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機構 日期 題名 作者
臺大學術典藏 2011 IKZF1 deletions predict a poor prognosis in children with B-cell progenitor acute lymphoblastic leukemia: A multicenter analysis in Taiwan Yang Y.-L. ;Hung C.-C. ;Chen J.-S. ;Lin K.-H. ;Jou S.-T. ;Hsiao C.-C. ;Sheen J.-M. ;Cheng C.-N. ;Wu K.-H. ;Lin S.-R. ;Yu S.-L. ;Chen H.-Y. ;Lu M.-Y. ;Wang S.-C. ;Hsiu-Hao Chang ;Lin S.-W. ;Su Y.-N. ;Lin D.-T.; Yang Y.-L.; Hung C.-C.; Chen J.-S.; Lin K.-H.; Jou S.-T.; Hsiao C.-C.; Sheen J.-M.; Cheng C.-N.; Wu K.-H.; Lin S.-R.; Yu S.-L.; Chen H.-Y.; Lu M.-Y.; Wang S.-C.; HSIU-HAO CHANG; Lin S.-W.; Su Y.-N.; Lin D.-T.
臺大學術典藏 2011 Genetic mutation in male patients with incontinentia pigmenti Lin S.-Y.;Po-Nien Tsao;Hsieh W.-S.;Hung C.-C.;Su Y.-N.; Lin S.-Y.; PO-NIEN TSAO; Hsieh W.-S.; Hung C.-C.; Su Y.-N.
臺大學術典藏 2011 IKZF1 deletions predict a poor prognosis in children with B-cell progenitor acute lymphoblastic leukemia: A multicenter analysis in Taiwan SHIANN-TANG JOU; Lin K.-H.; Chen J.-S.; Hung C.-C.; Yang Y.-L.; Lin D.-T.; Su Y.-N.; Lin S.-W.; Chang H.-H.; Wang S.-C.; Lu M.-Y.; Hsiao C.-C.; Sheen J.-M.; Cheng C.-N.; Wu K.-H.; Lin S.-R.; Yu S.-L.; Chen H.-Y.
臺大學術典藏 2010 Seventeen Y-chromosomal short tandem repeat haplotypes in seven groups of population living in Taiwan Hsiao-Lin Hwa;Tseng L.-H.;Ko T.-M.;Chang Y.-Y.;Yin H.-Y.;Su Y.-N.;Lee J.C.-I.; HSIAO-LIN HWA; Tseng L.-H.; Ko T.-M.; Chang Y.-Y.; Yin H.-Y.; Su Y.-N.; Lee J.C.-I.
臺大學術典藏 2010 Seventeen Y-chromosomal short tandem repeat haplotypes in seven groups of population living in Taiwan JAMES CHUN-I LEE; Su Y.-N.; Yin H.-Y.; Chang Y.-Y.; Ko T.-M.; Tseng L.-H.; Hwa H.-L.; Hwa H.-L.;Tseng L.-H.;Ko T.-M.;Chang Y.-Y.;Yin H.-Y.;Su Y.-N.;James Chun-I Lee
臺大學術典藏 2010 CYP1A1 modifies the effect of maternal exposure to environmental tobacco smoke on child behavior Hsieh C.-J.;Suh-Fang Jeng;Su Y.-N.;Liao H.-F.;Hsieh W.-S.;Wu K.-Y.;Chen P.-C.; Hsieh C.-J.; SUH-FANG JENG; Su Y.-N.; Liao H.-F.; Hsieh W.-S.; Wu K.-Y.; Chen P.-C.
臺大學術典藏 2010 Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosis Lin Y.-P.;Su Y.-N.;Weng W.-C.;Wang-Tso Lee; Lin Y.-P.; Su Y.-N.; Weng W.-C.; WANG-TSO LEE
臺大學術典藏 2010 Clinical and genetic analysis of Peutz-Jeghers syndrome patients in Taiwan Weng M.-T.; YEN-HSUAN NI; Su Y.-N.; Wong J.-M.; Wei S.-C.
臺大學術典藏 2009 Mesothelin inhibits paclitaxel-induced apoptosis through the PI3K pathway Hu Y.-H.; WEN-FANG CHENG; Su Y.-N.; Lee C.-N.; Hsieh C.-Y.; Chen C.-A.; Chang M.-C.
臺大學術典藏 2009 Neonatal and Pregnancy Outcome in Primary Antiphospholipid Syndrome: A 10-year Experience in One Medical Center Chou A.-K.; Hsieh S.-C.; Su Y.-N.; Jeng S.-F.; Chen C.-Y.; Chou H.-C.; PO-NIEN TSAO; Hsieh W.-S.
臺大學術典藏 2008 Connective tissue growth factor linked to the E7 tumor antigen generates potent antitumor immune responses mediated by an antiapoptotic mechanism Cheng W.-F.; Chang M.-C.; Sun W.-Z.; Lee C.-N.; Lin H.-W.; Su Y.-N.; Hsieh C.-Y.; CHI-AN CHEN
臺大學術典藏 2008 Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison Lee C.-N.; Lin C.-Y.; Cheng W.-F.; CHI-AN CHEN; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L.; Hung C.-C.
