IRIS

Sfoglia per Autore  

Opzioni
Mostrati risultati da 21 a 40 di 117
Titolo Data di pubblicazione Autore(i) File
Molecular stability of chemically modified collagen triple helices 1-gen-2003 Giudici, Camilla; Viola, Manuela; Tira, MARIA ENRICA; Forlino, Antonella; Tenni, Ruggero
Optimization of a capillary electrophoretic method to detect and quantify the Gly-Pro dipeptide in complex matrices from long term cultured prolidase deficiency fibroblasts 1-gen-2003 Lupi, ANNA LISA; DELLA TORRE, Sara; Rossi, Antonio; Cetta, Giuseppe; Forlino, Antonella
Effect of enamel matrix derivative on human periodontal fibroblasts: proliferation, morphology and root surface colonization. An in vitro study 1-gen-2003 Cattaneo, Vitaliano; Rota, C.; Silvestri, M.; Piacentini, Cesare; Forlino, Antonella; Gallanti, Angelo; Rasperini, G.; Cetta, Giuseppe
Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship. 1-gen-2004 Lupi, ANNA LISA; De Riso, A; DELLA TORRE, Sara; Rossi, Antonio; Campari, Elena; Vilarinho, L; Cetta, Giuseppe; Forlino, Antonella
Prolidase Deficiency: case reports of two Argentinian brothers. 1-gen-2004 Cabrera, Hn; Giovanna, Pd; Bozzini, Nf; Forlino, Antonella
Structure, stability and interactions of type I collagen with GLY349-CYS substitution in alpha 1(I) chain in a murine Osteogenesis Imperfecta model. 1-gen-2004 Kuznetsova, N. V.; Forlino, Antonella; Cabral, W. A.; Marini, J. C.; Leikin, S.
Brittle IV Mouse Model for Osteogenesis imperfecta IV Demonstrates Postpubertal Adaptations to Improve Whole Bone Strength. 1-gen-2004 Kozloff, K. M.; Carden, A.; Bergwitz, C.; Forlino, Antonella; Uveges, T.; Morris, M. D.; Marini, J. C.; Goldstein, S. A.
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
N-benzyloxycarbonyl-L-proline: an in vitro inhibitor of prolidase. 1-gen-2005 Lupi, ANNA LISA; Rossi, Antonio; Vaghi, Patrizia; Gallanti, Angelo; Cetta, Giuseppe; Forlino, Antonella
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
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
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
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
Systemic lupus erythematosus-like disease in a 6-year-old boy with prolidase deficiency 1-gen-2007 DI ROCCO, M.; Fantasia, A. R.; Taro, M.; Loy, A.; Forlino, Antonella; Martini, A.
Selective retention and degradation of molecules with a single mutant alpha1(I) chain in the Brtl IV mouse model of OI 1-gen-2007 Forlino, Antonella; Kuznetsova, N. V.; Marini, Jc; Leikin, S.
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 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
Consortium of Osteogenesis Imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans. 1-gen-2007 Marini, Jc; Forlino, Antonella; Cabral, Wa; Barnes, Am; SAN ANTONIO, Jd; Milgrom, S; Hyland, Jc; Korkko, J; Prockop, Dj; DE PAEPE, A; Coucke, P; Symoens, S; Glorieux, Fh; Roughley, Pj; Lund, Am; KUURILA SVAHN, K; Hartikka, H; Cohn, Dh; Krakow, D; Mottes, M; Schwarze, U; Chen, D; Yang, K; Kuslich, C; Troendle, J; Dalgleish, R; Byers, Ph
HEM dysplasia and ichthyosis are likely laminopathies and not due to 3beta-hydroxysterol Delta14-reductase deficiency. 1-gen-2007 Wassif, Ca; Brownson, Ke; Sterner, Al; Forlino, Antonella; Zerfaspm, ; Wilson, Wk; Starostmf, ; Porter, Fd
Mostrati risultati da 21 a 40 di 117
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile