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

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	Repositories
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	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

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	機構典藏計畫網站
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	臺大學術典藏NTU Scholars

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Institution	Date	Title	Author
臺大學術典藏	2021-07-26T10:00:48Z	Kinetin Detection Enhancement Based on Photonic Nanojets and Surface-Enhanced Raman Scattering	Lai H.-C;Wang Y.-J;Dai C.-A;Hsueh C.-H;Wang S.-J;Li J.-H.; Lai H.-C; Wang Y.-J; Dai C.-A; Hsueh C.-H; Wang S.-J; Li J.-H.; SHU-JEN WANG
臺大學術典藏	2021-05-31T06:18:06Z	Functional studies on three novel HCNH2 mutations in Taiwan: Identification of distinct mechanisms of channel defect and dissociation between glycosylation defect and assembly defect	Hsueh C.-H.; Chen W.-P.; Lin J.-L.; Liu Y.-B.; MING-JAI SU; Lai L.-P.
臺大學術典藏	2021-05-31T06:18:05Z	Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations	Hsueh C.-H.; Chen W.-P.; Lin J.-L.; Tsai C.-T.; Liu Y.-B.; Juang J.-M.; Tsao H.-M.; MING-JAI SU; Lai L.-P.
臺大學術典藏	2021-05-31T06:18:04Z	Piceatannol, a derivative of resveratrol, moderately slows l Na inactivation and exerts antiarrhythmic action in ischaemia-reperfused rat hearts	Chen W.-P.; Hung L.-M.; Hsueh C.-H.; Lai L.-P.; MING-JAI SU
臺大學術典藏	2021-04-15T07:52:48Z	Functional studies on three novel HCNH2 mutations in Taiwan: Identification of distinct mechanisms of channel defect and dissociation between glycosylation defect and assembly defect	Hsueh C.-H.; WEN-PIN CHEN; Lin J.-L.; Liu Y.-B.; Su M.-J.; Lai L.-P.
臺大學術典藏	2021-04-15T07:52:45Z	Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations	Hsueh C.-H.; WEN-PIN CHEN; Lin J.-L.; Tsai C.-T.; Liu Y.-B.; Juang J.-M.; Tsao H.-M.; Su M.-J.; Lai L.-P.
臺大學術典藏	2021-04-15T07:52:44Z	Piceatannol, a derivative of resveratrol, moderately slows l Na inactivation and exerts antiarrhythmic action in ischaemia-reperfused rat hearts	WEN-PIN CHEN; Hung L.-M.; Hsueh C.-H.; Lai L.-P.; Su M.-J.
臺大學術典藏	2021-04-15T07:52:33Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; WEN-PIN CHEN; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2021-03-11T04:29:40Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Juang J.-M.J.;Lu T.-P.;Lai L.-C.;Hsueh C.-H.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Hwang J.-J.;Fu-Tien Chiang;Yeh S.S.-F.;Chen W.-P.;Chuang E.Y.;Lai L.-P.;Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; FU-TIEN CHIANG; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-30T08:47:59Z	The g.762TC polymorphism of the NPC1L1 gene is common in Chinese and contributes to a higher promoter activity and higher serum cholesterol levels	Chen C.-W.; Hwang J.-J.; CHIA-TI TSAI; Su Y.-N.; Hsueh C.-H.; Shen M.J.; Lai L.-P.
臺大學術典藏	2020-12-30T08:47:56Z	Rimonabant inhibits TNF-α-induced endothelial IL-6 secretion via CB1 receptor and cAMP-dependent protein kinase pathway	Hsueh C.-H.; Liang Y.-J.; Lin J.-L.; CHIA-TI TSAI; Lai L.-P.; Huang N.-L.; Juang J.-M.; Wang Y.-H.
臺大學術典藏	2020-12-30T08:47:44Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Chiang F.-T.; Hwang J.-J.; Lin L.-Y.; Yu C.-C.; CHIA-TI TSAI; Liu Y.-B.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-30T07:47:54Z	Functional studies on three novel HCNH2 mutations in Taiwan: Identification of distinct mechanisms of channel defect and dissociation between glycosylation defect and assembly defect	Hsueh C.-H.; Chen W.-P.; Lin J.-L.; YEN BIN LIU; Su M.-J.; Lai L.-P.
臺大學術典藏	2020-12-30T07:47:53Z	Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations	Hsueh C.-H.; Chen W.-P.; Lin J.-L.; Tsai C.-T.; YEN BIN LIU; Juang J.-M.; Tsao H.-M.; Su M.-J.; Lai L.-P.
臺大學術典藏	2020-12-30T07:47:50Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Chuang E.Y.; Lai L.-P.; Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; YEN BIN LIU; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.
臺大學術典藏	2020-12-28T12:04:21Z	The g.762TC polymorphism of the NPC1L1 gene is common in Chinese and contributes to a higher promoter activity and higher serum cholesterol levels	Lai L.-P.; Shen M.J.; Hsueh C.-H.; Su Y.-N.; Tsai C.-T.; HWANG, JUEY-JEN; Chen C.-W.
臺大學術典藏	2020-12-28T12:04:03Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; HWANG, JUEY-JEN; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-28T10:02:49Z	Arrhythmogenic right ventricular dysplasia: Clinical characteristics and identification of novel desmosome gene mutations	Yang C.-T.; Juang J.-M.; Hwang J.-J.; Lin J.-L.; Lai L.-P.; CHIH-CHIEH YU; Yu C.-H.; Hsueh C.-H.
臺大學術典藏	2020-12-28T10:02:48Z	Erratum: Arrhythmogenic right ventricular dysplasia: Clinical characteristics and identification of novel desmosome gene mutations (Journal of the Formosan Medical Association (2008) vol. 107 (7) (548-558))	CHIH-CHIEH YU; Yu C.H.; Hsueh C.H.; Yang C.T.; Juang J.M.; Hwang J.J.; Lin J.L.; Lai L.P.
臺大學術典藏	2020-12-28T10:02:42Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; CHIH-CHIEH YU; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.
臺大學術典藏	2020-12-28T07:56:57Z	Arrhythmogenic right ventricular dysplasia: Clinical characteristics and identification of novel desmosome gene mutations	Yu C.-H.; Yu C.-C.; Hsueh C.-H.; Yang C.-T.; JYH-MING JIMMY JUANG; Hwang J.-J.; Lin J.-L.; Lai L.-P.
臺大學術典藏	2020-12-28T07:56:55Z	Rimonabant inhibits TNF-α-induced endothelial IL-6 secretion via CB1 receptor and cAMP-dependent protein kinase pathway	Lai L.-P.; Huang N.-L.; JYH-MING JIMMY JUANG; Wang Y.-H.; Hsueh C.-H.; Liang Y.-J.; Lin J.-L.; Tsai C.-T.
臺大學術典藏	2020-12-04T07:44:55Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; LIAN-YU LIN; Yu C.-C.; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-11-17T02:45:34Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Lin J.-L.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Hwang J.-J.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Hsueh C.-H.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;Yu C.-C.;Hwang J.-J.;Chiang F.-T.;Yeh S.S.-F.;Chen W.-P.;Chuang E.Y.;Lai L.-P.;Lin J.-L.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.
臺大學術典藏	2020-10-26T11:34:47Z	Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations	Chen W.-P.; Hsueh C.-H.; Lin J.-L.; Tsai C.-T.; Liu Y.-B.; JYH-MING JIMMY JUANG; Tsao H.-M.; Su M.-J.; Lai L.-P.

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