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PAGANINI, CHIARA

PAGANINI, CHIARA  

DIPARTIMENTO DI SANITA' PUBBLICA, MEDICINA SPERIMENTALE E FORENSE  

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Titolo Data di pubblicazione Autore(i) File
A Refractory Celiac Patient Successfully Treated With Mesenchymal Stem Cell Infusions 1-gen-2016 Ciccocioppo, Rachele; Gallia, Alessandra; Avanzini, Maria A.; Betti, Elena; Picone, Cristina; Vanoli, Alessandro; Paganini, Chiara; Biagi, Federico; Maccario, Rita; Corazza, GINO ROBERTO
A Refractory Celiac Patient Successfully Treated With Mesenchymal Stem Cell Infusions 1-gen-2016 Ciccocioppo, Rachele; Gallia, Alessandra; Avanzini, Maria A; Betti, Elena; Picone, Cristina; Vanoli, Alessandro; Paganini, Chiara; Biagi, Federico; Maccario, Rita; Corazza, Gino R
Analysis of Aggrecan Glycanation by Western Blot in Cell Culture 1-gen-2023 Gramegna Tota, Chiara; Leone, Alessandra; Rossi, Antonio; Paganini, Chiara
Analysis of Aggrecan Glycanation by Western Blot in Cell Culture 1-gen-2023 Gramegna Tota, Chiara; Leone, Alessandra; Rossi, Antonio; Paganini, Chiara
Analysis of proteoglycan synthesis and secretion in cell culture systems 1-gen-2019 Paganini, C.; Costantini, R.; Rossi, A.
Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy 1-gen-2022 Guasto, Alessandra; Dubail, Johanne; Aguilera-Albesa, Sergio; Paganini, Chiara; Vanhulle, Catherine; Haouari, Walid; Gorría-Redondo, Nerea; Aznal-Sainz, Elena; Boddaert, Nathalie; Planas-Serra, Laura; Schlüter, Agatha; Vélez-Santamaría, Valentina; Verdura, Edgard; Bruneel, Arnaud; Rossi, Antonio; Huber, Céline; Pujol, Aurora; Cormier-Daire, Valérie
Biallelic variants in the SLC13A1 sulfate transporter gene cause hyposulfatemia with a mild spondylo‐epi‐metaphyseal dysplasia 1-gen-2023 van de Kamp, Jiddeke M.; Bökenkamp, Arend; Smith, Desiree E. C.; Wamelink, Mirjam M. C.; Jansen, Erwin E. W.; Struys, Eduard A.; Waisfisz, Quinten; Verkleij, Marieke; Hartmann, Michaela F.; Wang, Rong; Wudy, Stefan A.; Paganini, Chiara; Rossi, Antonio; Finken, Martijn J. J.
Bone and connective tissue disorders caused by defects in glycosaminoglycan biosynthesis: a panoramic view 1-gen-2019 Paganini, Chiara; Costantini, Rossella; Superti-Furga, Andrea; Rossi, Antonio
Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification 1-gen-2019 Paganini, Chiara; Monti, Luca; Costantini, Rossella; Besio, Roberta; Lecci, Silvia; Biggiogera, Marco; Tian, Kun; Schwartz, Jean-Marc; Huber, Céline; Cormier-Daire, Valérie; Gibson, Beth G.; Pirog, Katarzyna A.; Forlino, Antonella; Rossi, Antonio
Cant1 Affects Cartilage Proteoglycan Properties: Aggrecan and Decorin Characterization in a Mouse Model of Desbuquois Dysplasia Type 1 1-gen-2024 Gramegna Tota, Chiara; Leone, Alessandra; Khan, Asifa; Forlino, Antonella; Rossi, Antonio; Paganini, Chiara
