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Mostrati risultati da 1 a 20 di 33
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Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I 1-gen-2010 Cellini, Barbara; Montioli, Riccardo; Paiardini, A.; Lorenzetto, Antonio; Maset, F.; Bellini, T.; Oppici, Elisa; Voltattorni, Carla
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant. 1-gen-2010 Cellini, Barbara; Lorenzetto, Antonio; Montioli, Riccardo; Oppici, Elisa; Voltattorni, Carla
Biochemical and computational approaches to improve the clinical treatment of Dopa decarboxylase-related diseases: an overview 1-gen-2012 Cellini, Barbara; Montioli, Riccardo; Oppici, Elisa; Voltattorni, Carla
Molecular insights into primary hyperoxaluria Type I pathogenesis. 1-gen-2012 Cellini, Barbara; Oppici, Elisa; Paiardini, A.; Montioli, Riccardo
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 associated with Primary Hyperoxaluria Type I. 1-gen-2012 Oppici, Elisa; Montioli, Riccardo; Lorenzetto, Antonio; Bianconi, Silvia; Voltattorni, Carla; Cellini, Barbara
Molecular and cellular insights into defects of human alanine:glyoxylate aminotransferase variants associated with Primary Hyperoxaluria Type I 1-gen-2013 Oppici, Elisa
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
Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase 1-gen-2013 Oppici, Elisa; Roncador, Alessandro; Montioli, Riccardo; Bianconi, Silvia; 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
Crystal structure of the S187F variant of human liver alanine: Aminotransferase associated with primary hyperoxaluria type I and its functional implications 1-gen-2013 Oppici, Elisa; Krisztian, Fodor; Alessandro, Paiardini; Chris, Williams; Voltattorni, Carla; Matthias, Wilmanns; Cellini, Barbara
Tat-mediated delivery of human alanine:glyoxylate aminotransferase in a cellular model of Primary Hyperoxaluria Type I 1-gen-2013 Roncador, A.; Oppici, E.; Montioli, R.; Maset, F.; Cellini, B.
The chaperone role of the pyridoxal 5′-phosphate and its implications for rare diseases involving B6-dependent enzymes 1-gen-2014 Cellini, Barbara; Montioli, Riccardo; Oppici, Elisa; Astegno, Alessandra; Voltattorni, Carla
S81 L and G170R mutations causing Primary Hyperoxaluria Type I in homozygosis and heterozygosis: an example of positive interallelic complementation. 1-gen-2014 Montioli, Riccardo; Roncador, Alessandro; Oppici, Elisa; Mandrile, G; Giachino, Df; Cellini, Barbara; Voltattorni, Cb
Liver peroxisomal alanine:glyoxylate aminotransferase and the effects of mutations associated with Primary Hyperoxaluria Type I: An overview. 1-gen-2015 Oppici, Elisa; Montioli, Riccardo; Cellini, Barbara
Pyridoxamine and pyridoxal are more effective than pyridoxine in rescuing folding-defective variants of human alanine:glyoxylate aminotransferase causing primary hyperoxaluria type I. 1-gen-2015 Oppici, Elisa; Fargue, S.; Reid, E. S.; Mills, P. B.; Clayton, P. T.; Danpure, C. J.; Cellini, Barbara
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
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
Gain-of-function mutant p53 enhances mitochondrial ROS through the inhibition of PGC-1α/UCP2 axis in cancer cells 1-gen-2016 Cordani, Marco; Butera, Giovanna; Butturini, Elena; Pacchiana, Raffaella; Oppici, Elisa; Mariotto, Sofia Giovanna; Cellini, Barbara; Donadelli, Massimo
A novel pathway for metabolism of the cardiovascular risk factor homoarginine by alanine:glyoxylate aminotransferase 2 1-gen-2016 Rodionov, Roman N.; Oppici, Elisa; Martens Lobenhoffer, Jens; Jarzebska, Natalia; Brilloff, Silke; Burdin, Dmitrii; Demyanov, Anton; Kolouschek, Anne; Leiper, James; Maas, Renke; Cellini, Barbara; Weiss, Norbert; Bode Böger, Stefanie M.
Mutant p53 proteins counteract autophagic mechanism sensitizing cancer cells to mTOR inhibition 1-gen-2016 Cordani, Marco; Oppici, Elisa; Dando, Ilaria; Butturini, Elena; DALLA POZZA, Elisa; Nadal Serrano, Mercedes; Oliver, Jordi; Roca, Pilar; Mariotto, Sofia Giovanna; Cellini, Barbara; Blandino, Giovanni; Palmieri, Marta; Di Agostino, Silvia; Donadelli, Massimo
Mostrati risultati da 1 a 20 di 33
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