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Frank Sielaff

Showing results (1-10 of 9) with videos related to

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Bioorganic & Medicinal Chemistry Letters|December 21, 2010
New furin inhibitors based on weakly basic amidinohydrazonesFrank Sielaff, Manuel E Than, Dorian Bevec, et al.
Journal of the American Society for Mass Spectrometry|August 8, 2012
Quantifying protein-ligand binding constants using electrospray ionization mass spectrometry: a systematic binding affinity study of a series of hydrophobically modified trypsin inhibitorsDragana Cubrilovic, Adam Biela, Frank Sielaff, et al.
Journal of Medicinal Chemistry|May 23, 2012
Ligand binding stepwise disrupts water network in thrombin: enthalpic and entropic changes reveal classical hydrophobic effectAdam Biela, Frank Sielaff, Felix Terwesten, et al.
The Biochemical Journal|March 27, 2013
Identification of the first synthetic inhibitors of the type II transmembrane serine protease TMPRSS2 suitable for inhibition of influenza virus activationDaniela Meyer, Frank Sielaff, Maya Hammami, et al.
Vaccine|October 18, 2012
Hemagglutinin activating host cell proteases provide promising drug targets for the treatment of influenza A and B virus infectionsEva Böttcher-Friebertshäuser, Yinghui Lu, Daniela Meyer, et al.
Bioorganic & Medicinal Chemistry Letters|July 12, 2011
Development of substrate analogue inhibitors for the human airway trypsin-like protease HATFrank Sielaff, Eva Böttcher-Friebertshäuser, Daniela Meyer, et al.
Biochimica Et Biophysica Acta|May 6, 2014
Impact of protein and ligand impurities on ITC-derived protein-ligand thermodynamicsStefan Grüner, Manuel Neeb, Luzi Jakob Barandun, et al.
Journal of Medicinal Chemistry|December 30, 2009
Potent inhibitors of furin and furin-like proprotein convertases containing decarboxylated P1 arginine mimeticsGero L Becker, Frank Sielaff, Manuel E Than, et al.
Journal of Virology|March 19, 2010
Cleavage of influenza virus hemagglutinin by airway proteases TMPRSS2 and HAT differs in subcellular localization and susceptibility to protease inhibitorsEva Böttcher-Friebertshäuser, Catharina Freuer, Frank Sielaff, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Bioorganic & Medicinal Chemistry Letters|December 21, 2010
New furin inhibitors based on weakly basic amidinohydrazonesFrank Sielaff, Manuel E Than, Dorian Bevec, et al.
Journal of the American Society for Mass Spectrometry|August 8, 2012
Quantifying protein-ligand binding constants using electrospray ionization mass spectrometry: a systematic binding affinity study of a series of hydrophobically modified trypsin inhibitorsDragana Cubrilovic, Adam Biela, Frank Sielaff, et al.
Journal of Medicinal Chemistry|May 23, 2012
Ligand binding stepwise disrupts water network in thrombin: enthalpic and entropic changes reveal classical hydrophobic effectAdam Biela, Frank Sielaff, Felix Terwesten, et al.
The Biochemical Journal|March 27, 2013
Identification of the first synthetic inhibitors of the type II transmembrane serine protease TMPRSS2 suitable for inhibition of influenza virus activationDaniela Meyer, Frank Sielaff, Maya Hammami, et al.
Vaccine|October 18, 2012
Hemagglutinin activating host cell proteases provide promising drug targets for the treatment of influenza A and B virus infectionsEva Böttcher-Friebertshäuser, Yinghui Lu, Daniela Meyer, et al.
Bioorganic & Medicinal Chemistry Letters|July 12, 2011
Development of substrate analogue inhibitors for the human airway trypsin-like protease HATFrank Sielaff, Eva Böttcher-Friebertshäuser, Daniela Meyer, et al.
Biochimica Et Biophysica Acta|May 6, 2014
Impact of protein and ligand impurities on ITC-derived protein-ligand thermodynamicsStefan Grüner, Manuel Neeb, Luzi Jakob Barandun, et al.
Journal of Medicinal Chemistry|December 30, 2009
Potent inhibitors of furin and furin-like proprotein convertases containing decarboxylated P1 arginine mimeticsGero L Becker, Frank Sielaff, Manuel E Than, et al.
Journal of Virology|March 19, 2010
Cleavage of influenza virus hemagglutinin by airway proteases TMPRSS2 and HAT differs in subcellular localization and susceptibility to protease inhibitorsEva Böttcher-Friebertshäuser, Catharina Freuer, Frank Sielaff, et al.
Pageof 1