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Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss.
Terrinoni A, Codispoti A, Serra V, Bruno E, Didona B, Paradisi M, Nisticò S, Campione E, Napolitano B, Diluvio L, Melino G. Terrinoni A, et al. Among authors: bruno e. Biochem Biophys Res Commun. 2010 Apr 23;395(1):25-30. doi: 10.1016/j.bbrc.2010.03.098. Epub 2010 Mar 20. Biochem Biophys Res Commun. 2010. PMID: 20307501
Role of p63 and the Notch pathway in cochlea development and sensorineural deafness.
Terrinoni A, Serra V, Bruno E, Strasser A, Valente E, Flores ER, van Bokhoven H, Lu X, Knight RA, Melino G. Terrinoni A, et al. Among authors: bruno e. Proc Natl Acad Sci U S A. 2013 Apr 30;110(18):7300-5. doi: 10.1073/pnas.1214498110. Epub 2013 Apr 15. Proc Natl Acad Sci U S A. 2013. PMID: 23589895 Free PMC article.
Role of the TAp63 Isoform in Recurrent Nasal Polyps.
Terrinoni A, Palombo R, Pitolli C, Caporali S, De Berardinis R, Ciccarone S, Lanzillotta A, Mauramati S, Porta G, Minieri M, Melino G, Bernardini S, Bruno E. Terrinoni A, et al. Among authors: bruno e. Folia Biol (Praha). 2019;65(4):170-180. doi: 10.14712/fb2019065040170. Folia Biol (Praha). 2019. PMID: 31903890 Free article.
533 results