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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Showing items 351-375 of 715  (29 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-03-05T08:16:44Z Overexpression of Placenta Growth Factor Contributes to the Pathogenesis of Pulmonary Emphysema Tsao P.-N.;Su Y.-N.;Li H.;Pei-Hsin Huang;Chien C.-T.;Lai Y.-L.;Lee C.-N.;Chen C.-A.;Cheng W.-F.;Wei S.-C.;Yu C.-J.;Hsieh F.-J.;Hsu S.-M.; Tsao P.-N.; Su Y.-N.; Li H.; PEI-HSIN HUANG; Chien C.-T.; Lai Y.-L.; Lee C.-N.; Chen C.-A.; Cheng W.-F.; Wei S.-C.; Yu C.-J.; Hsieh F.-J.; Hsu S.-M.
臺大學術典藏 2020-03-05T07:52:26Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Liu S.-Y.; Tsai W.-Y.; Lee N.-C.; Lee C.-T.; Tung Y.-C.; Hwu W.-L.; Shih J.-C.; Lin W.-H.; Wu M.-Z.; KUAN-TING KUO; Yang Y.-L.; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.
臺大學術典藏 2020-03-05T06:38:58Z Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma Yang C.-Y.; Liau J.-Y.; Huang W.-J.; Chang Y.-T.; Chang M.-C.; JEN-CHIEH LEE; Tsai J.-H.; Su Y.-N.; Hung C.-C.; Jeng Y.-M.
臺大學術典藏 2020-03-05T06:28:38Z Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma Hung C.-C.; Su Y.-N.; Tsai J.-H.; Lee J.-C.; Chang M.-C.; Chang Y.-T.; Huang W.-J.; JAU-YU LIAU; Yang C.-Y.; Yang C.-Y.;Jau-Yu Liau;Huang W.-J.;Chang Y.-T.;Chang M.-C.;Lee J.-C.;Tsai J.-H.;Su Y.-N.;Hung C.-C.;Jeng Y.-M.; Jeng Y.-M.
臺大學術典藏 2020-03-05T06:05:45Z Correlation of Survival Motor Neuron Expression in Leukocytes and Spinal Cord in Spinal Muscular Atrophy LI-KAI TSAI; Yang C.-C.; Ting C.-H.; Su Y.-N.; Hwu W.-L.; Li H.
臺大學術典藏 2020-03-05T03:20:31Z Soluble vascular endothelial growth factor receptor-1 protects mice in sepsis Tsao P.-N.;Chan F.-T.;Wei S.-C.;Hsieh W.-S.;Chou H.-C.;Su Y.-N.;Chen C.-Y.;Wen-Ming Hsu;Hsieh F.-J.;Hsu S.-M.; Tsao P.-N.; Chan F.-T.; Wei S.-C.; Hsieh W.-S.; Chou H.-C.; Su Y.-N.; Chen C.-Y.; WEN-MING HSU; Hsieh F.-J.; Hsu S.-M.
臺大學術典藏 2020-03-05T03:20:25Z Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome Lin S.-Y.;Lee C.-N.;Hung C.-C.;Tsai W.-Y.;Lin S.-P.;Li N.-C.;Hsieh W.-S.;Tung Y.-C.;Niu D.-M.;Wen-Ming Hsu;Chen L.-Y.;Fang M.-Y.;Tu M.-P.;Kuo P.-W.;Lin C.-Y.;Su Y.-N.;Ho H.-N.; Lin S.-Y.; Lee C.-N.; Hung C.-C.; Tsai W.-Y.; Lin S.-P.; Li N.-C.; Hsieh W.-S.; Tung Y.-C.; Niu D.-M.; WEN-MING HSU; Chen L.-Y.; Fang M.-Y.; Tu M.-P.; Kuo P.-W.; Lin C.-Y.; Su Y.-N.; Ho H.-N.
臺大學術典藏 2020-03-04T09:03:21Z LDLR and ApoB are major genetic causes of autosomal dominant hypercholesterolemia in a taiwanese population Yang K.-C.;Su Y.-N.;Shew J.-Y.;Yang K.-Y.;Tseng W.-K.;Chau-Chung Wu;Lee Y.-T.; Yang K.-C.; Su Y.-N.; Shew J.-Y.; Yang K.-Y.; Tseng W.-K.; CHAU-CHUNG WU; Lee Y.-T.
