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Alberto Podjarny

Showing results (31-40 of 52) with videos related to

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Human Molecular Genetics|June 20, 2013
Linear and extended: a common polyglutamine conformation recognized by the three antibodies MW1, 1C2 and 3B5H10Fabrice A C Klein, Gabrielle Zeder-Lutz, Alexandra Cousido-Siah, et al.
Acta Crystallographica. Section D, Biological Crystallography|October 15, 2010
X-ray-induced deterioration of disulfide bridges at atomic resolutionTatiana Petrova, Stephan Ginell, Andre Mitschler, et al.
Journal of Medicinal Chemistry|September 2, 2005
Factorizing selectivity determinants of inhibitor binding toward aldose and aldehyde reductases: structural and thermodynamic properties of the aldose reductase mutant Leu300Pro-fidarestat complexTatiana Petrova, Holger Steuber, Isabelle Hazemann, et al.
Proteins|May 18, 2004
Ultrahigh resolution drug design. II. Atomic resolution structures of human aldose reductase holoenzyme complexed with Fidarestat and Minalrestat: implications for the binding of cyclic imide inhibitorsOssama El-Kabbani, Connie Darmanin, Thomas R Schneider, et al.
Plos One|July 30, 2015
Substrate Specificity, Inhibitor Selectivity and Structure-Function Relationships of Aldo-Keto Reductase 1B15: A Novel Human Retinaldehyde ReductaseJoan Giménez-Dejoz, Michal H Kolář, Francesc X Ruiz, et al.
Angewandte Chemie (International Ed. in English)|May 4, 2018
Structural Basis of Outstanding Multivalent Effects in Jack Bean α-Mannosidase InhibitionEduardo Howard, Alexandra Cousido-Siah, Mathieu L Lepage, et al.
European Journal of Medicinal Chemistry|April 30, 2018
Design, synthesis, structure-activity relationships and X-ray structural studies of novel 1-oxopyrimido[4,5-c]quinoline-2-acetic acid derivatives as selective and potent inhibitors of human aldose reductaseIsidro Crespo, Joan Giménez-Dejoz, Sergio Porté, et al.
Chemico-Biological Interactions|February 6, 2017
Structural basis for the inhibition of AKR1B10 by the C3 brominated TTNPB derivative UVI2008Francesc X Ruiz, Isidro Crespo, Susana Álvarez, et al.
Scientific Reports|February 10, 2017
Structural variability of E. coli thioredoxin captured in the crystal structures of single-point mutantsMartín E Noguera, Diego S Vazquez, Gerardo Ferrer-Sueta, et al.
Proteins|July 4, 2012
Crystal packing modifies ligand binding affinity: the case of aldose reductaseAlexandra Cousido-Siah, Tatiana Petrova, Isabelle Hazemann, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|June 20, 2013
Linear and extended: a common polyglutamine conformation recognized by the three antibodies MW1, 1C2 and 3B5H10Fabrice A C Klein, Gabrielle Zeder-Lutz, Alexandra Cousido-Siah, et al.
Acta Crystallographica. Section D, Biological Crystallography|October 15, 2010
X-ray-induced deterioration of disulfide bridges at atomic resolutionTatiana Petrova, Stephan Ginell, Andre Mitschler, et al.
Journal of Medicinal Chemistry|September 2, 2005
Factorizing selectivity determinants of inhibitor binding toward aldose and aldehyde reductases: structural and thermodynamic properties of the aldose reductase mutant Leu300Pro-fidarestat complexTatiana Petrova, Holger Steuber, Isabelle Hazemann, et al.
Proteins|May 18, 2004
Ultrahigh resolution drug design. II. Atomic resolution structures of human aldose reductase holoenzyme complexed with Fidarestat and Minalrestat: implications for the binding of cyclic imide inhibitorsOssama El-Kabbani, Connie Darmanin, Thomas R Schneider, et al.
Plos One|July 30, 2015
Substrate Specificity, Inhibitor Selectivity and Structure-Function Relationships of Aldo-Keto Reductase 1B15: A Novel Human Retinaldehyde ReductaseJoan Giménez-Dejoz, Michal H Kolář, Francesc X Ruiz, et al.
Angewandte Chemie (International Ed. in English)|May 4, 2018
Structural Basis of Outstanding Multivalent Effects in Jack Bean α-Mannosidase InhibitionEduardo Howard, Alexandra Cousido-Siah, Mathieu L Lepage, et al.
European Journal of Medicinal Chemistry|April 30, 2018
Design, synthesis, structure-activity relationships and X-ray structural studies of novel 1-oxopyrimido[4,5-c]quinoline-2-acetic acid derivatives as selective and potent inhibitors of human aldose reductaseIsidro Crespo, Joan Giménez-Dejoz, Sergio Porté, et al.
Chemico-Biological Interactions|February 6, 2017
Structural basis for the inhibition of AKR1B10 by the C3 brominated TTNPB derivative UVI2008Francesc X Ruiz, Isidro Crespo, Susana Álvarez, et al.
Scientific Reports|February 10, 2017
Structural variability of E. coli thioredoxin captured in the crystal structures of single-point mutantsMartín E Noguera, Diego S Vazquez, Gerardo Ferrer-Sueta, et al.
Proteins|July 4, 2012
Crystal packing modifies ligand binding affinity: the case of aldose reductaseAlexandra Cousido-Siah, Tatiana Petrova, Isabelle Hazemann, et al.
Pageof 6