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Page 1
The Ercc1-/Δ mouse model of XFE progeroid syndrome undergoes accelerated retinal degeneration.
Narasimhan A, Min SH, Johnson LL, Roehrich H, Cho W, Her TK, Windschitl C, O'Kelly RD, Angelini L, Yousefzadeh MJ, McLoon LK, Hauswirth WW, Robbins PD, Skowronska-Krawczyk D, Niedernhofer LJ. Narasimhan A, et al. Among authors: min sh. Aging Cell. 2025 Mar;24(3):e14419. doi: 10.1111/acel.14419. Epub 2024 Nov 27. Aging Cell. 2025. PMID: 39604117 Free PMC article.
AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy.
Dinculescu A, Stupay RM, Deng WT, Dyka FM, Min SH, Boye SL, Chiodo VA, Abrahan CE, Zhu P, Li Q, Strettoi E, Novelli E, Nagel-Wolfrum K, Wolfrum U, Smith WC, Hauswirth WW. Dinculescu A, et al. Among authors: min sh. PLoS One. 2016 Feb 16;11(2):e0148874. doi: 10.1371/journal.pone.0148874. eCollection 2016. PLoS One. 2016. PMID: 26881841 Free PMC article.
Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.
Scalabrino ML, Boye SL, Fransen KM, Noel JM, Dyka FM, Min SH, Ruan Q, De Leeuw CN, Simpson EM, Gregg RG, McCall MA, Peachey NS, Boye SE. Scalabrino ML, et al. Among authors: min sh. Hum Mol Genet. 2015 Nov 1;24(21):6229-39. doi: 10.1093/hmg/ddv341. Epub 2015 Aug 26. Hum Mol Genet. 2015. PMID: 26310623 Free PMC article.
25 results