臺大學術典藏 2020-03-04T09:03:19Z Corrections to the LDLR gene polymorphisms identified in a Taiwanese population [3] Yang K.-C.; Su Y.-N.; Shew J.-Y.; Yang K.-Y.; Tseng W.-K.; CHAU-CHUNG WU; Lee Y.-T.
臺大學術典藏 2020-03-03T03:06:51Z Generation and characterization of an ascitogenic mesothelin-expressing tumor model Cheng W.-F.;Hung C.-F.;Chai C.-Y.;Chen C.-A.;Lee C.-N.;Su Y.-N.;Wen-Yih Tseng;Hsieh C.-Y.;Shih I.-M.;Wang T.-L.;Wu T.-C.; Cheng W.-F.; Hung C.-F.; Chai C.-Y.; Chen C.-A.; Lee C.-N.; Su Y.-N.; WEN-YIH TSENG; Hsieh C.-Y.; Shih I.-M.; Wang T.-L.; Wu T.-C.
臺大學術典藏 2020-03-03T02:33:35Z Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1. MING-JEN LEE; Su Y.N.; You H.L.; Chiou S.C.; Lin L.C.; Yang C.C.; Lee W.C.; Hwu W.L.; Hsieh F.J.; Stephenson D.A.; Yu C.L.
臺大學術典藏 2020-03-03T02:33:35Z Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C Yang C.-C.; Su Y.-N.; Chiou P.-C.; Fietz M.J.; Yu C.-L.; Hwu W.-L.; MING-JEN LEE
臺大學術典藏 2020-03-02T12:11:12Z Cardioembolic stroke related to limb-girdle muscular dystrophy 1B Chen C.-H; SUNG-CHUN TANG; Su Y.-N; Yang C.-C; Jeng J.-S.
臺大學術典藏 2020-03-02T08:11:25Z A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay Lin C.-Y.;Su Y.-N.;Lee C.-N.;Hung C.-C.;Cheng W.-F.;Lin W.-L.;Chen C.-A.;Sung-Tsang Hsieh; Lin C.-Y.; Su Y.-N.; Lee C.-N.; Hung C.-C.; Cheng W.-F.; Lin W.-L.; Chen C.-A.; SUNG-TSANG HSIEH
臺大學術典藏 2020-03-02T08:11:22Z Use of multiplex PCR and CE for gene dosage quantification and its biomedical application for SMN, PMP22, and α-globin genes Hung C.-C.;Chien S.-C.;Lin C.-Y.;Chang C.-H.;Chang Y.-F.;Jong Y.-J.;Sung-Tsang Hsieh;Hsieh W.-S.;Liu M.S.;Lin W.-L.;Lee C.-N.;Su Y.-N.; Hung C.-C.; Chien S.-C.; Lin C.-Y.; Chang C.-H.; Chang Y.-F.; Jong Y.-J.; SUNG-TSANG HSIEH; Hsieh W.-S.; Liu M.S.; Lin W.-L.; Lee C.-N.; Su Y.-N.
臺大學術典藏 2020-03-02T08:11:20Z Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison Hung C.-C.;Lee C.-N.;Lin C.-Y.;Cheng W.-F.;Chen C.-A.;Sung-Tsang Hsieh;Yang C.-C.;Jong Y.-J.;Su Y.-N.;Lin W.-L.; Hung C.-C.; Lee C.-N.; Lin C.-Y.; Cheng W.-F.; Chen C.-A.; SUNG-TSANG HSIEH; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L.
臺大學術典藏 2020-02-27T07:43:24Z Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Lo H.-M.; Huang S.K.S.; Lin J.-L.; Lin J.-L.;Huang S.K.S.;Lo H.-M.;Wu M.-H.;Lin T.-K.;Chen S.-A.;Tsao H.-M.;Lei M.-H.;Ueng K.-C.;Wu T.-J.;Ko Y.-L.;Wang C.-C.;Yeh S.-J.;WEN-JONE CHEN;Ho Y.-L.;Liu Y.-B.;Juang J.-M.;Chiang F.-T.;Su Y.-N.;Lai L.-P.; Lai L.-P.; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; WEN-JONE CHEN; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.
