GIOIA, ROBERTA

GIOIA, ROBERTA  

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Risultati 1 - 19 di 19 (tempo di esecuzione: 0.03 secondi).
Titolo Data di pubblicazione Autore(i) File
A Mn(II)-Mn(II) center in human prolidase 1-gen-2013 Besio, R; Baratto, Mc; Gioia, R; Monzani, E; Nicolis, S; Cucca, L; Profumo, A; Casella, L; Basosi, R; Tenni, R; Rossi, A; Forlino, A
Allele-specific Col1a1 silencing reduces mutant collagen in fibroblasts from Brtl mouse, a model for classical osteogenesis imperfecta. 1-gen-2014 Rousseau, J; Gioia, Roberta; Layrolle, P; Lieubeau, B; Heymann, D; Rossi, Antonio; Marini, Jc; Trichet, V; Forlino, Antonella
Altered cytoskeletal organization characterized lethal but not surviving Brtl+/- mice: insight on phenotypic variability in osteogenesis imperfecta 1-gen-2015 Bianchi, L; Gagliardi, A; Maruelli, S; Besio, R; Landi, C; Gioia, R; Kozloff, K M; Khoury, B M; Coucke, P J; Symoens, S; Marini, J C; Rossi, A; Bini, L; Forlino, A
Characterization of stress response in human retinal epithelial cells. 1-gen-2013 Giansanti, V; Rodriguez, Ge; Savoldelli, M; Gioia, Roberta; Forlino, Antonella; Mazzini, G; Pennati, M; Zaffaroni, N; Scovassi, Ai; Torriglia, A.
Crtap and p3h1 knock out zebrafish support defective collagen chaperoning as the cause of their osteogenesis imperfecta phenotype 1-gen-2020 Tonelli, F.; Cotti, S.; Leoni, L.; Besio, R.; Gioia, R.; Marchese, L.; Giorgetti, S.; Villani, S.; Gistelinck, C.; Wagener, R.; Kobbe, B.; Fiedler, I. A. K.; Larionova, D.; Busse, B.; Eyre, D.; Rossi, A.; Witten, P. E.; Forlino, A.
Differential response to intracellular stress in the skin from osteogenesis imperfecta Brtl mice with lethal and non lethal phenotype: a proteomic approach 1-gen-2012 Bianchi, L; Gagliardi, A; Gioia, R; Besio, Roberta; Tani, C; Landi, C; Cipriano, M; Gimigliano, A; Rossi, A; Marini, Jc; Forlino, A; Bini, L
Impaired osteoblastogenesis in a murine model of dominant osteogenesis imperfecta: a new target for osteogenesis imperfecta pharmacological therapy 1-gen-2012 Gioia, R; Panaroni, C; Besio, R; Palladini, G; Merlini, G; Giansanti, V; Scovassi, Ia; Villani, S; Villa, I; Villa, A; Vezzoni, P; Tenni, R; Rossi, A; Marini, Jc; Forlino, A
Improved prolidase activity assay allowed enzyme kinetic characterization and faster prolidase deficiency diagnosis 1-gen-2011 Besio, R; Monzani, E; Gioia, R; Nicolis, S; Rossi, A; Casella, L; Forlino, A
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knock-in murine model for classical, dominant osteogenesis imperfecta 1-gen-2009 Panaroni, C; Gioia, R; Lupi, A; Besio, R; Goldstein, S A; Kreider, J; Leikin, S; Vera, J C; Mertz, E L; Perilli, E; Baruffaldi, F; Villa, Ilaria; Farina, A; Casasco, M; Cetta, G; Rossi, A; Frattini, A; Marini, J C; Vezzoni, P; Forlino, A
Kinetic and structural evidences on human prolidase pathological mutants suggest strategies for enzyme functional rescue 1-gen-2013 Besio, R; Gioia, R; Cossu, F; Monzani, E; Nicolis, S; Cucca, L; Profumo, A; Casella, L; Tenni, R; Bolognesi, M; Rossi, A; Forlino, A
Knocking out TMEM38B in human foetal osteoblasts hFOB 1.19 by CRISPR/Cas9: A model for recessive OI type XIV 1-gen-2021 Leoni, L.; Tonelli, F.; Besio, R.; Gioia, R.; Moccia, F.; Rossi, A.; Forlino, A.
