English  |  正體中文  |  简体中文  |  Total items :0  
Visitors :  50947155    Online Users :  801
Project Commissioned by the Ministry of Education
Project Executed by National Taiwan University Library
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
About TAIR

Browse By

News

Copyright

Related Links

"su y n"

Return to Browse by Author
Sorting by Title Sort by Date

Showing items 131-180 of 715  (15 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
View [10|25|50] records per page

Institution Date Title Author
臺大學術典藏 2021-02-04T06:05:14Z Characterization of DNA vaccines encoding the domains of calreticulin for their ability to elicit tumor-specific immunity and antiangiogenesis Cheng W.-F.;Hung C.-F.;Chen C.-A.;Chien-Nan Lee;Su Y.-N.;Chai C.-Y.;Boyd D.A.K.;Hsieh C.-Y.;Wu T.-C.; Cheng W.-F.; Hung C.-F.; Chen C.-A.; CHIEN-NAN LEE; Su Y.-N.; Chai C.-Y.; Boyd D.A.K.; Hsieh C.-Y.; Wu T.-C.
臺大學術典藏 2021-02-04T06:05:13Z Antigen-specific CD8+ T lymphocytes generated from a DNA vaccine control tumors through the Fas-FasL pathway Cheng W.-F.;Chien-Nan Lee;Chang M.-C.;Su Y.-N.;Chen C.-A.;Hsieh C.-Y.; Cheng W.-F.; CHIEN-NAN LEE; Chang M.-C.; Su Y.-N.; Chen C.-A.; Hsieh C.-Y.
臺大學術典藏 2021-02-04T06:05:13Z Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: Application to the SMN1/SMN2 gene Hung C.-C.;Chien-Nan Lee;Chen C.-P.;Jong Y.-J.;Chen C.-A.;Cheng W.-F.;Lin W.-L.;Su Y.-N.; Hung C.-C.; CHIEN-NAN LEE; Chen C.-P.; Jong Y.-J.; Chen C.-A.; Cheng W.-F.; Lin W.-L.; Su Y.-N.
臺大學術典藏 2021-02-04T06:05:12Z Chimeric DNA vaccine reverses morphine-induced immunosuppression and tumorigenesis Cheng W.-F.;Chen L.-K.;Chen C.-A.;Chang M.-C.;Hsiao P.-N.;Su Y.-N.;Chien-Nan Lee;Jeng H.-J.;Hsieh C.-Y.;Sun W.-Z.; Cheng W.-F.; Chen L.-K.; Chen C.-A.; Chang M.-C.; Hsiao P.-N.; Su Y.-N.; CHIEN-NAN LEE; Jeng H.-J.; Hsieh C.-Y.; Sun W.-Z.
臺大學術典藏 2021-02-04T06:05:12Z 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.;Lin W.-L.;Chien-Nan Lee; Hung C.-C.; Su Y.-N.; Lin C.-Y.; Yang C.-C.; Lee W.-T.; Chien S.-C.; Lin W.-L.; CHIEN-NAN LEE
臺大學術典藏 2021-02-04T06:05:12Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Chien-Nan Lee;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Wu M.-H.;Hsieh F.-J.; CHIEN-NAN LEE; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J.
臺大學術典藏 2021-02-04T06:05:09Z Rapid genetic analysis of oculocutaneous albinism (OCA1) using denaturing high performance liquid chromatography (DHPLC) system Lin S.-Y.; Chien S.-C.; Su Y.-N.; CHIEN-NAN LEE; Chen C.-P.
臺大學術典藏 2021-02-04T06:05:09Z A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay Lin C.-Y.;Su Y.-N.;Chien-Nan Lee;Hung C.-C.;Cheng W.-F.;Lin W.-L.;Chen C.-A.;Hsieh S.-T.; Lin C.-Y.; Su Y.-N.; CHIEN-NAN LEE; Hung C.-C.; Cheng W.-F.; Lin W.-L.; Chen C.-A.; Hsieh S.-T.
臺大學術典藏 2021-02-04T06:05:08Z 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.;Lin W.-L.;Chien-Nan Lee; 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.; Lin W.-L.; CHIEN-NAN LEE