臺大學術典藏 2020-02-27T07:43:16Z Erratum: Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms (Journal of Human Genetics (2005) 50 (490-496) DOI: 10.1007/s10038-005-0283-3) Lin J.-L.;Huang S.K.S.;Lo H.-M.;Wu M.-H.;Lin T.-K.;Chen S.-A.;Tsao H.-M.;Lei M.-H.;Ueng K.-C.;Wu T.-J.;Ko Y.-L.;Wang C.-C.;Yeh S.-J.;WEN-JONE CHEN;Ho Y.-L.;Liu Y.-B.;Juang J.-M.;Chiang F.-T.;Hsieh F.-J.;Su Y.-N.;Lai L.-P.; Lai L.-P.; Su Y.-N.; Hsieh F.-J.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; WEN-JONE CHEN; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Lin J.-L.; Huang S.K.S.; Lo H.-M.; Wu M.-H.; Chen S.-A.; Lin T.-K.
臺大學術典藏 2020-02-27T06:39:34Z A hospital-based study of clinical and genetic features of Crohn's disease Wei S.-C. ;Ni Y.-H. ;Yang H.-I. ;Su Y.-N. ;Chang M.-C. ;Chang Y.-T. ;Ming-Jium Shieh ;Wang C.-Y. ;Wong J.-M.; Wei S.-C.; Ni Y.-H.; Yang H.-I.; Su Y.-N.; Chang M.-C.; Chang Y.-T.; MING-JIUM SHIEH; Wang C.-Y.; Wong J.-M.
臺大學術典藏 2020-02-26T09:01:10Z Denaturing HPLC coupled with multiplex PCR for rapid detection of large deletions in Duchenne muscular dystrophy carriers Hung C.-C.;Su Y.-N.;Lin C.-Y.;Yang C.-C.;Lee W.-T.;Chien S.-C.;Win-Li Lin;Lee C.-N.; Hung C.-C.; Su Y.-N.; Lin C.-Y.; Yang C.-C.; Lee W.-T.; Chien S.-C.; Win-Li Lin; Lee C.-N.
臺大學術典藏 2020-02-26T09:01:10Z Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: Application to the SMN1/SMN2 gene Lee C.-N.; Chen C.-P.; Jong Y.-J.; Chen C.-A.; Cheng W.-F.; Win-Li Lin; Su Y.-N.; Hung C.-C.;Lee C.-N.;Chen C.-P.;Jong Y.-J.;Chen C.-A.;Cheng W.-F.;Win-Li Lin;Su Y.-N.; Hung C.-C.
臺大學術典藏 2020-02-26T09:01:10Z Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: A highly efficient and reliable carrier-screening test Su Y.-N.;Hung C.-C.;Li H.;Lee C.-N.;Cheng W.-F.;Tsao P.-N.;Chang M.-C.;Yu C.-L.;Hsieh W.-S.;Win-Li Lin;Hsu S.-M.; Su Y.-N.; Hung C.-C.; Li H.; Lee C.-N.; Cheng W.-F.; Tsao P.-N.; Chang M.-C.; Yu C.-L.; Hsieh W.-S.; Win-Li Lin; Hsu S.-M.
臺大學術典藏 2020-02-26T09:01:09Z A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay Chen C.-A.; Hsieh S.-T.; Lin C.-Y.;Su Y.-N.;Lee C.-N.;Hung C.-C.;Cheng W.-F.;Win-Li Lin;Chen C.-A.;Hsieh S.-T.; Lee C.-N.; Su Y.-N.; Lin C.-Y.; Win-Li Lin; Hung C.-C.; Cheng W.-F.
臺大學術典藏 2020-02-26T09:01:07Z Molecular and clinical analyses of 84 patients with tuberous sclerosis complex Hung C.-C.;Su Y.N.;Chien S.-C.;Liou H.-H.;Chen C.-C.;Chen P.-C.;Hsieh C.-J.;Chen C.-P.;Lee W.-T.;Win-Li Lin;Lee C.-N.; Hung C.-C.; Su Y.N.; Chien S.-C.; Liou H.-H.; Chen C.-C.; Chen P.-C.; Hsieh C.-J.; Chen C.-P.; Lee W.-T.; Win-Li Lin; Lee C.-N.
臺大學術典藏 2020-02-26T09:01:05Z Denaturing high-performance liquid chromatography: An efficient screening approach in the genetic diagnosis of hemoglobin Hammersmith Hung C.-C.;Chien S.-C.;Su Y.-N.;Chern J.P.S.;Lin K.-H.;Win-Li Lin; Hung C.-C.; Chien S.-C.; Su Y.-N.; Chern J.P.S.; Lin K.-H.; Win-Li Lin

Showing items 351-375 of 715  (29 Page(s) Totally)
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