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Elisa Oppici

Showing results (1-10 of 30) with videos related to

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Biochimica Et Biophysica Acta|January 27, 2015
Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overviewElisa Oppici, Riccardo Montioli, Barbara Cellini
Current Drug Targets|March 3, 2016
Natural and Unnatural Compounds Rescue Folding Defects of Human Alanine: Glyoxylate Aminotransferase Leading to Primary Hyperoxaluria Type IElisa Oppici, Riccardo Montioli, Mirco Dindo, et al.
Frontiers in Bioscience (Landmark Edition)|December 29, 2011
Molecular insights into primary hyperoxaluria type 1 pathogenesisBarbara Cellini, Elisa Oppici, Alessandro Paiardini, et al.
The Open Biochemistry Journal|December 25, 2012
Biochemical and computational approaches to improve the clinical treatment of dopa decarboxylase-related diseases: an overviewBarbara Cellini, Riccardo Montioli, Elisa Oppici, et al.
Biochimica Et Biophysica Acta|September 24, 2013
Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferaseElisa Oppici, Alessandro Roncador, Riccardo Montioli, et al.
Clinical Biochemistry|December 21, 2013
The chaperone role of the pyridoxal 5'-phosphate and its implications for rare diseases involving B6-dependent enzymesBarbara Cellini, Riccardo Montioli, Elisa Oppici, et al.
Journal of Inherited Metabolic Disease|November 8, 2017
Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B<sub>6</sub>Mirco Dindo, Elisa Oppici, Daniele Dell'Orco, et al.
Handbook of Experimental Pharmacology|October 27, 2017
Folding Defects Leading to Primary HyperoxaluriaElisa Oppici, Mirco Dindo, Carolina Conter, et al.
Biomed Research International|June 20, 2013
Interaction of human Dopa decarboxylase with L-Dopa: spectroscopic and kinetic studies as a function of pHRiccardo Montioli, Barbara Cellini, Mirco Dindo, et al.
Biochimie|August 18, 2010
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variantBarbara Cellini, Antonio Lorenzetto, Riccardo Montioli, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Biochimica Et Biophysica Acta|January 27, 2015
Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overviewElisa Oppici, Riccardo Montioli, Barbara Cellini
Current Drug Targets|March 3, 2016
Natural and Unnatural Compounds Rescue Folding Defects of Human Alanine: Glyoxylate Aminotransferase Leading to Primary Hyperoxaluria Type IElisa Oppici, Riccardo Montioli, Mirco Dindo, et al.
Frontiers in Bioscience (Landmark Edition)|December 29, 2011
Molecular insights into primary hyperoxaluria type 1 pathogenesisBarbara Cellini, Elisa Oppici, Alessandro Paiardini, et al.
The Open Biochemistry Journal|December 25, 2012
Biochemical and computational approaches to improve the clinical treatment of dopa decarboxylase-related diseases: an overviewBarbara Cellini, Riccardo Montioli, Elisa Oppici, et al.
Biochimica Et Biophysica Acta|September 24, 2013
Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferaseElisa Oppici, Alessandro Roncador, Riccardo Montioli, et al.
Clinical Biochemistry|December 21, 2013
The chaperone role of the pyridoxal 5'-phosphate and its implications for rare diseases involving B6-dependent enzymesBarbara Cellini, Riccardo Montioli, Elisa Oppici, et al.
Journal of Inherited Metabolic Disease|November 8, 2017
Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B<sub>6</sub>Mirco Dindo, Elisa Oppici, Daniele Dell'Orco, et al.
Handbook of Experimental Pharmacology|October 27, 2017
Folding Defects Leading to Primary HyperoxaluriaElisa Oppici, Mirco Dindo, Carolina Conter, et al.
Biomed Research International|June 20, 2013
Interaction of human Dopa decarboxylase with L-Dopa: spectroscopic and kinetic studies as a function of pHRiccardo Montioli, Barbara Cellini, Mirco Dindo, et al.
Biochimie|August 18, 2010
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variantBarbara Cellini, Antonio Lorenzetto, Riccardo Montioli, et al.
Pageof 3