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Novel nonsense mutation causes analbuminemia in a Moroccan family. 1-gen-2005 Campagnoli, Monica; Sala, Alberto; Romano, Assunta; Rossi, Antonio; Nauta, J.; Koot, B. G.; Minchiotti, Lorenzo; Galliano, Monica
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
Adesion proteins in CHO cells. 1-gen-2006 Seppi, Claudio; Mancini, FRANCESCA ROBERTA; Balduini, Cesare; Cetta, Giuseppe; Rossi, Antonio
Cartilage histogenesis in a murine model of chondrodysplasia 1-gen-2006 ICARO CORNAGLIA, Antonia; Casasco, Marco; Riva, Federica; Farina, Aurora; Giannella, PAOLA ANTONIA; Forlino, Antonella; Rossi, Antonio; Cetta, Giuseppe; Gualeni, Benedetta; Pecora, Fabio; Casasco, Andrea; Calligaro, Alberto
Self-aggregation of fibrillar collagens I and II involves lysine side chains. 1-gen-2006 Tenni, Ruggero; Sonaggere, Myriam; Viola, Manuela; Bartolini, Barbara; Tira, MARIA ENRICA; Rossi, Antonio; Orsini, E.; Ruggeri, A.; Ottani, V.
Insights from a transgenic mouse model on the role of SLC26A2 in health and disease. 1-gen-2006 Forlino, Antonella; Gualeni, Benedetta; Pecora, Fabio; DELLA TORRE, Sara; Piazza, ROCCO GIOVANNI; Tiveron, Cecilia; Tatangelo, Laura; SUPERTI FURGA, Andrea; Cetta, Giuseppe; Rossi, Antonio
Collagen plays an active role in the aggregation of beta 2-microglobulin under physio-pathological conditions of dialysis-related amyloidosis. 1-gen-2006 Relini, A; Canale, C; DE STEFANO, S; Rolandi, R; Giorgetti, Sofia; Stoppini, Monica; Rossi, Antonio; Fogolari, F; Corazza, A; Esposito, G; Gliozzi, A; Bellotti, Vittorio
Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family. 1-gen-2006 Lupi, ANNA LISA; Rossi, Antonio; Campari, Elena; Pecora, Fabio; Lund, A. M.; Elcioglu, N. h.; Gultepe, M.; Di Rocco, M.; Cetta, Giuseppe; Forlino, Antonella
In vivo contribution of amino acid sulfur to cartilage proteoglycan sulfation. 1-gen-2006 Pecora, Fabio; Gualeni, Benedetta; Forlino, Antonella; SUPERTI FURGA, A.; Tenni, Ruggero; Cetta, Giuseppe; Rossi, Antonio
Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies. 1-gen-2006 Lupi, Anna; Della Torre, S.; Campari, Elena; Tenni, Ruggero; Cetta, Giuseppe; Rossi, Antonio; Forlino, Antonella
Ultrastructural aspects of cartilage histogenesis in a model of chondrodysplasia 1-gen-2007 ICARO CORNAGLIA, Antonia; Casasco, Marco; Riva, Federica; Gualeni, B.; Necchi, Vittorio; Farina, Aurora; Giannella, PAOLA ANTONIA; Rossi, Antonio
Methionine sulfoxide reductase enzymes (Msr): a comparative analysis of the levels of expression in human blood cells 1-gen-2007 Achilli, Cesare; Ciana, Annarita; Rossi, Antonio; Balduini, Cesare; Minetti, Giampaolo
Comparative analysis of the expression of methionine sulfoxide reductase enzymes in human blood cells 1-gen-2007 Achilli, Cesare; Ciana, Annarita; Rossi, Antonio; Balduini, Cesare; Minetti, Giampaolo
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
Differential expression of both extracellular and intracellular proteins is involved in the lethal or nonlethal phenotypic variation of BrtlIV, a murine model for osteogenesis imperfecta 1-gen-2007 Forlino, Antonella; Tani, C.; Rossi, Antonio; Lupi, ANNA LISA; Campari, Elena; Gualeni, Benedetta; Bianchi, L.; Armini, A.; Cetta, Giuseppe; Bini, L.; Marini, J. C.
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
Heparin strongly enhances the formation of beta 2-microglobulin amyloid fibrils in the presence of type I collagen 1-gen-2008 Relini, A.; De Stefano, S.; Torrassa, S.; Cavalleri, O.; Rolandi, R.; Gliozzi, A.; Giorgetti, Sofia; Raimondi, Sara; Marchese, Loredana; Verga, L.; Rossi, Antonio; Stoppini, Monica; Bellotti, Vittorio
Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis. 1-gen-2008 Hermanns, P; Unger, S; Rossi, Antonio; Perez Aytes, A; Cortina, H; Bonafé, L; Boccone, L; Setzu, V; Dutoit, M; Sangiorgi, L; Pecora, Fabio; Reicherter, K; Nishimura, G; Spranger, J; Zabel, B; Superti Furga, A.
Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations 1-gen-2008 Lupi, ANNA LISA; Tenni, Ruggero; Rossi, Antonio; Cetta, Giuseppe; Forlino, Antonella
Neutrophil granulocytes uniquely express, among human blood cells, high levels of Methionine-sulfoxide-reductase enzymes. 1-gen-2008 Achilli, Cesare; Ciana, Annarita; Rossi, Antonio; Balduini, Cesare; Minetti, Giampaolo
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