DINDO, MIRCO
DINDO, MIRCO
DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO
A comprehensive picture of the mutations associated with aromatic amino acid decarboxylase deficiency: from molecular mechanisms to therapy implications
2014-01-01 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
2019-01-01 Conter, Carolina; Oppici, Elisa; Dindo, Mirco; Rossi, Luigia; Magnani, Mauro; 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
2018-01-01 Dindo, Mirco; Oppici, Elisa; Dell'Orco, Daniele; Montone, Rosa; Cellini, Barbara
Crystal structure of Aspergillus fumigatus AroH, an aromatic amino acid aminotransferase
2022-01-01 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
2021-01-01 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
2016-01-01 Dindo, Mirco; Montioli, Riccardo; Busato, Mirko; Giorgetti, Alejandro; Cellini, Barbara; Voltattorni, Carla Borri
Evolution of chalcone isomerase from a noncatalytic ancestor
2018-01-01 Kaltenbach, Miriam; Burke, Jason R; Dindo, Mirco; Pabis, Anna; Munsberg, Fabian S; Rabin, Avigayel; Kamerlin, Shina C L; Noel, Joseph P; Tawfik, Dan S
Interaction of Human Dopa Decarboxylase with L-Dopa: Spectroscopic and Kinetic Studies as a Function of pH
2013-01-01 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
2015-01-01 Montioli, Riccardo; Oppici, Elisa; Dindo, Mirco; Roncador, Alessandro; Gotte, Giovanni; Cellini, Barbara; Borri Voltattorni, Carla
Molecular basis of primary hyperoxaluria: clues to innovative treatments
2019-01-01 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
2016-01-01 Oppici, Elisa; Montioli, Riccardo; Dindo, Mirco; Cellini, Barbara
New variants of AADC deficiency expand the knowledge of enzymatic phenotypes
2020-01-01 Montioli, Riccardo; Bisello, Giovanni; Dindo, Mirco; Rossignoli, Giada; 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
2017-01-01 Dindo, Mirco; Conter, Carolina; Cellini, Barbara
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine
2013-01-01 Montioli, Riccardo; Oppici, Elisa; Cellini, Barbara; Roncador, Alessandro; Dindo, Mirco; Voltattorni, Carla
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
The ILE56 mutation on different genetic backgrounds of alanine: Glyoxylate aminotransferase: Clinical features and biochemical characterization
2020-01-01 Dindo, Mirco; Mandrile, Giorgia; Conter, Carolina; Montone, Rosa; Giachino, Daniela; Pelle, Alessandra; Costantini, Claudio; Cellini, Barbara
The novel R347g pathogenic mutation Of aromatic amino acid decarboxylase provides additional molecular insights into enzyme catalysis and deficiency
2016-01-01 Montioli, Riccardo; Paiardini, Alessandro; Kurian, Manju A.; Dindo, Mirco; Rossignoli, Giada; Heales, Simon J. R.; Pope, Simon; Voltattorni, Carla Borri; Bertoldi, Mariarita
| 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 | |
| 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-2022 | 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 | |
| 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 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 | |
| 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 | |
| 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 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 | |
| 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 | |
| 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 |