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Vicki Nienaber

Showing results (1-10 of 11) with videos related to

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Current Topics in Medicinal Chemistry|November 26, 2009
Start small and stay small. Minimizing attrition in the clinic with a focus on CNS therapeuticsVicki Nienaber
Drug Discovery Today|July 12, 2002
Is X-ray crystallography a viable tool for lead discovery?Vicki Nienaber
Methods in Enzymology|January 23, 2016
Fragment-Based Screening for Enzyme Inhibitors Using CalorimetryMichael I Recht, Vicki Nienaber, Francisco E Torres
The Journal of Biological Chemistry|July 2, 2010
X-ray crystal structures of monomeric and dimeric peptide inhibitors in complex with the human neonatal Fc receptor, FcRnAdam R Mezo, Vandana Sridhar, John Badger, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|July 29, 2011
The structure of LpxD from Pseudomonas aeruginosa at 1.3 Å resolutionJohn Badger, Barbara Chie-Leon, Cheyenne Logan, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|January 9, 2013
Structure determination of LpxD from the lipopolysaccharide-synthesis pathway of Acinetobacter baumanniiJohn Badger, Barbara Chie-Leon, Cheyenne Logan, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|November 30, 2012
Structure determination of LpxA from the lipopolysaccharide-synthesis pathway of Acinetobacter baumanniiJohn Badger, Barbara Chie-Leon, Cheyenne Logan, et al.
Journal of Biomolecular Screening|January 7, 2012
Fragment-based screening for inhibitors of PDE4A using enthalpy arrays and X-ray crystallographyMichael I Recht, Vandana Sridhar, John Badger, et al.
Journal of Biomolecular Screening|December 31, 2013
Identification and optimization of PDE10A inhibitors using fragment-based screening by nanocalorimetry and X-ray crystallographyMichael I Recht, Vandana Sridhar, John Badger, et al.
Bioorganic & Medicinal Chemistry Letters|May 20, 2004
Interaction with the S1 beta-pocket of urokinase: 8-heterocycle substituted and 6,8-disubstituted 2-naphthamidine urokinase inhibitorsMichael D Wendt, Andrew Geyer, William J McClellan, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Current Topics in Medicinal Chemistry|November 26, 2009
Start small and stay small. Minimizing attrition in the clinic with a focus on CNS therapeuticsVicki Nienaber
Drug Discovery Today|July 12, 2002
Is X-ray crystallography a viable tool for lead discovery?Vicki Nienaber
Methods in Enzymology|January 23, 2016
Fragment-Based Screening for Enzyme Inhibitors Using CalorimetryMichael I Recht, Vicki Nienaber, Francisco E Torres
The Journal of Biological Chemistry|July 2, 2010
X-ray crystal structures of monomeric and dimeric peptide inhibitors in complex with the human neonatal Fc receptor, FcRnAdam R Mezo, Vandana Sridhar, John Badger, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|July 29, 2011
The structure of LpxD from Pseudomonas aeruginosa at 1.3 Å resolutionJohn Badger, Barbara Chie-Leon, Cheyenne Logan, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|January 9, 2013
Structure determination of LpxD from the lipopolysaccharide-synthesis pathway of Acinetobacter baumanniiJohn Badger, Barbara Chie-Leon, Cheyenne Logan, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|November 30, 2012
Structure determination of LpxA from the lipopolysaccharide-synthesis pathway of Acinetobacter baumanniiJohn Badger, Barbara Chie-Leon, Cheyenne Logan, et al.
Journal of Biomolecular Screening|January 7, 2012
Fragment-based screening for inhibitors of PDE4A using enthalpy arrays and X-ray crystallographyMichael I Recht, Vandana Sridhar, John Badger, et al.
Journal of Biomolecular Screening|December 31, 2013
Identification and optimization of PDE10A inhibitors using fragment-based screening by nanocalorimetry and X-ray crystallographyMichael I Recht, Vandana Sridhar, John Badger, et al.
Bioorganic & Medicinal Chemistry Letters|May 20, 2004
Interaction with the S1 beta-pocket of urokinase: 8-heterocycle substituted and 6,8-disubstituted 2-naphthamidine urokinase inhibitorsMichael D Wendt, Andrew Geyer, William J McClellan, et al.
Pageof 2