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Felix Reisen

Showing results (1-10 of 16) with videos related to

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Journal of Biomolecular Screening|September 19, 2013
Benchmarking of multivariate similarity measures for high-content screening fingerprints in phenotypic drug discoveryFelix Reisen, Xian Zhang, Daniela Gabriel, et al.
Journal of Proteome Research|October 2, 2010
Self-organizing fuzzy graphs for structure-based comparison of protein pocketsFelix Reisen, Martin Weisel, Jan M Kriegl, et al.
Molecular Informatics|July 28, 2016
Automated Docking of Flexible Molecules Into Receptor Binding Sites by Ligand Self-Organization In SituAlexander Klenner, Martin Weisel, Felix Reisen, et al.
Plos One|August 14, 2015
In Silico Adoption of an Orphan Nuclear Receptor NR4A1Harald Lanig, Felix Reisen, David Whitley, et al.
Assay and Drug Development Technologies|August 11, 2015
Linking phenotypes and modes of action through high-content screen fingerprintsFelix Reisen, Amelie Sauty de Chalon, Martin Pfeifer, et al.
Journal of Medicinal Chemistry|May 20, 2011
Discovery and biological evaluation of a novel class of dual microsomal prostaglandin E2 synthase-1/5-lipoxygenase inhibitors based on 2-[(4,6-diphenethoxypyrimidin-2-yl)thio]hexanoic acidMartina Hieke, Christine Greiner, Michaela Dittrich, et al.
Plos Computational Biology|February 24, 2012
DOGS: reaction-driven de novo design of bioactive compoundsMarkus Hartenfeller, Heiko Zettl, Miriam Walter, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 6, 2012
Phenotype-based high-content chemical library screening identifies statins as inhibitors of in vivo lymphangiogenesisMartin Michael Peter Schulz, Felix Reisen, Silvana Zgraggen, et al.
Journal of Computational Chemistry|December 14, 2011
Virtual screening for compounds that mimic protein-protein interface epitopesTim Geppert, Felix Reisen, Max Pillong, et al.
Journal of Chemical Information and Modeling|February 18, 2014
Targeting dynamic pockets of HIV-1 protease by structure-based computational screening for allosteric inhibitorsJens Kunze, Nickolay Todoroff, Petra Schneider, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Biomolecular Screening|September 19, 2013
Benchmarking of multivariate similarity measures for high-content screening fingerprints in phenotypic drug discoveryFelix Reisen, Xian Zhang, Daniela Gabriel, et al.
Journal of Proteome Research|October 2, 2010
Self-organizing fuzzy graphs for structure-based comparison of protein pocketsFelix Reisen, Martin Weisel, Jan M Kriegl, et al.
Molecular Informatics|July 28, 2016
Automated Docking of Flexible Molecules Into Receptor Binding Sites by Ligand Self-Organization In SituAlexander Klenner, Martin Weisel, Felix Reisen, et al.
Plos One|August 14, 2015
In Silico Adoption of an Orphan Nuclear Receptor NR4A1Harald Lanig, Felix Reisen, David Whitley, et al.
Assay and Drug Development Technologies|August 11, 2015
Linking phenotypes and modes of action through high-content screen fingerprintsFelix Reisen, Amelie Sauty de Chalon, Martin Pfeifer, et al.
Journal of Medicinal Chemistry|May 20, 2011
Discovery and biological evaluation of a novel class of dual microsomal prostaglandin E2 synthase-1/5-lipoxygenase inhibitors based on 2-[(4,6-diphenethoxypyrimidin-2-yl)thio]hexanoic acidMartina Hieke, Christine Greiner, Michaela Dittrich, et al.
Plos Computational Biology|February 24, 2012
DOGS: reaction-driven de novo design of bioactive compoundsMarkus Hartenfeller, Heiko Zettl, Miriam Walter, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 6, 2012
Phenotype-based high-content chemical library screening identifies statins as inhibitors of in vivo lymphangiogenesisMartin Michael Peter Schulz, Felix Reisen, Silvana Zgraggen, et al.
Journal of Computational Chemistry|December 14, 2011
Virtual screening for compounds that mimic protein-protein interface epitopesTim Geppert, Felix Reisen, Max Pillong, et al.
Journal of Chemical Information and Modeling|February 18, 2014
Targeting dynamic pockets of HIV-1 protease by structure-based computational screening for allosteric inhibitorsJens Kunze, Nickolay Todoroff, Petra Schneider, et al.
Pageof 2