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機構 日期 題名 作者
臺大學術典藏 2022-04-20T07:19:17Z Concurrent analysis of copy number variation and gene expression: Application in paired non-smoking female lung cancer patients Chen P.-C.; Lu T.-P.; Chang J.-C.; Lai L.-C.; Tsai M.-H.; CHUHSING KATE HSIAO; Chuang E.Y.
臺大學術典藏 2022-04-20T07:19:16Z Identification of genes with consistent methylation levels across different human tissues Lu T.-P.; Chen K.T.; Tsai M.-H.; Kuo K.-T.; CHUHSING KATE HSIAO; Lai L.-C.; Chuang E.Y.
臺大學術典藏 2022-04-20T07:19:15Z SNP rs10248565 in HDAC9 as a novel genomic aberration biomarker of lung adenocarcinoma in non-smoking women Lai L.-C.; Tsai M.-H.; Chen P.-C.; Chen L.H.; Hsiao J.-H.; Chen S.-K.; Lu T.-P.; Lee J.-M.; Hsu C.-P.; CHUHSING KATE HSIAO; Chuang E.Y.
臺大學術典藏 2022-04-20T07:19:14Z Identification of regulatory SNPs associated with genetic modifications in lung adenocarcinoma Bioinformatics Lu T.-P.; CHUHSING KATE HSIAO; Lai L.-C.; Tsai M.-H.; Hsu C.-P.; Lee J.-M.; Chuang E.Y.
臺大學術典藏 2022-03-31T02:39:25Z A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity Lin S.-Y.; Hsieh S.-C.; Lin Y.-C.; Lee C.-N.; Tsai M.-H.; Lai L.-C.; Chuang E.Y.; PAU-CHUNG CHEN; Hung C.-C.; Chen L.-Y.; Hsieh W.S.; Niu D.-M.; Su Y.-N.; Ho H.-N.
臺大學術典藏 2022-02-23T08:10:41Z 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.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; HUI-CHUN HUANG; 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 2022-01-12T07:07:26Z Prognostic significance of NPM1 mutation-modulated microRNA-mRNA regulation in acute myeloid leukemia Chiu Y.-C.; Tsai M.-H.; Chou W.-C.; Liu Y.-C.; Kuo Y.-Y.; HSIN-AN HOU; Lu T.-P.; Lai L.-C.; Chen Y.; Tien H.-F.; Chuang E.Y.
臺大學術典藏 2022-01-07T06:05:57Z IL-1β-driven neutrophilia preserves antibacterial defense in the absence of the kinase IKKβ Hsu L.-C.; Enzler T.; Seita J.; Timmer A.M.; CHIH-YUAN LEE; Lai T.-Y.; Yu G.-Y.; Lai L.-C.; Temkin V.; Sinzig U.; Aung T.; Nizet V.; Weissman I.L.; Karin M.
臺大學術典藏 2021-09-09T07:52:45Z 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 2021-09-09T07:52:45Z 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.; CHIH-CHIEH YU; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.

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