Antonio Lorenzetto

Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I

Barbara Cellini, Riccardo Montioli, Alessandro Paiardini et al. · Proceedings of the National Academy of Sciences · 2010 · 70 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation

Barbara Cellini, Riccardo Montioli, Alessandro Paiardini et al. · Journal of Biological Chemistry · 2009 · 58 citations · Full text

Life Sciences, Biochemistry, Genetics +17

Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant

Barbara Cellini, Antonio Lorenzetto, Riccardo Montioli et al. · Biochimie · 2010 · 57 citations

Life Sciences, Genetics, Molecular Genetics +17

Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I

Elisa Oppici, Riccardo Montioli, Antonio Lorenzetto et al. · Molecular Genetics and Metabolism · 2011 · 41 citations

Life Sciences, Biochemistry, Genetics +13

The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I

Elisa Oppici, Riccardo Montioli, Mirco Dindo et al. · ACS Chemical Biology · 2015 · 23 citations

Life Sciences, Biochemistry, Molecular Biology +14