| Evolution of chalcone isomerase from a noncatalytic ancestor M Kaltenbach, JR Burke, M Dindo, A Pabis, FS Munsberg, A Rabin, ... Nature chemical biology 14 (6), 548-555, 2018 | 128 | 2018 |
| Molecular basis of primary hyperoxaluria: clues to innovative treatments M Dindo, C Conter, E Oppici, V Ceccarelli, L Marinucci, B Cellini Urolithiasis 47, 67-78, 2019 | 68 | 2019 |
| A comprehensive picture of the mutations associated with aromatic amino acid decarboxylase deficiency: from molecular mechanisms to therapy implications R Montioli, M Dindo, A Giorgetti, S Piccoli, B Cellini, CB Voltattorni Human Molecular Genetics 23 (20), 5429-5440, 2014 | 60 | 2014 |
| Sustained enzymatic activity and flow in crowded protein droplets A Testa, M Dindo, AA Rebane, B Nasouri, RW Style, R Golestanian, ... Nature communications 12 (1), 6293, 2021 | 57 | 2021 |
| A systems genomics approach identifies SIGLEC15 as a susceptibility factor in recurrent vulvovaginal candidiasis M Jaeger, M Pinelli, M Borghi, C Constantini, M Dindo, L Van Emst, ... Science Translational Medicine 11 (496), eaar3558, 2019 | 41 | 2019 |
| S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxine R Montioli, E Oppici, B Cellini, A Roncador, M Dindo, CB Voltattorni Human Molecular Genetics 22 (8), 1615-1624, 2013 | 33 | 2013 |
| Pyridoxal 5′-phosphate-dependent enzymes at the crossroads of host–microbe tryptophan metabolism B Cellini, T Zelante, M Dindo, MM Bellet, G Renga, L Romani, ... International Journal of Molecular Sciences 21 (16), 5823, 2020 | 25 | 2020 |
| Non-enzymatic and highly sensitive lactose detection utilizing graphene field-effect transistors E Danielson, M Dindo, AJ Porkovich, P Kumar, Z Wang, P Jain, T Mete, ... Biosensors and Bioelectronics 165, 112419, 2020 | 24 | 2020 |
| Correlation between the molecular effects of mutations at the dimer interface of alanine–glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular … M Dindo, E Oppici, D Dell’Orco, R Montone, B Cellini Journal of Inherited Metabolic Disease 41, 263-275, 2018 | 24 | 2018 |
| Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine: glyoxylate aminotransferase and chaperoning activity of pyridoxine R Montioli, E Oppici, M Dindo, A Roncador, G Gotte, B Cellini, ... Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics 1854 (10), 1280-1289, 2015 | 24 | 2015 |
| The chaperoning activity of amino-oxyacetic acid on folding-defective variants of human alanine: glyoxylate aminotransferase causing primary hyperoxaluria type I E Oppici, R Montioli, M Dindo, L Maccari, V Porcari, A Lorenzetto, ... ACS chemical biology 10 (10), 2227-2236, 2015 | 22 | 2015 |
| Interaction of human Dopa decarboxylase with L-Dopa: spectroscopic and kinetic studies as a function of pH R Montioli, B Cellini, M Dindo, E Oppici, CB Voltattorni BioMed Research International 2013, 2013 | 19 | 2013 |
| New variants of AADC deficiency expand the knowledge of enzymatic phenotypes R Montioli, G Bisello, M Dindo, G Rossignoli, CB Voltattorni, M Bertoldi Archives of biochemistry and biophysics 682, 108263, 2020 | 18 | 2020 |
| Electrostatic interactions drive native‐like aggregation of human alanine: glyoxylate aminostransferase M Dindo, C Conter, B Cellini The FEBS journal 284 (21), 3739-3764, 2017 | 18 | 2017 |
| The novel R347g pathogenic mutation of aromatic amino acid decarboxylase provides additional molecular insights into enzyme catalysis and deficiency R Montioli, A Paiardini, MA Kurian, M Dindo, G Rossignoli, SJR Heales, ... Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics 1864 (6), 676-682, 2016 | 18 | 2016 |
| Biochemical properties and oxalate‐degrading activity of oxalate decarboxylase from bacillus subtilis at neutral pH C Conter, E Oppici, M Dindo, L Rossi, M Magnani, B Cellini IUBMB life 71 (7), 917-927, 2019 | 17 | 2019 |
| Effects of interface mutations on the dimerization of alanine glyoxylate aminotransferase and implications in the mistargeting of the pathogenic variants F152I and I244T M Dindo, R Montioli, M Busato, A Giorgetti, B Cellini, CB Voltattorni Biochimie 131, 137-148, 2016 | 17 | 2016 |
| Folding defects leading to primary hyperoxaluria E Oppici, M Dindo, C Conter, C Borri Voltattorni, B Cellini Targeting Trafficking in Drug Development, 313-343, 2018 | 15 | 2018 |
| The ILE56 mutation on different genetic backgrounds of alanine: glyoxylate aminotransferase: clinical features and biochemical characterization M Dindo, G Mandrile, C Conter, R Montone, D Giachino, A Pelle, ... Molecular genetics and metabolism 131 (1-2), 171-180, 2020 | 12 | 2020 |
| Cycloserine enantiomers are reversible inhibitors of human alanine: glyoxylate aminotransferase: implications for Primary Hyperoxaluria type 1 M Dindo, S Grottelli, G Annunziato, G Giardina, M Pieroni, G Pampalone, ... Biochemical Journal 476 (24), 3751-3768, 2019 | 11 | 2019 |
