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ACS Central Science|July 31, 2023
Proximity-Based Modalities for Biology and MedicineXingui Liu, 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 AbellFuture Medicinal Chemistry|May 20, 2016
Selectivity on-target of bromodomain chemical probes by structure-guided medicinal chemistry and chemical biologyCarles Galdeano, Alessio CiulliCurrent Opinion in Structural Biology|December 3, 2020
Building ubiquitination machineries: E3 ligase multi-subunit assembly and substrate targeting by PROTACs and molecular gluesSarath Ramachandran, Alessio CiulliAnnual Review of Biochemistry|March 23, 2022
Driving E3 Ligase Substrate Specificity for Targeted Protein Degradation: Lessons from Nature and the LaboratoryAngus D Cowan, Alessio CiulliEssays in Biochemistry|November 10, 2017
Molecular recognition of ternary complexes: a new dimension in the structure-guided design of chemical degradersScott J Hughes, Alessio CiulliChemical Society Reviews|August 19, 2022
Discovery of small molecule ligands for the von Hippel-Lindau (VHL) E3 ligase and their use as inhibitors and PROTAC degradersClaudia J Diehl, Alessio CiulliProgress in Biophysics and Molecular Biology|September 2, 2014
NMR approaches in structure-based lead discovery: recent developments and new frontiers for targeting multi-protein complexesDavid M Dias, Alessio CiulliChemical Communications (Cambridge, England)|January 16, 2019
Spy vs. spy: selecting the best reporter for 19F NMR competition experimentsGuilherme Vieira de Castro, Alessio CiulliPageof 16