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Showing items 281-290 of 353  (36 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-02-12T04:06:08Z Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison Lin W.-L.;Su Y.-N;Jong Y.-J;Yang C.-C;Hsieh S.-T;Chen C.-A;Cheng W.-F;Lin C.-Y;CHIEN-NAN LEE;Hung C.-C; Hung C.-C; CHIEN-NAN LEE; Lin C.-Y; Cheng W.-F; Chen C.-A; Hsieh S.-T; Yang C.-C; Jong Y.-J; Su Y.-N; Lin W.-L.
臺大學術典藏 2020-02-06T08:32:09Z Two separate functions of NME3 critical for cell survival underlie a neurodegenerative disorder Chen C.-W.;Wang H.-L.;Huang C.-W.;Huang C.-Y.;Lim W.K.;Chen Tu I.;Koorapati A.;Hsieh S.-T.;Kan H.-W.;Shiou-Ru Tzeng;Liao J.-C.;Chong W.M.;Naroditzky I.;Kidron D.;Eran A.;Nijim Y.;Sela E.;Feldman H.B.;Kalfon L.;Raveh-Barak H.;Falik-Zaccai T.C.;Elpeleg O.;Mandel H.;Chang Z.-F.; Chen C.-W.; Wang H.-L.; Huang C.-W.; Huang C.-Y.; Lim W.K.; Chen Tu I.; Koorapati A.; Hsieh S.-T.; Kan H.-W.; SHIOU-RU TZENG; Liao J.-C.; Chong W.M.; Naroditzky I.; Kidron D.; Eran A.; Nijim Y.; Sela E.; Feldman H.B.; Kalfon L.; Raveh-Barak H.; Falik-Zaccai T.C.; Elpeleg O.; Mandel H.; Chang Z.-F.
臺大學術典藏 2020-02-06T06:49:52Z Preimplantation genetic diagnosis and screening: Current status and future challenges Chen H.-F;Shee-Uan Chen;Ma G.-C;Hsieh S.-T;Tsai H.-D;Yang Y.-S;Chen M.; Chen H.-F; SHEE-UAN CHEN; Ma G.-C; Hsieh S.-T; Tsai H.-D; Yang Y.-S; Chen M.
臺大學術典藏 2020-02-06T06:49:51Z Preimplantation genetic diagnosis of neurodegenerative diseases: Review of methodologies and report of our experience as a regional reference laboratory Liao C.-H;Chang M.-Y;Ma G.-C;Chang S.-P;Lin C.-F;Lin W.-H;Chen H.-F;Shee-Uan Chen;Lee Y.-C;Chao C.-C;Chen M;Hsieh S.-T.; Liao C.-H; Chang M.-Y; Ma G.-C; Chang S.-P; Lin C.-F; Lin W.-H; Chen H.-F; SHEE-UAN CHEN; Lee Y.-C; Chao C.-C; Chen M; Hsieh S.-T.
臺大學術典藏 2020-02-06T05:22:27Z A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay Hsieh S.-T.;Chen C.-A.;Lin W.-L.;WEN-FANG CHENG;Hung C.-C.;Lee C.-N.;Su Y.-N.;Lin C.-Y.; Lin C.-Y.; Su Y.-N.; Lee C.-N.; Hung C.-C.; WEN-FANG CHENG; Lin W.-L.; Chen C.-A.; Hsieh S.-T.; Lin C.-Y.; Su Y.-N.; Lee C.-N.; Hung C.-C.; WEN-FANG CHENG; Lin W.-L.; Chen C.-A.; Hsieh S.-T.
臺大學術典藏 2020-02-06T05:22:22Z Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison Lin W.-L.;Su Y.-N.;Jong Y.-J.;Yang C.-C.;Hsieh S.-T.;Chen C.-A.;WEN-FANG CHENG;Lin C.-Y.;Lee C.-N.;Hung C.-C.; Hung C.-C.; Lee C.-N.; Lin C.-Y.; WEN-FANG CHENG; Chen C.-A.; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L.; Hung C.-C.; Lee C.-N.; Lin C.-Y.; WEN-FANG CHENG; Chen C.-A.; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L.
臺大學術典藏 2020 Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser Lai H.-J.;Huang K.-C.;Liang Y.-C.;Kuo-Liong Chien;Lee M.-J.;Hsieh S.-T.;Chao C.-C.;Yang C.-C.; Lai H.-J.; Huang K.-C.; Liang Y.-C.; KUO-LIONG CHIEN; Lee M.-J.; Hsieh S.-T.; Chao C.-C.; Yang C.-C.
臺大學術典藏 2020 Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser Lai H.-J.;Huang K.-C.;Liang Y.-C.;Chien K.-L.;Lee M.-J.;Hsieh S.-T.;Chi-Chao Chao;Yang C.-C.; Lai H.-J.; Huang K.-C.; Liang Y.-C.; Chien K.-L.; Lee M.-J.; Hsieh S.-T.; CHI-CHAO CHAO; Yang C.-C.
臺大學術典藏 2019-11-29T03:04:22Z Auditory agnosia caused by a tectal germinoma Pan C.-L.;Meng-Fai Kuo;Hsieh S.-T.; Pan C.-L.; MENG-FAI KUO; Hsieh S.-T.
臺大學術典藏 2019 Skin nerve pathology: Biomarkers of premanifest and manifest amyloid neuropathy Hsieh S.-T.; Cheng Y.-Y.; Lin Y.-H.; Yeh T.-Y.; Lin W.-M.; Chiang H.; Jiang H.-H.; Liao C.-H.; Kan H.-W.; Hsueh H.-W.; CHI-CHAO CHAO; Chi-Chao Chao;Hsueh H.-W.;Kan H.-W.;Liao C.-H.;Jiang H.-H.;Chiang H.;Lin W.-M.;Yeh T.-Y.;Lin Y.-H.;Cheng Y.-Y.;Hsieh S.-T.

Showing items 281-290 of 353  (36 Page(s) Totally)
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