DINDO, MIRCO

DINDO, MIRCO  

DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO  

Mostra records
Risultati 1 - 20 di 20 (tempo di esecuzione: 0.062 secondi).
Titolo Data di pubblicazione Autore(i) File
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
Biochemical properties and oxalate-degrading activity of oxalate decarboxylase from Bacillus Subtilis at neutral pH 1-gen-2019 Conter, Carolina; Oppici, Elisa; Dindo, Mirco; Rossi, Luigia; Magnani, Mauro; Cellini, Barbara
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
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 B6 1-gen-2018 Dindo, Mirco; Oppici, Elisa; Dell'Orco, Daniele; Montone, Rosa; Cellini, Barbara
Crystal structure of Aspergillus fumigatus AroH, an aromatic amino acid aminotransferase 1-gen-2021 Spizzichino, Sharon; Pampalone, Gioena; Dindo, Mirco; Bruno, Agostino; Romani, Luigina; Cutruzzolà, Francesca; Zelante, Teresa; Pieroni, Marco; Cellini, Barbara; Giardina, Giorgio
Dimerization drives proper folding of human Alanine:Glyoxylate aminotransferase but is dispensable for peroxisomal targeting 1-gen-2021 Dindo, Mirco; Ambrosini, Giulia; Oppici, Elisa; Pey, Angel L; O'Toole, Peter J; Marrison, Joanne L; Morrison, Ian E G; Butturini, Elena; Grottelli, Silvia; Costantini, Claudio; 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
Evolution of chalcone isomerase from a noncatalytic ancestor 1-gen-2018 Kaltenbach, Miriam; Burke, Jason R; Dindo, Mirco; Pabis, Anna; Munsberg, Fabian S; Rabin, Avigayel; Kamerlin, Shina C L; Noel, Joseph P; Tawfik, Dan S
Folding defects leading to primary hyperoxaluria 1-gen-2018 Oppici, Elisa; Dindo, Mirco; Conter, Carolina; Voltattorni, Carla; Cellini, Barbara
The ILE56 mutation on different genetic backgrounds of alanine: Glyoxylate aminotransferase: Clinical features and biochemical characterization 1-gen-2020 Dindo, Mirco; Mandrile, Giorgia; Conter, Carolina; Montone, Rosa; Giachino, Daniela; Pelle, Alessandra; Costantini, Claudio; 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
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
Molecular analysis of the dimerization and aggregation processes of human alanine:glyoxylate aminotransferase and effect of mutations leading to Primary Hyperoxaluria Type I 1-gen-2017 Dindo, Mirco
Molecular basis of primary hyperoxaluria: clues to innovative treatments 1-gen-2019 Dindo, Mirco; Conter, Carolina; Oppici, Elisa; Ceccarelli, Veronica; Marinucci, Lorella; Cellini, Barbara
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
New variants of AADC deficiency expand the knowledge of enzymatic phenotypes 1-gen-2020 Montioli, Riccardo; Bisello, Giovanni; Dindo, Mirco; Rossignoli, Giada; Voltattorni, Carla Borri; 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
Opposite effect of polymorphic mutations on the electrostatic aggregation of human alanine:glyoxylate aminotransferase: implications for the pathogenesis of Primary Hyperoxaluria Type I 1-gen-2017 Dindo, Mirco; Conter, Carolina; Cellini, Barbara
Pathogenic variants of human Aromatic L-Amino Acid Decarboxylase: evidences of misfolding in functionally active variants 1-gen-2018 Bisello, Giovanni; Montioli, Riccardo; Dindo, Mirco; Voltattorni Carla, Borri; Bertoldi, Mariarita
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