oxidized Animal Toxins in Escherichia coliYoan Duhoo, Ana Filipa Sequeira, Natalie J Saez, et al.Chemmedchem|August 19, 2022
Phenotypic Screening of Histone Deacetylase (HDAC) Inhibitors against Schistosoma mansoniMuhammad Murtaza Hassan, Abootaleb Sedighi, Olasunkanmi O Olaoye, et al.ACS Infectious Diseases|October 7, 2025
Benzodeazaoxaflavin Sirtuin Inhibitors Inhibit Schistosoma mansoni Sirt2 and Cause Phenotypic Changes and Lethality in Schistosomula and Adult Worm StagesRoberto Gimmelli, Giuliana Papoff, Emanuele Fabbrizi, et al.Chemmedchem|December 10, 2019
Structure-Based Design, Synthesis, and Biological Evaluation of Triazole-Based smHDAC8 InhibitorsDmitrii V Kalinin, Sunit K Jana, Maxim Pfafenrot, et al.Pageof 17