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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Showing items 326-335 of 727 (73 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-12-30T08:47:36Z	Renal Denervation Decreases Susceptibility to Arrhythmogenic Cardiac Alternans and Ventricular Arrhythmia in a Rat Model of Post-Myocardial Infarction Heart Failure	Chang S.-N.; Chang S.-H.; Yu C.-C.; Wu C.-K.; Lai L.-P.; Chiang F.-T.; Hwang J.-J.; Lin J.-L.; CHIA-TI TSAI
臺大學術典藏	2020-12-30T08:47:35Z	Biomarkers and echocardiography for evaluating the improvement of the ventricular diastolic function after surgical relief of hydronephrosis	Yeh H.-M.; Lin T.-T.; Yeh C.-F.; Huang H.-S.; Chang S.-N.; Lin J.-W.; CHIA-TI TSAI; Lai L.-P.; Huang Y.-Y.; Chu C.-L.
臺大學術典藏	2020-12-30T08:47:32Z	The effect and molecular mechanism of statins on the expression of human anti-coagulation genes	CHIA-TI TSAI; Chang S.-N.; Wu C.-K.; Lai L.-P.; Chiang F.-T.; Hwang J.-J.
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	2020-12-30T07:47:54Z	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	2020-12-30T07:47:51Z	Prevalence of atrial fibrillation in patients with brugada syndrome in Taiwan	Juang J.-M.J.; Chen C.-Y.; YEN BIN LIU; Lin L.-Y.; Chen W.-J.; Lai L.-P.; Tsai C.-T.; Lin J.-L.
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	2020-12-30T07:47:50Z	Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations	YEN BIN LIU; Yu C.-C.; Yeh H.-M.; Chiu W.-Y.; Chen C.-Y.; Juang J.-M.J.; Tsai C.-T.; Lo L.-W.; Yeh S.-F.S.; Lai L.-P.

Showing items 326-335 of 727 (73 Page(s) Totally)
<< < 28 29 30 31 32 33 34 35 36 37 > >>
View [10|25|50] records per page