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A nonhuman primate model of inherited retinal disease.
Moshiri A, Chen R, Kim S, Harris RA, Li Y, Raveendran M, Davis S, Liang Q, Pomerantz O, Wang J, Garzel L, Cameron A, Yiu G, Stout JT, Huang Y, Murphy CJ, Roberts J, Gopalakrishna KN, Boyd K, Artemyev NO, Rogers J, Thomasy SM. Moshiri A, et al. Among authors: wang j. J Clin Invest. 2019 Feb 1;129(2):863-874. doi: 10.1172/JCI123980. Epub 2019 Jan 22. J Clin Invest. 2019. PMID: 30667376 Free PMC article.
Correlation of Outer Retinal Degeneration and Choriocapillaris Loss in Stargardt Disease Using En Face Optical Coherence Tomography and Optical Coherence Tomography Angiography.
Alabduljalil T, Patel RC, Alqahtani AA, Gao SS, Gale MJ, Zhang M, Jia Y, Huang D, Chiang PW, Chen R, Wang J, Weleber RG, Pennesi ME, Yang P. Alabduljalil T, et al. Among authors: wang j. Am J Ophthalmol. 2019 Jun;202:79-90. doi: 10.1016/j.ajo.2019.02.007. Epub 2019 Feb 14. Am J Ophthalmol. 2019. PMID: 30771335 Free PMC article.
Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy.
Bertrand RE, Wang J, Xiong KH, Thangavel C, Qian X, Ba-Abbad R, Liang Q, Simões RT, Sampaio SAM, Carss KJ, Lucy Raymond F, Robson AG, Webster AR, Arno G, Porto FBO, Chen R. Bertrand RE, et al. Among authors: wang j. Genet Med. 2021 Mar;23(3):488-497. doi: 10.1038/s41436-020-01003-x. Epub 2020 Oct 20. Genet Med. 2021. PMID: 33077892 Free PMC article.
Transcript isoforms of Reep6 have distinct functions in the retina.
Liang Q, Wu N, Zaneveld S, Liu H, Fu S, Wang K, Bertrand R, Wang J, Li Y, Chen R. Liang Q, et al. Among authors: wang k, wang j. Hum Mol Genet. 2021 Oct 13;30(21):1907-1918. doi: 10.1093/hmg/ddab157. Hum Mol Genet. 2021. PMID: 34104971 Free PMC article.
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