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Molecular insights into primary hyperoxaluria Type I pathogenesis. 1-gen-2012 Cellini, Barbara; Oppici, Elisa; Paiardini, A.; Montioli, Riccardo
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. 1-gen-2012 Oppici, Elisa; Montioli, Riccardo; Lorenzetto, Antonio; Bianconi, Silvia; Voltattorni, Carla; Cellini, Barbara
Interaction of Human Dopa Decarboxylase with L-Dopa: Spectroscopic and Kinetic Studies as a Function of pH 1-gen-2013 Montioli, Riccardo; Cellini, Barbara; Dindo, Mirco; Oppici, Elisa; Voltattorni, Carla
Tat-mediated delivery of human alanine:glyoxylate aminotransferase in a cellular model of Primary Hyperoxaluria Type I 1-gen-2013 Roncador, A.; Oppici, E.; Montioli, R.; Maset, F.; Cellini, B.
Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase 1-gen-2013 Oppici, Elisa; Roncador, Alessandro; Montioli, Riccardo; Bianconi, Silvia; Cellini, Barbara
Evidence for dimer/tetramer equilibrium in Trypanosoma brucei 6-phosphogluconate dehydrogenase 1-gen-2013 Hanau, S.; Proietti d'Empaire, L.; Capone, . I.; Alberighi, S.; Montioli, R.; Dallocchio, F.
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine 1-gen-2013 Montioli, Riccardo; Oppici, Elisa; Cellini, Barbara; Roncador, Alessandro; Dindo, Mirco; Voltattorni, Carla
The chaperone role of the pyridoxal 5′-phosphate and its implications for rare diseases involving B6-dependent enzymes 1-gen-2014 Cellini, Barbara; Montioli, Riccardo; Oppici, Elisa; Astegno, Alessandra; Voltattorni, Carla
A comprehensive picture of the mutations associated with aromatic amino acid decarboxylase deficiency: from molecular mechanisms to therapy implications 1-gen-2014 Montioli, R.; Dindo, Mirco; Giorgetti, Alejandro; Piccoli, Stefano; Cellini, Barbara; Voltattorni, Carla
S81 L and G170R mutations causing Primary Hyperoxaluria Type I in homozygosis and heterozygosis: an example of positive interallelic complementation. 1-gen-2014 Montioli, Riccardo; Roncador, Alessandro; Oppici, Elisa; Mandrile, G; Giachino, Df; Cellini, Barbara; Voltattorni, Cb
Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview. 1-gen-2015 Oppici, Elisa; Montioli, Riccardo; Cellini, Barbara
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine 1-gen-2015 Montioli, Riccardo; Oppici, Elisa; Dindo, Mirco; Roncador, Alessandro; Gotte, Giovanni; Cellini, Barbara; Borri Voltattorni, Carla
The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I 1-gen-2015 Oppici, Elisa; Montioli, Riccardo; Dindo, Mirco; Maccari, Laura; Porcari, Valentina; Lorenzetto, Antonio; Chellini, Sara; Voltattorni, Carla Borri; Cellini, Barbara
Parkinson's Disease: recent updates in the identification of human dopa decarboxylase inhibitors 1-gen-2016 Montioli, Riccardo; Voltattorni, Carla B; Bertoldi, Mariarita
The novel R347g pathogenic mutation Of aromatic amino acid decarboxylase provides additional molecular insights into enzyme catalysis and deficiency 1-gen-2016 Montioli, Riccardo; Paiardini, Alessandro; Kurian, Manju A.; Dindo, Mirco; Rossignoli, Giada; Heales, Simon J. R.; Pope, Simon; Voltattorni, Carla Borri; Bertoldi, Mariarita
Natural and unnatural compounds rescue folding defects of human alanine:glyoxylate aminotransferase leading to Primary Hyperoxaluria Type I 1-gen-2016 Oppici, Elisa; Montioli, Riccardo; Dindo, Mirco; Cellini, Barbara
Effects of interface mutations on the dimerization of alanine glyoxylate aminotransferase and implications in the mistargeting of the pathogenic variants F152I and I244T 1-gen-2016 Dindo, Mirco; Montioli, Riccardo; Busato, Mirko; Giorgetti, Alejandro; Cellini, Barbara; Voltattorni, Carla Borri
Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism 1-gen-2016 Mesa Torres, Noel; Calvo, Ana C; Oppici, Elisa; Titelbaum, Nicholas; Montioli, Riccardo; Miranda Vizuete, Antonio; Cellini, Barbara; Salido, Eduardo; Pey, Angel L.
Extensive deamidation of RNase A inhibits its oligomerization through 3D domain swapping 1-gen-2017 Fagagnini, Andrea; Montioli, Riccardo; Caloiu, Andra; Ribó, Marc; Laurents, Douglas V.; Gotte, Giovanni
Radiation damage at the active site of human alanine:glyoxylate aminotransferase reveals that the cofactor position is finely tuned during catalysis 1-gen-2017 Giardina, Giorgio; Paiardini, Alessandro; Montioli, Riccardo; Cellini, Barbara; Borri Voltattorni, Carla; Cutruzzolà, Francesca
Mostrati risultati da 21 a 40 di 61
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