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

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	造訪人次 : 51191440 線上人數 : 834 教育部委託研究計畫計畫執行:國立臺灣大學圖書館

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

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機構	日期	題名	作者
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	2020-12-30T08:47:56Z	Association between genetic polymorphisms in the renin-angiotensin system and systolic heart failure revised by a propensity score-based analysis	Chiang F.-T.; Hwang J.-J.; Chang S.-N.; Lin J.-W.; Juang J.-M.; CHIA-TI TSAI
臺大學術典藏	2020-12-30T08:47:49Z	Angiotensin II regulates the LARG/RhoA/MYPT1 axis in rat vascular smooth muscle in vitro	Chiu W.-C.; Juang J.-M.; Chang S.-N.; Wu C.-K.; CHIA-TI TSAI; Tseng Y.-Z.; Chiang F.-T.
臺大學術典藏	2020-12-30T08:47:37Z	Non-carriers of reduced-function CYP2C19 alleles are most susceptible to impairment of the anti-platelet effect of clopidogrel by proton-pump inhibitors: A pilot study	Lee J.-K.; Wu C.-K.; Juang J.-M.; CHIA-TI TSAI; Hwang J.-J.; Lin J.-L.; Chiang F.-T.
臺大學術典藏	2020-12-30T08:47:37Z	KCNN2 polymorphisms and cardiac tachyarrhythmias	Yu C.-C.; CHIA-TI TSAI; Chen P.-L.; Wu C.-K.; Chiu F.-C.; Chiang F.-T.; Chen P.-S.; Chen C.-L.; Lin L.-Y.; Juang J.-M.; Ho L.-T.; La L.-P.; Yang W.-S.; Lin J.-L.
臺大學術典藏	2020-12-30T07:47:57Z	Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms	Ko Y.-L.; Wang C.-C.; Chen W.-J.; Yeh S.-J.; Ho Y.-L.; YEN BIN LIU; Lai L.-P.; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.; Lin J.-L.
臺大學術典藏	2020-12-30T07:47:57Z	Erratum: Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms (Journal of Human Genetics (2005) 50 (490-496) DOI: 10.1007/s10038-005-0283-3)	Lin J.-L.; Lai L.-P.; Su Y.-N.; Hsieh F.-J.; Chiang F.-T.; Juang J.-M.; YEN BIN LIU; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.
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	2020-12-28T12:04:30Z	The association of human connexin 40 genetic polymorphisms with atrial fibrillation	Chern Y.-R.; Juang J.-M.; Lai L.-P.; Tsai C.-T.; Chiang F.-T.; Lin J.-L.; HWANG, JUEY-JEN; Hsu K.-L.; Tseng C.-D.; Tseng Y.-Z.
臺大學術典藏	2020-12-28T12:04:15Z	Association between genetic polymorphisms in the renin-angiotensin system and systolic heart failure revised by a propensity score-based analysis	Juang J.-M.; Tsai C.-T.; HWANG, JUEY-JEN; Chiang F.-T.; Chang S.-N.; Lin J.-W.

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