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Plos One|February 21, 2013
Myotonia congenita mutation enhances the degradation of human CLC-1 chloride channelsTing-Ting Lee, Xiao-Dong Zhang, Chao-Chin Chuang, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|May 21, 2016
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis PigmentosaWen-Hsuan Wu, Yi-Ting Tsai, Sally Justus, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 29, 2020
PKM2 ablation enhanced retinal function and survival in a preclinical model of retinitis pigmentosaEthan Zhang, Joseph Ryu, Sarah R Levi, et al.Journal of Virology|October 29, 2005
Assembly of severe acute respiratory syndrome coronavirus RNA packaging signal into virus-like particles is nucleocapsid dependentPing-Kun Hsieh, Shin C Chang, Chu-Chun Huang, et al.Molecular Cell|May 19, 2018
C-Terminal End-Directed Protein Elimination by CRL2 Ubiquitin LigasesHsiu-Chuan Lin, Chi-Wei Yeh, Yen-Fu Chen, et al.Ophthalmology|May 16, 2018
Clustered Regularly Interspaced Short Palindromic Repeats-Based Genome Surgery for the Treatment of Autosomal Dominant Retinitis PigmentosaYi-Ting Tsai, Wen-Hsuan Wu, Ting-Ting Lee, et al.Nature Cell Biology|March 27, 2025
Proteostasis and lysosomal repair deficits in transdifferentiated neurons of Alzheimer's diseaseChing-Chieh Chou, Ryan Vest, Miguel A Prado, et al.Biorxiv : the Preprint Server for Biology|April 10, 2023
Proteostasis and lysosomal repair deficits in transdifferentiated neurons of Alzheimer's diseaseChing-Chieh Chou, Ryan Vest, Miguel A Prado, et al.Research Square|June 10, 2024
Human tNeurons reveal aging-linked proteostasis deficits driving Alzheimer's phenotypesChing-Chieh Chou, Ryan Vest, Miguel A Prado, et al.Science (New York, N.Y.)|October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiCFlorian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.Pageof 10