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Markus Kroemer

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Acta Crystallographica. Section D, Biological Crystallography|April 27, 2002
The structure of L-rhamnulose-1-phosphate aldolase (class II) solved by low-resolution SIR phasing and 20-fold NCS averagingMarkus Kroemer, Georg E Schulz
Biochemistry|September 10, 2003
Structure and catalytic mechanism of L-rhamnulose-1-phosphate aldolaseMarkus Kroemer, Iris Merkel, Georg E Schulz
Acta Crystallographica. Section D, Biological Crystallography|August 31, 2004
APRV - a program for automated data processing, refinement and visualizationMarkus Kroemer, Matthias K Dreyer, K Ulrich Wendt
Acta Crystallographica. Section D, Biological Crystallography|October 8, 2014
Using textons to rank crystallization droplets by the likely presence of crystalsJia Tsing Ng, Carien Dekker, Markus Kroemer, et al.
Bioorganic & Medicinal Chemistry Letters|January 12, 2010
Novel 3-aminopyrazole inhibitors of MK-2 discovered by scaffold hopping strategyJuraj Velcicky, Roland Feifel, Stuart Hawtin, et al.
Structure (London, England : 1993)|August 15, 2006
Structural basis of ubiquitin recognition by the deubiquitinating protease USP2Martin Renatus, Shirley Gil Parrado, Allan D'Arcy, et al.
Nature Structural & Molecular Biology|March 15, 2006
Structural basis for the activation of flaviviral NS3 proteases from dengue and West Nile virusPaul Erbel, Nikolaus Schiering, Allan D'Arcy, et al.
Chemmedchem|August 8, 2006
Structural basis for the exceptional in vivo efficacy of bisphosphonate drugsJean-Michel Rondeau, Francis Bitsch, Emmanuelle Bourgier, et al.
Bioorganic & Medicinal Chemistry Letters|July 2, 2010
In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part IILaszlo Revesz, Achim Schlapbach, Reiner Aichholz, et al.
Bioorganic & Medicinal Chemistry Letters|July 3, 2010
In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part ILaszlo Revesz, Achim Schlapbach, Reiner Aichholz, et al.
Pageof 1

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

Sort By:
Pageof 1
Acta Crystallographica. Section D, Biological Crystallography|April 27, 2002
The structure of L-rhamnulose-1-phosphate aldolase (class II) solved by low-resolution SIR phasing and 20-fold NCS averagingMarkus Kroemer, Georg E Schulz
Biochemistry|September 10, 2003
Structure and catalytic mechanism of L-rhamnulose-1-phosphate aldolaseMarkus Kroemer, Iris Merkel, Georg E Schulz
Acta Crystallographica. Section D, Biological Crystallography|August 31, 2004
APRV - a program for automated data processing, refinement and visualizationMarkus Kroemer, Matthias K Dreyer, K Ulrich Wendt
Acta Crystallographica. Section D, Biological Crystallography|October 8, 2014
Using textons to rank crystallization droplets by the likely presence of crystalsJia Tsing Ng, Carien Dekker, Markus Kroemer, et al.
Bioorganic & Medicinal Chemistry Letters|January 12, 2010
Novel 3-aminopyrazole inhibitors of MK-2 discovered by scaffold hopping strategyJuraj Velcicky, Roland Feifel, Stuart Hawtin, et al.
Structure (London, England : 1993)|August 15, 2006
Structural basis of ubiquitin recognition by the deubiquitinating protease USP2Martin Renatus, Shirley Gil Parrado, Allan D'Arcy, et al.
Nature Structural & Molecular Biology|March 15, 2006
Structural basis for the activation of flaviviral NS3 proteases from dengue and West Nile virusPaul Erbel, Nikolaus Schiering, Allan D'Arcy, et al.
Chemmedchem|August 8, 2006
Structural basis for the exceptional in vivo efficacy of bisphosphonate drugsJean-Michel Rondeau, Francis Bitsch, Emmanuelle Bourgier, et al.
Bioorganic & Medicinal Chemistry Letters|July 2, 2010
In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part IILaszlo Revesz, Achim Schlapbach, Reiner Aichholz, et al.
Bioorganic & Medicinal Chemistry Letters|July 3, 2010
In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part ILaszlo Revesz, Achim Schlapbach, Reiner Aichholz, et al.
Pageof 1