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Francesc Xavier Ruiz

Showing results (1-10 of 15) with videos related to

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Current Opinion in Structural Biology|January 15, 2020
Evolving understanding of HIV-1 reverse transcriptase structure, function, inhibition, and resistanceFrancesc Xavier Ruiz, Eddy Arnold
Metabolites|December 23, 2021
Perspective on the Structural Basis for Human Aldo-Keto Reductase 1B10 InhibitionFrancesc Xavier Ruiz, Xavier Parés, Jaume Farrés
Chemico-Biological Interactions|January 9, 2013
X-ray structure of the V301L aldo-keto reductase 1B10 complexed with NADP(+) and the potent aldose reductase inhibitor fidarestat: implications for inhibitor binding and selectivityFrancesc Xavier Ruiz, Alexandra Cousido-Siah, André Mitschler, et al.
Journal of Medicinal Chemistry|November 5, 2024
Structure-Based Design of Covalent SARS-CoV-2 Papain-like Protease InhibitorsBin Tan, Xueying Liang, Ahmadullah Ansari, et al.
Analytical Biochemistry|November 1, 2011
Validation of surface plasmon resonance screening of a diverse chemical library for the discovery of protein tyrosine phosphatase 1b bindersGabrielle Zeder-Lutz, Laurence Choulier, Marie Besse, et al.
Nature Communications|February 13, 2025
Design of quinoline SARS-CoV-2 papain-like protease inhibitors as oral antiviral drug candidatesPrakash Jadhav, Xueying Liang, Ahmadullah Ansari, et al.
Science Advances|July 20, 2022
Cryo-EM structure of the HIV-1 Pol polyprotein provides insights into virion maturationJerry Joe E K Harrison, Dario Oliveira Passos, Jessica F Bruhn, et al.
Biorxiv : the Preprint Server for Biology|April 16, 2025
Crystallographic fragment screening of the dengue virus polymerase reveals multiple binding sites for the development of non-nucleoside antiflaviviralsManisha Saini, Jasmin C Aschenbrenner, Francesc Xavier Ruiz, et al.
Journal of Medicinal Chemistry|September 2, 2025
Crystallographic Fragment Screening of the Dengue Virus Polymerase Reveals Multiple Binding Sites for the Development of Non-nucleoside AntiflaviviralsManisha Saini, Jasmin C Aschenbrenner, Francesc Xavier Ruiz, et al.
Science (New York, N.Y.)|March 28, 2024
Design of a SARS-CoV-2 papain-like protease inhibitor with antiviral efficacy in a mouse modelBin Tan, Xiaoming Zhang, Ahmadullah Ansari, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Current Opinion in Structural Biology|January 15, 2020
Evolving understanding of HIV-1 reverse transcriptase structure, function, inhibition, and resistanceFrancesc Xavier Ruiz, Eddy Arnold
Metabolites|December 23, 2021
Perspective on the Structural Basis for Human Aldo-Keto Reductase 1B10 InhibitionFrancesc Xavier Ruiz, Xavier Parés, Jaume Farrés
Chemico-Biological Interactions|January 9, 2013
X-ray structure of the V301L aldo-keto reductase 1B10 complexed with NADP(+) and the potent aldose reductase inhibitor fidarestat: implications for inhibitor binding and selectivityFrancesc Xavier Ruiz, Alexandra Cousido-Siah, André Mitschler, et al.
Journal of Medicinal Chemistry|November 5, 2024
Structure-Based Design of Covalent SARS-CoV-2 Papain-like Protease InhibitorsBin Tan, Xueying Liang, Ahmadullah Ansari, et al.
Analytical Biochemistry|November 1, 2011
Validation of surface plasmon resonance screening of a diverse chemical library for the discovery of protein tyrosine phosphatase 1b bindersGabrielle Zeder-Lutz, Laurence Choulier, Marie Besse, et al.
Nature Communications|February 13, 2025
Design of quinoline SARS-CoV-2 papain-like protease inhibitors as oral antiviral drug candidatesPrakash Jadhav, Xueying Liang, Ahmadullah Ansari, et al.
Science Advances|July 20, 2022
Cryo-EM structure of the HIV-1 Pol polyprotein provides insights into virion maturationJerry Joe E K Harrison, Dario Oliveira Passos, Jessica F Bruhn, et al.
Biorxiv : the Preprint Server for Biology|April 16, 2025
Crystallographic fragment screening of the dengue virus polymerase reveals multiple binding sites for the development of non-nucleoside antiflaviviralsManisha Saini, Jasmin C Aschenbrenner, Francesc Xavier Ruiz, et al.
Journal of Medicinal Chemistry|September 2, 2025
Crystallographic Fragment Screening of the Dengue Virus Polymerase Reveals Multiple Binding Sites for the Development of Non-nucleoside AntiflaviviralsManisha Saini, Jasmin C Aschenbrenner, Francesc Xavier Ruiz, et al.
Science (New York, N.Y.)|March 28, 2024
Design of a SARS-CoV-2 papain-like protease inhibitor with antiviral efficacy in a mouse modelBin Tan, Xiaoming Zhang, Ahmadullah Ansari, et al.
Pageof 2