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Martin Marek

Showing results (41-50 of 63) with videos related to

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Computational and Structural Biotechnology Journal|April 7, 2022
Computer-aided engineering of staphylokinase toward enhanced affinity and selectivity for plasminDmitri Nikitin, Jan Mican, Martin Toul, et al.
Archiv Der Pharmazie|June 23, 2017
Isophthalic Acid-Based HDAC Inhibitors as Potent Inhibitors of HDAC8 from Schistosoma mansoniKatharina Stenzel, Alokta Chakrabarti, Jelena Melesina, 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.
Nature|January 28, 2014
ANP32E is a histone chaperone that removes H2A.Z from chromatinArnaud Obri, Khalid Ouararhni, Christophe Papin, et al.
Protein Science : a Publication of the Protein Society|August 14, 2023
Multimeric structure of a subfamily III haloalkane dehalogenase-like enzyme solved by combination of cryo-EM and x-ray crystallographyKlaudia Chmelova, Tadeja Gao, Martin Polak, et al.
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.
Journal of Molecular Biology|March 25, 2014
Molecular basis for the antiparasitic activity of a mercaptoacetamide derivative that inhibits histone deacetylase 8 (HDAC8) from the human pathogen schistosoma mansoniDiana A Stolfa, Martin Marek, Julien Lancelot, et al.
Chemmedchem|May 29, 2018
Synthesis, Crystallization Studies, and in vitro Characterization of Cinnamic Acid Derivatives as SmHDAC8 Inhibitors for the Treatment of SchistosomiasisTheresa Bayer, Alokta Chakrabarti, Julien Lancelot, 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.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Computational and Structural Biotechnology Journal|April 7, 2022
Computer-aided engineering of staphylokinase toward enhanced affinity and selectivity for plasminDmitri Nikitin, Jan Mican, Martin Toul, et al.
Archiv Der Pharmazie|June 23, 2017
Isophthalic Acid-Based HDAC Inhibitors as Potent Inhibitors of HDAC8 from Schistosoma mansoniKatharina Stenzel, Alokta Chakrabarti, Jelena Melesina, 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.
Nature|January 28, 2014
ANP32E is a histone chaperone that removes H2A.Z from chromatinArnaud Obri, Khalid Ouararhni, Christophe Papin, et al.
Protein Science : a Publication of the Protein Society|August 14, 2023
Multimeric structure of a subfamily III haloalkane dehalogenase-like enzyme solved by combination of cryo-EM and x-ray crystallographyKlaudia Chmelova, Tadeja Gao, Martin Polak, et al.
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.
Journal of Molecular Biology|March 25, 2014
Molecular basis for the antiparasitic activity of a mercaptoacetamide derivative that inhibits histone deacetylase 8 (HDAC8) from the human pathogen schistosoma mansoniDiana A Stolfa, Martin Marek, Julien Lancelot, et al.
Chemmedchem|May 29, 2018
Synthesis, Crystallization Studies, and in vitro Characterization of Cinnamic Acid Derivatives as SmHDAC8 Inhibitors for the Treatment of SchistosomiasisTheresa Bayer, Alokta Chakrabarti, Julien Lancelot, 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.
Pageof 7