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

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顯示項目 201-250 / 539 (共11頁)
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機構	日期	題名	作者
臺大學術典藏	2020-12-30T08:47:44Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Chiang F.-T.; Hwang J.-J.; Lin L.-Y.; Yu C.-C.; CHIA-TI TSAI; Liu Y.-B.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.
臺大學術典藏	2020-12-30T08:47:43Z	Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome	Lin J.-L.; Chuang E.Y.; Lai L.-P.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; CHIA-TI TSAI; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.
臺大學術典藏	2020-12-30T08:47:41Z	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.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.; CHIA-TI TSAI; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Juang J.-M.J.
臺大學術典藏	2020-12-30T08:47:38Z	Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation	Chiang F.-T.; Lin J.-L.; Hwang J.-J.; Tseng C.-D.; CHIA-TI TSAI; 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.
臺大學術典藏	2020-12-30T08:47:32Z	Prevalence of sudden arrhythmic death syndrome-related genetic mutations in an Asian cohort of whole genome sequence	Chiu F.-C.; Wu C.-K.; Hwang J.-J.; Chuang E.Y.; CHIA-TI TSAI; Huang P.-S.; Hsieh C.-S.; Chang S.-N.; Chen J.-J.
臺大學術典藏	2020-12-30T07:47:50Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	Chuang E.Y.; Lai L.-P.; Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; YEN BIN LIU; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.
臺大學術典藏	2020-12-30T07:47:49Z	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.; YEN BIN LIU; Tsai C.-T.; Lin L.-Y.; 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	2020-12-30T07:47:46Z	Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry	Jyh-Ming J.-J.; YEN BIN LIU; 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 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	2020-12-30T07:47:44Z	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.; YEN BIN LIU; 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	2020-12-29T08:15:53Z	MiR-338-5p inhibits cell proliferation, colony formation, migration and cisplatin resistance in esophageal squamous cancer cells by targeting FERMT2	Hsieh, Y.-C.; Chen, L.-H.; Lin, W.-C.; Lin, W.-C.;Chen, L.-H.;Hsieh, Y.-C.;Yang, P.-W.;Lai, L.-C.;Chuang, E.Y.;Lee, J.-M.;Tsai, M.-H.; Yang, P.-W.; Lai, L.-C.; Chuang, E.Y.; Lee, J.-M.; Tsai, M.-H.; LI-HAN CHEN
臺大學術典藏	2020-12-28T12:04:07Z	Next-generation sequencing in the genetics of human atrial fibrillation	Hsieh C.-S.; Chuang E.Y.; Juang J.-M.J.; HWANG, JUEY-JEN; Tseng C.-D.; Chiang F.-T.; Lai L.-P.; Lin J.-L.; Tsai C.-T.
臺大學術典藏	2020-12-28T12:04:03Z	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	2020-12-28T12:03:59Z	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.; Lin L.-Y.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-28T12:03:54Z	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	2020-12-28T12:03:19Z	Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry	Lin J.-L.; Yang D.-H.; Chuang J.-Y.; Sherri Yeh S.-F.; Chen J.-J.; Liao M.-T.; Jyh-Ming J.-J.; 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.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.
臺大學術典藏	2020-12-28T12:03:16Z	GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death	Antzelevitch C.; Rivolta I.; Chuang E.Y.; Lai L.-P.; Yeh S.-F.S.; Lai L.-C.; Lu T.-P.; Huang H.-C.; Chen C.-Y.J.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Liu Y.-B.; Juang J.-M.J.; Binda A.; Lee S.-J.; HWANG, JUEY-JEN; Chen W.-J.
臺大學術典藏	2020-12-28T12:03:15Z	Prevalence of sudden arrhythmic death syndrome-related genetic mutations in an Asian cohort of whole genome sequence	Chiu F.-C.; Wu C.-K.; HWANG, JUEY-JEN; Chuang E.Y.; Tsai C.-T.; Huang P.-S.; Hsieh C.-S.; Chang S.-N.; Chen J.-J.