臺大學術典藏 2021-02-04T06:05:07Z Serum mesothelin in epithelial ovarian carcinoma: A new screening marker and prognostic factor Huang C.-Y.;Cheng W.-F.;Chien-Nan Lee;Su Y.-N.;Chien S.-C.;Tzeng Y.-L.;Hsieh C.-Y.;Chen C.-A.; Huang C.-Y.; Cheng W.-F.; CHIEN-NAN LEE; Su Y.-N.; Chien S.-C.; Tzeng Y.-L.; Hsieh C.-Y.; Chen C.-A.
臺大學術典藏 2021-02-04T06:05:07Z Sindbis virus replicon particles encoding calreticulin linked to a tumor antigen generate long-term tumor-specific immunity Cheng W.-F.; CHIEN-NAN LEE; Su Y.-N.; Chai C.-Y.; Chang M.-C.; Polo J.M.; Hung C.-F.; Wu T.-C.; Hsieh C.-Y.; Chen C.-A.
臺大學術典藏 2021-02-04T06:05:06Z Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in prader-willi syndrome and duchenne muscular dystrophy Hung C.-C.;Chen C.-P.;Lin S.-P.;Chien S.-C.;Chien-Nan Lee;Cheng W.-F.;Hsieh W.-S.;Liu M.S.;Su Y.-N.;Lin W.-L.; Hung C.-C.; Chen C.-P.; Lin S.-P.; Chien S.-C.; CHIEN-NAN LEE; Cheng W.-F.; Hsieh W.-S.; Liu M.S.; Su Y.-N.; Lin W.-L.
臺大學術典藏 2021-02-04T06:05:04Z Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy Huang W.-Y.;Hung C.-C.;Chien-Nan Lee;Su Y.-N.;Chen C.-P.; Huang W.-Y.; Hung C.-C.; CHIEN-NAN LEE; Su Y.-N.; Chen C.-P.
臺大學術典藏 2021-02-04T06:05:04Z Molecular assay of -α3.7 and -α4.2 deletions causing α-thalassemia by denaturing high-performance liquid chromatography Hung C.-C.;Chien-Nan Lee;Chen C.-P.;Jong Y.-J.;Hsieh W.-S.;Lin W.-L.;Su Y.-N.;Hsu S.-M.; Hung C.-C.; CHIEN-NAN LEE; Chen C.-P.; Jong Y.-J.; Hsieh W.-S.; Lin W.-L.; Su Y.-N.; Hsu S.-M.
臺大學術典藏 2021-02-04T06:05:03Z 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.;Hsieh S.-T.;Hsieh W.-S.;Liu M.S.;Lin W.-L.;Chien-Nan Lee;Su Y.-N.; Hung C.-C.; Chien S.-C.; Lin C.-Y.; Chang C.-H.; Chang Y.-F.; Jong Y.-J.; Hsieh S.-T.; Hsieh W.-S.; Liu M.S.; Lin W.-L.; CHIEN-NAN LEE; Su Y.-N.
臺大學術典藏 2021-02-04T06:05:02Z DNA vaccine encoding heat shock protein 60 co-linked to HPV16 E6 and E7 tumor antigens generates more potent immunotherapeutic effects than respective E6 or E7 tumor antigens Huang C.-Y.;Chen C.-A.;Chien-Nan Lee;Chang M.-C.;Su Y.-N.;Lin Y.-C.;Hsieh C.-Y.;Cheng W.-F.; Huang C.-Y.; Chen C.-A.; CHIEN-NAN LEE; Chang M.-C.; Su Y.-N.; Lin Y.-C.; Hsieh C.-Y.; Cheng W.-F.
臺大學術典藏 2021-02-04T06:05:02Z IL-6-encoding tumor antigen generates potent cancer immunotherapy through antigen processing and anti-apoptotic pathways Hsieh C.-Y.;Chen C.-A.;Huang C.-Y.;Chang M.-C.;Chien-Nan Lee;Su Y.-N.;Cheng W.-F.; Hsieh C.-Y.; Chen C.-A.; Huang C.-Y.; Chang M.-C.; CHIEN-NAN LEE; Su Y.-N.; Cheng W.-F.
臺大學術典藏 2021-02-04T06:05:01Z PGD of β-thalassaemia and HLA haplotypes using OmniPlex whole genome amplification Chen S.-U.;Su Y.-N.;Fang M.-Y.;Chang L.-J.;Tsai Y.-Y.;Lin L.-T.;Chien-Nan Lee;Yang Y.-S.; Chen S.-U.; Su Y.-N.; Fang M.-Y.; Chang L.-J.; Tsai Y.-Y.; Lin L.-T.; CHIEN-NAN LEE; Yang Y.-S.
臺大學術典藏 2021-02-04T06:05:00Z 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.;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.; 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 2021-02-04T06:04:59Z Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM Lin S.-Y.;Su Y.-N.;Hung C.-C.;Tsay W.;Chiou S.-S.;Chang C.-T.;Ho H.-N.;Chien-Nan Lee; Lin S.-Y.; Su Y.-N.; Hung C.-C.; Tsay W.; Chiou S.-S.; Chang C.-T.; Ho H.-N.; CHIEN-NAN LEE
