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Anja Vogelmann

Showing results (1-10 of 7) with videos related to

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Current Opinion in Chemical Biology|March 9, 2020
Proteolysis targeting chimeras (PROTACs) for epigenetics researchAnja Vogelmann, Dina Robaa, Wolfgang Sippl, et al.
ACS Pharmacology & Translational Science|February 21, 2022
Comparison of Cellular Target Engagement Methods for the Tubulin Deacetylases Sirt2 and HDAC6: NanoBRET, CETSA, Tubulin Acetylation, and PROTACsAnja Vogelmann, Manfred Jung, Finn K Hansen, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 30, 2020
Syntheses of Thailandepsin B Pseudo-Natural Products: Access to New Highly Potent HDAC Inhibitors via Late-Stage ModificationJana Brosowsky, Monika Lutterbeck, Amelie Liebich, et al.
SLAS Discovery : Advancing Life Sciences R & D|March 15, 2026
A versatile acoustic droplet ejection mass spectrometry platform enables drug discovery for the solute carrier (SLC) target familyAnja Vogelmann, M Florian Rudolph, Yuting Wang, et al.
ACS Chemical Neuroscience|November 11, 2024
Aromatic Amino Acid Hydroxylases as Off-Targets of Histone Deacetylase InhibitorsAnne Baumann, Niklas Papenkordt, Dina Robaa, et al.
Journal of Medicinal Chemistry|June 7, 2024
Structure-Activity Studies of 1,2,4-Oxadiazoles for the Inhibition of the NAD<sup>+</sup>-Dependent Lysine Deacylase Sirtuin 2Arianna Colcerasa, Florian Friedrich, Jelena Melesina, et al.
Journal of Medicinal Chemistry|October 30, 2023
Development of First-in-Class Dual Sirt2/HDAC6 Inhibitors as Molecular Tools for Dual Inhibition of Tubulin DeacetylationLaura Sinatra, Anja Vogelmann, Florian Friedrich, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Current Opinion in Chemical Biology|March 9, 2020
Proteolysis targeting chimeras (PROTACs) for epigenetics researchAnja Vogelmann, Dina Robaa, Wolfgang Sippl, et al.
ACS Pharmacology & Translational Science|February 21, 2022
Comparison of Cellular Target Engagement Methods for the Tubulin Deacetylases Sirt2 and HDAC6: NanoBRET, CETSA, Tubulin Acetylation, and PROTACsAnja Vogelmann, Manfred Jung, Finn K Hansen, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 30, 2020
Syntheses of Thailandepsin B Pseudo-Natural Products: Access to New Highly Potent HDAC Inhibitors via Late-Stage ModificationJana Brosowsky, Monika Lutterbeck, Amelie Liebich, et al.
SLAS Discovery : Advancing Life Sciences R & D|March 15, 2026
A versatile acoustic droplet ejection mass spectrometry platform enables drug discovery for the solute carrier (SLC) target familyAnja Vogelmann, M Florian Rudolph, Yuting Wang, et al.
ACS Chemical Neuroscience|November 11, 2024
Aromatic Amino Acid Hydroxylases as Off-Targets of Histone Deacetylase InhibitorsAnne Baumann, Niklas Papenkordt, Dina Robaa, et al.
Journal of Medicinal Chemistry|June 7, 2024
Structure-Activity Studies of 1,2,4-Oxadiazoles for the Inhibition of the NAD<sup>+</sup>-Dependent Lysine Deacylase Sirtuin 2Arianna Colcerasa, Florian Friedrich, Jelena Melesina, et al.
Journal of Medicinal Chemistry|October 30, 2023
Development of First-in-Class Dual Sirt2/HDAC6 Inhibitors as Molecular Tools for Dual Inhibition of Tubulin DeacetylationLaura Sinatra, Anja Vogelmann, Florian Friedrich, et al.
Pageof 1