about
The role of histone demethylases in cancer therapySubstituted 2-(2-aminopyrimidin-4-yl)pyridine-4-carboxylates as potent inhibitors of JumonjiC domain-containing histone demethylases4-Biphenylalanine- and 3-Phenyltyrosine-Derived Hydroxamic Acids as Inhibitors of the JumonjiC-Domain-Containing Histone Demethylase KDM4A.Development of Erasin: a chromone-based STAT3 inhibitor which induces apoptosis in Erlotinib-resistant lung cancer cells.On the physical origin of the cation-anion intermediate bond in ionic liquids Part I. Placing a (weak) hydrogen bond between two charges.Tetrazolylhydrazides as Selective Fragment-Like Inhibitors of the JumonjiC-Domain-Containing Histone Demethylase KDM4A.Coupled Cluster in Condensed Phase. Part I: Static Quantum Chemical Calculations of Hydrogen Fluoride ClustersCoupled Cluster in Condensed Phase. Part II: Liquid Hydrogen Fluoride from Quantum Cluster Equilibrium TheoryThe Clinically Used Iron Chelator Deferasirox Is an Inhibitor of Epigenetic JumonjiC Domain-Containing Histone DemethylasesStructure-Based Screening of Tetrazolylhydrazide Inhibitors versus KDM4 Histone Demethylases
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description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-9274-1433
@en
name
Martin Roatsch
@ast
Martin Roatsch
@de
Martin Roatsch
@en
Martin Roatsch
@es
Martin Roatsch
@nl
type
label
Martin Roatsch
@ast
Martin Roatsch
@de
Martin Roatsch
@en
Martin Roatsch
@es
Martin Roatsch
@nl
prefLabel
Martin Roatsch
@ast
Martin Roatsch
@de
Martin Roatsch
@en
Martin Roatsch
@es
Martin Roatsch
@nl
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1105481492
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0000-0002-9274-1433
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viaf-246146822108107380986