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Molecules (Basel, Switzerland)|August 29, 2024
Novel Quinazoline Derivatives as Highly Effective A2A Adenosine Receptor AntagonistsAmélie Laversin, Robin Dufossez, Raphaël Bolteau, et al.
Journal of Medicinal Chemistry|April 7, 2020
Interrogating the Lactate Dehydrogenase Tetramerization Site Using (Stapled) PeptidesLéopold Thabault, Lucie Brisson, Chiara Brustenga, et al.
European Journal of Medicinal Chemistry|August 7, 2022
High ligand efficiency quinazoline compounds as novel A<sub>2A</sub> adenosine receptor antagonistsRaphaël Bolteau, Romain Duroux, Amélie Laversin, et al.
European Journal of Medicinal Chemistry|September 12, 2021
Discovery of a cryptic site at the interface 2 of TEAD - Towards a new family of YAP/TAZ-TEAD inhibitorsManon Sturbaut, Fabrice Bailly, Mathilde Coevoet, et al.
Cancers|November 27, 2021
The EGF Domains of MUC4 Oncomucin Mediate HER2 Binding Affinity and Promote Pancreatic Cancer Cell TumorigenesisNicolas Stoup, Maxime Liberelle, Céline Schulz, et al.
Protein Science : a Publication of the Protein Society|April 22, 2025
Structural insights into the interaction between testis-specific Y-encoded-like protein 5 and ubiquitin-specific protease 7Marine Ancia, Khadija Wahni, Joudy Chakrowf, et al.
Cell Death & Disease|October 17, 2024
PAK6 rescues pathogenic LRRK2-mediated ciliogenesis and centrosomal cohesion defects in a mutation-specific mannerLucia Iannotta, Rachel Fasiczka, Giulia Favetta, et al.
Cells|March 25, 2022
A Phosphosite Mutant Approach on LRRK2 Links Phosphorylation and Dephosphorylation to Protective and Deleterious Markers, RespectivelyAntoine Marchand, Alessia Sarchione, Panagiotis S Athanasopoulos, et al.
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