TA-NMT-0116-0692-COLU/FFB/Foundation Fighting Blindness/United States[Grants and Funding] - Search Results

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Comparative Analysis of Functional and Structural Decline in Retinitis Pigmentosas.

Cabral T, Lima de Carvalho JR Jr, Kim J, Oh JK, Levi SR, Park KS, Duong JK, Park J, Boudreault K, Belfort R Jr, Tsang SH. Cabral T, et al. Int J Mol Sci. 2020 Apr 15;21(8):2730. doi: 10.3390/ijms21082730. Int J Mol Sci. 2020. PMID: 32326409 Free PMC article.

Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy.

Soucy M, Kolesnikova M, Kim AH, Tsang SH. Soucy M, et al. Doc Ophthalmol. 2023 Jun;146(3):267-272. doi: 10.1007/s10633-022-09916-5. Epub 2023 Jan 7. Doc Ophthalmol. 2023. PMID: 36609934

Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a Rho^D190N mutation.

Sancho-Pelluz J, Cui X, Lee W, Tsai YT, Wu WH, Justus S, Washington I, Hsu CW, Park KS, Koch S, Velez G, Bassuk AG, Mahajan VB, Lin CS, Tsang SH. Sancho-Pelluz J, et al. Cell Mol Life Sci. 2019 Sep;76(18):3657-3665. doi: 10.1007/s00018-019-03090-9. Epub 2019 Apr 11. Cell Mol Life Sci. 2019. PMID: 30976840 Free PMC article.

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