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Markus Kaiser

Showing results (71-80 of 203) with videos related to

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Journal of Molecular Biology|December 10, 2002
Navigation inside a protease: substrate selection and product exit in the tricorn protease from Thermoplasma acidophilumJeong Sun Kim, Michael Groll, Hans Jürgen Musiol, et al.
BMC Genomics|October 6, 2019
A homology-guided, genome-based proteome for improved proteomics in the alloploid Nicotiana benthamianaJiorgos Kourelis, Farnusch Kaschani, Friederike M Grosse-Holz, et al.
Chemistry & Biodiversity|December 29, 2006
TMC-95A analogues with endocyclic biphenyl ether group as proteasome inhibitorsMarkus Kaiser, Alexander G Milbradt, Carlo Siciliano, et al.
Plant Biotechnology Journal|February 12, 2019
Activity-based proteomics reveals nine target proteases for the recombinant protein-stabilizing inhibitor SlCYS8 in Nicotiana benthamianaPhilippe V Jutras, Friederike Grosse-Holz, Farnusch Kaschani, et al.
LGBT Health|October 31, 2025
Timing and Satisfaction in Chest Masculinization Surgery: A Transgender Quality of Life Questionnaire-Based Analysis of Age-Related OutcomesAndrej Wehle, Sabrina Caecilia, Markus Kaiser, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2009
Synthetic and structural studies on syringolin A and B reveal critical determinants of selectivity and potency of proteasome inhibitionJérôme Clerc, Michael Groll, Damir J Illich, et al.
Chembiochem : a European Journal of Chemical Biology|August 23, 2014
Peptidyl succinimidyl peptides as taspase 1 inhibitorsJohannes van den Boom, Marija Mamić, Daniele Baccelliere, et al.
Angewandte Chemie (International Ed. in English)|May 18, 2017
Tailored Ahp-cyclodepsipeptides as Potent Non-covalent Serine Protease InhibitorsSteffen Köcher, Juliana Rey, Jens Bongard, et al.
Biological Chemistry|March 7, 2020
Targeting of parvulin interactors by diazirine mediated cross-linking discloses a cellular role of human Par14/17 in actin polymerizationAnna Goehring, Irina Michin, Tina Gerdes, et al.
Chembiochem : a European Journal of Chemical Biology|September 26, 2012
Sulfonyl fluoride analogues as activity-based probes for serine proteasesD Alexander Shannon, Christian Gu, Christopher J McLaughlin, et al.
Pageof 21

Showing results (71-80 of 203) with videos related to

Sort By:
Pageof 21
Journal of Molecular Biology|December 10, 2002
Navigation inside a protease: substrate selection and product exit in the tricorn protease from Thermoplasma acidophilumJeong Sun Kim, Michael Groll, Hans Jürgen Musiol, et al.
BMC Genomics|October 6, 2019
A homology-guided, genome-based proteome for improved proteomics in the alloploid Nicotiana benthamianaJiorgos Kourelis, Farnusch Kaschani, Friederike M Grosse-Holz, et al.
Chemistry & Biodiversity|December 29, 2006
TMC-95A analogues with endocyclic biphenyl ether group as proteasome inhibitorsMarkus Kaiser, Alexander G Milbradt, Carlo Siciliano, et al.
Plant Biotechnology Journal|February 12, 2019
Activity-based proteomics reveals nine target proteases for the recombinant protein-stabilizing inhibitor SlCYS8 in Nicotiana benthamianaPhilippe V Jutras, Friederike Grosse-Holz, Farnusch Kaschani, et al.
LGBT Health|October 31, 2025
Timing and Satisfaction in Chest Masculinization Surgery: A Transgender Quality of Life Questionnaire-Based Analysis of Age-Related OutcomesAndrej Wehle, Sabrina Caecilia, Markus Kaiser, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2009
Synthetic and structural studies on syringolin A and B reveal critical determinants of selectivity and potency of proteasome inhibitionJérôme Clerc, Michael Groll, Damir J Illich, et al.
Chembiochem : a European Journal of Chemical Biology|August 23, 2014
Peptidyl succinimidyl peptides as taspase 1 inhibitorsJohannes van den Boom, Marija Mamić, Daniele Baccelliere, et al.
Angewandte Chemie (International Ed. in English)|May 18, 2017
Tailored Ahp-cyclodepsipeptides as Potent Non-covalent Serine Protease InhibitorsSteffen Köcher, Juliana Rey, Jens Bongard, et al.
Biological Chemistry|March 7, 2020
Targeting of parvulin interactors by diazirine mediated cross-linking discloses a cellular role of human Par14/17 in actin polymerizationAnna Goehring, Irina Michin, Tina Gerdes, et al.
Chembiochem : a European Journal of Chemical Biology|September 26, 2012
Sulfonyl fluoride analogues as activity-based probes for serine proteasesD Alexander Shannon, Christian Gu, Christopher J McLaughlin, et al.
Pageof 21