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Iscience|March 4, 2022
Ligands with different dimeric configurations potently activate the EphA2 receptor and reveal its potential for biased signalingMaricel Gomez-Soler, Marina P Gehring, Bernhard C Lechtenberg, et al.ACS Medicinal Chemistry Letters|July 26, 2017
Structure-Guided Strategy for the Development of Potent Bivalent ERK InhibitorsBernhard C Lechtenberg, Peter D Mace, E Hampton Sessions, et al.ACS Medicinal Chemistry Letters|September 24, 2016
Modifications of a Nanomolar Cyclic Peptide Antagonist for the EphA4 Receptor To Achieve High Plasma StabilityErika J Olson, Bernhard C Lechtenberg, Chunxia Zhao, et al.The Journal of Biological Chemistry|June 17, 2021
A cancer mutation promotes EphA4 oligomerization and signaling by altering the conformation of the SAM domainTaylor P Light, Maricel Gomez-Soler, Zichen Wang, et al.European Journal of Medicinal Chemistry|November 4, 2024
Lipidation and PEGylation strategies to prolong the in vivo half-life of a nanomolar EphA4 receptor antagonistMaricel Gomez-Soler, Erika J Olson, Elena Rubio de la Torre, et al.Life Science Alliance|April 1, 2025
The RBR E3 ubiquitin ligase HOIL-1 can ubiquitinate diverse non-protein substrates in vitroXiangyi S Wang, Jenny Jiou, Anthony Cerra, et al.European Journal of Medicinal Chemistry|March 25, 2024
Lipidation and PEGylation Strategies to Prolong the in Vivo Half-Life of a Nanomolar EphA4 Receptor AntagonistMaricel Gomez-Soler, Erika J Olson, Elena Rubio de la Torre, et al.Nature Communications|June 19, 2023
Structural mapping of PEAK pseudokinase interactions identifies 14-3-3 as a molecular switch for PEAK3 signalingMichael J Roy, Minglyanna G Surudoi, Ashleigh Kropp, et al.Redox Biology|December 6, 2022
Design and characterization of a heterobifunctional degrader of KEAP1Hao Chen, Nghi H Nguyen, Charlene M Magtoto, et al.Nature|April 22, 2026
Ubiquitination of glycogen and metabolites in cells and tissuesMarco Jochem, Simon A Cobbold, Craig A Goodman, et al.Pageof 4