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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
Identifying the structure of the active sites of human recombinant prolidase 1-gen-2010 Besio, R; Alleva, S; Forlino, A; Lupi, A; Meneghini, C; Miniozzi, V; Profumo, A; Stellato, Francesco; Tenni, R; Morante, S
Prolidase deficiency may be reversed by hematopietic stem cell transplantation: CE analysis of dipeptides in urine and monitoring of prolidase activity in blood. 1-gen-2011 Colombo, Raffaella; Bertoletti, Laura; Forlino, Antonella; Besio, Roberta; DE LORENZI, Ersilia
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
Partial rescue of biochemical parameters after hematopoietic stem cell transplantation in a patient with prolidase deficiency due to two novel PEPD mutations 1-gen-2012 Caselli, Désirée; Cimaz, Rolando; Besio, Roberta; Rossi, Antonio; DE LORENZI, Ersilia; Colombo, Raffaella; Cantarini, Luca; Riva, Silvia; Spada, Marco; Forlino, Antonella; Aricò, Maurizio
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
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
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
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
Role of the advanced glycation end products receptor in Crohn’s disease inflammation 1-gen-2013 Ciccocioppo, R.; Vanoli, Alessandro; Klersy, C.; Imbesi, V.; Boccaccio, V.; Manca, R.; Betti, E.; Cangemi, GIUSEPPINA CRISTINA; Strada, E.; Besio, Roberta; Rossi, Antonio; Falcone, Colomba; Ardizzone, S.; Fociani, P.; Danelli, P.; Corazza, GINO ROBERTO
Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasis 1-gen-2014 Gruenwald, K; Castagnola, P; Besio, R; Dimori, M; Chen, Y; Akel, N S; Swain, F L; Skinner, R A; Eyre, D R; Gaddy, D; Suva, L J; Morello, R
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
Treatment options for osteogenesis imperfecta 1-gen-2015 Besio, R; Forlino, A
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
A Rare Cause of Lower Extremity Ulcers: Prolidase Deficiency 1-gen-2016 Adlşen, E; Erduran, F B; Ezgü, F S; Kasapkara, Ç S; Besio, R; Forlino, A; Gürer, M A
Sc65-null mice provide evidence for a novel endoplasmic reticulum complex regulating collagen lysyl hydroxylation 1-gen-2016 Heard, M E; Cofirst, ; Besio, R; Cofirst, ; Weis, M A; Rai, J; Hudson, D M; Dimori, M; Zimmerman, S M; Kamykowski, J A; Hogue, W R; Swain, F L; Burdine, M S; Mackintosh, S G; Tackett, A J; Suva, L J; Eyre, D R; Morello, R
Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective 1-gen-2017 Gagliardi, A; Cofirst, ; Besio, R; Cofirst, ; Carnemolla, C; Landi, C; Armini, A; Aglan, M; Otaify, G; Temtamy, S A; Forlino, A; Bini, L; Bianchi, L
The scavenging chemokine receptor ACKR2 has a significant impact on acute mortality rate and early lesion development after traumatic brain injury 1-gen-2017 Woodcock T, M.; Frugier, T; Nguyen, T T; Semple, B D; Bye, N; Massara, M; Savino, B; Besio, R; Sobacchi, C; Locati, M; Morganti-Kossmann, M C
Expression characterization and functional implication of the collagen-modifying Leprecan proteins in mouse gonadal tissue and mature sperm 1-gen-2018 Zimmerman, Sarah M; Besio, Roberta; Heard-Lipsmeyer, Melissa E; Dimori, Milena; Castagnola, Patrizio; Swain, Frances L; Gaddy, Dana; Diekman, Alan B; Morello, Roy
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
Mostrati risultati da 1 a 20 di 38
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