臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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机构	日期	题名	作者
臺大學術典藏	2020-06-30T07:15:28Z	Deactivation retards recovery from inactivation in Shaker K+ channels	Chung-Chin Kuo; Chung-Chin Kuo
臺大學術典藏	2020-06-30T07:15:28Z	Carbamazepine inhibition of neuronal Na+ currents: Quantitative distinction from phenytoin and possible therapeutic implications	Chung-Chin Kuo;Chen R.-S.;Lu L.;Chen R.-C.; Chung-Chin Kuo; Chen R.-S.; Lu L.; Chen R.-C.
臺大學術典藏	2020-06-30T07:15:27Z	Facilitation of recovery from inactivation by external NA+ and location of the activation gate in neuronal NA+ channels	Chung-Chin Kuo;Liao S.-Y.; Chung-Chin Kuo; Liao S.-Y.
臺大學術典藏	2020-06-30T07:15:27Z	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.; Chung-Chin Kuo; Huang R.-C.; Lou B.-S.
臺大學術典藏	2020-06-30T07:15:27Z	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; Shieh R.-C.; Chang J.-C.; Chung-Chin Kuo
臺大學術典藏	2020-06-30T07:15:27Z	Zn2+ modulation of neuronal transient K+ current: Fast and selective binding to the deactivated channels	Chung-Chin Kuo;Chen F.-P.; Chung-Chin Kuo; Chen F.-P.
臺大學術典藏	2020-06-30T07:15:26Z	The position of the fourth segment of domain 4 determines status of the inactivation gate in Na+ channels	Yang Y.-C.;Chung-Chin Kuo; Yang Y.-C.; Chung-Chin Kuo
臺大學術典藏	2020-06-30T07:15:26Z	Effect of Na+ flow on Cd2+ block of tetrodotoxin-resistant Na+ channels	Chung-Chin Kuo;Lin T.-J.;Hsieh C.-P.; Chung-Chin Kuo; Lin T.-J.; Hsieh C.-P.
臺大學術典藏	2020-06-30T07:15:26Z	Recovery from inactivation of T-type Ca2+ channels in rat thalamic neurons	Chung-Chin Kuo;Yang S.; Chung-Chin Kuo; Yang S.
臺大學術典藏	2020-06-30T07:15:26Z	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; Yang Y.-C.; Chung-Chin Kuo

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