Di Iorio E - Search Results

1

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.

Melchionda S, Ahituv N, Bisceglia L, Sobe T, Glaser F, Rabionet R, Arbones ML, Notarangelo A, Di Iorio E, Carella M, Zelante L, Estivill X, Avraham KB, Gasparini P. Melchionda S, et al. Among authors: di iorio e. Am J Hum Genet. 2001 Sep;69(3):635-40. doi: 10.1086/323156. Epub 2001 Jul 20. Am J Hum Genet. 2001. PMID: 11468689 Free PMC article.

2

A new locus (DFNA47) for autosomal dominant non-syndromic inherited hearing loss maps to 9p21-22 in a large Italian family.

D'Adamo P, Donaudy F, D'Eustacchio A, Di Iorio E, Melchionda S, Gasparini P. D'Adamo P, et al. Among authors: di iorio e. Eur J Hum Genet. 2003 Feb;11(2):121-4. doi: 10.1038/sj.ejhg.5200929. Eur J Hum Genet. 2003. PMID: 12634859

3

Hearing loss: frequency and functional studies of the most common connexin26 alleles.

D'Andrea P, Veronesi V, Bicego M, Melchionda S, Zelante L, Di Iorio E, Bruzzone R, Gasparini P. D'Andrea P, et al. Among authors: di iorio e. Biochem Biophys Res Commun. 2002 Aug 23;296(3):685-91. doi: 10.1016/s0006-291x(02)00891-4. Biochem Biophys Res Commun. 2002. PMID: 12176036

4

Expression of VSX1 in human corneal keratocytes during differentiation into myofibroblasts in response to wound healing.

Barbaro V, Di Iorio E, Ferrari S, Bisceglia L, Ruzza A, De Luca M, Pellegrini G. Barbaro V, et al. Among authors: di iorio e. Invest Ophthalmol Vis Sci. 2006 Dec;47(12):5243-50. doi: 10.1167/iovs.06-0185. Invest Ophthalmol Vis Sci. 2006. PMID: 17122109

5

A novel de novo missense mutation in TP63 underlying germline mosaicism in AEC syndrome: implications for recurrence risk and prenatal diagnosis.

Barbaro V, Nardiello P, Castaldo G, Willoughby CE, Ferrari S, Ponzin D, Amato F, Bonifazi E, Parekh M, Calistri A, Parolin C, Di Iorio E. Barbaro V, et al. Among authors: di iorio e. Am J Med Genet A. 2012 Aug;158A(8):1957-61. doi: 10.1002/ajmg.a.35414. Epub 2012 Jun 27. Am J Med Genet A. 2012. PMID: 22740388

6

Isoforms of DeltaNp63 and the migration of ocular limbal cells in human corneal regeneration.

Di Iorio E, Barbaro V, Ruzza A, Ponzin D, Pellegrini G, De Luca M. Di Iorio E, et al. Proc Natl Acad Sci U S A. 2005 Jul 5;102(27):9523-8. doi: 10.1073/pnas.0503437102. Epub 2005 Jun 27. Proc Natl Acad Sci U S A. 2005. PMID: 15983386 Free PMC article.

7

Reconstruction of a human hemicornea through natural scaffolds compatible with the growth of corneal epithelial stem cells and stromal keratocytes.

Barbaro V, Ferrari S, Fasolo A, Ponzin D, Di Iorio E. Barbaro V, et al. Among authors: di iorio e. Mol Vis. 2009 Oct 17;15:2084-93. Mol Vis. 2009. PMID: 19862337 Free PMC article.

8

Q-FIHC: quantification of fluorescence immunohistochemistry to analyse p63 isoforms and cell cycle phases in human limbal stem cells.

Di Iorio E, Barbaro V, Ferrari S, Ortolani C, De Luca M, Pellegrini G. Di Iorio E, et al. Microsc Res Tech. 2006 Dec;69(12):983-91. doi: 10.1002/jemt.20375. Microsc Res Tech. 2006. PMID: 16972233

9

C/EBPdelta regulates cell cycle and self-renewal of human limbal stem cells.

Barbaro V, Testa A, Di Iorio E, Mavilio F, Pellegrini G, De Luca M. Barbaro V, et al. Among authors: di iorio e. J Cell Biol. 2007 Jun 18;177(6):1037-49. doi: 10.1083/jcb.200703003. Epub 2007 Jun 11. J Cell Biol. 2007. PMID: 17562792 Free PMC article.

10

Evaluation of ocular surface disorders: a new diagnostic tool based on impression cytology and confocal laser scanning microscopy.

Barbaro V, Ferrari S, Fasolo A, Pedrotti E, Marchini G, Sbabo A, Nettis N, Ponzin D, Di Iorio E. Barbaro V, et al. Among authors: di iorio e. Br J Ophthalmol. 2010 Jul;94(7):926-32. doi: 10.1136/bjo.2009.164152. Epub 2009 Sep 8. Br J Ophthalmol. 2010. PMID: 19740872

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