Histone deacetylase inhibitors modulate hormesis in leukemic cells with mutant FMS-like tyrosine kinase-3
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
1 Online-Ressource.
- Sprache
-
Englisch
- Erschienen in
-
Histone deacetylase inhibitors modulate hormesis in leukemic cells with mutant FMS-like tyrosine kinase-3 ; volume:37 ; number:11 ; day:21 ; month:9 ; year:2023 ; pages:2319-2323 ; date:11.2023
Leukemia ; 37, Heft 11 (21.9.2023), 2319-2323, 11.2023
- Urheber
-
Zeyn, Yanira
Hausmann, Kristin
Halilovic, Melisa
Beyer, Mandy
Ibrahim, Hany S.
Brenner, Walburgis
Mahboobi, Siavosh
Bros, Matthias
Sippl, Wolfgang
Krämer, Oliver Holger
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41375-023-02036-2
- URN
-
urn:nbn:de:101:1-2024012211522681947876
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:27 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Zeyn, Yanira
- Hausmann, Kristin
- Halilovic, Melisa
- Beyer, Mandy
- Ibrahim, Hany S.
- Brenner, Walburgis
- Mahboobi, Siavosh
- Bros, Matthias
- Sippl, Wolfgang
- Krämer, Oliver Holger
- SpringerLink (Online service)
Ähnliche Objekte (12)
Molecular Modelling Untersuchungen zum Bindungsverhalten von Histamin H2- und H3-Rezeptor-Liganden
Epigenetic targets in drug discovery
Structure-based design of inhibitors of the zinc-dependent enzymes histone deacetylase (HDAC) and UDP-3-O-(R-3-hydroxymyristoylyl)-N-acetylglucosamine deacetylase (LpxC)
Methionine 274 Is Not the Determining Factor for Selective Inhibition of Histone Deacetylase 8 (HDAC8) by L-Shaped Inhibitors
Exploring aromatic cage flexibility of the histone methyllysine reader protein Spindlin1 and its impact on binding mode prediction: an in silico study
Aromatic amino acid hydroxylases as off-targets of histone deacetylase inhibitors
Design, Synthese und Charakterisierung neuer Sirtuin Inhibitoren
Structure based design, synthesis and characterization of small molecules as inhibitors of parasitic targets
Application of computer-based methods to guide the development of novel sirtuin inhibitors : [kumulative Dissertation]
Applications of computational methods and African natural product databases to search for novel inhibitors of histone deacetylases ; [kumulative Dissertation]
Design and synthesis of antimycobacterial agents targeting the mycobacterial electron transport chain and the cell wall synthesis, and in vitro testing against different mycobacterial species
Class I HDAC selective modulators : design, synthesis, and biological characterization
Molecular Modelling Untersuchungen zum Bindungsverhalten von Histamin H2- und H3-Rezeptor-Liganden
Epigenetic targets in drug discovery
Structure-based design of inhibitors of the zinc-dependent enzymes histone deacetylase (HDAC) and UDP-3-O-(R-3-hydroxymyristoylyl)-N-acetylglucosamine deacetylase (LpxC)
Methionine 274 Is Not the Determining Factor for Selective Inhibition of Histone Deacetylase 8 (HDAC8) by L-Shaped Inhibitors
Exploring aromatic cage flexibility of the histone methyllysine reader protein Spindlin1 and its impact on binding mode prediction: an in silico study
Aromatic amino acid hydroxylases as off-targets of histone deacetylase inhibitors
Design, Synthese und Charakterisierung neuer Sirtuin Inhibitoren
Structure based design, synthesis and characterization of small molecules as inhibitors of parasitic targets
Application of computer-based methods to guide the development of novel sirtuin inhibitors : [kumulative Dissertation]
Applications of computational methods and African natural product databases to search for novel inhibitors of histone deacetylases ; [kumulative Dissertation]
Design and synthesis of antimycobacterial agents targeting the mycobacterial electron transport chain and the cell wall synthesis, and in vitro testing against different mycobacterial species
Class I HDAC selective modulators : design, synthesis, and biological characterization
Molecular Modelling Untersuchungen zum Bindungsverhalten von Histamin H2- und H3-Rezeptor-Liganden
Epigenetic targets in drug discovery
Structure-based design of inhibitors of the zinc-dependent enzymes histone deacetylase (HDAC) and UDP-3-O-(R-3-hydroxymyristoylyl)-N-acetylglucosamine deacetylase (LpxC)
Methionine 274 Is Not the Determining Factor for Selective Inhibition of Histone Deacetylase 8 (HDAC8) by L-Shaped Inhibitors
Exploring aromatic cage flexibility of the histone methyllysine reader protein Spindlin1 and its impact on binding mode prediction: an in silico study
Aromatic amino acid hydroxylases as off-targets of histone deacetylase inhibitors
Design, Synthese und Charakterisierung neuer Sirtuin Inhibitoren
Structure based design, synthesis and characterization of small molecules as inhibitors of parasitic targets
Application of computer-based methods to guide the development of novel sirtuin inhibitors : [kumulative Dissertation]
Applications of computational methods and African natural product databases to search for novel inhibitors of histone deacetylases ; [kumulative Dissertation]
Design and synthesis of antimycobacterial agents targeting the mycobacterial electron transport chain and the cell wall synthesis, and in vitro testing against different mycobacterial species