Search results (136)
« Back to PublicationsUbiquitin E3 ligase KLHL6 brings exhausted T-cells back into action
Journal article
Chen Z. et al, (2026), Immunity & Inflammation, 2
Fragment-Based Drug Discovery of Novel High-affinity, Selective, and Anti-inflammatory Inhibitors of the Keap1-Nrf2 Protein-Protein Interaction.
Journal article
Lin C. et al, (2025), Angewandte Chemie (International ed. in English), 64
Structural mimicry of UM171 and neomorphic cancer mutants co-opts E3 ligase KBTBD4 for HDAC1/2 recruitment.
Journal article
Chen Z. et al, (2025), Nature communications, 16
Toward target 2035: EUbOPEN - a public–private partnership to enable & unlock biology in the open
Journal article
Tredup C. et al, (2025), RSC Medicinal Chemistry, 16, 457 - 464
Covalent Inhibitors of KEAP1 with Exquisite Selectivity.
Journal article
Fejes I. et al, (2024), Journal of medicinal chemistry, 67, 21208 - 21222
Structure-Guided Conformational Restriction Leading to High-Affinity, Selective, and Cell-Active Tetrahydroisoquinoline-Based Noncovalent Keap1-Nrf2 Inhibitors.
Journal article
Qin Y. et al, (2024), Journal of medicinal chemistry, 67, 18828 - 18864
BTB extension and ion-binding domain contribute to the pentameric structure and TFAP2A binding of KCTD1
Journal article
Pinkas DM. et al, (2024), Structure, 32, 1586 - 1593.e4
Discovery of Two Highly Selective Structurally Orthogonal Chemical Probes for Activin Receptor-like Kinases 1 and 2.
Journal article
Němec V. et al, (2024), Journal of medicinal chemistry, 67, 12632 - 12659
Discovery and Characterization of a Chemical Probe for Cyclin-Dependent Kinase-Like 2.
Journal article
Bashore FM. et al, (2024), ACS medicinal chemistry letters, 15, 1325 - 1333
BTB extension and ion-binding domain contribute to the pentameric structure and TFAP2A binding of KCTD1
Preprint
Pinkas DM. et al, (2024)
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome
Journal article
Miller KA. et al, (2024), Journal of Medical Genetics, 61, 490 - 501
Still in Search for an EAAT Activator: GT949 Does Not Activate EAAT2, nor EAAT3 in Impedance and Radioligand Uptake Assays
Journal article
van Veggel L. et al, (2024), ACS Chemical Neuroscience, 15, 1424 - 1431
Discovery of Conformationally Constrained ALK2 Inhibitors.
Journal article
González-Álvarez H. et al, (2024), Journal of medicinal chemistry, 67, 4707 - 4725
Correction: CIS is a potent checkpoint in NK cell-mediated tumor immunity.
Journal article
Delconte RB. et al, (2024), Nature immunology, 25, 371 - 372
PRMT5 inhibition shows in vitro efficacy against H3K27M-altered diffuse midline glioma, but does not extend survival in vivo.
Journal article
Brown EJ. et al, (2024), Scientific reports, 14