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

	English \| 正體中文 \| 简体中文 \| Total items :2856704
	Visitors : 53703955 Online Users : 1670 Project Commissioned by the Ministry of Education Project Executed by National Taiwan University Library

Scope

Adv. Search

Login

Administrator

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

About TAIR
	About TAIR

Browse By
	Institution
	Author
	Title
	Date
	Statistics Chart
	Institution Facts
	Trend

News
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

Copyright
	Publisher & Journal Policy
	TAIR Copyright Conference Minutes

Related Links
	機構典藏計畫網站
	ROAR
	OpenDOAR
	SHERPA
	OAIster
	JAIRO
	Ira
	DSPACE
	RWWR
	臺大學術典藏NTU Scholars

"hsueh c h"

Return to Browse by Author
Sorting by Title	Sort by Date

Showing items 51-60 of 146 (15 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
View [10|25|50] records per page

Institution	Date	Title	Author
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.

Showing items 51-60 of 146 (15 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
View [10|25|50] records per page