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公開日期
標題
作者
來源出版物
scopus
WOS
全文
1993
G-protein modulation of ion permeation through N-type calcium channels
Chung-Chin Kuo
; Bean B.P.
Nature
60
68
2014
Gating of the Kir2.1 Channel at the Bundle Crossing Region by Intracellular Spermine and Other Cations
Huang C.-W.; Chung-Chin Kuo
Journal of Cellular Physiology
4
4
2022
The genesis and functional consequences of cortico-subthalamic beta augmentation and excessive subthalamic burst discharges after dopaminergic deprivation
Lai, Hsing-Jung; Deng, Chuan-Rou; Wang, Ren-Wei; Lee, Lan-Hsin Nancy; CHUNG-CHIN KUO
Experimental neurology
1
0
2021
Glutamate transmission rather than cellular pacemaking propels excitatory-inhibitory resonance for ictogenesis in amygdala
Wang G.-H.; Chou P.; Hsueh S.-W.; Yang Y.-C.; CHUNG-CHIN KUO
Neurobiology of Disease
6
5
2021
How Can an Na+ Channel Inhibitor Ameliorate Seizures in Lennox–Gastaut Syndrome?
Lin Y.-C.; Lai Y.-C.; Chou P.; Hsueh S.-W.; Lin T.-H.; Huang C.-S.; Wang R.-W.; Yang Y.-C.; CHUNG-CHIN KUO
Annals of Neurology
5
3
2007
A hydrophobic element secures S4 voltage sensor in position in resting Shaker K+ channels
Yang Y.-C.; Own C.-J.; Chung-Chin Kuo
Journal of Physiology
11
10
2020
Hyperpolarization of the subthalamic nucleus alleviates hyperkinetic movement disorders
CHUN-HWEI TAI
; MING-KAI PAN
; SHENG-HONG TSENG
; Wang T.-R.; Chung-Chin Kuo
Scientific Reports
7
7
1998
Imipramine inhibition of transient K+ current: An external open channel blocker preventing fast inactivation
Chung-Chin Kuo
Biophysical Journal
30
31
2005
An inactivation stabilizer of the Na+ channel acts as an opportunistic pore blocker modulated by external Na+
Yang Y.-C.; Chung-Chin Kuo
Journal of General Physiology
21
19
2002
Inhibition of Na + current by imipramine and related compounds: Different binding kinetics as an inactivation stabilizer and as an open channel blocker
Yang Y.-C.; Chung-Chin Kuo
Molecular Pharmacology
55
52
2000
Inhibition of Na+ current by diphenhydramine and other diphenyl compounds: Molecular determinants of selective binding to the inactivated channels
Chung-Chin Kuo
; Huang R.-C.; Lou B.-S.
Molecular Pharmacology
81
78
2020
Inhibition of neuronal Na+ currents by lacosamide: Differential binding affinity and kinetics to different inactivated states
Peng Y.-S.; Wu H.-T.; Lai Y.-C.; Chen J.-L.; Yang Y.-C.; CHUNG-CHIN KUO
Neuropharmacology
7
5
2024
Inhibition of resurgent Na+ currents by rufinamide
Chen, Jian-Lin; CHUNG-CHIN KUO
Neuropharmacology
1993
Ion permeation through the L-type Ca2+ channel in rat phaeochromocytoma cells: two sets of ion binding sites in the pore.
Chung-Chin Kuo
; Hess P.
The Journal of Physiology
98
99
2010
Ionic flow enhances low-affinity binding: a revised mechanistic view into Mg2+ block of NMDA receptors
Yang Y.-C.; Lee C.-H.; Chung-Chin Kuo
Journal of Physiology
13
12
1999
K + binding sites and interactions between permeating K+ ions at the external pore mouth of an inward rectifier K+ channel (Kir2.1)
Shieh R.-C.; Chang J.-C.; Chung-Chin Kuo
Journal of Biological Chemistry
17
16
2010
Lidocaine, carbamazepine, and imipramine have partially overlapping binding sites and additive inhibitory effect on neuronal Na+ channels
Yang Y.-C.; Huang C.-S.; Chung-Chin Kuo
Anesthesiology
42
42
2016
Modulation of NMDA channel gating by Ca2+ and Cd2+ binding to the external pore mouth
Tu Y.-C.; Yang Y.-C.; Chung-Chin Kuo
Scientific Reports
9
8
2011
Modulation of subthalamic T-type Ca2+ channels remedies locomotor deficits in a rat model of Parkinson disease
CHUN-HWEI TAI
; Yang Y.-C.; MING-KAI PAN
; Huang C.-S.; Chung-Chin Kuo
Journal of Clinical Investigation
59
58
2008
Molecular determinants of the anticonvulsant felbamate binding site in the N-methyl-D-aspartate receptor
Chang H.-R.; Chung-Chin Kuo
Journal of Medicinal Chemistry
21
13