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Methods in Enzymology|February 10, 2023
Crystallization of VHL-based PROTAC-induced ternary complexesAndre J Wijaya, William Farnaby, Alessio CiulliCurrent Opinion in Pharmacology|April 2, 2021
Transforming targeted cancer therapy with PROTACs: A forward-looking perspectiveWilliam Farnaby, Manfred Koegl, Darryl B McConnell, et al.Current Opinion in Structural Biology|February 22, 2023
Breaking free from the crystal lattice: Structural biology in solution to study protein degradersKevin Haubrich, Valentina A Spiteri, William Farnaby, et al.ACS Chemical Biology|February 6, 2019
SPR-Measured Dissociation Kinetics of PROTAC Ternary Complexes Influence Target Degradation RateMichael J Roy, Sandra Winkler, Scott J Hughes, et al.Methods in Molecular Biology (Clifton, N.J.)|June 5, 2013
Biophysical screening for the discovery of small-molecule ligandsAlessio CiulliCurrent Opinion in Structural Biology|January 29, 2017
Recognition of substrate degrons by E3 ubiquitin ligases and modulation by small-molecule mimicry strategiesXavier Lucas, Alessio CiulliChemical Reviews|May 14, 2026
Methods to Study the Molecular Mechanism and Drive the Design of Protein DegradersCharlotte Crowe, Alessio CiulliCurrent Opinion in Chemical Biology|August 17, 2019
Bifunctional chemical probes inducing protein-protein interactionsChiara Maniaci, Alessio CiulliRSC Medicinal Chemistry|May 27, 2021
Recent advances in synthetic and medicinal chemistry of phosphotyrosine and phosphonate-based phosphotyrosine analoguesNikolai Makukhin, Alessio CiulliThe Biochemical Journal|April 18, 2015
Targeting Cullin-RING E3 ubiquitin ligases for drug discovery: structure, assembly and small-molecule modulationEmil Bulatov, Alessio CiulliPageof 16