E
Enzo Di Iorio
Researcher at University of Padua
Publications - 45
Citations - 2849
Enzo Di Iorio is an academic researcher from University of Padua. The author has contributed to research in topics: Stem cell & Cornea. The author has an hindex of 18, co-authored 43 publications receiving 2499 citations.
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Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells
Fulvio Mavilio,Graziella Pellegrini,Stefano Ferrari,Francesca Di Nunzio,Enzo Di Iorio,Alessandra Recchia,Giulietta Maruggi,Giuliana Ferrari,Elena Provasi,Chiara Bonini,Sergio Capurro,Andrea Conti,Cristina Magnoni,Alberto Giannetti,Michele De Luca +14 more
TL;DR: Ex vivo gene therapy of JEB is feasible and leads to full functional correction of the disease, and retroviral integration site analysis indicated that the regenerated epidermis is maintained by a defined repertoire of transduced stem cells.
Journal ArticleDOI
Retinitis Pigmentosa: Genes and Disease Mechanisms
Francesco Parmeggiani,Francesco Sorrentino,Diego Ponzin,Vanessa Barbaro,Stefano Ferrari,Enzo Di Iorio +5 more
TL;DR: Which genes are involved in the genesis of RP and how mutations can lead to retinal degeneration are reviewed to reveal important information with respect to the likelihood of disease development and choices of therapy.
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Isoforms of ΔNp63 and the migration of ocular limbal cells in human corneal regeneration
Enzo Di Iorio,Vanessa Barbaro,Alessandro Ruzza,Diego Ponzin,Graziella Pellegrini,Michele De Luca +5 more
TL;DR: The concept that the alpha isoform of p63 is necessary for the maintenance of the proliferative potential of limbal stem cells and their ability to migrate over the cornea is supported.
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MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss
Salvatore Melchionda,Nadav Ahituv,Luigi Bisceglia,Tama Sobe,Fabian Glaser,Raquel Rabionet,Maria L. Arbonés,Angelo Notarangelo,Enzo Di Iorio,Massimo Carella,Leopoldo Zelante,Xavier Estivill,Karen B. Avraham,Paolo Gasparini +13 more
TL;DR: The mapping of a new deafness locus, DFNA22, on chromosome 6q13 in a family affected by a nonsyndromic dominant form of deafness (NSAD), and the subsequent identification of a missense mutation in the MYO6 gene in all members of the family with hearing loss are described.
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C/EBPδ regulates cell cycle and self-renewal of human limbal stem cells
Vanessa Barbaro,Anna Testa,Enzo Di Iorio,Fulvio Mavilio,Graziella Pellegrini,Michele De Luca +5 more
TL;DR: In this paper, CCAAT enhancer binding protein δ (C/EBPδ), Bmi1, and ΔNp63α identifies mitotically quiescent limbal stem cells, which generate holoclones in culture.