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Thomas Wein

Showing results (11-20 of 28) with videos related to

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Nature Communications|April 11, 2026
Structural optimization of drug molecules with incrementally trained language modelsTim Hörmann, Domenic Mayer, Max Lewandowski, et al.
Chemmedchem|January 26, 2016
Different Binding Modes of Small and Large Binders of GAT1Thomas Wein, Marilena Petrera, Lars Allmendinger, et al.
Angewandte Chemie (International Ed. in English)|September 9, 2024
A High-Quality Photoswitchable Probe that Selectively and Potently Regulates the Transcription Factor RORγMartin Reynders, Sabine Willems, Julian A Marschner, et al.
Chemmedchem|December 20, 2015
Development of Highly Potent GAT1 Inhibitors: Synthesis of Nipecotic Acid Derivatives by Suzuki-Miyaura Cross-Coupling ReactionsMarilena Petrera, Thomas Wein, Lars Allmendinger, et al.
Journal of Medicinal Chemistry|June 21, 2018
Development of New Photoswitchable Azobenzene Based γ-Aminobutyric Acid (GABA) Uptake Inhibitors with Distinctly Enhanced Potency upon PhotoactivationToni Lutz, Thomas Wein, Georg Höfner, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 7, 2011
The glutamic acid-rich protein is a gating inhibitor of cyclic nucleotide-gated channelsStylianos Michalakis, Xiangang Zong, Elvir Becirovic, et al.
Communications Chemistry|May 21, 2025
Structural and mechanistic profiling of Nurr1 modulation by vidofludimus enables structure-guided ligand designÚrsula López-García, Jan Vietor, Julian A Marschner, et al.
Journal of Medicinal Chemistry|February 7, 2025
A Nurr1 Agonist Derived from the Natural Ligand DHI Induces Neuroprotective Gene ExpressionMarkus Egner, Romy Busch, Úrsula López-García, et al.
Current Computer-Aided Drug Design|July 4, 2018
New Resensitizers for the Nicotinic Acetylcholine Receptor by Ligand-Based Pharmacophore ModelingThomas Wein, Klaus T Wanner, Sebastian Rappenglück, et al.
Bioorganic Chemistry|September 26, 2022
Fragment-based discovery of orphan nuclear receptor Nur77/NGFI-B ligandsSilvia Arifi, Daniel Zaienne, Jan Heering, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Nature Communications|April 11, 2026
Structural optimization of drug molecules with incrementally trained language modelsTim Hörmann, Domenic Mayer, Max Lewandowski, et al.
Chemmedchem|January 26, 2016
Different Binding Modes of Small and Large Binders of GAT1Thomas Wein, Marilena Petrera, Lars Allmendinger, et al.
Angewandte Chemie (International Ed. in English)|September 9, 2024
A High-Quality Photoswitchable Probe that Selectively and Potently Regulates the Transcription Factor RORγMartin Reynders, Sabine Willems, Julian A Marschner, et al.
Chemmedchem|December 20, 2015
Development of Highly Potent GAT1 Inhibitors: Synthesis of Nipecotic Acid Derivatives by Suzuki-Miyaura Cross-Coupling ReactionsMarilena Petrera, Thomas Wein, Lars Allmendinger, et al.
Journal of Medicinal Chemistry|June 21, 2018
Development of New Photoswitchable Azobenzene Based γ-Aminobutyric Acid (GABA) Uptake Inhibitors with Distinctly Enhanced Potency upon PhotoactivationToni Lutz, Thomas Wein, Georg Höfner, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 7, 2011
The glutamic acid-rich protein is a gating inhibitor of cyclic nucleotide-gated channelsStylianos Michalakis, Xiangang Zong, Elvir Becirovic, et al.
Communications Chemistry|May 21, 2025
Structural and mechanistic profiling of Nurr1 modulation by vidofludimus enables structure-guided ligand designÚrsula López-García, Jan Vietor, Julian A Marschner, et al.
Journal of Medicinal Chemistry|February 7, 2025
A Nurr1 Agonist Derived from the Natural Ligand DHI Induces Neuroprotective Gene ExpressionMarkus Egner, Romy Busch, Úrsula López-García, et al.
Current Computer-Aided Drug Design|July 4, 2018
New Resensitizers for the Nicotinic Acetylcholine Receptor by Ligand-Based Pharmacophore ModelingThomas Wein, Klaus T Wanner, Sebastian Rappenglück, et al.
Bioorganic Chemistry|September 26, 2022
Fragment-based discovery of orphan nuclear receptor Nur77/NGFI-B ligandsSilvia Arifi, Daniel Zaienne, Jan Heering, et al.
Pageof 3