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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.
Plos One|August 23, 2012
14-3-3θ is a binding partner of rat Eag1 potassium channelsPo-Hao Hsu, Shi-Chuen Miaw, Chau-Ching Chuang, et al.
International Journal of Molecular Sciences|November 30, 2018
FKBP8 Enhances Protein Stability of the CLC-1 Chloride Channel at the Plasma MembraneYi-Jheng Peng, Yi-Ching Lee, Ssu-Ju Fu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 8, 2017
Ubiquitin Ligase RNF138 Promotes Episodic Ataxia Type 2-Associated Aberrant Degradation of Human Cav2.1 (P/Q-Type) Calcium ChannelsSsu-Ju Fu, Chung-Jiuan Jeng, Chia-Hao Ma, et al.
Journal of Molecular Endocrinology|July 13, 2026
Novel gain-of-function CLCN2 germline mutation associated with nonclassical lateralizing primary aldosteronismSsu-Ju Fu, Kang-Yung Peng, Ya-Hui Hu, et al.
The Journal of Biological Chemistry|March 1, 2021
Identification of MKRN1 as a second E3 ligase for Eag1 potassium channels reveals regulation via differential degradationYa-Ching Fang, Ssu-Ju Fu, Po-Hao Hsu, et al.
Plos Genetics|December 3, 2025
A fly model of SCA36 reveals combinatorial neurotoxicity of hexanucleotide and dipeptide repeatsCheng-Tsung Hsiao, Ssu-Ju Fu, Ting-Ni Guo, et al.
NPJ Parkinson'S Disease|January 15, 2026
UQCRC1 deficiency impairs mitophagy via PINK1-dependent mechanisms in Parkinson's diseaseJeng-Lin Li, Shu-Yi Huang, Po-Yu Huang, et al.
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