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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机构	日期	题名	作者
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.
臺大學術典藏	2022-09-06T02:42:26Z	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	2022-09-06T02:42:23Z	Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome	Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; LIAN-YU LIN; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L.
臺大學術典藏	2022-09-06T02:42:05Z	Genome-wide methylation profiles in coronary artery ectasia	Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; LIAN-YU LIN; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J.
臺大學術典藏	2022-09-06T02:41:58Z	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.; LIAN-YU LIN; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C.
臺大學術典藏	2022-09-06T02:41:47Z	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 J.-J.; Chen W.-J.; Liu Y.-B.; LIAN-YU LIN; 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	2022-09-06T02:41:46Z	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.; LIAN-YU LIN; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; Hwang J.-J.; 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	2022-09-06T02:41:42Z	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.; LIAN-YU LIN; Chen Y.-S.; Lin Y.-H.; Hwang J.-J.; 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.
臺大學術典藏	2022-08-19T00:20:42Z	Epithelioid Trophoblastic Tumor Around an Abdominal Cesarean Scar: A Pathologic and Molecular Genetic Analysis	Hsiue E.H.-C.; CHIUN HSU; Tseng L.-H.; Lu T.-P.; Kuo K.-T.

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