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Showing items 11-35 of 727  (30 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2022-09-20T06:49:58Z The association of human connexin 40 genetic polymorphisms with atrial fibrillation Juang J.-M.; Chern Y.-R.; Tsai C.-T.; Chiang F.-T.; Lin J.-L.; HWANG, JUEY-JEN; Hsu K.-L.; Tseng C.-D.; Tseng Y.-Z.; Lai L.-P.
臺大學術典藏 2022-09-20T06:49:57Z ATP-binding cassette transporter A1 gene I823M polymorphism affects plasma high-density lipoprotein cholesterol level and modifies the effect of low high-density lipoprotein cholesterol on the risk of coronary artery disease Tsai C.-T.; HWANG, JUEY-JEN; Chiang F.-T.; Tseng C.-D.; Lin J.-L.; Tseng Y.-Z.; Lai L.-P.
臺大學術典藏 2022-09-20T06:49:57Z Angiotensin II increases expression of α1C subunit of L-type calcium channel through a reactive oxygen species and cAMP response element-binding protein-dependent pathway in HL-1 myocytes Tsai C.-T.; Wang D.L.; Chen W.-P.; HWANG, JUEY-JEN; Hsieh C.-S.; Hsu K.-L.; Tseng C.-D.; Lai L.-P.; Tseng Y.-Z.; Chiang F.-T.; Lin J.-L.
臺大學術典藏 2022-09-20T06:49:56Z Morphologic and Topologic Characteristics of Coronary Venous System Delineated by Noninvasive Multidetector Computed Tomography in Chronic Systolic Heart Failure Patients Chen J.-J.; Lee W.-J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; HWANG, JUEY-JEN; Lin J.-L.
臺大學術典藏 2022-09-20T06:49:56Z Coexistence and exercise exacerbation of intraleft ventricular contractile dyssynchrony in hypertensive patients with diastolic heart failure Wang Y.-C.; HWANG, JUEY-JEN; Lai L.-P.; Tsai C.-T.; Lin L.-C.; Katra R.; Lin J.-L.
臺大學術典藏 2022-09-20T06:49:49Z Renin-angiotensin system gene polymorphisms and diastolic heart failure Wu C.-K.; Tsai C.-T.; HWANG, JUEY-JEN; Luo J.-L.; Juang J.J.-M.; Hsu K.-L.; Lai L.-P.; Lin J.-L.; Tseng C.-D.; Chiang F.-T.
臺大學術典藏 2022-09-20T06:49:48Z 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)) Yu C.C.; Yu C.H.; Hsueh C.H.; Yang C.T.; Juang J.M.; HWANG, JUEY-JEN; Lin J.L.; Lai L.P.
臺大學術典藏 2022-09-20T06:49:46Z The clinical implications of blood adiponectin in cardiometabolic disorders Chang L.-C.; Huang K.-C.; Wu Y.-W.; Kao H.-L.; Chen C.-L.; Lai L.-P.; HWANG, JUEY-JEN; Yang W.-S.
臺大學術典藏 2022-09-20T06:49:31Z Significant association of rs13376333 in KCNN3 on chromosome 1q21 with atrial fibrillation in a Taiwanese population Chang S.-H.; Chang S.-N.; HWANG, JUEY-JEN; Chiang F.-T.; Tseng C.-D.; Lee J.-K.; Lai L.-P.; Lin J.-L.; Wu C.-K.; Tsai C.-T.
臺大學術典藏 2022-09-20T06:49:30Z A functional variant in the promoter region regulates the C-reactive protein gene and is a potential candidate for increased risk of atrial fibrillation Chang S.-N.; Tsai C.-T.; Wu C.-K.; Lee J.-K.; Lai L.-P.; Huang S.-W.; Huang L.-Y.; Tseng C.-D.; Lin J.-L.; Chiang F.-T.; HWANG, JUEY-JEN
臺大學術典藏 2022-09-20T06:49:29Z Impact of ventricular dyssynchrony on postexercise accommodation of systolic myocardial motion in hypertensive patients with heart failure and a normal ejection fraction: A tissue-Doppler echocardiography study Wang Y.-C.; Yu C.-C.; Chiu F.-C.; Klepfer R.; Hilpisch K.; Splett V.; Tsai C.-T.; Lai L.-P.; HWANG, JUEY-JEN; Lin J.-L.
臺大學術典藏 2022-09-20T06:49:21Z 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 2022-09-20T06:49:20Z Additive effect of the metabolic syndrome score to the conventional CHADS2 score for the thromboembolic risk stratification of patients with atrial fibrillation Tsai C.-T.; Chang S.-H.; Chang S.-N.; HWANG, JUEY-JEN; Wu C.-K.; Wang Y.-C.; Tseng C.-D.; Yeh H.-M.; Lai L.-P.; Chiang F.-T.; Lin J.-L.
臺大學術典藏 2022-09-20T06:49:19Z Anti-anxiety drugs use and cardiovascular outcomes in patients with myocardial infarction: A national wide assessment Wu C.-K.; Huang Y.-T.; Lee J.-K.; Jimmy Juang J.-M.; Tsai C.-T.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L.; Chen P.-C.; Lin L.-Y.