Enzyme replacement therapy in mice lacking arylsulfatase B targets bone-remodeling cells, but not chondrocytes 1-gen-2020 Hendrickx, G.; Danyukova, T.; Baranowsky, A.; Rolvien, T.; Angermann, A.; Schweizer, M.; Keller, J.; Schroder, J.; Meyer-Schwesinger, C.; Muschol, N.; Paganini, C.; Rossi, A.; Amling, M.; Pohl, S.; Schinke, T.
Identification of potential non-invasive biomarkers in diastrophic dysplasia 1-gen-2023 Paganini, Chiara; Carroll, Ricki S.; Gramegna Tota, Chiara; Schelhaas, Andrea J.; Leone, Alessandra; Duker, Angela L.; O'Connell, David A.; Coghlan, Ryan F.; Johnstone, Brian; Ferreira, Carlos R.; Peressini, Sabrina; Albertini, Riccardo; Forlino, Antonella; Bonafé, Luisa; Campos-Xavier, Ana Belinda; Superti-Furga, Andrea; Zankl, Andreas; Rossi, Antonio; Bober, Michael B.
Impaired proteoglycan glycosylation, elevated TGF-β signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplastica 1-gen-2018 Chan, Wing Lee; Steiner, Magdalena; Witkos, Tomasz; Egerer, Johannes; Busse, Björn; Mizumoto, Shuji; Pestka, Jan M.; Zhang, Haikuo; Hausser, Ingrid; Khayal, Layal Abo; Ott, Claus-Eric; Kolanczyk, Mateusz; Willie, Bettina; Schinke, Thorsten; Paganini, Chiara; Rossi, Antonio; Sugahara, Kazuyuki; Amling, Michael; Knaus, Petra; Chan, Danny; Lowe, Martin; Mundlos, Stefan; Kornak, Uwe
Improvement of the skeletal phenotype in a mouse model of diastrophic dysplasia after postnatal treatment with N-acetylcysteine 1-gen-2021 Paganini, C.; Gramegna Tota, C.; Monti, L.; Monti, I.; Maurizi, A.; Capulli, M.; Bourmaud, M.; Teti, A.; Cohen-Solal, M.; Villani, S.; Forlino, A.; Superti-Furga, A.; Rossi, A.
N-acetylcysteine treatment ameliorates the skeletal phenotype of a mouse model of diastrophic dysplasia 1-gen-2015 Monti, Luca; Paganini, Chiara; Lecci, Silvia; DE LEONARDIS, Fabio; Hay, Eric; Cohen Solal, Martine; Villani, Simona; Superti Furga, Andrea; Tenni, Ruggero; Forlino, Antonella; Rossi, Antonio
Phenotypic characterization of immortalized chondrocytes from a desbuquois dysplasia type 1 mouse model: A tool for studying defects in glycosaminoglycan biosynthesis 1-gen-2021 Tota, C. G.; Valenti, B.; Forlino, A.; Rossi, A.; Paganini, C.
Polyethylene Glycol-Poly-Lactide-co-Glycolide Block Copolymer-Based Nanoparticles as a Potential Tool for Off-Label Use of N-Acetylcysteine in the Treatment of Diastrophic Dysplasia 1-gen-2017 Chiesa, Enrica; Monti, Luca; Paganini, Chiara; Dorati, Rossella; Conti, Bice; Modena, Tiziana; Rossi, Antonio; Genta, Ida
Report on the 23rd FEBS Young Scientists’ Forum 2024 1-gen-2024 Miggiano, Riccardo; Ippolito, Luigi; Paganini, Chiara; Paone, Alessio; Tonelli, Francesca; Trojan and Irene D, Sonia; ıaz-Moreno,
Skeletal Dysplasias Caused by Sulfation Defects 1-gen-2020 Paganini, Chiara; Gramegna Tota, Chiara; Superti-Furga, Andrea; Rossi, Antonio
Testing the Cre-mediated genetic switch for the generation of conditional knock-in mice 1-gen-2019 Capulli, M.; Costantini, R.; Sonntag, S.; Maurizi, A.; Paganini, C.; Monti, L.; Forlino, A.; Shmerling, D.; Teti, A.; Rossi, A.