Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jutta Blank

Showing results (1-10 of 23) with videos related to

Pageof 3
Sort By:
Immunity|March 19, 2020
Structural Analysis Reveals that the Cytokine IL-17F Forms a Homodimeric Complex with Receptor IL-17RC to Drive IL-17RA-Independent SignalingArnaud Goepfert, Sylvie Lehmann, Jutta Blank, et al.
Journal of Biomolecular Screening|June 9, 2006
Readout technologies for highly miniaturized kinase assays applicable to high-throughput screening in a 1536-well formatMartin Klumpp, Andreas Boettcher, Damaris Becker, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|March 3, 2006
Purification, crystallization and preliminary crystallographic analysis of Arabidopsis thaliana imidazoleglycerol-phosphate dehydrataseSteven E Glynn, Patrick J Baker, Svetlana E Sedelnikova, et al.
Journal of Molecular Biology|February 28, 2012
Structural determinants of MALT1 protease activityChristian Wiesmann, Lukas Leder, Jutta Blank, et al.
Chemmedchem|February 9, 2024
Challenges for the Discovery of Non-Covalent WRN Helicase InhibitorsAlisa Heuser, Wassim Abdul Rahman, Elisabeth Bechter, et al.
Medchemcomm|August 16, 2018
Approaches to selective fibroblast growth factor receptor 4 inhibition through targeting the ATP-pocket middle-hinge regionRobin A Fairhurst, Thomas Knoepfel, Catherine Leblanc, et al.
Journal of Medicinal Chemistry|January 21, 2012
[1,2,4]triazol-3-ylsulfanylmethyl)-3-phenyl-[1,2,4]oxadiazoles: antagonists of the Wnt pathway that inhibit tankyrases 1 and 2 via novel adenosine pocket bindingMichael D Shultz, Christina A Kirby, Travis Stams, et al.
Chembiochem : a European Journal of Chemical Biology|October 17, 2015
Gift from Nature: Cyclomarin A Kills Mycobacteria and Malaria Parasites by Distinct Modes of ActionNathalie Bürstner, Silvio Roggo, Nils Ostermann, et al.
Bioorganic & Medicinal Chemistry Letters|May 16, 2018
N-aryl-piperidine-4-carboxamides as a novel class of potent inhibitors of MALT1 proteolytic activityAchim Schlapbach, Laszlo Revesz, Carole Pissot Soldermann, et al.
Cancer Research|June 24, 2011
A drug resistance screen using a selective MET inhibitor reveals a spectrum of mutations that partially overlap with activating mutations found in cancer patientsRalph Tiedt, Elisa Degenkolbe, Pascal Furet, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Immunity|March 19, 2020
Structural Analysis Reveals that the Cytokine IL-17F Forms a Homodimeric Complex with Receptor IL-17RC to Drive IL-17RA-Independent SignalingArnaud Goepfert, Sylvie Lehmann, Jutta Blank, et al.
Journal of Biomolecular Screening|June 9, 2006
Readout technologies for highly miniaturized kinase assays applicable to high-throughput screening in a 1536-well formatMartin Klumpp, Andreas Boettcher, Damaris Becker, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|March 3, 2006
Purification, crystallization and preliminary crystallographic analysis of Arabidopsis thaliana imidazoleglycerol-phosphate dehydrataseSteven E Glynn, Patrick J Baker, Svetlana E Sedelnikova, et al.
Journal of Molecular Biology|February 28, 2012
Structural determinants of MALT1 protease activityChristian Wiesmann, Lukas Leder, Jutta Blank, et al.
Chemmedchem|February 9, 2024
Challenges for the Discovery of Non-Covalent WRN Helicase InhibitorsAlisa Heuser, Wassim Abdul Rahman, Elisabeth Bechter, et al.
Medchemcomm|August 16, 2018
Approaches to selective fibroblast growth factor receptor 4 inhibition through targeting the ATP-pocket middle-hinge regionRobin A Fairhurst, Thomas Knoepfel, Catherine Leblanc, et al.
Journal of Medicinal Chemistry|January 21, 2012
[1,2,4]triazol-3-ylsulfanylmethyl)-3-phenyl-[1,2,4]oxadiazoles: antagonists of the Wnt pathway that inhibit tankyrases 1 and 2 via novel adenosine pocket bindingMichael D Shultz, Christina A Kirby, Travis Stams, et al.
Chembiochem : a European Journal of Chemical Biology|October 17, 2015
Gift from Nature: Cyclomarin A Kills Mycobacteria and Malaria Parasites by Distinct Modes of ActionNathalie Bürstner, Silvio Roggo, Nils Ostermann, et al.
Bioorganic & Medicinal Chemistry Letters|May 16, 2018
N-aryl-piperidine-4-carboxamides as a novel class of potent inhibitors of MALT1 proteolytic activityAchim Schlapbach, Laszlo Revesz, Carole Pissot Soldermann, et al.
Cancer Research|June 24, 2011
A drug resistance screen using a selective MET inhibitor reveals a spectrum of mutations that partially overlap with activating mutations found in cancer patientsRalph Tiedt, Elisa Degenkolbe, Pascal Furet, et al.
Pageof 3