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miR-181a/b downregulation: a mutation-independent therapeutic approach for inherited retinal diseases.
Carrella S, Di Guida M, Brillante S, Piccolo D, Ciampi L, Guadagnino I, Garcia Piqueras J, Pizzo M, Marrocco E, Molinari M, Petrogiannakis G, Barbato S, Ezhova Y, Auricchio A, Franco B, De Leonibus E, Surace EM, Indrieri A, Banfi S. Carrella S, et al. Among authors: surace em. EMBO Mol Med. 2022 Nov 8;14(11):e15941. doi: 10.15252/emmm.202215941. Epub 2022 Oct 4. EMBO Mol Med. 2022. PMID: 36194668 Free PMC article.
Inhibition of ocular neovascularization by hedgehog blockade.
Surace EM, Balaggan KS, Tessitore A, Mussolino C, Cotugno G, Bonetti C, Vitale A, Ali RR, Auricchio A. Surace EM, et al. Mol Ther. 2006 Mar;13(3):573-9. doi: 10.1016/j.ymthe.2005.10.010. Epub 2005 Dec 15. Mol Ther. 2006. PMID: 16343995 Free article.
Novel adeno-associated virus serotypes efficiently transduce murine photoreceptors.
Allocca M, Mussolino C, Garcia-Hoyos M, Sanges D, Iodice C, Petrillo M, Vandenberghe LH, Wilson JM, Marigo V, Surace EM, Auricchio A. Allocca M, et al. Among authors: surace em. J Virol. 2007 Oct;81(20):11372-80. doi: 10.1128/JVI.01327-07. Epub 2007 Aug 15. J Virol. 2007. PMID: 17699581 Free PMC article.
Versatility of AAV vectors for retinal gene transfer.
Surace EM, Auricchio A. Surace EM, et al. Vision Res. 2008 Feb;48(3):353-9. doi: 10.1016/j.visres.2007.07.027. Epub 2007 Oct 17. Vision Res. 2008. PMID: 17923143 Free article. Review.
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration.
Simonelli F, Maguire AM, Testa F, Pierce EA, Mingozzi F, Bennicelli JL, Rossi S, Marshall K, Banfi S, Surace EM, Sun J, Redmond TM, Zhu X, Shindler KS, Ying GS, Ziviello C, Acerra C, Wright JF, McDonnell JW, High KA, Bennett J, Auricchio A. Simonelli F, et al. Among authors: surace em. Mol Ther. 2010 Mar;18(3):643-50. doi: 10.1038/mt.2009.277. Epub 2009 Dec 1. Mol Ther. 2010. PMID: 19953081 Free PMC article. Clinical Trial.
63 results