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Cell Communication and Signaling : CCS|November 28, 2024
Pin1 promotes human CaV2.1 channel polyubiquitination by RNF138: pathophysiological implication for episodic ataxia type 2Ssu-Ju Fu, Kai-Min Cheng, Cheng-Tsung Hsiao, et al.Cellular and Molecular Life Sciences : CMLS|April 28, 2025
Restoration of Shal/KV4 proteostasis and motor function in a Drosophila model of spinocerebellar ataxia type 19/22Cheng-Tsung Hsiao, Ssu-Ju Fu, Kai-Min Cheng, et al.Frontiers in Neurology|March 3, 2020
Defective Gating and Proteostasis of Human ClC-1 Chloride Channel: Molecular Pathophysiology of Myotonia CongenitaChung-Jiuan Jeng, Ssu-Ju Fu, Chia-Ying You, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|August 28, 2022
Clinical and genetic characterization of NEFL-related neuropathy in TaiwanHua-Chuan Chao, Cheng-Tsung Hsiao, Kuan-Lin Lai, et al.Neurology. Genetics|April 29, 2016
Spinocerebellar ataxia type 36 in the Han ChineseYi-Chung Lee, Pei-Chien Tsai, Yuh-Cherng Guo, et al.Annals of Clinical and Translational Neurology|June 5, 2024
Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegiaCheng-Tsung Hsiao, Tzu-Yun Tsai, Ting-Yi Shen, et al.Scientific Reports|November 12, 2017
Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited NeuropathyYi-Chu Liao, Pei-Chien Tsai, Thy-Sheng Lin, et al.International Journal of Molecular Sciences|June 2, 2021
Regulation of ClC-2 Chloride Channel Proteostasis by Molecular Chaperones: Correction of Leukodystrophy-Associated DefectSsu-Ju Fu, Meng-Chun Hu, Cheng-Tsung Hsiao, et al.Human Mutation|July 12, 2019
Novel SCA19/22-associated KCND3 mutations disrupt human KV 4.3 protein biosynthesis and channel gatingCheng-Tsung Hsiao, Ssu-Ju Fu, Yo-Tsen Liu, et al.Parkinsonism & Related Disorders|October 14, 2021
Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotypeShao-Lun Hsu, Ying-Hao Chen, Cheng-Ta Chou, et al.Pageof 4