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Rob L M van Montfort

Showing results (11-20 of 51) with videos related to

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Cell Cycle (Georgetown, Tex.)|April 8, 2010
Targeting HSP70: the second potentially druggable heat shock protein and molecular chaperone?Marissa V Powers, Keith Jones, Caterina Barillari, et al.
Angewandte Chemie (International Ed. in English)|February 23, 2017
An Irreversible Inhibitor of HSP72 that Unexpectedly Targets Lysine-56Jonathan Pettinger, Yann-Vaï Le Bihan, Marcella Widya, et al.
Bioorganic & Medicinal Chemistry|August 8, 2013
Synthesis and evaluation of heteroaryl substituted diazaspirocycles as scaffolds to probe the ATP-binding site of protein kinasesCharlotte E Allen, Chiau L Chow, John J Caldwell, et al.
Journal of Molecular Biology|January 7, 2009
Insights into the conformational variability and regulation of human Nek2 kinaseIsaac Westwood, Donna-Marie Cheary, Joanne E Baxter, et al.
The Biochemical Journal|August 15, 2019
Structural and functional characterisation of human RNA helicase DHX8 provides insights into the mechanism of RNA-stimulated ADP releaseCatarina Felisberto-Rodrigues, Jemima C Thomas, Craig McAndrew, et al.
Bioorganic & Medicinal Chemistry|October 13, 2012
Benzimidazole inhibitors of the protein kinase CHK2: clarification of the binding mode by flexible side chain docking and protein-ligand crystallographyCornelis Matijssen, M Cris Silva-Santisteban, Isaac M Westwood, et al.
ACS Chemical Biology|August 22, 2018
Evaluation of APOBEC3B Recognition Motifs by NMR Reveals Preferred SubstratesManjuan Liu, Aurélie Mallinger, Marcello Tortorici, et al.
Journal of Medicinal Chemistry|March 4, 2011
Benzimidazole inhibitors induce a DFG-out conformation of never in mitosis gene A-related kinase 2 (Nek2) without binding to the back pocket and reveal a nonlinear structure-activity relationshipSavade Solanki, Paolo Innocenti, Corine Mas-Droux, et al.
Scientific Reports|November 20, 2025
Discovery of first-in-class inhibitors of the TRF1:TIN2 protein:protein interaction by fragment screeningGiacomo Casale, Manjuan Liu, Yann-Vaï Le Bihan, et al.
Journal of Medicinal Chemistry|February 17, 2006
Application of fragment screening and fragment linking to the discovery of novel thrombin inhibitorsNigel Howard, Chris Abell, Wendy Blakemore, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Cell Cycle (Georgetown, Tex.)|April 8, 2010
Targeting HSP70: the second potentially druggable heat shock protein and molecular chaperone?Marissa V Powers, Keith Jones, Caterina Barillari, et al.
Angewandte Chemie (International Ed. in English)|February 23, 2017
An Irreversible Inhibitor of HSP72 that Unexpectedly Targets Lysine-56Jonathan Pettinger, Yann-Vaï Le Bihan, Marcella Widya, et al.
Bioorganic & Medicinal Chemistry|August 8, 2013
Synthesis and evaluation of heteroaryl substituted diazaspirocycles as scaffolds to probe the ATP-binding site of protein kinasesCharlotte E Allen, Chiau L Chow, John J Caldwell, et al.
Journal of Molecular Biology|January 7, 2009
Insights into the conformational variability and regulation of human Nek2 kinaseIsaac Westwood, Donna-Marie Cheary, Joanne E Baxter, et al.
The Biochemical Journal|August 15, 2019
Structural and functional characterisation of human RNA helicase DHX8 provides insights into the mechanism of RNA-stimulated ADP releaseCatarina Felisberto-Rodrigues, Jemima C Thomas, Craig McAndrew, et al.
Bioorganic & Medicinal Chemistry|October 13, 2012
Benzimidazole inhibitors of the protein kinase CHK2: clarification of the binding mode by flexible side chain docking and protein-ligand crystallographyCornelis Matijssen, M Cris Silva-Santisteban, Isaac M Westwood, et al.
ACS Chemical Biology|August 22, 2018
Evaluation of APOBEC3B Recognition Motifs by NMR Reveals Preferred SubstratesManjuan Liu, Aurélie Mallinger, Marcello Tortorici, et al.
Journal of Medicinal Chemistry|March 4, 2011
Benzimidazole inhibitors induce a DFG-out conformation of never in mitosis gene A-related kinase 2 (Nek2) without binding to the back pocket and reveal a nonlinear structure-activity relationshipSavade Solanki, Paolo Innocenti, Corine Mas-Droux, et al.
Scientific Reports|November 20, 2025
Discovery of first-in-class inhibitors of the TRF1:TIN2 protein:protein interaction by fragment screeningGiacomo Casale, Manjuan Liu, Yann-Vaï Le Bihan, et al.
Journal of Medicinal Chemistry|February 17, 2006
Application of fragment screening and fragment linking to the discovery of novel thrombin inhibitorsNigel Howard, Chris Abell, Wendy Blakemore, et al.
Pageof 6