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ACS Central Science|July 31, 2023
Proximity-Based Modalities for Biology and MedicineXingui Liu, Alessio CiulliBioorganic & Medicinal Chemistry Letters|June 28, 2024
Stereochemical inversion at a 1,4-cyclohexyl PROTAC linker fine-tunes conformation and binding affinityMartina Pierri, Xingui Liu, Alena Kroupova, 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 CiulliSLAS Discovery : Advancing Life Sciences R & D|November 4, 2020
E3 Ligase Ligands for PROTACs: How They Were Found and How to Discover New OnesTasuku Ishida, Alessio CiulliCurrent Opinion in Biotechnology|October 26, 2007
Fragment-based approaches to enzyme inhibitionAlessio Ciulli, Chris AbellPageof 18