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Martin Neuenschwander

Showing results (11-20 of 57) with videos related to

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Plos One|July 29, 2024
Identification of drug-like molecules targeting the ATPase activity of dynamin-like EHD4Saif Mohd, Andreas Oder, Edgar Specker, et al.
Journal of Computer-Aided Molecular Design|April 17, 2020
Revealing cytotoxic substructures in molecules using deep learningHenry E Webel, Talia B Kimber, Silke Radetzki, et al.
Molecular Diversity|August 15, 2012
Sustainable synthesis and automated deposition: an accessible discovery screening library of fragment-like purinesChristoph Kamper, Katharina Korpis, Edgar Specker, et al.
Epidemiologia E Psichiatria Sociale|July 9, 2005
Prevalence of mental disorders in the Zurich Cohort Study: a twenty year prospective studyJules Angst, Alex Gamma, Martin Neuenschwander, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 1, 2026
Cell Painting Protocol to Characterize Morphological Profiles of Large Compound Collections Using the EU-OPENSCREEN LibraryChristopher Wolff, Martin Neuenschwander, Michelle Müller, et al.
Plos One|June 12, 2018
Drug discovery with an RBM20 dependent titin splice reporter identifies cardenolides as lead structures to improve cardiac fillingMartin Liss, Michael H Radke, Jamina Eckhard, et al.
Journal of Bacteriology|March 2, 2002
Rubredoxins involved in alkane oxidationJan B van Beilen, Martin Neuenschwander, Theo H M Smits, et al.
Molecular Diversity|August 18, 2009
Design of chemical libraries with potentially bioactive molecules applying a maximum common substructure conceptMichael Lisurek, Bernd Rupp, Jörg Wichard, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
Metabolic engineering of a genetic selection system with tunable stringencyAndreas C Kleeb, Maryam Hansson Edalat, Marianne Gamper, et al.
European Journal of Medicinal Chemistry|March 10, 2026
DFT guided design of novel quinone bioisosteres as inhibitors of the clathrin N-terminal domain-amphiphysin protein-protein interaction. Dihydroquinazolin-4(1H)-ones and quinazolin-3(4H)-onesNicholas S O'Brien, Jing Xue, Claudia Bahnik, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Plos One|July 29, 2024
Identification of drug-like molecules targeting the ATPase activity of dynamin-like EHD4Saif Mohd, Andreas Oder, Edgar Specker, et al.
Journal of Computer-Aided Molecular Design|April 17, 2020
Revealing cytotoxic substructures in molecules using deep learningHenry E Webel, Talia B Kimber, Silke Radetzki, et al.
Molecular Diversity|August 15, 2012
Sustainable synthesis and automated deposition: an accessible discovery screening library of fragment-like purinesChristoph Kamper, Katharina Korpis, Edgar Specker, et al.
Epidemiologia E Psichiatria Sociale|July 9, 2005
Prevalence of mental disorders in the Zurich Cohort Study: a twenty year prospective studyJules Angst, Alex Gamma, Martin Neuenschwander, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 1, 2026
Cell Painting Protocol to Characterize Morphological Profiles of Large Compound Collections Using the EU-OPENSCREEN LibraryChristopher Wolff, Martin Neuenschwander, Michelle Müller, et al.
Plos One|June 12, 2018
Drug discovery with an RBM20 dependent titin splice reporter identifies cardenolides as lead structures to improve cardiac fillingMartin Liss, Michael H Radke, Jamina Eckhard, et al.
Journal of Bacteriology|March 2, 2002
Rubredoxins involved in alkane oxidationJan B van Beilen, Martin Neuenschwander, Theo H M Smits, et al.
Molecular Diversity|August 18, 2009
Design of chemical libraries with potentially bioactive molecules applying a maximum common substructure conceptMichael Lisurek, Bernd Rupp, Jörg Wichard, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
Metabolic engineering of a genetic selection system with tunable stringencyAndreas C Kleeb, Maryam Hansson Edalat, Marianne Gamper, et al.
European Journal of Medicinal Chemistry|March 10, 2026
DFT guided design of novel quinone bioisosteres as inhibitors of the clathrin N-terminal domain-amphiphysin protein-protein interaction. Dihydroquinazolin-4(1H)-ones and quinazolin-3(4H)-onesNicholas S O'Brien, Jing Xue, Claudia Bahnik, et al.
Pageof 6