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VALLI, MAURIZIA

VALLI, MAURIZIA  

DIPARTIMENTO DI MEDICINA MOLECOLARE  

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Risultati 1 - 20 di 49 (tempo di esecuzione: 0.029 secondi).
Titolo Data di pubblicazione Autore(i) File
"In vitro" fibril formation of type I collagen from different sources: biochemical and morphological aspects. 1-gen-1986 Valli, Maurizia; Leonardi, L; Strocchi, R; Tenni, Ruggero; Guizzardi, S; Ruggeri, A; Balduini, Cesare
5-METHYL-PYRROLIDINONE CHITOSAN FILMS AS CARRIRERS FOR BUCCAL ADMINISTRATION OF PROTEINS 1-gen-2006 Colonna, Claudia; Genta, Ida; Perugini, Paola; Pavanetto, Franca; Modena, Tiziana; Valli, Maurizia; Muzzarelli, C; Conti, Bice
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 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 specific nanobody prevents amyloidogenesis of D76N β2-microglobulin in vitro and modifies its tissue distribution in vivo 1-gen-2017 Raimondi, Sara; Porcari, Riccardo; Mangione, Palma; Verona, Guglielmo; Marcoux, Julien; Giorgetti, Sofia; Taylor, Graham W.; Ellmerich, Stephan; Ballico, Maurizio; Zanini, Stefano; Pardon, Els; Al Shawi, Raya; Simons, J. Paul; Corazza, Alessandra; Fogolari, Federico; Leri, Manuela; Stefani, Massimo; Bucciantini, Monica; Gillmore, Julian D.; Hawkins, Philip N.; Valli, Maurizia; Stoppini, Monica; Robinson, Carol V.; Steyaert, Jan; Esposito, Gennaro; Bellotti, Vittorio
An in vitro test predictive of bioadhesive properties of chitosan films for buccal application 1-gen-2003 Conti, Bice; Valli, Maurizia; Perugini, Paola; Pavanetto, Franca; Modena, Tiziana; Genta, Ida
Anomalous cysteine in type I collagen. Localisation by chemical cleavage of the protein using 2-nitro-5-thiocyanobenzoic acid and by mismatch analysis of cDNA heteroduplexes. 1-gen-1990 Tenni, Ruggero; Rossi, Antonio; Valli, Maurizia; Mottes, M; Pignatti, Pf; Cetta, Giuseppe
Bioadhesive chitosan films for buccal release of proteins 1-gen-2005 Colonna, Claudia; Conti, Bice; Valli, Maurizia; Perugini, Paola; Pavanetto, Franca; Modena, Tiziana; Genta, Ida
Bioadhesive films for buccal release of proteins 1-gen-2005 Colonna, Claudia; Conti, Bice; Valli, Maurizia; Perugini, Paola; Pavanetto, Franca; Modena, Tiziana
Cardiac valve disease: an unreported feature in Ehlers Danlos syndrome arthrocalasia type? 1-gen-2012 Melis, D.; Cappuccio, G.; Ginocchio, V. M.; Minopoli, G.; Valli, Maurizia
Characterization of protein loaded 5-methyl-pyrrolidinone chitosan films 1-gen-2005 Colonna, Claudia; Conti, Bice; Valli, Maurizia; Perugini, Paola; Pavanetto, Franca; Modena, Tiziana; Muzzarelli, R. A. A.; Genta, Ida
Co-fibrillogenesis of Wild-type and D76N β2-Microglobulin: THE CRUCIAL ROLE OF FIBRILLAR SEEDS 1-gen-2016 Natalello, Antonino; Mangione, Palma; Giorgetti, Sofia; Porcari, Riccardo; Marchese, Loredana; Zorzoli, Irene; Relini, Annalisa; Ami, Diletta; Faravelli, Giulia; Valli, Maurizia; Stoppini, Monica; Doglia, Silvia M; Bellotti, Vittorio; Raimondi, Sara
Cutaneous metaplastic synovial cyst in Ehlers-Danlos syndrome: report of a second case. 1-gen-2008 Guala, A; Viglio, Simona; Ottinetti, A; Angeli, G; Canova, G; Colombo, E; Dardano, F; Danesino, Cesare; Valli, Maurizia
Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix. 1-gen-2012 Valli, Maurizia; Barnes, A; Gallanti, Angelo; Cabral, W; Viglio, Simona; Weis, M; Makareeva, E; Eyre, David; Leikin, S; Antoniazzi, Franco; Marini, Joan; Mottes, Monica
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. 1-gen-1996 Dyne, KATHARINE MARY; Valli, Maurizia; Forlino, Antonella; Mottes, Monica; Kresse, Hans; Cetta, Giuseppe
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. 1-gen-1993 Cetta, Giuseppe; Rossi, Antonio; Tenni, Ruggero; Valli, Maurizia; Forlino, Antonella; Zanaboni, Giuseppe; Dyne, KATHARINE MARY; R., Burgio
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: Clinical findings and novel COL3A1 mutations 1-gen-2011 Bruno, Drera; Nicoletta, Zoppi; Marco, Ritelli; Sergio, Barlati; Marina, Colombi; Gianluca, Tadini; Marina, Venturini; Piergiacomo Calzavara, Pinton; Anita, Wischmeijer; Maria Anna, Nicolazzi; Alfredo, Musumeci; Silvana, Penco; Loredana, Buscemi; Sara, Crivelli; Danesino, Cesare; Maurizio, Clementi; Viglio, Simona; Valli, Maurizia
Dipeptide loaded liposomes in photoaging: evaluation of cellular viability 1-gen-2006 Vettor, MANUELA TERESA; Perugini, Paola; Colonna, Claudia; Conti, Bice; Valli, Maurizia; Genta, Ida; Modena, Tiziana; Pavanetto, Franca
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis 1-gen-1997 G., Zanaboni; Viglio, Simona; K., Dyne; R., Grimm; Valli, Maurizia; Cetta, Giuseppe; Iadarola, Paolo