检索结果 - Cellini, Barbara

Biochemical and Computational Approaches to Improve the Clinical Treatment of Dopa Decarboxylase-Related Diseases: An Overview 由 Cellini, Barbara, Montioli, Riccardo, Oppici, Elisa, Voltattorni, Carla Borri

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PLP-Dependent Enzymes 由 Paiardini, Alessandro, Contestabile, Roberto, Buckle, Ashley M., Cellini, Barbara

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Oligomeric State and Thermal Stability of Apo- and Holo- Human Ornithine δ-Aminotransferase 由 Montioli, Riccardo, Zamparelli, Carlotta, Borri Voltattorni, Carla, Cellini, Barbara

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Folding pathway of the pyridoxal 5′-phosphate C-S lyase MalY from Escherichia coli 由 Bertoldi, Mariarita, Cellini, Barbara, Laurents, Douglas V., Borri Voltattorni, Carla

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Characterization of C-S Lyase from C. diphtheriae: A Possible Target for New Antimicrobial Drugs 由 Astegno, Alessandra, Giorgetti, Alejandro, Allegrini, Alessandra, Cellini, Barbara, Dominici, Paola

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Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications 由 Cellini, Barbara, Bertoldi, Mariarita, Montioli, Riccardo, Paiardini, Alessandro, Borri Voltattorni, Carla

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Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation 由 Cellini, Barbara, Montioli, Riccardo, Paiardini, Alessandro, Lorenzetto, Antonio, Voltattorni, Carla Borri

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Interaction of Human Dopa Decarboxylase with L-Dopa: Spectroscopic and Kinetic Studies as a Function of pH 由 Montioli, Riccardo, Cellini, Barbara, Dindo, Mirco, Oppici, Elisa, Voltattorni, Carla Borri

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Treponema denticola cystalysin exhibits significant alanine racemase activity accompanied by transamination: mechanistic implications. 由 Bertoldi, Mariarita, Cellini, Barbara, Paiardini, Alessandro, Di Salvo, Martino, Borri Voltattorni, Carla

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Biochemical properties and oxalate‐degrading activity of oxalate decarboxylase from bacillus subtilis at neutral pH 由 Conter, Carolina, Oppici, Elisa, Dindo, Mirco, Rossi, Luigia, Magnani, Mauro, Cellini, Barbara

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Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associate... 由 Oppici, Elisa, Montioli, Riccardo, Lorenzetto, Antonio, Bianconi, Silvia, Borri Voltattorni, Carla, Cellini, Barbara

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Radiation damage at the active site of human alanine:glyoxylate aminotransferase reveals that the cofactor position is finely tuned during catalysis 由 Giardina, Giorgio, Paiardini, Alessandro, Montioli, Riccardo, Cellini, Barbara, Voltattorni, Carla Borri, Cutruzzolà, Francesca

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Allele-specific Characterization of Alanine: Glyoxylate Aminotransferase Variants Associated with Primary Hyperoxaluria 由 Lage, Melissa D., Pittman, Adrianne M. C., Roncador, Alessandro, Cellini, Barbara, Tucker, Chandra L.

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Open conformation of human DOPA decarboxylase reveals the mechanism of PLP addition to Group II decarboxylases 由 Giardina, Giorgio, Montioli, Riccardo, Gianni, Stefano, Cellini, Barbara, Paiardini, Alessandro, Voltattorni, Carla Borri, Cutruzzolà, Francesca

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Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications 由 Oppici, Elisa, Fodor, Krisztian, Paiardini, Alessandro, Williams, Chris, Voltattorni, Carla Borri, Wilmanns, Matthias, Cellini, Barbara

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Evolutionary Divergent Suppressor Mutations in Conformational Diseases 由 Mesa-Torres, Noel, Betancor-Fernández, Isabel, Oppici, Elisa, Cellini, Barbara, Salido, Eduardo, Pey, Angel L.

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Pyridoxal 5′-Phosphate-Dependent Enzymes at the Crossroads of Host–Microbe Tryptophan Metabolism 由 Cellini, Barbara, Zelante, Teresa, Dindo, Mirco, Bellet, Marina M., Renga, Giorgia, Romani, Luigina, Costantini, Claudio

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S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementation 由 Montioli, Riccardo, Roncador, Alessandro, Oppici, Elisa, Mandrile, Giorgia, Giachino, Daniela Francesca, Cellini, Barbara, Borri Voltattorni, Carla

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Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and Retina 由 Montioli, Riccardo, Sgaravizzi, Giada, Desbats, Maria Andrea, Grottelli, Silvia, Voltattorni, Carla Borri, Salviati, Leonardo, Cellini, Barbara

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Identification of Human Alanine–Glyoxylate Aminotransferase Ligands as Pharmacological Chaperones for Variants Associated with Primary Hyperoxaluria Type 1 由 Grottelli, Silvia, Annunziato, Giannamaria, Pampalone, Gioena, Pieroni, Marco, Dindo, Mirco, Ferlenghi, Francesca, Costantino, Gabriele, Cellini, Barbara

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