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

Markus G Rudolph

Showing results (31-40 of 66) with videos related to

Pageof 7
Sort By:
Acta Crystallographica. Section D, Biological Crystallography|September 4, 2013
The structure of human α-2,6-sialyltransferase reveals the binding mode of complex glycansBernd Kuhn, Jörg Benz, Michael Greif, et al.
Acta Crystallographica. Section D, Biological Crystallography|March 25, 2004
Combined pseudo-merohedral twinning, non-crystallographic symmetry and pseudo-translation in a monoclinic crystal form of the gammadelta T-cell ligand T10Markus G Rudolph, Christer Wingren, Michael P Crowley, et al.
Nucleic Acids Research|December 5, 2012
Crystal structures of Thermotoga maritima reverse gyrase: inferences for the mechanism of positive DNA supercoilingMarkus G Rudolph, Yoandris del Toro Duany, Stefan P Jungblut, et al.
Acta Crystallographica. Section D, Structural Biology|May 3, 2018
Domain swap in the C-terminal ubiquitin-like domain of human doublecortinArne C Rufer, Eric Kusznir, Dominique Burger, et al.
Nucleic Acids Research|April 30, 2013
Recognition of two distinct elements in the RNA substrate by the RNA-binding domain of the T. thermophilus DEAD box helicase HeraLenz Steimer, Jan Philip Wurm, Martin H Linden, et al.
Journal of Medicinal Chemistry|April 28, 2017
Correction to Design of Potent and Druglike Nonphenolic Inhibitors for Catechol O-Methyltransferase Derived from a Fragment Screening Approach Targeting the S-Adenosyl-l-methionine PocketChristian Lerner, Roland Jakob-Roetne, Bernd Buettelmann, et al.
The Journal of Biological Chemistry|February 3, 2005
Crystal structure of human pFGE, the paralog of the Calpha-formylglycine-generating enzymeAchim Dickmanns, Bernhard Schmidt, Markus G Rudolph, et al.
Journal of Molecular Biology|February 6, 2010
Structure of the human fatty acid synthase KS-MAT didomain as a framework for inhibitor designGünter Pappenberger, Jörg Benz, Bernard Gsell, et al.
The Journal of Experimental Medicine|May 8, 2002
Structural comparison of allogeneic and syngeneic T cell receptor-peptide-major histocompatibility complex complexes: a buried alloreactive mutation subtly alters peptide presentation substantially increasing V(beta) InteractionsJohn G Luz, Mingdong Huang, K Christopher Garcia, et al.
ACS Medicinal Chemistry Letters|July 19, 2023
Discovery of a Series of Indane-Containing NBTIs with Activity against Multidrug-Resistant Gram-Negative PathogensJohn G Cumming, Lukas Kreis, Holger Kühne, et al.
Pageof 7

Showing results (31-40 of 66) with videos related to

Sort By:
Pageof 7
Acta Crystallographica. Section D, Biological Crystallography|September 4, 2013
The structure of human α-2,6-sialyltransferase reveals the binding mode of complex glycansBernd Kuhn, Jörg Benz, Michael Greif, et al.
Acta Crystallographica. Section D, Biological Crystallography|March 25, 2004
Combined pseudo-merohedral twinning, non-crystallographic symmetry and pseudo-translation in a monoclinic crystal form of the gammadelta T-cell ligand T10Markus G Rudolph, Christer Wingren, Michael P Crowley, et al.
Nucleic Acids Research|December 5, 2012
Crystal structures of Thermotoga maritima reverse gyrase: inferences for the mechanism of positive DNA supercoilingMarkus G Rudolph, Yoandris del Toro Duany, Stefan P Jungblut, et al.
Acta Crystallographica. Section D, Structural Biology|May 3, 2018
Domain swap in the C-terminal ubiquitin-like domain of human doublecortinArne C Rufer, Eric Kusznir, Dominique Burger, et al.
Nucleic Acids Research|April 30, 2013
Recognition of two distinct elements in the RNA substrate by the RNA-binding domain of the T. thermophilus DEAD box helicase HeraLenz Steimer, Jan Philip Wurm, Martin H Linden, et al.
Journal of Medicinal Chemistry|April 28, 2017
Correction to Design of Potent and Druglike Nonphenolic Inhibitors for Catechol O-Methyltransferase Derived from a Fragment Screening Approach Targeting the S-Adenosyl-l-methionine PocketChristian Lerner, Roland Jakob-Roetne, Bernd Buettelmann, et al.
The Journal of Biological Chemistry|February 3, 2005
Crystal structure of human pFGE, the paralog of the Calpha-formylglycine-generating enzymeAchim Dickmanns, Bernhard Schmidt, Markus G Rudolph, et al.
Journal of Molecular Biology|February 6, 2010
Structure of the human fatty acid synthase KS-MAT didomain as a framework for inhibitor designGünter Pappenberger, Jörg Benz, Bernard Gsell, et al.
The Journal of Experimental Medicine|May 8, 2002
Structural comparison of allogeneic and syngeneic T cell receptor-peptide-major histocompatibility complex complexes: a buried alloreactive mutation subtly alters peptide presentation substantially increasing V(beta) InteractionsJohn G Luz, Mingdong Huang, K Christopher Garcia, et al.
ACS Medicinal Chemistry Letters|July 19, 2023
Discovery of a Series of Indane-Containing NBTIs with Activity against Multidrug-Resistant Gram-Negative PathogensJohn G Cumming, Lukas Kreis, Holger Kühne, et al.
Pageof 7