公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2020 | Defective Gating and Proteostasis of Human ClC-1 Chloride Channel: Molecular Pathophysiology of Myotonia Congenita | Jeng C.-J.; Fu S.-J.; You C.-Y.; Peng Y.-J.; Hsiao C.-T.; Chen T.-Y.; CHIH-YUNG TANG | Frontiers in Neurology | 13 | 11 | |
2016 | The episodic ataxia type 1 mutation I262T alters voltage-dependent gating and disrupts protein biosynthesis of human Kv1.1 potassium channels | Chen S.-H.; Fu S.-J.; Huang J.-J.; CHIH-YUNG TANG | Scientific Reports | 10 | 8 | |
2018 | FKBP8 enhances protein stability of the CLC-1 chloride channel at the plasma membrane | Peng Y.-J.; Lee Y.-C.; Fu S.-J.; Chien Y.-C.; Liao Y.-F.; Chen T.-Y.; Jeng C.-J.; CHIH-YUNG TANG | International Journal of Molecular Sciences | 6 | 6 | |
2021 | Identification of MKRN1 as a second E3 ligase for Eag1 potassium channels reveals regulation via differential degradation | Fang Y.-C.; Fu S.-J.; Hsu P.-H.; Chang P.-T.; Huang J.-J.; Chiu Y.-C.; Liao Y.-F.; Jow G.-M.; CHIH-YUNG TANG ; Jeng C.-J. | Journal of Biological Chemistry | 7 | 6 | |
2021 | Neuronal Exosomes Secreted under Oxygen–Glucose Deprivation/Reperfusion Presenting Differentially Expressed miRNAs and Affecting Neuronal Survival and Neurite Outgrowth | Chiang C.-S.; Fu S.-J.; CHIA-LANG HSU ; Jeng C.-J.; CHIH-YUNG TANG ; Huang Y.-S.; SUNG-CHUN TANG | NeuroMolecular Medicine | 10 | 9 | |
2021 | Novel KCND3 variant underlying nonprogressive congenital ataxia or SCA19/22 disrupt KV4.3 protein expression and K+ currents with variable effects on channel properties | Zanni G.; Hsiao C.-T.; Fu S.-J.; CHIH-YUNG TANG ; Capuano A.; Bosco L.; Graziola F.; Bellacchio E.; Servidei S.; Primiano G.; Soong B.-W.; Jeng C.-J. | International Journal of Molecular Sciences | 11 | 9 | |
2019 | Novel SCA19/22-associated KCND3 mutations disrupt human KV4.3 protein biosynthesis and channel gating | Hsiao C.-T.; Fu S.-J.; Liu Y.-T.; Lu Y.-H.; Zhong C.-Y.; CHIH-YUNG TANG ; Soong B.-W.; Jeng C.-J. | Human Mutation | 14 | 13 | |
2021 | Rare gain-of-function kcnd3 variant associated with cerebellar ataxia, parkinsonism, cognitive dysfunction, and brain iron accumulation | Hsiao C.-T.; Tropea T.F.; Fu S.-J.; Bardakjian T.M.; Gonzalez-Alegre P.; Soong B.-W.; CHIH-YUNG TANG ; Jeng C.-J. | International Journal of Molecular Sciences | 6 | 6 | |
2017 | Ubiquitin ligase RNF138 promotes episodic ataxia type 2-associated aberrant degradation of human Cav2.1 (P/Q-type) calcium channels | Fu S.-J.; Jeng C.-J.; Ma C.-H.; Peng Y.-J.; Lee C.-M.; Fang Y.-C.; Lee Y.-C.; SUNG-CHUN TANG ; MENG-CHUN HU ; CHIH-YUNG TANG | 5 | 4 |