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AAV-ie enables safe and efficient gene transfer to inner ear cells.
Tan F, Chu C, Qi J, Li W, You D, Li K, Chen X, Zhao W, Cheng C, Liu X, Qiao Y, Su B, He S, Zhong C, Li H, Chai R, Zhong G. Tan F, et al. Nat Commun. 2019 Aug 19;10(1):3733. doi: 10.1038/s41467-019-11687-8. Nat Commun. 2019. PMID: 31427575 Free PMC article.
Efficient expansion and CRISPR-Cas9-mediated gene correction of patient-derived hepatocytes for treatment of inherited liver diseases.
Zhang K, Wan P, Wang L, Wang Z, Tan F, Li J, Ma X, Cen J, Yuan X, Liu Y, Sun Z, Cheng X, Liu Y, Liu X, Hu J, Zhong G, Li D, Xia Q, Hui L. Zhang K, et al. Among authors: tan f. Cell Stem Cell. 2024 May 13:S1934-5909(24)00177-2. doi: 10.1016/j.stem.2024.04.022. Online ahead of print. Cell Stem Cell. 2024. PMID: 38772378 Free article.
AAV-ie-K558R mediated cochlear gene therapy and hair cell regeneration.
Tao Y, Liu X, Yang L, Chu C, Tan F, Yu Z, Ke J, Li X, Zheng X, Zhao X, Qi J, Lin CP, Chai R, Zhong G, Wu H. Tao Y, et al. Among authors: tan f. Signal Transduct Target Ther. 2022 Apr 22;7(1):109. doi: 10.1038/s41392-022-00938-8. Signal Transduct Target Ther. 2022. PMID: 35449181 Free PMC article.
2,274 results