ROSSI, ANTONIO
ROSSI, ANTONIO
DIPARTIMENTO DI MEDICINA MOLECOLARE
4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretion
2018-01-01 Besio, R; Iula, G; Garibaldi, N; Cipolla, L; Sabbioneda, S; Biggiogera, M; Marini, Jc.; Rossi, A; Forlino, A
A chondrodysplasia family produced by mutations in the diastrophic dysplasia sulfate transporter gene: genotype/phenotype correlations
1996-01-01 SUPERTI FURGA, A.; Rossi, Antonio; Steinmann, B.; Gitzelmann, R.
A de novo G to T transversion in a pro-a1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain.
1991-01-01 Valli, Maurizia; M., Mottes; Tenni, Ruggero; A., Sangalli; M., Gomez Lyra; Rossi, Antonio; F., Antoniazzi; Cetta, Giuseppe; P. F., Pignatti
A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype
2005-01-01 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 family of chondrodysplasias caused by mutations in the diastrophic dysplasia sulfate transporter gene and associated with impaired sulfation of proteoglycans.
1996-01-01 Superti Furga, A; Hästbacka, J; Rossi, Antonio; van der Harten, Jj; Wilcox, Wr; Cohn, Dh; Rimoin, Dl; Steinmann, B; Lander, Es; Gitzelmann, R.
A Mn(II)-Mn(II) center in human prolidase
2013-01-01 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.
2008-01-01 Bonafé, L; Hastbacka, J; de la Chapelle, A; Campos Xavier, Ab; Chiesa, C; Forlino, Antonella; Superti Furga, A; Rossi, Antonio
A novel splicing mutation causes an undescribed type of analbuminemia.
2002-01-01 Campagnoli, Monica; Rossi, Antonio; Palmqvist, L; Flisberg, A; Niklasson, A; Minchiotti, Lorenzo; Galliano, Monica
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges.
2001-01-01 Minchiotti, Lorenzo; Campagnoli, Monica; Rossi, Antonio; Cosulich, MARIA ELISABETTA; Galliano, Monica; Monti, M; Pucci, P; Kragh Hansen, U.; Granel, B; Disdier, P; Weiller, P. j.
A quantitative and qualitative method for direct 2-DE analysis of murine cartilage
2007-01-01 Pecora, Fabio; Forlino, Antonella; Gualeni, Benedetta; Lupi, ANNA LISA; Giorgetti, Sofia; Marchese, Loredana; Stoppini, Monica; Tenni, Ruggero; Cetta, Giuseppe; Rossi, Antonio
Achondrogenesis type 1B is caused by mutations in the diastrophic dysplasia sulfate transporter gene
1996-01-01 SUPERTI FURGA, A.; Hastbacka, J.; Wilcox, W. R.; Cohn, D. H.; VAN DER HARTEN, H. J.; Rossi, Antonio; Blau, N.; Rimoin, D. L.; Steinmann, B.; Lander, E. S.; Gitzelamann, R.
Adesion proteins in CHO cells.
2006-01-01 Seppi, Claudio; Mancini, FRANCESCA ROBERTA; Balduini, Cesare; Cetta, Giuseppe; Rossi, Antonio
Allele-specific Col1a1 silencing reduces mutant collagen in fibroblasts from Brtl mouse, a model for classical osteogenesis imperfecta.
2014-01-01 Rousseau, J; Gioia, Roberta; Layrolle, P; Lieubeau, B; Heymann, D; Rossi, Antonio; Marini, Jc; Trichet, V; Forlino, Antonella
Alteration of proteoglycan sulfation affects bone growth and remodeling.
2013-01-01 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
2015-01-01 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.
2014-01-01 DE LEONARDIS, Fabio; Monti, Luca; Gualeni, Benedetta; Tenni, Ruggero; Forlino, Antonella; Rossi, Antonio
Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene.
2005-01-01 Campagnoli, Monica; Sala, Alberto; Labo', Sara; Rossi, Antonio; Neuhaus, T. J.; Braegger, C. P.; Minchiotti, Lorenzo; Galliano, Monica
Analysis of Aggrecan Glycanation by Western Blot in Cell Culture
2023-01-01 Gramegna Tota, Chiara; Leone, Alessandra; Rossi, Antonio; Paganini, Chiara
Analysis of Aggrecan Glycanation by Western Blot in Cell Culture
2023-01-01 Gramegna Tota, Chiara; Leone, Alessandra; Rossi, Antonio; Paganini, Chiara
Analysis of proteoglycan synthesis and secretion in cell culture systems
2019-01-01 Paganini, C.; Costantini, R.; Rossi, A.
| 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 chondrodysplasia family produced by mutations in the diastrophic dysplasia sulfate transporter gene: genotype/phenotype correlations | 1-gen-1996 | SUPERTI FURGA, A.; Rossi, Antonio; Steinmann, B.; Gitzelmann, R. | |
| A de novo G to T transversion in a pro-a1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain. | 1-gen-1991 | Valli, Maurizia; M., Mottes; Tenni, Ruggero; A., Sangalli; M., Gomez Lyra; Rossi, Antonio; F., Antoniazzi; Cetta, Giuseppe; P. F., Pignatti | |
| 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 family of chondrodysplasias caused by mutations in the diastrophic dysplasia sulfate transporter gene and associated with impaired sulfation of proteoglycans. | 1-gen-1996 | Superti Furga, A; Hästbacka, J; Rossi, Antonio; van der Harten, Jj; Wilcox, Wr; Cohn, Dh; Rimoin, Dl; Steinmann, B; Lander, Es; Gitzelmann, R. | |
| 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 novel splicing mutation causes an undescribed type of analbuminemia. | 1-gen-2002 | Campagnoli, Monica; Rossi, Antonio; Palmqvist, L; Flisberg, A; Niklasson, A; Minchiotti, Lorenzo; Galliano, Monica | |
| A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. | 1-gen-2001 | Minchiotti, Lorenzo; Campagnoli, Monica; Rossi, Antonio; Cosulich, MARIA ELISABETTA; Galliano, Monica; Monti, M; Pucci, P; Kragh Hansen, U.; Granel, B; Disdier, P; Weiller, P. j. | |
| 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 | |
| Achondrogenesis type 1B is caused by mutations in the diastrophic dysplasia sulfate transporter gene | 1-gen-1996 | SUPERTI FURGA, A.; Hastbacka, J.; Wilcox, W. R.; Cohn, D. H.; VAN DER HARTEN, H. J.; Rossi, Antonio; Blau, N.; Rimoin, D. L.; Steinmann, B.; Lander, E. S.; Gitzelamann, R. | |
| Adesion proteins in CHO cells. | 1-gen-2006 | Seppi, Claudio; Mancini, FRANCESCA ROBERTA; Balduini, Cesare; Cetta, Giuseppe; Rossi, Antonio | |
| 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 | |
| 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 | |
| Analbuminemia in a Swiss family is caused by a C --> T transition at nucleotide 4446 of the albumin gene. | 1-gen-2005 | Campagnoli, Monica; Sala, Alberto; Labo', Sara; Rossi, Antonio; Neuhaus, T. J.; Braegger, C. P.; Minchiotti, Lorenzo; Galliano, Monica | |
| 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. |