臺大學術典藏 2022-09-20T06:49:15Z TNF-α down-regulates sarcoplasmic reticulum Ca2+ ATPase expression and leads to left ventricular diastolic dysfunction through binding of NF-κB to promoter response element Tsai C.-T.; Wu C.-K.; Lee J.-K.; Chang S.-N.; Kuo Y.-M.; Wang Y.-C.; Lai L.-P.; Chiang F.-T.; HWANG, JUEY-JEN; Lin J.-L.
臺大學術典藏 2022-09-20T06:49:14Z Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan Juang J.M.J.; Tsai C.-T.; Lin L.-Y.; Liu Y.-B.; Yu C.-C.; HWANG, JUEY-JEN; Chen J.-J.; Chiu F.-C.; Chen W.-J.; Tseng C.-D.; Chiang F.-T.; Yeh H.-M.; Sherri Yeh S.-F.; Lai L.-P.; Lin J.-L.
臺大學術典藏 2022-09-20T06:49:12Z Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease Ho L.-T.; Lin L.-Y.; Yang Y.-H.; Wu C.-K.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L.; Chen P.-C.
臺大學術典藏 2022-09-20T06:49:10Z Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy Chung Y.-W.; Yang Y.-H.; Wu C.-K.; Yu C.-C.; Juang J.-M.J.; Wang Y.-C.; Tsai C.-T.; Lin L.-Y.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Chen P.-C.; Lin J.-L.
臺大學術典藏 2022-09-20T06:49:08Z Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Ueng K.-C.; Tsai C.-F.; Lin T.-H.; Wu C.-K.; Lee J.-K.; Lin L.-Y.; Wang Y.-C.; Yu C.-C.; Lai L.-P.; Tseng C.-D.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L.
臺大學術典藏 2022-09-20T06:48:41Z Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry Chen C.-Y.J.; Lu T.-P.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; HWANG, JUEY-JEN; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏 2022-09-20T06:48:39Z Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry Chen C.-Y.J.; Juang J.-M.J.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Yu C.-C.; Huang H.-C.; Lin T.-T.; Liao M.-C.; Chen J.-J.; HWANG, JUEY-JEN; Chen W.-J.; Yeh S.-F.S.; Yang D.-H.; Chiang F.-T.; Lin J.-L.; Lai L.-P.; Horie M.; Wu M.-H.; Wu T.-J.; Chen S.-A.; Wang C.-C.; Chang K.-C.; Feng A.-N.; Lin Y.-J.; Ueng K.-C.; Tsao H.-M.; Huang J.-L.; Tsai W.-C.; Tsai C.-F.; Chang S.-L.; Lo L.-W.; Hu Y.-F.; Chung F.-P.; Chang C.-J.; Lo H.-M.; Chiang M.-C.; Hsia C.-P.; Liu J.-F.; Chiu S.-N.; Lin M.-T.; Chua S.-K.; Hsieh Y.-C.; Li C.-H.; Liao Y.-C.; Lin H.-H.; Liu Z.-Z.; Ye G.-H.; Chiu W.-R.; Chang J.-R.; Feng W.-J.; Chang S.-X.; Lei M.-H.; Ko W.-C.; Kong C.-W.; Kuo C.-T.; Huang B.-X.; Li K.-T.; Chen W.-D.; Luo J.-L.; Lin J.-Y.; Tsai T.-N.; Hsu C.-T.; Lin L.-R.; Chen R.-Y.; Li P.-T.; Stephen Huang S.K.; SADS-TW BrS Registry
臺大學術典藏 2022-09-20T06:48:36Z The effect and molecular mechanism of statins on the expression of human anti-coagulation genes Chang S.-N.; Wu C.-K.; Lai L.-P.; Chiang F.-T.; HWANG, JUEY-JEN; Tsai C.-T.
臺大學術典藏 2022-09-20T06:48:31Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death Juang J.-M.J.; Binda A.; Lee S.-J.; HWANG, JUEY-JEN; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C.
臺大學術典藏 2022-09-20T06:48:30Z Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry Jimmy Juang J.-M.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; HWANG, JUEY-JEN; Lin T.-T.; Liao M.-T.; Chen J.-J.; Sherri Yeh S.-F.; Chuang J.-Y.; Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.
臺大學術典藏 2022-09-20T06:48:27Z Long-term outcomes and left ventricular diastolic function of sarcomere mutation-positive and mutation-negative patients with hypertrophic cardiomyopathy: a prospective cohort study Chen C.-Y.J.; Su M.-Y.M.; Liao Y.-C.; Chang F.-L.; Wu C.-K.; Lin L.-Y.; Chen Y.-S.; Lin Y.-H.; HWANG, JUEY-JEN; Yu S.-L.; Kao H.-L.; Chen W.-J.; Lu T.-P.; Shih C.-Y.; Yeh S.-F.S.; Yang D.-H.; Lai L.-P.; Juang J.-M.J.

Showing items 11-35 of 727  (30 Page(s) Totally)
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