Sfoglia per Autore
Personalized stem cell therapy to correct corneal defects due to a unique homozygous-heterozygous mosaicism of ectrodactyly-ectodermal dysplasia-clefting syndrome
2016 Barbaro, Vanessa; Nasti, ANNAMARIA ASSUNTA; Raffa, Paolo; Migliorati, Angelo; Nespeca, Patrizia; Ferrari, Stefano; Palumbo, Elisa; Bertolin, Marina; Breda, Claudia; Miceli, Francesco; Russo, Antonella; Caenazzo, Luciana; Ponzin, Diego; Palu', Giorgio; Parolin, MARIA CRISTINA; DI IORIO, MARIO VINCENZO
Safety outcomes and long-term effectiveness of ex vivo autologous cultured limbal epithelial transplantation for limbal stem cell deficiency
2016 Adriano, Fasolo; Emilio, Pedrotti; Mattia, Passilongo; Giorgio, Marchini; Cristina, Monterosso; Roberto, Zampini; Elisabetta, Bohm; Federica, Birattari; Antonella, Franch; Vanessa, Barbaro; Marina, Bertolin; Claudia, Breda; DI IORIO, MARIO VINCENZO; Barbara, Ferrari; Stefano, Ferrari; Mauro, Meneguzzi; Diego, Ponzin .
Identification of novel X-linked gain-of-function RPGR-ORF15 mutation in Italian family with retinitis pigmentosa and pathologic myopia
2016 Parmeggiani, Francesco; Barbaro, Vanessa; De Nadai, Katia; Lavezzo, Enrico; Toppo, Stefano; Chizzolini, Marzio; Palu', Giorgio; Parolin, MARIA CRISTINA; DI IORIO, MARIO VINCENZO
Correction of Mutant p63 in EEC Syndrome Using siRNA Mediated Allele-Specific Silencing Restores Defective Stem Cell Function
2016 Barbaro, Vanessa; Nasti, ANNAMARIA ASSUNTA; DEL VECCHIO, Claudia; Ferrari, Stefano; Migliorati, Angelo; Raffa, Paolo; Lariccia, Vincenzo; Nespeca, Patrizia; Biasolo, Mariangela; Willoughby, Colin E.; Ponzin, Diego; Palu', Giorgio; Parolin, MARIA CRISTINA; DI IORIO, MARIO VINCENZO
Visualization of DNA G-quadruplexes in herpes simplex virus 1-infected cells
2016 Artusi, Sara; Perrone, Rosalba; Lago, Sara; Raffa, Paolo; DI IORIO, MARIO VINCENZO; Palu', Giorgio; Richter, Sara
In Vivo Confocal Microscopy 1 Year after Autologous Cultured Limbal Stem Cell Grafts
2015 Pedrotti, E.; Passilongo, M.; Fasolo, A.; Nubile, M.; Parisi, G.; Mastropasqua, R.; Ficial, S.; Bertolin, M.; Di Iorio, E.; Ponzin, D.; Marchini, G.
Dissecting the molecular mechanisms accounting for the Feline Immunodeficiency Virus Envelope Glycoprotein ability to antagonize feline tetherin restriction
2015 Celestino, Michele; Calistri, Arianna; DI IORIO, MARIO VINCENZO; Palu', Giorgio; Parolin, MARIA CRISTINA
Gene transfer of integration defective anti-HSV-1 meganuclease to human corneas ex vivo
2014 H. M., Elbadawy; M., Gailledrat; C., Desseaux; G., Salvalaio; DI IORIO, MARIO VINCENZO; B., Ferrari; M., Bertolin; V., Barbaro; M., Parekh; R., Gayon; Munegato, Denis; Franchin, Elisa; Calistri, Arianna; Palu', Giorgio; Parolin, MARIA CRISTINA; D., Ponzin; S., Ferrari
Gene Therapy approaches for corneal diseases
2013 DI IORIO, MARIO VINCENZO; Vanessa, Barbaro; DEL VECCHIO, Claudia; Mohit, Parekh; Alvisi, Gualtiero; Poletti, Valentina; Palu', Giorgio; Parolin, MARIA CRISTINA
Nuclear Akt2 opposes limbal keratinocyte stem cell self-renewal by repressing a FOXO-mTORC1 signaling pathway.
2013 Saoncella, S; Tassone, B; Deklic, E; Avolio, F; Jon, C; Tornillo, G; De Luca, E; DI IORIO, MARIO VINCENZO; Piva, R; Cabodi, S; Turco, E; Pandolfi, Pp; Calautti, E.
Laser Scanning Confocal Microscopy: Application in Manufacturing and Research of Corneal Stem Cells
2013 V., Barbaro; S., Ferrari; M., Parekh; D., Ponzin; Parolin, MARIA CRISTINA; DI IORIO, MARIO VINCENZO
Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations.
2012 DI IORIO, MARIO VINCENZO; Kaye, Sb; Ponzin, D; Barbaro, V; Ferrari, S; Böhm, E; Nardiello, P; Castaldo, G; Mcgrath, Ja; Willoughby, Ce
Targeting corneal disorders using gene therapy
2012 M., Parekh; S., Ferrari; DI IORIO, MARIO VINCENZO; V., Barbrao; M., Bertolin; B., Ferrari; D., Ponzin
Long-term effectiveness of autologous cultured limbal stem cell grafts in patients with limbal stem cell deficiency due to chemical burns.
2012 Marchini, G; Pedrotti, E; Pedrotti, M; Barbaro, V; DI IORIO, MARIO VINCENZO; Ferrari, S; Bertolin, M; Ferrari, B; Passilongo, M; Fasolo, A; Ponzin, D.
Development of an allele-specific real-time PCR assay for discrimination and quantification of p63 R279H mutation in EEC syndrome.
2012 Barbaro, V; Confalonieri, L; Vallini, I; Ferrari, S; Ponzin, D; Mantero, G; Willoughby, Ce; Parekh, M; DI IORIO, MARIO VINCENZO
A Simplified Technique for In situ Excision of Cornea and Evisceration of Retinal Tissue from Human Ocular Globe.
2012 Parekh, M; Ferrari, S; DI IORIO, MARIO VINCENZO; Barbaro, V; Camposampiero, D; Karali, M; Ponzin, D; Salvalaio, G.
A novel de novo missense mutation in TP63 underlying germline mosaicism in AEC syndrome: implications for recurrence risk and prenatal diagnosis
2012 Barbaro, V; Nardiello, P; Castaldo, G; Willoughby, Ce; Ferrari, S; Ponzin, D; Amato, F; Bonifazi, E; Parekh, M; Calistri, Arianna; Parolin, MARIA CRISTINA; DI IORIO, MARIO VINCENZO
Retinitis pigmentosa: genes and disease mechanisms.
2011 Ferrari, S; DI IORIO, MARIO VINCENZO; Barbaro, V; Ponzin, D; Sorrentino, Fs; Parmeggiani, F.
Localization and expression of CHST6 and keratan sulfate proteoglycans in the human cornea.
2010 DI IORIO, MARIO VINCENZO; Barbaro, V; Volpi, N; Bertolin, M; Ferrari, B; Fasolo, A; Arnaldi, R; Brusini, P; Prosdocimo, G; Ponzin, D; Ferrari, S.
Evaluation of ocular surface disorders: a new diagnostic tool based on impression cytology and confocal laser scanning microscopy.
2010 Barbaro, V; Ferrari, S; Fasolo, A; Pedrotti, E; Marchini, G; Sbabo, A; Nettis, N; Ponzin, D; DI IORIO, MARIO VINCENZO
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