臺大學術典藏 2008 Association of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) mutation/variant/haplotype and Tumor Necrosis Factor (TNF) promoter polymorphism in hyperlipidemic pancreatitis Wei S.-C.; Wong J.-M.; Kuo C.-H.; Su Y.-N.; Chang Y.-T.; Chang M.-C.; Su T.-C.; PO-CHIN LIANG
臺大學術典藏 2008 Diagnosis of BSEP/ABCB11 Mutations in Asian Patients with Cholestasis Using Denaturing High Performance Liquid Chromatography Chen H.-L.; Liu Y.-J.; Su Y.-N.; Wang N.-Y.; Wu S.-H.; Ni Y.-H.; Hsu H.-Y.; Wu T.-C.; MEI-HWEI CHANG
國立臺灣大學 2007 P1-120 Influential factors of the development in infants and toddlers application of the “International Classification of Functioning, Disability and Health” framework Hwang, A.-W.; Liao, H.-F.; Hsieh, W.-S.; Chen, P.-C.; Su, Y.-N.; Weng, L.-J.
臺大學術典藏 2007 Molecular assay of -α3.7 and -α4.2 deletions causing α-thalassemia by denaturing high-performance liquid chromatography Hung C.-C.;Lee C.-N.;Chen C.-P.;Jong Y.-J.;Hsieh W.-S.;Win-Li Lin;Su Y.-N.;Hsu S.-M.; Hung C.-C.; Lee C.-N.; Chen C.-P.; Jong Y.-J.; Hsieh W.-S.; Win-Li Lin; Su Y.-N.; Hsu S.-M.
臺大學術典藏 2007 Congenital central hypoventilation syndrome with PHOX2B gene mutation in a Taiwanese infant Chen, L.-R.;Tsao, P.-N.;Su, Y.-N.;Fan, P.-C.;Chou, H.-C.;Chen, C.-Y.;Chang, Y.-H.;Hsieh, W.-S.; WU-SHIUN HSIEH
臺大學術典藏 2007 Unequal crossover recombination - Population screening for PHOX2B gene polyalanine polymorphism using CE Hung C.-C.;Su Y.-N.;Tsao P.-N.;Chen P.-C.;Lin S.-J.;Lin C.-H.;Mu S.-C.;Liu C.-A.;Chang Y.-C.;Win-Li Lin;Hsieh W.-S.;Hsu S.-M.; Hung C.-C.; Su Y.-N.; Tsao P.-N.; Chen P.-C.; Lin S.-J.; Lin C.-H.; Mu S.-C.; Liu C.-A.; Chang Y.-C.; Win-Li Lin; Hsieh W.-S.; Hsu S.-M.
臺大學術典藏 2007 Congenital central hypoventilation syndrome with PHOX2B gene mutation in a Taiwanese infant Chen L.-R.; PO-NIEN TSAO; Su Y.-N.; Fan P.-C.; Chou H.-C.; Chen C.-Y.; Chang Y.-H.; Hsieh W.-S.
臺大學術典藏 2007 Perinatal and infant health outcomes among neonates born to aboriginal parents in Taiwan Chang Y.-H.;Chen P.-C.;Hsieh C.-J.;Jeng S.-F.;Liao H.-F.;Su Y.-N.;Lin S.-J.;Hung-Chieh Chou;Lin Y.-P.;Hsieh W.-S.; Chang Y.-H.; Chen P.-C.; Hsieh C.-J.; Jeng S.-F.; Liao H.-F.; Su Y.-N.; Lin S.-J.; HUNG-CHIEH CHOU; Lin Y.-P.; Hsieh W.-S.
國立臺灣大學 2006-03 Determination of SMN1/SMN2 Gene Dosage by a Quantitative Genotyping Platform Combining Capillary Electrophoresis and MALDI-TOF Mass Spectrometry Kao, H.-Y.; Su, Y.-N.; Liao, H.-K.; Liu, M.S.; Chen, Y.-J.
臺大學術典藏 2006 Sindbis virus replicon particles encoding calreticulin linked to a tumor antigen generate long-term tumor-specific immunity CHI-AN CHEN; Hsieh C.-Y.; Wu T.-C.; Cheng W.-F.;Lee C.-N.;Su Y.-N.;Chai C.-Y.;Chang M.-C.;Polo J.M.;Hung C.-F.;Wu T.-C.;Hsieh C.-Y.;Chi-An Chen; Cheng W.-F.; Lee C.-N.; Su Y.-N.; Chai C.-Y.; Chang M.-C.; Polo J.M.; Hung C.-F.
臺大學術典藏 2006 A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay Hsieh S.-T.; CHI-AN CHEN; Lin C.-Y.;Su Y.-N.;Lee C.-N.;Hung C.-C.;Cheng W.-F.;Lin W.-L.;Chi-An Chen;Hsieh S.-T.; Lin C.-Y.; Su Y.-N.; Lee C.-N.; Hung C.-C.; Cheng W.-F.; Lin W.-L.
臺大學術典藏 2006 Septic shock after intracervical laminaria insertion Lee C.-N.; Chen C.-A; Su Y.-N; Cheng W.-F; SHIN-YU LIN; Shin-Yu Lin;Cheng W.-F;Su Y.-N;Chen C.-A;Lee C.-N.
臺大學術典藏 2006 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.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; Wu M.-H.; Wang C.-C.; Yeh S.-J.; Chen W.-J.; Liu Y.-B.; Ho Y.-L.; JYH-MING JIMMY JUANG; Chiang F.-T.; Su Y.-N.; Hsieh F.-J.; Lai L.-P.

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