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Scientific Reports|January 19, 2016
The episodic ataxia type 1 mutation I262T alters voltage-dependent gating and disrupts protein biosynthesis of human Kv1.1 potassium channelsSzu-Han Chen, Ssu-Ju Fu, Jing-Jia Huang, et al.
Acta Neurologica Taiwanica|June 16, 2025
Intrafamilial Phenotypic Variation in Taiwanese Patients with Hereditary Spastic Paraplegia and Charcot-Marie-Tooth Disease Due to KIF5A Mutations: A Cross-Sectional Observational StudyPo-Yu Lin, Cheng-Tsung Hsiao, Han-Wei Huang, et al.
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.
Plos One|October 22, 2014
The Eag domain regulates the voltage-dependent inactivation of rat Eag1 K+ channelsTing-Feng Lin, Guey-Mei Jow, Hsin-Yu Fang, et al.
Reproduction (Cambridge, England)|July 19, 2025
Regulation of testosterone synthesis in Leydig cells by ClC-2 chloride channelSsu-Ju Fu, Min-Shan Syu, Chih-Yu Tang, et al.
Neuromolecular Medicine|January 3, 2021
Neuronal Exosomes Secreted under Oxygen-Glucose Deprivation/Reperfusion Presenting Differentially Expressed miRNAs and Affecting Neuronal Survival and Neurite OutgrowthChien-Sung Chiang, Ssu-Ju Fu, Chia-Lang Hsu, 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.
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.
International Journal of Molecular Sciences|August 7, 2021
Rare Gain-of-Function KCND3 Variant Associated with Cerebellar Ataxia, Parkinsonism, Cognitive Dysfunction, and Brain Iron AccumulationCheng-Tsung Hsiao, Thomas F Tropea, Ssu-Ju Fu, et al.
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