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Barbara Cellini

Showing results (51-60 of 104) with videos related to

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Biochimica Et Biophysica Acta. Proteins and Proteomics|October 17, 2020
Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspectsRiccardo Montioli, Ilaria Bellezza, Maria Andrea Desbats, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 7, 2011
Open conformation of human DOPA decarboxylase reveals the mechanism of PLP addition to Group II decarboxylasesGiorgio Giardina, Riccardo Montioli, Stefano Gianni, et al.
Proteins|April 17, 2013
Crystal structure of the S187F variant of human liver alanine: glyoxylate [corrected] aminotransferase associated with primary hyperoxaluria type I and its functional implicationsElisa Oppici, Krisztian Fodor, Alessandro Paiardini, 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.
Genes|July 18, 2018
Evolutionary Divergent Suppressor Mutations in Conformational DiseasesNoel Mesa-Torres, Isabel Betancor-Fernández, Elisa Oppici, et al.
The FEBS Journal|April 9, 2019
R180T variant of δ-ornithine aminotransferase associated with gyrate atrophy: biochemical, computational, X-ray and NMR studies provide insight into its catalytic featuresRiccardo Montioli, Alessandro Paiardini, Giorgio Giardina, et al.
Frontiers in Molecular Biosciences|August 16, 2021
Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and RetinaRiccardo Montioli, Giada Sgaravizzi, Maria Andrea Desbats, 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.
Pageof 11

Showing results (51-60 of 104) with videos related to

Sort By:
Pageof 11
Biochimica Et Biophysica Acta. Proteins and Proteomics|October 17, 2020
Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspectsRiccardo Montioli, Ilaria Bellezza, Maria Andrea Desbats, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 7, 2011
Open conformation of human DOPA decarboxylase reveals the mechanism of PLP addition to Group II decarboxylasesGiorgio Giardina, Riccardo Montioli, Stefano Gianni, et al.
Proteins|April 17, 2013
Crystal structure of the S187F variant of human liver alanine: glyoxylate [corrected] aminotransferase associated with primary hyperoxaluria type I and its functional implicationsElisa Oppici, Krisztian Fodor, Alessandro Paiardini, 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.
Genes|July 18, 2018
Evolutionary Divergent Suppressor Mutations in Conformational DiseasesNoel Mesa-Torres, Isabel Betancor-Fernández, Elisa Oppici, et al.
The FEBS Journal|April 9, 2019
R180T variant of δ-ornithine aminotransferase associated with gyrate atrophy: biochemical, computational, X-ray and NMR studies provide insight into its catalytic featuresRiccardo Montioli, Alessandro Paiardini, Giorgio Giardina, et al.
Frontiers in Molecular Biosciences|August 16, 2021
Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and RetinaRiccardo Montioli, Giada Sgaravizzi, Maria Andrea Desbats, 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.
Pageof 11