Lack of prolidase causes a bone phenotype both in human and in mouse 1-gen-2015 Besio, R; Maruelli, S; Gioia, R; Villa, I; Grabowski, P; Gallagher, O; Bishop, N J; Foster, S; De Lorenzi, E; Colombo, R; Diaz, J L; Moore-Barton, H; Deshpande, C; Aydin, H I; Tokatli, A; Kwiek, B; Kasapkara, C S; Adisen, E O; Gurer, M A; Di Rocco, M; Phang, J M; Gunn, T M; Tenni, R; Rossi, A; Forlino, A
Regulation of NAD(P) synthesis in Bacillus subtilis 1-gen-2007 Gamba, Pamela; Marinoni, Ilaria; Barbieri, Giulia; Pozzi, Camilla; Gioia, Roberta; Laureti, Luisa; Cecchini, DAVIDE AGOSTINO; Albertini, Alessandra
Severely impaired bone material quality in chihuahua zebrafish resembles classical dominant human Osteogenesis Imperfecta 1-gen-2018 Fiedler, I A K; Schmidt, F N; Wölfel, E M; Plumeyer, C; Milovanovic, P; Gioia, R; Tonelli, F; Bale H, A.; Jähn, K; Besio, R; Forlino, A; Busse, B
Structure, evolution and expression of zebrafish cartilage oligomeric matrix protein (COMP, TSP5). CRISPR-Cas mutants show a dominant phenotype in myosepta 1-gen-2022 Forte-Gomez, Helena Fabiana; Gioia, Roberta; Tonelli, Francesca; Kobbe, Birgit; Koch, Peter; Bloch, Wilhelm; Paulsson, Mats; Zaucke, Frank; Forlino, Antonella; Wagener, Raimund
The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta 1-gen-2017 Gioia, Roberta; Tonelli, Francesca; Ceppi, Ilaria; Biggiogera, Marco; Leikin, Sergey; Fisher, Shannon; Tenedini, Elena; Yorgan, Timur A; Schinke, Thorsten; Tian, Kun; Schwartz, Jean Marc; Forte, Fabiana; Wagener, Raimund; Villani, Simona; Rossi, Antonio; Forlino, Antonella
TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophy. 1-gen-2014 Difrancesco, Jc; Novara, Francesca; Zuffardi, Orsetta; Forlino, Antonella; Gioia, Roberta; Cossu, F; Bolognesi, M; Andreoni, S; Saracchi, E; Frigeni, B; Stellato, T; Tolnay, M; Winkler, Dt; Remida, P; Isimbaldi, G; Ferrarese, C.
Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin 1-gen-2016 Gistelinck, C.; Gioia, Roberta; Gagliardi, A.; Tonelli, Francesca; Marchese, Loredana; Bianchi, L.; Landi, C.; Bini, L.; Huysseune, A.; Witten, P. E.; Staes, A.; Gevaert, K.; De Rocker, N.; Menten, B.; Malfait, F.; Leikin, S.; Carra, S.; Tenni, Ruggero; Rossi, Antonio; De Paepe, A.; Coucke, P.; Willaert, A.; Forlino, Antonella
Zebrafish Tric-b is required for skeletal development and bone cells differentiation 1-gen-2023 Tonelli, Francesca; Leoni, Laura; Daponte, Valentina; Gioia, Roberta; Cotti, Silvia; Fiedler, Imke A K; Larianova, Daria; Willaert, Andy; Coucke, Paul J; Villani, Simona; Busse, Björn; Besio, Roberta; Rossi, Antonio; Witten, P Eckhard; Forlino, Antonella