Retinal Degeneration

Displaying 1 - 15 of 15CSV
Fu, C., Yang, N., Chuang, J.-Z., Nakajima, N., Iraha, S., Roy, N., Wu, Z., Jiang, Z., Otsu, W., Radu, R. A., Yang, H. H., Lee, M. P., Worgall, T. S., Xiong, W.-C., & Sung, C.-H. (2024). Mutant mice with rod-specific VPS35 deletion exhibit retinal α-synuclein pathology-associated degeneration. Nature Communications, 15(1). https://doi.org/10.1038/s41467-024-50189-0
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Wu, J.-H., Moghimi, S., Walker, E., Nishida, T., Brye, N., Mahmoudinezhad, G., Liebmann, J. M., Fazio, M., Girkin, C. A., Zangwill, L. M., & Weinreb, R. N. (2024). Time to Glaucoma Progression Detection by Optical Coherence Tomography in Individuals of African and European Descents. American Journal of Ophthalmology, 260, 60–69. https://doi.org/10.1016/j.ajo.2023.12.002
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Chang, Y.-H., Kang, E. Y.-C., Liu, L., Jenny, L. A., Khang, R., Seo, G. H., Lee, H., Chen, K.-J., Wu, W.-C., Hsiao, M.-C., & Wang, N.-K. (2023). Maternal mosaicism in SSBP1 causing optic atrophy with retinal degeneration: implications for genetic counseling. Orphanet Journal of Rare Diseases, 18(1). https://doi.org/10.1186/s13023-023-02748-9
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Lin, T.-Y., Wu, P.-L., Kang, E. Y.-C., Chi, Y.-C., Jenny, L. A., Lin, P.-H., Lee, C.-Y., Liu, C.-H., Liu, L., Yeh, L.-K., Chen, K.-J., Hwang, Y.-S., Wu, W.-C., Lai, C.-C., Hsiao, M.-C., Liu, P.-K., & Wang, N.-K. (2023). Clinical Characteristics and Genetic Variants in Taiwanese Patients With PROM1-Related Inherited Retinal Disorders. Investigative Opthalmology & Visual Science, 64(14), 25. https://doi.org/10.1167/iovs.64.14.25
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Wu, J.-H., Moghimi, S., Walker, E., Nishida, T., Liebmann, J. M., Fazio, M., Girkin, C. A., Zangwill, L. M., & Weinreb, R. N. (2023). Clinical Factors Associated With Long-Term OCT Variability in Glaucoma. American Journal of Ophthalmology, 255, 98–106. https://doi.org/10.1016/j.ajo.2023.07.011
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da Costa, B. L., Jenny, L. A., Maumenee, I. H., Tsang, S. H., & Quinn, P. M. J. (2023). Analysis of CRB1 Pathogenic Variants Correctable with CRISPR Base and Prime Editing. Retinal Degenerative Diseases XIX, 103–107. https://doi.org/10.1007/978-3-031-27681-1_16
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Caruso, S. M., Tsai, Y.-T., da Costa, B. L., Kolesnikova, M., Jenny, L. A., Tsang, S. H., & Quinn, P. M. J. (2023). Prime Editing Strategy to Install the PRPH2 c.828+1G>A Mutation. Retinal Degenerative Diseases XIX, 97–102. https://doi.org/10.1007/978-3-031-27681-1_15
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Kolesnikova, M., Lima de Carvalho, J. R., Parmann, R., Kim, A. H., Mahajan, V. B., Tsang, S. H., & Sparrow, J. R. (2022). Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence. Molecular Genetics & Genomic Medicine, 10(11). Portico. https://doi.org/10.1002/mgg3.2038
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Wang, Y., Ma, X., Muthuraman, P., Raja, A., Jayaraman, A., Petrukhin, K., Cioffi, C. L., Ma, J.-X., & Moiseyev, G. (2022). The novel visual cycle inhibitor (±)-RPE65-61 protects retinal photoreceptors from light-induced degeneration. PLOS ONE, 17(10), e0269437. https://doi.org/10.1371/journal.pone.0269437
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Verra, D. M., Spinnhirny, P., Sandu, C., Grégoire, S., Acar, N., Berdeaux, O., Brétillon, L., Sparrow, J. R., & Hicks, D. (2022). Intrinsic differences in rod and cone membrane composition: implications for cone degeneration. Graefe’s Archive for Clinical and Experimental Ophthalmology, 260(10), 3131–3148. https://doi.org/10.1007/s00417-022-05684-9
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Avrutsky, M. I., Lawson, J. M., Smart, J. E., Chen, C. W., & Troy, C. M. (2022). Noninvasive Ophthalmic Imaging Measures Retinal Degeneration and Vision Deficits in Ndufs4−/− Mouse Model of Mitochondrial Complex I Deficiency. Translational Vision Science & Technology, 11(8), 5. https://doi.org/10.1167/tvst.11.8.5
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Cui, X., Kim, H. J., Cheng, C.-H., Jenny, L. A., Lima de Carvalho, J. R., Chang, Y.-J., Kong, Y., Hsu, C.-W., Huang, I.-W., Ragi, S. D., Lin, C.-S., Li, X., Sparrow, J. R., & Tsang, S. H. (2022). Long-term vitamin A supplementation in a preclinical mouse model forRhoD190N-associated retinitis pigmentosa. Human Molecular Genetics, 31(14), 2438–2451. https://doi.org/10.1093/hmg/ddac032
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Wu, W.-H., Tsai, Y.-T., Huang, I.-W., Cheng, C.-H., Hsu, C.-W., Cui, X., Ryu, J., Quinn, P. M. J., Caruso, S. M., Lin, C.-S., & Tsang, S. H. (2022). CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa. Molecular Therapy, 30(4), 1407–1420. https://doi.org/10.1016/j.ymthe.2022.02.010
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Nolan, N. D., Caruso, S. M., Cui, X., & Tsang, S. H. (2022). Renormalization of metabolic coupling treats age-related degenerative disorders: an oxidative RPE niche fuels the more glycolytic photoreceptors. Eye, 36(2), 278–283. https://doi.org/10.1038/s41433-021-01726-4
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