| CRISPR repair reveals causative mutation in a preclinical model of retinitis pigmentosa WH Wu, YT Tsai, S Justus, TT Lee, L Zhang, CS Lin, AG Bassuk, ... Molecular Therapy 24 (8), 1388-1394, 2016 | 122 | 2016 |
| Clustered regularly interspaced short palindromic repeats-based genome surgery for the treatment of autosomal dominant retinitis pigmentosa YT Tsai, WH Wu, TT Lee, WP Wu, CL Xu, KS Park, X Cui, S Justus, CS Lin, ... Ophthalmology 125 (9), 1421-1430, 2018 | 119 | 2018 |
| Myotonia congenita mutation enhances the degradation of human CLC-1 chloride channels TT Lee, XD Zhang, CC Chuang, JJ Chen, YA Chen, SC Chen, TY Chen, ... PloS one 8 (2), e55930, 2013 | 28 | 2013 |
| Dominantly inherited myotonia congenita resulting from a mutation that increases open probability of the muscle chloride channel CLC-1 DP Richman, Y Yu, TT Lee, PY Tseng, WP Yu, RA Maselli, CY Tang, ... Neuromolecular medicine 14, 328-337, 2012 | 11 | 2012 |
| PKM2 ablation enhanced retinal function and survival in a preclinical model of retinitis pigmentosa JRLCSHT Ethan Zhang, Joseph Ryu, Sarah R. Levi, Jin Kyun Oh,Chun Wei Hsu ... Mammalian Genome 31, 77–85, 2020 | 10 | 2020 |
| Distal end of carboxyl terminus is not essential for the assembly of rat Eag1 potassium channels IH Chen, JH Hu, GM Jow, CC Chuang, TT Lee, DC Liu, CJ Jeng Journal of Biological Chemistry 286 (31), 27183-27196, 2011 | 10 | 2011 |
| Ribotoxic collisions on CAG expansions disrupt proteostasis and stress responses in Huntington’s Disease R Aviner, TT Lee, VB Masto, D Gestaut, KH Li, R Andino, J Frydman BiorXiv, 2022.05. 04.490528, 2022 | 7 | 2022 |
| CRISPR-based genome surgery for the treatment of autosomal dominant retinitis pigmentosa YT Tsai, WH Wu, TT Lee, WP Wu, CL Xu, KS Park, X Cui, S Justus, CS Lin, ... Ophthalmology 125 (9), 1421, 2018 | 6 | 2018 |
| Polyglutamine-mediated ribotoxicity disrupts proteostasis and stress responses in Huntington’s disease R Aviner, TT Lee, VB Masto, KH Li, R Andino, J Frydman Nature Cell Biology, 1-11, 2024 | | 2024 |
