LORENZETTO, Antonio
LORENZETTO, Antonio
DIPARTIMENTO DI SCIENZE DELLA VITA E DELLA RIPRODUZIONE (attivo dal 01/01/2000 al 31/12/2015)
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.
2012-01-01 Oppici, Elisa; Montioli, Riccardo; Lorenzetto, Antonio; Bianconi, Silvia; Voltattorni, Carla; Cellini, Barbara
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant.
2010-01-01 Cellini, Barbara; Lorenzetto, Antonio; Montioli, Riccardo; Oppici, Elisa; Voltattorni, Carla
Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I
2010-01-01 Cellini, Barbara; Montioli, Riccardo; Paiardini, A.; Lorenzetto, Antonio; Maset, F.; Bellini, T.; Oppici, Elisa; Voltattorni, Carla
Molecular insight into the synergism between the minor allele of human liver peroxisomal alanine: glyoxylate aminotransferase and the f152i mutation
2009-01-01 Cellini, Barbara; Montioli, Riccardo; Alessandro, Paiardini; Lorenzetto, Antonio; Voltattorni, Carla
Molecular insight into the synergism between the minor allele of human liver peroxisomal alanine: Glyoxylate aminotransferase and the F152I mutation
2009-01-01 Cellini, Barbara; Montioli, Riccardo; A., Paiardini; Lorenzetto, Antonio; Voltattorni, Carla
SHEDDING LIGHT ON THE MOLECULAR DEFECT OF TWOALANINE:GLYOXYLATE AMINOTRANSFERASE PATHOGENIC VARIANTS:A BIOCHEMICAL APPROACH.
2011-01-01 Lorenzetto, Antonio
The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I
2015-01-01 Oppici, Elisa; Montioli, Riccardo; Dindo, Mirco; Maccari, Laura; Porcari, Valentina; Lorenzetto, Antonio; Chellini, Sara; Voltattorni, Carla Borri; Cellini, Barbara