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Alessio Ciulli

Showing results (71-80 of 163) with videos related to

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Journal of Chemical Information and Modeling|November 29, 2021
Automated Determination of Nuclear Magnetic Resonance Chemical Shift Perturbations in Ligand Screening Experiments: The PICASSO Web ServerVincenzo Laveglia, Andrea Giachetti, Linda Cerofolini, et al.
Journal of Medicinal Chemistry|April 25, 2017
Allosteric Targeting of the Fanconi Anemia Ubiquitin-Conjugating Enzyme Ube2T by Fragment ScreeningFrancesca E Morreale, Alessio Bortoluzzi, Viduth K Chaugule, et al.
Journal of Medicinal Chemistry|September 22, 2017
Mind the Metal: A Fragment Library-Derived Zinc Impurity Binds the E2 Ubiquitin-Conjugating Enzyme Ube2T and Induces Structural RearrangementsFrancesca E Morreale, Andrea Testa, Viduth K Chaugule, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
Native Mass Spectrometry Analysis of Cullin RING Ubiquitin E3 Ligase Complexes in the Context of Targeted Protein DegradationLouise M Sternicki, Charlotte Crowe, Lianne H E Wieske, et al.
Angewandte Chemie (International Ed. in English)|September 26, 2009
Application of fragment growing and fragment linking to the discovery of inhibitors of Mycobacterium tuberculosis pantothenate synthetaseAlvin W Hung, H Leonardo Silvestre, Shijun Wen, et al.
EMBO Reports|August 23, 2024
Combination of AID2 and BromoTag expands the utility of degron-based protein knockdownsYuki Hatoyama, Moutushi Islam, Adam G Bond, et al.
Journal of the American Chemical Society|March 18, 2010
Optimization of the interligand Overhauser effect for fragment linking: application to inhibitor discovery against Mycobacterium tuberculosis pantothenate synthetasePawel Sledz, H Leonardo Silvestre, Alvin W Hung, et al.
ACS Chemical Biology|August 29, 2019
Design and Characterization of SGK3-PROTAC1, an Isoform Specific SGK3 Kinase PROTAC DegraderHannah Tovell, Andrea Testa, Houjiang Zhou, et al.
Molecular Cell|August 22, 2025
Opportunities in proximity modulation: Bridging academia and industryIvan Dikic, Cristina Mayor-Ruiz, Georg E Winter, et al.
The Biochemical Journal|September 2, 2024
The pro-drug C13 activates AMPK by two distinct mechanismsJordana B Freemantle, Dinesh Shah, Dylan M Lynch, et al.
Pageof 17

Showing results (71-80 of 163) with videos related to

Sort By:
Pageof 17
Journal of Chemical Information and Modeling|November 29, 2021
Automated Determination of Nuclear Magnetic Resonance Chemical Shift Perturbations in Ligand Screening Experiments: The PICASSO Web ServerVincenzo Laveglia, Andrea Giachetti, Linda Cerofolini, et al.
Journal of Medicinal Chemistry|April 25, 2017
Allosteric Targeting of the Fanconi Anemia Ubiquitin-Conjugating Enzyme Ube2T by Fragment ScreeningFrancesca E Morreale, Alessio Bortoluzzi, Viduth K Chaugule, et al.
Journal of Medicinal Chemistry|September 22, 2017
Mind the Metal: A Fragment Library-Derived Zinc Impurity Binds the E2 Ubiquitin-Conjugating Enzyme Ube2T and Induces Structural RearrangementsFrancesca E Morreale, Andrea Testa, Viduth K Chaugule, et al.
Biorxiv : the Preprint Server for Biology|January 16, 2026
Native Mass Spectrometry Analysis of Cullin RING Ubiquitin E3 Ligase Complexes in the Context of Targeted Protein DegradationLouise M Sternicki, Charlotte Crowe, Lianne H E Wieske, et al.
Angewandte Chemie (International Ed. in English)|September 26, 2009
Application of fragment growing and fragment linking to the discovery of inhibitors of Mycobacterium tuberculosis pantothenate synthetaseAlvin W Hung, H Leonardo Silvestre, Shijun Wen, et al.
EMBO Reports|August 23, 2024
Combination of AID2 and BromoTag expands the utility of degron-based protein knockdownsYuki Hatoyama, Moutushi Islam, Adam G Bond, et al.
Journal of the American Chemical Society|March 18, 2010
Optimization of the interligand Overhauser effect for fragment linking: application to inhibitor discovery against Mycobacterium tuberculosis pantothenate synthetasePawel Sledz, H Leonardo Silvestre, Alvin W Hung, et al.
ACS Chemical Biology|August 29, 2019
Design and Characterization of SGK3-PROTAC1, an Isoform Specific SGK3 Kinase PROTAC DegraderHannah Tovell, Andrea Testa, Houjiang Zhou, et al.
Molecular Cell|August 22, 2025
Opportunities in proximity modulation: Bridging academia and industryIvan Dikic, Cristina Mayor-Ruiz, Georg E Winter, et al.
The Biochemical Journal|September 2, 2024
The pro-drug C13 activates AMPK by two distinct mechanismsJordana B Freemantle, Dinesh Shah, Dylan M Lynch, et al.
Pageof 17