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	2020-12-28T10:02:41Z	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.; Lin L.-Y.; CHIH-CHIEH YU; 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	2020-12-28T08:14:22Z	SLCO3A1, a novel Crohn's disease-associated gene, regulates NF-κB activity and associates with intestinal perforation	Wei S.-C.; Podolsky D.K.; Wong J.-M.; Tan Y.-Y.; Weng M.-T.; Lai L.-C.; Hsiao J.-H.; Chuang E.Y.; Shun C.-T.; Wu D.-C.; Kao A.-W.; Chuang C.-S.; YEN-HSUAN NI; Shieh M.-J.; Tung C.-C.; Chen Y.; Wang C.-Y.; Xavier R.J.
臺大學術典藏	2020-12-28T08:14:12Z	SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKC?-dependent Pathway	Shun C.-T.; YEN-HSUAN NI; Chuang E.Y.; Hsiao J.-H.; Lai L.-C.; Yu L.C.H.; Wei S.-C.; Yang-Yen H.-F.; Tsao P.-N.; Weng M.-T.; Tung C.-C.; Xavier R.J.; Podolsky D.K.; Yen J.J.Y.; Wong J.-M.
臺大學術典藏	2020-12-28T07:56:49Z	Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation	Lin L.-Y.; JYH-MING JIMMY JUANG; Chuang E.Y.; Chang S.-N.; Hsieh C.-S.; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-28T07:56:42Z	An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases	Huang S.-H.; Chang Y.-S.; JYH-MING JIMMY JUANG; Chang K.-W.; Tsai M.-H.; Lu T.-P.; Lai L.-C.; Chuang E.Y.; Huang N.-T.
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.

显示项目 221-230 / 539 (共54页)
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