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David Lagorce

Showing results (11-20 of 29) with videos related to

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Plos One|October 24, 2014
Rational design of small-molecule stabilizers of spermine synthase dimer by virtual screening and free energy-based approachZhe Zhang, Virginie Martiny, David Lagorce, et al.
Plos One|June 25, 2011
Tyrosine kinase syk non-enzymatic inhibitors and potential anti-allergic drug-like compounds discovered by virtual and in vitro screeningBruno O Villoutreix, Guillaume Laconde, David Lagorce, et al.
Current Protein & Peptide Science|August 19, 2007
Free resources to assist structure-based virtual ligand screening experimentsBruno O Villoutreix, Nicolas Renault, David Lagorce, et al.
Molecular Pharmaceutics|October 18, 2012
In silico prediction of aqueous solubility: a multimodel protocol based on chemical similarityFlorent Chevillard, David Lagorce, Christelle Reynès, et al.
Plos One|September 17, 2013
In silico mechanistic profiling to probe small molecule binding to sulfotransferasesVirginie Y Martiny, Pablo Carbonell, David Lagorce, et al.
Progress in Biophysics and Molecular Biology|March 10, 2015
In silico design of low molecular weight protein-protein interaction inhibitors: Overall concept and recent advancesMélaine A Kuenemann, Olivier Sperandio, Céline M Labbé, et al.
Oncogene|June 19, 2003
Hepatitis B virus-related insertional mutagenesis occurs frequently in human liver cancers and recurrently targets human telomerase genePatrizia Paterlini-Bréchot, Kenichi Saigo, Yoshiki Murakami, et al.
Bioinformatics (Oxford, England)|June 4, 2011
The FAF-Drugs2 server: a multistep engine to prepare electronic chemical compound collectionsDavid Lagorce, Julien Maupetit, Jonathan Baell, et al.
Nucleic Acids Research|January 16, 2003
Identification and functional characterization of a new member of the human Mcm protein family: hMcm8Devrim Gozuacik, Mounia Chami, David Lagorce, et al.
Molecular Informatics|September 26, 2014
Drug-Like Protein-Protein Interaction Modulators: Challenges and Opportunities for Drug Discovery and Chemical BiologyBruno O Villoutreix, Melaine A Kuenemann, Jean-Luc Poyet, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Plos One|October 24, 2014
Rational design of small-molecule stabilizers of spermine synthase dimer by virtual screening and free energy-based approachZhe Zhang, Virginie Martiny, David Lagorce, et al.
Plos One|June 25, 2011
Tyrosine kinase syk non-enzymatic inhibitors and potential anti-allergic drug-like compounds discovered by virtual and in vitro screeningBruno O Villoutreix, Guillaume Laconde, David Lagorce, et al.
Current Protein & Peptide Science|August 19, 2007
Free resources to assist structure-based virtual ligand screening experimentsBruno O Villoutreix, Nicolas Renault, David Lagorce, et al.
Molecular Pharmaceutics|October 18, 2012
In silico prediction of aqueous solubility: a multimodel protocol based on chemical similarityFlorent Chevillard, David Lagorce, Christelle Reynès, et al.
Plos One|September 17, 2013
In silico mechanistic profiling to probe small molecule binding to sulfotransferasesVirginie Y Martiny, Pablo Carbonell, David Lagorce, et al.
Progress in Biophysics and Molecular Biology|March 10, 2015
In silico design of low molecular weight protein-protein interaction inhibitors: Overall concept and recent advancesMélaine A Kuenemann, Olivier Sperandio, Céline M Labbé, et al.
Oncogene|June 19, 2003
Hepatitis B virus-related insertional mutagenesis occurs frequently in human liver cancers and recurrently targets human telomerase genePatrizia Paterlini-Bréchot, Kenichi Saigo, Yoshiki Murakami, et al.
Bioinformatics (Oxford, England)|June 4, 2011
The FAF-Drugs2 server: a multistep engine to prepare electronic chemical compound collectionsDavid Lagorce, Julien Maupetit, Jonathan Baell, et al.
Nucleic Acids Research|January 16, 2003
Identification and functional characterization of a new member of the human Mcm protein family: hMcm8Devrim Gozuacik, Mounia Chami, David Lagorce, et al.
Molecular Informatics|September 26, 2014
Drug-Like Protein-Protein Interaction Modulators: Challenges and Opportunities for Drug Discovery and Chemical BiologyBruno O Villoutreix, Melaine A Kuenemann, Jean-Luc Poyet, et al.
Pageof 3