臺大學術典藏	2020-12-28T10:52:55Z	Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry	Liu Y.-B.; Jyh-Ming J.-J.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; HUI-CHUN HUANG; 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	2020-12-28T10:52:54Z	GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death	Binda A.; Juang J.-M.J.; 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	2020-12-28T10:02:42Z	Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome	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.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.
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.
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.
臺大學術典藏	2020-12-02T11:04:33Z	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.; CHO-KAI WU; Lee J.-K.; Lin L.-Y.; 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	2020-12-02T11:04:23Z	Prevalence of sudden arrhythmic death syndrome-related genetic mutations in an Asian cohort of whole genome sequence	Huang P.-S.; Hsieh C.-S.; Chang S.-N.; Chen J.-J.; Chiu F.-C.; CHO-KAI WU; Hwang J.-J.; Chuang E.Y.; Tsai C.-T.
臺大學術典藏	2020-12-02T09:15:18Z	Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation	Lin T.-H.; Tsai C.-F.; Ueng K.-C.; Chuang E.Y.; Chang S.-N.; Hsieh C.-S.; Tsai C.-T.; Wu C.-K.; Lee J.-K.; Lin L.-Y.; YI-CHIH WANG; Yu C.-C.; Lai L.-P.; Tseng C.-D.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-02T02:34:42Z	Duodenal ulcer-related antigens from Helicobacter pylori: Immunoproteome and protein microarray approaches	Lin Y.-F.;Chen C.-Y.;Tsai M.-H.;Wu M.-S.;Wang Y.-C.;Chuang E.Y.;Lin J.-T.;Pan-Chyr Yang;Chow L.-P.; Lin Y.-F.; Chen C.-Y.; Tsai M.-H.; Wu M.-S.; Wang Y.-C.; Chuang E.Y.; Lin J.-T.; PAN-CHYR YANG; Chow L.-P.
臺大學術典藏	2020-12-02T02:34:34Z	A probe-density-based analysis method for array CGH data: Simulation, normalization and centralization	Chen H.-I.H.; Hsu F.-H.; Jiang Y.; Tsai M.-H.; PAN-CHYR YANG; Meltzer P.S.; Chuang E.Y.; Chen Y.
臺大學術典藏	2020-12-02T02:34:32Z	Erratum: A probe-density-based analysis method for array CGH data: Simulation, normalization and centralization (Bioinformatics (2008) vol. 24 (16) (1749-1756))	Chen H.-I.H.; Hsu F.-H.; Jiang Y.; Tsai M.-H.; PAN-CHYR YANG; Meltzer P.S.; Chuang E.Y.; Chen Y.
臺大學術典藏	2020-12-02T02:34:15Z	Identification of a novel biomarker, SEMA5A, for non-small cell lung carcinoma in nonsmoking women	Lu T.-P.;Tsai M.-H.;Lee J.-M.;Hsu C.-P.;Chen P.-C.;Lin C.-W.;Shih J.-Y.;Pan-Chyr Yang;Hsiao C.K.;Lai L.-C.;Chuang E.Y.; Lu T.-P.; Tsai M.-H.; Lee J.-M.; Hsu C.-P.; Chen P.-C.; Lin C.-W.; Shih J.-Y.; PAN-CHYR YANG; Hsiao C.K.; Lai L.-C.; Chuang E.Y.
臺大學術典藏	2020-11-27T03:28:34Z	Altered gut microbiota and inflammatory cytokine responses in patients with Parkinson's disease	Lin C.-H.; CHIEH-CHANG CHEN; Chiang H.-L.; Liou J.-M.; Chang C.-M.; Lu T.-P.; Chuang E.Y.; Tai Y.-C.; Cheng C.; Lin H.-Y.; Wu M.-S.
