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Mirco Dindo

Showing results (11-20 of 38) with videos related to

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Archives of Biochemistry and Biophysics|January 19, 2020
New variants of AADC deficiency expand the knowledge of enzymatic phenotypesRiccardo Montioli, Giovanni Bisello, Mirco Dindo, et al.
Biochimie|October 11, 2016
Effects of interface mutations on the dimerization of alanine glyoxylate aminotransferase and implications in the mistargeting of the pathogenic variants F152I and I244TMirco Dindo, Riccardo Montioli, Mirko Busato, et al.
Human Molecular Genetics|May 29, 2014
A comprehensive picture of the mutations associated with aromatic amino acid decarboxylase deficiency: from molecular mechanisms to therapy implicationsRiccardo Montioli, Mirco Dindo, Alejandro Giorgetti, et al.
Human Molecular Genetics|January 17, 2013
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxineRiccardo Montioli, Elisa Oppici, Barbara Cellini, et al.
International Journal of Molecular Sciences|August 23, 2020
Pyridoxal 5'-Phosphate-Dependent Enzymes at the Crossroads of Host-Microbe Tryptophan MetabolismBarbara Cellini, Teresa Zelante, Mirco Dindo, et al.
Biochimica Et Biophysica Acta|July 8, 2015
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxineRiccardo Montioli, Elisa Oppici, Mirco Dindo, et al.
Journal of Medicinal Chemistry|July 13, 2022
Identification of Human Alanine-Glyoxylate Aminotransferase Ligands as Pharmacological Chaperones for Variants Associated with Primary Hyperoxaluria Type 1Silvia Grottelli, Giannamaria Annunziato, Gioena Pampalone, et al.
Molecular Genetics and Metabolism|August 15, 2020
The ILE56 mutation on different genetic backgrounds of alanine:glyoxylate aminotransferase: Clinical features and biochemical characterizationMirco Dindo, Giorgia Mandrile, Carolina Conter, et al.
Frontiers in Molecular Biosciences|May 9, 2024
Harnessing inter-kingdom metabolic disparities at the human-fungal interface for novel therapeutic approachesClaudio Costantini, Marilena Pariano, Matteo Puccetti, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Enzyme Activity Regulates Substrate Diffusion by Modulating Viscosity in Crowded MilieuAlessandro Bevilacqua, Mauricio Rios Maciel, Mark V Sullivan, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Archives of Biochemistry and Biophysics|January 19, 2020
New variants of AADC deficiency expand the knowledge of enzymatic phenotypesRiccardo Montioli, Giovanni Bisello, Mirco Dindo, et al.
Biochimie|October 11, 2016
Effects of interface mutations on the dimerization of alanine glyoxylate aminotransferase and implications in the mistargeting of the pathogenic variants F152I and I244TMirco Dindo, Riccardo Montioli, Mirko Busato, et al.
Human Molecular Genetics|May 29, 2014
A comprehensive picture of the mutations associated with aromatic amino acid decarboxylase deficiency: from molecular mechanisms to therapy implicationsRiccardo Montioli, Mirco Dindo, Alejandro Giorgetti, et al.
Human Molecular Genetics|January 17, 2013
S250F variant associated with aromatic amino acid decarboxylase deficiency: molecular defects and intracellular rescue by pyridoxineRiccardo Montioli, Elisa Oppici, Barbara Cellini, et al.
International Journal of Molecular Sciences|August 23, 2020
Pyridoxal 5'-Phosphate-Dependent Enzymes at the Crossroads of Host-Microbe Tryptophan MetabolismBarbara Cellini, Teresa Zelante, Mirco Dindo, et al.
Biochimica Et Biophysica Acta|July 8, 2015
Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxineRiccardo Montioli, Elisa Oppici, Mirco Dindo, et al.
Journal of Medicinal Chemistry|July 13, 2022
Identification of Human Alanine-Glyoxylate Aminotransferase Ligands as Pharmacological Chaperones for Variants Associated with Primary Hyperoxaluria Type 1Silvia Grottelli, Giannamaria Annunziato, Gioena Pampalone, et al.
Molecular Genetics and Metabolism|August 15, 2020
The ILE56 mutation on different genetic backgrounds of alanine:glyoxylate aminotransferase: Clinical features and biochemical characterizationMirco Dindo, Giorgia Mandrile, Carolina Conter, et al.
Frontiers in Molecular Biosciences|May 9, 2024
Harnessing inter-kingdom metabolic disparities at the human-fungal interface for novel therapeutic approachesClaudio Costantini, Marilena Pariano, Matteo Puccetti, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Enzyme Activity Regulates Substrate Diffusion by Modulating Viscosity in Crowded MilieuAlessandro Bevilacqua, Mauricio Rios Maciel, Mark V Sullivan, et al.
Pageof 4