Sfoglia per Autore
Techniques for culture and assessment of limbal stem cell grafts.
2010 DI IORIO, MARIO VINCENZO; Ferrari, S; Fasolo, A; Böhm, E; Ponzin, D; Barbaro, V.
Different expression levels of MUC1 in conjunctiva and cornea for the assessment of ocular surface disorders.
2010 Barbaro, V; Ferrari, S; Fasolo, A; Pedrotti, E; Marchini, G; Sbabo, A; Nettis, N; Ponzin, D; DI IORIO, MARIO VINCENZO
Reconstruction of a human hemicornea through natural scaffolds compatible with the growth of corneal epithelial stem cells and stromal keratocytes.
2009 Barbaro, V; Ferrari, S; Fasolo, A; Ponzin, D; DI IORIO, MARIO VINCENZO
Advances in corneal surgery and cell therapy: challenges and perspectives for eye banks
2009 S., Ferrari; V., Barbaro; DI IORIO, MARIO VINCENZO; A., Fasolo; D., Ponzin
USE OF SYNTHETIC AND NATURAL SCAFFOLDS TO DEVELOP NEW CLINICAL APPLICATIONS FOR CORNEAL EPITHELIAL STEM CELLS
2008 V., Barbaro; DI IORIO, MARIO VINCENZO; S., Ferrari; D., Ponzin
Correction of laminin-5 deficiency in human epidermal stem cells by transcriptionally targeted retroviral vectors
2008 G., Maruggi; F., Di Nunzio; Cavazza, ; A. Cavazza S., Ferrari; DI IORIO, MARIO VINCENZO; M., Garcia; M., De Luca; G., Pellegrini; M., Del Rio; F., Larcher; F., Mavilio
Custom phototherapeutic keratectomy and autologous fibrin-cultured limbal stem cell autografting: a combined approach.
2008 Vinciguerra, P; Albè, E; Rosetta, P; DI IORIO, MARIO VINCENZO; Pellegrini, G.
Correction of laminin-5 deficiency in human epidermal stem cells by transcriptionally targeted lentiviral vectors.
2008 Di Nunzio, F; Maruggi, G; Ferrari, S; DI IORIO, MARIO VINCENZO; Poletti, V; Garcia, M; Del Rio, M; De Luca, M; Larcher, F; Pellegrini, G; Mavilio, F.
C/EBPdelta regulates cell cycle and self-renewal of human limbal stem cells.
2007 Barbaro, V; Testa, A; DI IORIO, MARIO VINCENZO; Mavilio, F; Pellegrini, G; De Luca, M.
Development of a hemicornea from human primary cell cultures for pharmacotoxicology testing.
2007 Builles, N; Bechetoille, N; Justin, V; André, V; Barbaro, V; DI IORIO, MARIO VINCENZO; Auxenfans, C; Hulmes, Dj; Damour, O.
Q-FIHC: quantification of fluorescence immunohistochemistry to analyse p63 isoforms and cell cycle phases in human limbal stem cells.
2006 DI IORIO, MARIO VINCENZO; Barbaro, V; Ferrari, S; Ortolani, C; De Luca, M; Pellegrini, G.
Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells.
2006 Mavilio, F; Pellegrini, G; Ferrari, S; Di Nunzio, F; DI IORIO, MARIO VINCENZO; Recchia, A; Maruggi, G; Ferrari, G; Provasi, E; Bonini, C; Capurro, S; Conti, A; Magnoni, C; Giannetti, A; De Luca, M.
Expression of VSX1 in human corneal keratocytes during differentiation into myofibroblasts in response to wound healing.
2006 Barbaro, V; DI IORIO, MARIO VINCENZO; Ferrari, S; Bisceglia, L; Ruzza, A; De Luca, M; Pellegrini, G.
Isoforms of DeltaNp63 and the migration of ocular limbal cells in human corneal regeneration.
2005 DI IORIO, MARIO VINCENZO; Barbaro, V; Ruzza, A; Ponzin, D; Pellegrini, G; De Luca, M.
Sordità. Malattie genetiche. Molecole e geni. Diagnosi, prevenzione e terapia.
2004 Gasparini, P; DI IORIO, MARIO VINCENZO; Melchionda, S.
A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family.
2003 D'Adamo, P; Donaudy, F; D'Eustacchio, A; DI IORIO, MARIO VINCENZO; Melchionda, S; Gasparini, P.
Hearing loss: frequency and functional studies of the most common connexin26 alleles.
2002 D'Andrea, P; Veronesi, V; Bicego, M; Melchionda, S; Zelante, L; DI IORIO, MARIO VINCENZO; Bruzzone, R; Gasparini, P.
Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients.
2002 Wattenhofer, M; DI IORIO, MARIO VINCENZO; Rabionet, R; Dougherty, L; Pampanos, A; Schwede, T; Montserrat Sentis, B; Arbones, Ml; Iliades, T; Pasquadibisceglie, A; D'Amelio, M; Alwan, S; Rossier, C; Dahl, Hh; Petersen, Mb; Estivill, X; Gasparini, P; Scott, Hs; Antonarakis, Se
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.
2001 Melchionda, S; Ahituv, N; Bisceglia, L; Sobe, T; Glaser, F; Rabionet, R; Arbones, Ml; Notarangelo, A; DI IORIO, MARIO VINCENZO; Carella, M; Zelante, L; Estivill, X; Avraham, Kb; Gasparini, P.
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