臺大學術典藏	2020-11-27T03:28:33Z	Long-term changes of gut microbiota, antibiotic resistance, and metabolic parameters after Helicobacter pylori eradication: a multicentre, open-label, randomised trial	Liou J.-M.; CHIEH-CHANG CHEN; Chang C.-M.; Fang Y.-J.; Bair M.-J.; Chen P.-Y.; Chang C.-Y.; Hsu Y.-C.; Chen M.-J.; Chien-Chuan Chen; Lee J.-Y.; Yang T.-H.; Luo J.-C.; Chen C.-Y.; Hsu W.-F.; Chen Y.-N.; Wu J.-Y.; Lin J.-T.; Lu T.-P.; Chuang E.Y.; El-Omar E.M.; Wu M.-S.; Taiwan Gastrointestinal Disease; Helicobacter Consortium
臺大學術典藏	2020-11-27T03:28:32Z	Comparison of DNA stabilizers and storage conditions on preserving fecal microbiota profiles	Liou J.-M.; Fang Y.-J.; Chuang E.Y.; Wu M.-S.; CHIEH-CHANG CHEN; Wu W.-K.; Chang C.-M.; Panyod S.; Lu T.-P.
臺大學術典藏	2020-11-18T05:27:46Z	Genetic loci associated with an earlier age at onset in multiplex schizophrenia	Chuang E.Y.; Chang L.-C.; Chen C.-H.; Wu J.-Y.; Tsuang M.T.; Chen W.J.; Lu T.-P.; Hwu H.-G.; Liu C.-M.; Lien Y.-J.; Wang S.-H.; Woolston A.L.;Hsiao P.-C.;Po-Hsiu Kuo;Wang S.-H.;Lien Y.-J.;Liu C.-M.;Hwu H.-G.;Lu T.-P.;Chuang E.Y.;Chang L.-C.;Chen C.-H.;Wu J.-Y.;Tsuang M.T.;Chen W.J.; Woolston A.L.; Hsiao P.-C.; PO-HSIU KUO
臺大學術典藏	2020-11-17T02:45:38Z	Distinct Signaling Pathways After Higher or Lower Doses of Radiation in Three Closely Related Human Lymphoblast Cell Lines	TZU-PIN LU; Lai L.-C.; Lin B.-I.; Chen L.-H.; Hsiao T.-H.; Liber H.L.; Cook J.A.; Mitchell J.B.; Tsai M.-H.; Chuang E.Y.
臺大學術典藏	2020-11-17T02:45:37Z	Down-regulation of NDRG1 promotes migration of cancer cells during reoxygenation	Chuang E.Y.; Lee C.-Y.; TZU-PIN LU; Sher Y.-P.; Tsai M.-H.; Chen K.-C.; Su Y.-Y.; Lai L.-C.
臺大學術典藏	2020-11-17T02:45:37Z	Concurrent analysis of copy number variations and expression profiles to identify genes associated with tumorigenesis and survival outcome in lung adenocarcinoma	Tzu-Pin Lu ;Chen P.-C.;Lai L.-C.;Tsai M.-H.;Hsiao C.K.;Chuang E.Y.; TZU-PIN LU; Chen P.-C.; Lai L.-C.; Tsai M.-H.; Hsiao C.K.; Chuang E.Y.
臺大學術典藏	2020-11-17T02:45:37Z	Concurrent analysis of copy number variation and gene expression: Application in paired non-smoking female lung cancer patients	Chen P.-C.; Chang J.-C.;Lai L.-C.;Tzu-Pin Lu ;Tsai M.-H.;Chuang E.Y.;Hsiao C.K.;Chen P.-C.; Chang J.-C.; Lai L.-C.; TZU-PIN LU; Tsai M.-H.; Chuang E.Y.; Hsiao C.K.

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	造訪人次 : 51994070 線上人數 : 771 教育部委託研究計畫計畫執行:國立臺灣大學圖書館