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

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	造訪人次 : 51995487 線上人數 : 819 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	2020-12-28T07:56:41Z	VariED: The first integrated database of gene annotation and expression profiles for variants related to human diseases	Tsai M.-H.; Lai L.-C.; Chiang L.-M.; JYH-MING JIMMY JUANG; Chattopadhyay A.; Lee C.-Y.; Lu T.-P.; Chuang E.Y.
臺大學術典藏	2020-12-28T07:56:37Z	GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death	Huang H.-C.; Yu C.-C.; Ho L.-T.; Liu Y.-B.; Lin L.-Y.; Chen W.-J.; Hwang J.-J.; JYH-MING JIMMY JUANG; Binda A.; Lee S.-J.; 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	2020-12-22T03:29:15Z	SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKC?-dependent Pathway	Ni Y.-H.; Shun C.-T.; Chuang E.Y.; Hsiao J.-H.; Yu L.C.H.; Lai L.-C.; Tung C.-C.; Weng M.-T.; PO-NIEN TSAO; Yang-Yen H.-F.; Wei S.-C.; Wei S.-C.;Yang-Yen H.-F.;Po-Nien Tsao;Weng M.-T.;Tung C.-C.;Yu L.C.H.;Lai L.-C.;Hsiao J.-H.;Chuang E.Y.;Shun C.-T.;Ni Y.-H.;Xavier R.J.;Podolsky D.K.;Yen J.J.Y.;Wong J.-M.; Xavier R.J.; Podolsky D.K.; Yen J.J.Y.; Wong J.-M.
臺大學術典藏	2020-12-21T08:16:30Z	Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome	Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; WEN-JONE CHEN; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.
臺大學術典藏	2020-12-04T07:44:55Z	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	2020-12-04T07:44:54Z	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	2020-12-04T07:44:53Z	Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation	Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Juang J.-M.J.; LIAN-YU LIN; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-04T07:44:49Z	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.; LIAN-YU LIN; Wang Y.-C.; Yu C.-C.; Lai L.-P.; Tseng C.-D.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-04T07:44:31Z	Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry	Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.; Jyh-Ming J.-J.; 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.
臺大學術典藏	2020-12-04T07:44:29Z	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.

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