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Molecules (Basel, Switzerland)|March 3, 2018
A Novel Class of Schistosoma mansoni Histone Deacetylase 8 (HDAC8) Inhibitors Identified by Structure-Based Virtual Screening and In Vitro TestingConrad V Simoben, Dina Robaa, Alokta Chakrabarti, et al.
Nucleic Acids Research|May 31, 2021
The structure of the mouse ADAT2/ADAT3 complex reveals the molecular basis for mammalian tRNA wobble adenosine-to-inosine deaminationElizabeth Ramos-Morales, Efil Bayam, Jordi Del-Pozo-Rodríguez, et al.
Bioorganic Chemistry|December 3, 2014
Hydroxamates of para-aminobenzoic acid as selective inhibitors of HDAC8Umasankar Kulandaivelu, Laxmi Manasa Chilakamari, Surender Singh Jadav, et al.
EMBO Reports|July 17, 2010
The structural plasticity of SCA7 domains defines their differential nucleosome-binding propertiesJacques Bonnet, Ying-Hui Wang, Gianpiero Spedale, et al.
Nature|January 28, 2014
ANP32E is a histone chaperone that removes H2A.Z from chromatinArnaud Obri, Khalid Ouararhni, Christophe Papin, et al.
International Journal of Molecular Sciences|July 27, 2022
Design, Synthesis and Biological Characterization of Histone Deacetylase 8 (HDAC8) Proteolysis Targeting Chimeras (PROTACs) with Anti-Neuroblastoma ActivitySalma Darwish, Ehab Ghazy, Tino Heimburg, et al.
Journal of Medicinal Chemistry|June 6, 2017
Alkoxyurea-Based Histone Deacetylase Inhibitors Increase Cisplatin Potency in Chemoresistant Cancer Cell LinesKatharina Stenzel, Alexandra Hamacher, Finn K Hansen, et al.
Journal of Medicinal Chemistry|March 4, 2016
Structure-Based Design and Synthesis of Novel Inhibitors Targeting HDAC8 from Schistosoma mansoni for the Treatment of SchistosomiasisTino Heimburg, Alokta Chakrabarti, Julien Lancelot, et al.
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