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David House

Showing results (41-50 of 52) with videos related to

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Nature Communications|January 2, 2025
Robust proteome profiling of cysteine-reactive fragments using label-free chemoproteomicsGeorge S Biggs, Emma E Cawood, Aini Vuorinen, et al.
Angewandte Chemie (International Ed. in English)|August 4, 2020
A Photoaffinity-Based Fragment-Screening Platform for Efficient Identification of Protein LigandsEmma K Grant, David J Fallon, Michael M Hann, et al.
Nature Microbiology|May 19, 2025
The fast-evolving FIKK kinase family of Plasmodium falciparum can be inhibited by a single compoundHugo Belda, David Bradley, Evangelos Christodoulou, et al.
Bioorganic & Medicinal Chemistry Letters|July 10, 2007
Non-steroidal glucocorticoid agonists: the discovery of aryl pyrazoles as A-ring mimeticsMargaret Clackers, Diane M Coe, Derek A Demaine, et al.
Nature Chemical Biology|October 25, 2019
Author Correction: MCT2 mediates concentration-dependent inhibition of glutamine metabolism by MOGLouise Fets, Paul C Driscoll, Fiona Grimm, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 14, 2009
Design and x-ray crystal structures of high-potency nonsteroidal glucocorticoid agonists exploiting a novel binding site on the receptorKeith Biggadike, Randy K Bledsoe, Diane M Coe, et al.
Nature Chemical Biology|October 10, 2018
MCT2 mediates concentration-dependent inhibition of glutamine metabolism by MOGLouise Fets, Paul C Driscoll, Fiona Grimm, et al.
Bioorganic & Medicinal Chemistry Letters|January 25, 2011
Discovery of a potent series of non-steroidal non α-trifluoromethyl carbinol glucocorticoid receptor agonists with reduced lipophilicityHawa Diallo, Davina C Angell, Heather A Barnett, et al.
Angewandte Chemie (International Ed. in English)|April 20, 2026
A Synergistic Inhibitor Development Strategy Against Human UDP-Galactose-4-EpimeraseWilliam M Browne, Jonathan Pettinger, Teresa Weckwerth, et al.
Journal of Medicinal Chemistry|November 28, 2007
Nonsteroidal glucocorticoid agonists: tetrahydronaphthalenes with alternative steroidal A-ring mimetics possessing dissociated (transrepression/transactivation) efficacy selectivityKeith Biggadike, Mohamed Boudjelal, Margaret Clackers, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Nature Communications|January 2, 2025
Robust proteome profiling of cysteine-reactive fragments using label-free chemoproteomicsGeorge S Biggs, Emma E Cawood, Aini Vuorinen, et al.
Angewandte Chemie (International Ed. in English)|August 4, 2020
A Photoaffinity-Based Fragment-Screening Platform for Efficient Identification of Protein LigandsEmma K Grant, David J Fallon, Michael M Hann, et al.
Nature Microbiology|May 19, 2025
The fast-evolving FIKK kinase family of Plasmodium falciparum can be inhibited by a single compoundHugo Belda, David Bradley, Evangelos Christodoulou, et al.
Bioorganic & Medicinal Chemistry Letters|July 10, 2007
Non-steroidal glucocorticoid agonists: the discovery of aryl pyrazoles as A-ring mimeticsMargaret Clackers, Diane M Coe, Derek A Demaine, et al.
Nature Chemical Biology|October 25, 2019
Author Correction: MCT2 mediates concentration-dependent inhibition of glutamine metabolism by MOGLouise Fets, Paul C Driscoll, Fiona Grimm, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 14, 2009
Design and x-ray crystal structures of high-potency nonsteroidal glucocorticoid agonists exploiting a novel binding site on the receptorKeith Biggadike, Randy K Bledsoe, Diane M Coe, et al.
Nature Chemical Biology|October 10, 2018
MCT2 mediates concentration-dependent inhibition of glutamine metabolism by MOGLouise Fets, Paul C Driscoll, Fiona Grimm, et al.
Bioorganic & Medicinal Chemistry Letters|January 25, 2011
Discovery of a potent series of non-steroidal non α-trifluoromethyl carbinol glucocorticoid receptor agonists with reduced lipophilicityHawa Diallo, Davina C Angell, Heather A Barnett, et al.
Angewandte Chemie (International Ed. in English)|April 20, 2026
A Synergistic Inhibitor Development Strategy Against Human UDP-Galactose-4-EpimeraseWilliam M Browne, Jonathan Pettinger, Teresa Weckwerth, et al.
Journal of Medicinal Chemistry|November 28, 2007
Nonsteroidal glucocorticoid agonists: tetrahydronaphthalenes with alternative steroidal A-ring mimetics possessing dissociated (transrepression/transactivation) efficacy selectivityKeith Biggadike, Mohamed Boudjelal, Margaret Clackers, et al.
Pageof 6