FORLINO, ANTONELLA

FORLINO, ANTONELLA  

DIPARTIMENTO DI MEDICINA MOLECOLARE  

Mostra records
Risultati 1 - 20 di 115 (tempo di esecuzione: 0.025 secondi).
Titolo Data di pubblicazione Autore(i) File
4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretion 1-gen-2018 Besio, R; Iula, G; Garibaldi, N; Cipolla, L; Sabbioneda, S; Biggiogera, M; Marini, Jc.; Rossi, A; Forlino, A
A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI. 1-gen-1995 Zolezzi, Francesca; Forlino, Antonella; Mottes, Monica; Valli, Maurizia; Sensi, Alberto; Calzolari, Elisa; Pignatti, Pierfrancesc; Cetta, Giuseppe
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta. 1-gen-1994 Mottes, M; Sangalli, A; Valli, Maurizia; Forlino, Antonella; Gomez Lira, M; Antoniazzi, F; Constantinou Deltas, Cd; Cetta, Giuseppe; Pignatti, Pf
A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype 1-gen-2005 Forlino, Antonella; Piazza, ROCCO GIOVANNI; Tiveron, C.; Torre, S. D.; Tatangelo, L.; Bonafe, L.; Gualeni, Benedetta; Romano, Assunta; Pecora, Fabio; SUPERTI FURGA, A.; Cetta, Giuseppe; Rossi, Antonio
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
A novel mutation in the sulphate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia. 1-gen-2008 Bonafé, L; Hastbacka, J; de la Chapelle, A; Campos Xavier, Ab; Chiesa, C; Forlino, Antonella; Superti Furga, A; Rossi, Antonio
A quantitative and qualitative method for direct 2-DE analysis of murine cartilage 1-gen-2007 Pecora, Fabio; Forlino, Antonella; Gualeni, Benedetta; Lupi, ANNA LISA; Giorgetti, Sofia; Marchese, Loredana; Stoppini, Monica; Tenni, Ruggero; Cetta, Giuseppe; Rossi, Antonio
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
A standard set of outcome measures for the comprehensive assessment of osteogenesis imperfecta 1-gen-2021 Nijhuis, W.; Franken, A.; Ayers, K.; Damas, C.; Folkestad, L.; Forlino, A.; Fraschini, P.; Hill, C.; Janus, G.; Kruse, R.; Lande Wekre, L.; Michiels, L.; Montpetit, K.; Panzeri, L.; Porquet-Bordes, V.; Rauch, F.; Sakkers, R.; Salles, J. -P.; Semler, O.; Sun, J.; To, M.; Tosi, L.; Yao, Y.; Yeung, E. H. K.; Zhytnik, L.; Zillikens, M. C.; Verhoef, M.
Absence of Dipeptidyl Peptidase 3 increases oxidative stress and causes bone loss 1-gen-2019 Menale, Ciro; Robinson, Lisa J; Palagano, Eleonora; Rigoni, Rosita; Erreni, Marco; Almarza, Alejandro J; Strina, Dario; Mantero, Stefano; Lizier, Michela; Forlino, Antonella; Besio, Roberta; Monari, Marta; Vezzoni, Paolo; Cassani, Barbara; Blair, Harry C; Villa, Anna; Sobacchi, Cristina
Activity of alpha 1-antitrypsin and cigarette smoking in subarachnoid haemorrhage from ruptured aneurysm. 1-gen-1996 Gaetani, P; Tartara, F; Tancioni, F; Klersy, C; Forlino, Antonella; Baena, Rr
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
Alpha 1-antitrypsin activity in subarachnoid hemorrhage. 1-gen-1996 Tartara, F; Gaetani, P; Tancioni, F; Guagliano, A; Klersy, C; Forlino, Antonella; Marzatico, Fulvio; Rodriguez, Y. BAENA R.
Alteration of proteoglycan sulfation affects bone growth and remodeling. 1-gen-2013 Gualeni, Benedetta; de Vernejoul, Mc; Marty Morieux, C; DE LEONARDIS, Fabio; Franchi, M; Monti, L; Forlino, Antonella; Houillier, P; Rossi, Antonio; Geoffroy, V.
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
Altered signaling in the G1 phase deregulates chondrocyte growth in a mouse model with proteoglycan undersulfation. 1-gen-2014 DE LEONARDIS, Fabio; Monti, Luca; Gualeni, Benedetta; Tenni, Ruggero; Forlino, Antonella; Rossi, Antonio
Alternative splicing in COL1A1 mRNA leads to a partial null allele and two in-frame forms with structural defects in non-lethal osteogenesis imperfecta. 1-gen-1996 Wang, Q; Forlino, Antonella; Marini, Jc
An alpha 2(I) glycine to aspartate substitution is responsible for the presence of a kink in type I collagen in a lethal case of osteogenesis imperfecta. 1-gen-1998 Forlino, Antonella; Keene, Dr; Schmidt, K; Marini, Jc
Appendage regeneration in vertebrates: What makes this possible? 1-gen-2021 Daponte, V.; Tylzanowski, P.; Forlino, A.
Bone biology: insights from osteogenesis imperfecta and related rare fragility syndromes 1-gen-2019 Besio, Roberta; Chow, Chi-Wing; Tonelli, Francesca; Marini, Joan C; Forlino, Antonella