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Rens M J M de Vries

Showing results (1-10 of 9) with videos related to

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Chemmedchem|February 14, 2020
Elucidation of an Allosteric Mode of Action for a Thienopyrazole RORγt Inverse AgonistRens M J M de Vries, Richard G Doveston, Femke A Meijer, et al.
Molecular and Cellular Endocrinology|February 1, 2019
Allosteric small molecule modulators of nuclear receptorsFemke A Meijer, Iris A Leijten-van de Gevel, Rens M J M de Vries, et al.
The Biochemical Journal|February 17, 2017
Structural interface between LRRK2 and 14-3-3 proteinLoes M Stevers, Rens M J M de Vries, Richard G Doveston, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 4, 2021
Cooperativity between the orthosteric and allosteric ligand binding sites of RORγtRens M J M de Vries, Femke A Meijer, Richard G Doveston, et al.
Bioorganic & Medicinal Chemistry|June 17, 2022
Indazole MRL-871 interacts with PPARγ via a binding mode that induces partial agonismIris A Leijten-van de Gevel, Kim H N van Herk, Rens M J M de Vries, et al.
ACS Chemical Neuroscience|July 11, 2017
Ligand Dependent Switch from RXR Homo- to RXR-NURR1 HeterodimerizationMarcel Scheepstra, Sebastian A Andrei, Rens M J M de Vries, et al.
Journal of Medicinal Chemistry|December 11, 2019
Ligand-Based Design of Allosteric Retinoic Acid Receptor-Related Orphan Receptor γt (RORγt) Inverse AgonistsFemke A Meijer, Richard G Doveston, Rens M J M de Vries, et al.
Journal of Medicinal Chemistry|May 19, 2021
Structure-Activity Relationship Studies of Trisubstituted Isoxazoles as Selective Allosteric Ligands for the Retinoic-Acid-Receptor-Related Orphan Receptor γtFemke A Meijer, Annet O W M Saris, Richard G Doveston, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 19, 2016
Characterization and small-molecule stabilization of the multisite tandem binding between 14-3-3 and the R domain of CFTRLoes M Stevers, Chan V Lam, Seppe F R Leysen, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Chemmedchem|February 14, 2020
Elucidation of an Allosteric Mode of Action for a Thienopyrazole RORγt Inverse AgonistRens M J M de Vries, Richard G Doveston, Femke A Meijer, et al.
Molecular and Cellular Endocrinology|February 1, 2019
Allosteric small molecule modulators of nuclear receptorsFemke A Meijer, Iris A Leijten-van de Gevel, Rens M J M de Vries, et al.
The Biochemical Journal|February 17, 2017
Structural interface between LRRK2 and 14-3-3 proteinLoes M Stevers, Rens M J M de Vries, Richard G Doveston, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 4, 2021
Cooperativity between the orthosteric and allosteric ligand binding sites of RORγtRens M J M de Vries, Femke A Meijer, Richard G Doveston, et al.
Bioorganic & Medicinal Chemistry|June 17, 2022
Indazole MRL-871 interacts with PPARγ via a binding mode that induces partial agonismIris A Leijten-van de Gevel, Kim H N van Herk, Rens M J M de Vries, et al.
ACS Chemical Neuroscience|July 11, 2017
Ligand Dependent Switch from RXR Homo- to RXR-NURR1 HeterodimerizationMarcel Scheepstra, Sebastian A Andrei, Rens M J M de Vries, et al.
Journal of Medicinal Chemistry|December 11, 2019
Ligand-Based Design of Allosteric Retinoic Acid Receptor-Related Orphan Receptor γt (RORγt) Inverse AgonistsFemke A Meijer, Richard G Doveston, Rens M J M de Vries, et al.
Journal of Medicinal Chemistry|May 19, 2021
Structure-Activity Relationship Studies of Trisubstituted Isoxazoles as Selective Allosteric Ligands for the Retinoic-Acid-Receptor-Related Orphan Receptor γtFemke A Meijer, Annet O W M Saris, Richard G Doveston, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 19, 2016
Characterization and small-molecule stabilization of the multisite tandem binding between 14-3-3 and the R domain of CFTRLoes M Stevers, Chan V Lam, Seppe F R Leysen, et al.
Pageof 1