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Antimicrobial Agents and Chemotherapy|October 21, 2015
Structural Basis of Metallo-β-Lactamase Inhibition by Captopril StereoisomersJürgen Brem, Sander S van Berkel, David Zollman, et al.Bioorganic & Medicinal Chemistry|January 23, 2024
Selective targeting of human TET1 by cyclic peptide inhibitors: Insights from biochemical profilingKlemensas Šimelis, Hilal Saraç, Eidarus Salah, et al.Journal of Molecular Biology|August 5, 2010
Crystal structure of the 2-oxoglutarate- and Fe(II)-dependent lysyl hydroxylase JMJD6Monica Mantri, Tobias Krojer, Eleanor A Bagg, et al.The Journal of Biological Chemistry|September 15, 2011
Structural and evolutionary basis for the dual substrate selectivity of human KDM4 histone demethylase familyLars Hillringhaus, Wyatt W Yue, Nathan R Rose, et al.Nucleic Acids Research|June 11, 2014
Jumonji domain containing protein 6 (Jmjd6) modulates splicing and specifically interacts with arginine-serine-rich (RS) domains of SR- and SR-like proteinsAstrid Heim, Christina Grimm, Udo Müller, et al.Communications Biology|November 28, 2024
JmjC catalysed histone H2a N-methyl arginine demethylation and C4-arginine hydroxylation reveals importance of sequence-reactivity relationshipsJoanna Bonnici, Razanne Oueini, Eidarus Salah, et al.Antimicrobial Agents and Chemotherapy|July 13, 2016
Interaction of Avibactam with Class B Metallo-β-LactamasesMartine I Abboud, Christian Damblon, Jürgen Brem, et al.The Journal of Biological Chemistry|November 6, 2025
Cellular and functional insights into FIH-mediated hydroxylation of TRPA1Tao Guo, Dianne Marquez Lopez, Siyuan Wang, et al.Proceedings of the National Academy of Sciences of the United States of America|August 5, 2022
Widespread hydroxylation of unstructured lysine-rich protein domains by JMJD6Matthew E Cockman, Yoichiro Sugimoto, Hamish B Pegg, et al.Chemical Communications (Cambridge, England)|July 3, 2018
Human histone demethylase KDM6B can catalyse sequential oxidationsRichard J Hopkinson, Gareth W Langley, Roman Belle, et al.Pageof 59