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Onconase Dimerization Through 3D Domain Swapping: Structural Investigations and Increase Of The Apoptotic Effect In Cancer Cells 1-gen-2017 Fagagnini, Andrea; Pica, Andrea; Fasoli, Sabrina; Montioli, Riccardo; Donadelli, Massimo; Cordani, Marco; Butturini, Elena; Acquasaliente, Laura; Picone, Delia; Gotte, Giovanni
Extensive deamidation of RNase A inhibits its oligomerization through 3D domain swapping 1-gen-2017 Fagagnini, Andrea; Montioli, Riccardo; Caloiu, Andra; Ribó, Marc; Laurents, Douglas V.; Gotte, Giovanni
Pathogenic variants of human Aromatic L-Amino Acid Decarboxylase: evidences of misfolding in functionally active variants 1-gen-2018 Bisello, Giovanni; Montioli, Riccardo; Dindo, Mirco; Voltattorni Carla, Borri; Bertoldi, Mariarita
Cysteine 180 Is a Redox Sensor Modulating the Activity of Human Pyridoxal 5'-Phosphate Histidine Decarboxylase 1-gen-2018 Rossignoli, Giada; Grottesi, Alessandro; Bisello, Giovanni; Montioli, Riccardo; Borri Voltattorni, Carla; Paiardini, Alessandro; Bertoldi, Mariarita
Molecular and cellular basis of ornithine δ-aminotransferase deficiency caused by the V332M mutation associated with gyrate atrophy of the choroid and retina 1-gen-2018 Montioli, Riccardo; Desbats, Maria Andrea; Grottelli, Silvia; Doimo, Mara; Bellezza, Ilaria; Borri Voltattorni, Carla; Salviati, Leonardo; Cellini, Barbara
Properties of RNase A monomer and dimers depend on the oligomerization pathway followed. 1-gen-2018 Fasoli, Sabrina; Fagagnini, Andrea; Montioli, Riccardo; Raineri, Alice; Gotte, Giovanni
Heterozygosis in aromatic amino acid decarboxylase deficiency: Evidence for a positive interallelic complementation between R347Q and R358H mutations 1-gen-2018 Montioli, Riccardo; Janson, Giacomo; Paiardini, Alessandro; Bertoldi, Mariarita; Borri Voltattorni, Carla
Aromatic amino acid decarboxylase deficiency: Molecular and metabolic basis and therapeutic outlook 1-gen-2019 Himmelreich, Nastassja; Montioli, Riccardo; Bertoldi, Mariarita; Carducci, Carla; Leuzzi, Vincenzo; Gemperle, Corinne; Berner, Todd; Hyland, Keith; Thöny, Beat; Hoffmann, Georg F; Borri Voltattorni, Carla; Blau, Nenad
A novel compound heterozygous genotype associated with aromatic amino acid decarboxylase deficiency: Clinical aspects and biochemical studies 1-gen-2019 Montioli, Riccardo; Battini, Roberta; Paiardini, Alessandro; Tolve, Manuela; Bertoldi, Mariarita; Carducci, Carla; Leuzzi, Vincenzo; Borri Voltattorni, Carla
R180T variant of δ-ornithine aminotransferase associated with gyrate atrophy: biochemical, computational, X-RAY and NMR studies provide insight into its catalytic features 1-gen-2019 Montioli, Riccardo; Paiardini, Alessandro; Giardina, Giorgio; Zanzoni, Serena; Cutruzzola, Francesca; Cellini, Barbara; Borri Voltattorni, Carla
Deciphering the fate of slan+ -monocytes in human tonsils by gene expression profiling 1-gen-2020 Bianchetto-Aguilera, Francisco; Tamassia, Nicola; Gasperini, Sara; Calzetti, Federica; Finotti, Giulia; Gardiman, Elisa; Montioli, Riccardo; Bresciani, Debora; Vermi, William; Cassatella, Marco Antonio
New variants of AADC deficiency expand the knowledge of enzymatic phenotypes 1-gen-2020 Montioli, Riccardo; Bisello, Giovanni; Dindo, Mirco; Rossignoli, Giada; Voltattorni, Carla Borri; Bertoldi, Mariarita
RNase A domain-swapped dimers produced through different methods: structure–catalytic properties and antitumor activity 1-gen-2021 Montioli, Riccardo; Campagnari, Rachele; Fasoli, Sabrina; Fagagnini, Andrea; Caloiu, Andra; Smania, Marcello; Menegazzi, Marta; Gotte, Giovanni
Dimerization of human angiogenin and of variants involved in neurodegenerative diseases 1-gen-2021 Fasoli, Sabrina; Bettin, Ilaria; Montioli, Riccardo; Fagagnini, Andrea; Peterle, Daniele; Laurents, Douglas V; Gotte, Giovanni
Deficit of human ornithine aminotransferase in gyrate atrophy: Molecular, cellular, and clinical aspects 1-gen-2021 Montioli, Riccardo; Bellezza, Ilaria; Desbats, Maria Andrea; Voltattorni, Carla Borri; Salviati, Leonardo; Cellini, Barbara
Molecular and cellular studies reveal folding defects of human ornithine aminotransferase variants associated with gyrate atrophy of the choroid and retina 1-gen-2021 Montioli, Riccardo; Sgaravizzi, Giada; Desbats, Maria Andrea; Grottelli, Silvia; Voltattorni, Carla Borri; Salviati, Leonardo; Cellini, Barbara
Aromatic amino acid decarboxylase deficiency: the added value of biochemistry 1-gen-2021 Montioli, Riccardo; Borri Voltattorni, Carla
Compound heterozygosis in AADC deficiency: A complex phenotype dissected through comparison among heterodimeric and homodimeric AADC proteins 1-gen-2021 Longo, Carmen; Montioli, Riccardo; Bisello, Giovanni; Palazzi, Luana; Mastrangelo, Mario; Brennenstuhl, Heiko; de Laureto, Patrizia Polverino; Opladen, Thomas; Leuzzi, Vincenzo; Bertoldi, Mariarita
Spectrum of DDC variants causing aromatic l-amino acid decarboxylase (AADC) deficiency and pathogenicity interpretation using ACMG-AMP/ACGS recommendations 1-gen-2022 Himmelreich, Nastassja; Montioli, Riccardo; Garbade, Sven F; Kopesky, Jeffrey; Elsea, Sarah H; Carducci, Carla; Voltattorni, Carla B; Blau, Nenad
Human RNase 1 can extensively oligomerize through 3D domain swapping thanks to the crucial contribution of its C-terminus 1-gen-2023 Noro, Irene; Bettin, Ilaria; Fasoli, Sabrina; Smania, Marcello; Lunardi, Luca; Giannini, Michele; Andreoni, Leonardo; Montioli, Riccardo; Gotte, Giovanni
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