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Vittorio Limongelli

Showing results (41-50 of 82) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|February 25, 2017
Ligand binding to telomeric G-quadruplex DNA investigated by funnel-metadynamics simulationsFederica Moraca, Jussara Amato, Francesco Ortuso, et al.
Nucleic Acids Research|November 8, 2014
G-triplex structure and formation propensityLinda Cerofolini, Jussara Amato, Andrea Giachetti, et al.
Biochimica Et Biophysica Acta|January 5, 2010
Membrane charge dependent states of the beta-amyloid fragment Abeta (16-35) with differently charged micelle aggregatesManuela Grimaldi, Mario Scrima, Cinzia Esposito, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 13, 2012
Sampling protein motion and solvent effect during ligand bindingVittorio Limongelli, Luciana Marinelli, Sandro Cosconati, et al.
Nature Communications|July 26, 2020
Protein-ligand binding with the coarse-grained Martini modelPaulo C T Souza, Sebastian Thallmair, Paolo Conflitti, et al.
Journal of Chemical Information and Modeling|December 16, 2021
Discovery of Bile Acid Derivatives as Potent ACE2 Activators by Virtual Screening and Essential DynamicsBianca Fiorillo, Silvia Marchianò, Federica Moraca, et al.
Journal of Medicinal Chemistry|January 7, 2014
Design, synthesis, and biological evaluation of potent dual agonists of nuclear and membrane bile acid receptorsClaudio D'Amore, Francesco Saverio Di Leva, Valentina Sepe, et al.
Molecules (Basel, Switzerland)|March 20, 2019
Introduction of Nonacidic Side Chains on 6-Ethylcholane Scaffolds in the Identification of Potent Bile Acid Receptor Agonists with Improved Pharmacokinetic PropertiesClaudia Finamore, Giuliana Baronissi, Silvia Marchianò, et al.
Journal of Medicinal Chemistry|May 3, 2008
Acetic acid aldose reductase inhibitors bearing a five-membered heterocyclic core with potent topical activity in a visual impairment rat modelConcettina La Motta, Stefania Sartini, Silvia Salerno, et al.
Journal of Medicinal Chemistry|May 10, 2013
Binding mechanism of the farnesoid X receptor marine antagonist suvanine reveals a strategy to forestall drug modulation on nuclear receptors. Design, synthesis, and biological evaluation of novel ligandsFrancesco Saverio Di Leva, Carmen Festa, Claudio D'Amore, et al.
Pageof 9

Showing results (41-50 of 82) with videos related to

Sort By:
Pageof 9
Proceedings of the National Academy of Sciences of the United States of America|February 25, 2017
Ligand binding to telomeric G-quadruplex DNA investigated by funnel-metadynamics simulationsFederica Moraca, Jussara Amato, Francesco Ortuso, et al.
Nucleic Acids Research|November 8, 2014
G-triplex structure and formation propensityLinda Cerofolini, Jussara Amato, Andrea Giachetti, et al.
Biochimica Et Biophysica Acta|January 5, 2010
Membrane charge dependent states of the beta-amyloid fragment Abeta (16-35) with differently charged micelle aggregatesManuela Grimaldi, Mario Scrima, Cinzia Esposito, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 13, 2012
Sampling protein motion and solvent effect during ligand bindingVittorio Limongelli, Luciana Marinelli, Sandro Cosconati, et al.
Nature Communications|July 26, 2020
Protein-ligand binding with the coarse-grained Martini modelPaulo C T Souza, Sebastian Thallmair, Paolo Conflitti, et al.
Journal of Chemical Information and Modeling|December 16, 2021
Discovery of Bile Acid Derivatives as Potent ACE2 Activators by Virtual Screening and Essential DynamicsBianca Fiorillo, Silvia Marchianò, Federica Moraca, et al.
Journal of Medicinal Chemistry|January 7, 2014
Design, synthesis, and biological evaluation of potent dual agonists of nuclear and membrane bile acid receptorsClaudio D'Amore, Francesco Saverio Di Leva, Valentina Sepe, et al.
Molecules (Basel, Switzerland)|March 20, 2019
Introduction of Nonacidic Side Chains on 6-Ethylcholane Scaffolds in the Identification of Potent Bile Acid Receptor Agonists with Improved Pharmacokinetic PropertiesClaudia Finamore, Giuliana Baronissi, Silvia Marchianò, et al.
Journal of Medicinal Chemistry|May 3, 2008
Acetic acid aldose reductase inhibitors bearing a five-membered heterocyclic core with potent topical activity in a visual impairment rat modelConcettina La Motta, Stefania Sartini, Silvia Salerno, et al.
Journal of Medicinal Chemistry|May 10, 2013
Binding mechanism of the farnesoid X receptor marine antagonist suvanine reveals a strategy to forestall drug modulation on nuclear receptors. Design, synthesis, and biological evaluation of novel ligandsFrancesco Saverio Di Leva, Carmen Festa, Claudio D'Amore, et al.
Pageof 9