臺大學術典藏 2021-02-04T06:04:55Z Preimplantation genetic diagnosis of β-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes Hung C.-C.;Chen S.-U.;Lin S.-Y.;Fang M.-Y.;Chang L.-J.;Tsai Y.-Y.;Lin L.-T.;Yang Y.-S.;Chien-Nan Lee;Su Y.-N.; Hung C.-C.; Chen S.-U.; Lin S.-Y.; Fang M.-Y.; Chang L.-J.; Tsai Y.-Y.; Lin L.-T.; Yang Y.-S.; CHIEN-NAN LEE; Su Y.-N.
臺大學術典藏 2021-02-04T06:04:55Z Second-trimester Maternal Serum Quadruple Test for Down Syndrome Screening: A Taiwanese Population-based Study Shaw S.W.S.;Lin S.-Y.;Lin C.-H.;Su Y.-N.;Cheng P.-J.;Chien-Nan Lee;Chen C.-P.; Shaw S.W.S.; Lin S.-Y.; Lin C.-H.; Su Y.-N.; Cheng P.-J.; CHIEN-NAN LEE; Chen C.-P.
臺大學術典藏 2021-02-04T06:04:55Z Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome Lin S.-Y.;Chien-Nan Lee;Hung C.-C.;Tsai W.-Y.;Lin S.-P.;Li N.-C.;Hsieh W.-S.;Tung Y.-C.;Niu D.-M.;Hsu W.-M.;Chen L.-Y.;Fang M.-Y.;Tu M.-P.;Kuo P.-W.;Lin C.-Y.;Su Y.-N.;Ho H.-N.; Lin S.-Y.; CHIEN-NAN LEE; Hung C.-C.; Tsai W.-Y.; Lin S.-P.; Li N.-C.; Hsieh W.-S.; Tung Y.-C.; Niu D.-M.; Hsu W.-M.; 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 2021-02-04T06:04:25Z Long-term growth and bone development in children of HBV-infected mothers with and without fetal exposure to tenofovir disoproxil fumarate Wen W.-H.;Chen H.-L.;Shih T.T.-F.;Wu J.-F.;Ni Y.-H.;Chien-Nan Lee;Zhao L.-L.;Lai M.-W.;Mu S.-C.;Tung Y.-C.;Hsu H.-Y.;Chang M.-H.;Shyu M.K.;Hwa H.L.;Su Y.N.;Shih J.C.;Chao K.H.;Chiu Y.C.;Chang K.C.;Liu C.J.;Su T.H.;Chen D.S.;Chen S.M.;Lin C.C.;Lin P.Y.;Yang W.R.;Hu J.J.;Yang C.K.;Chang Y.K.;Chen K.H.;Lin H.H.;Lin Y.H.;Chen H.J.;Pan H.S.;Lau B.H.;Lee C.L.;Cheng P.J.;Chang Y.L.;Chiueh H.Y.;Wang T.H.;Hsu J.J.;Lo L.M.;Hsieh C.L.;Cheng S.W.;Tsai M.S.;Lin L.H.;She B.Q.;Peng F.S.;Lin Y.C.;Chen C.P.;Huang J.P.;Yeung C.Y.;Taiwan Study Group For The Prevention Of Mother-To-Infant Transmission Of Hbv (Premit Study); Wen W.-H.; Chen H.-L.; Shih T.T.-F.; Wu J.-F.; Ni Y.-H.; CHIEN-NAN LEE; Zhao L.-L.; Lai M.-W.; Mu S.-C.; Tung Y.-C.; Hsu H.-Y.; Chang M.-H.; Shyu M.K.; Hwa H.L.; Su Y.N.; Shih J.C.; Chao K.H.; Chiu Y.C.; Chang K.C.; Liu C.J.; Su T.H.; Chen D.S.; Chen S.M.; Lin C.C.; Lin P.Y.; Yang W.R.; Hu J.J.; Yang C.K.; Chang Y.K.; Chen K.H.; Lin H.H.; Lin Y.H.; Chen H.J.; Pan H.S.; Lau B.H.; Lee C.L.; Cheng P.J.; Chang Y.L.; Chiueh H.Y.; Wang T.H.; Hsu J.J.; Lo L.M.; Hsieh C.L.; Cheng S.W.; Tsai M.S.; Lin L.H.; She B.Q.; Peng F.S.; Lin Y.C.; Chen C.P.; Huang J.P.; Yeung C.Y.; Taiwan Study Group for the Prevention of Mother-to-Infant Transmission of HBV (PreMIT study)
臺大學術典藏 2021-01-27T01:38:22Z Rapid detection of β-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC Su Y.-N.;Lee C.-N.;Hung C.-C.;Chen C.-A.;Cheng W.-F.;Tsao P.-N.;Chia-Li Yu;Hsieh F.-J.; Su Y.-N.; Lee C.-N.; Hung C.-C.; Chen C.-A.; Cheng W.-F.; Tsao P.-N.; CHIA-LI YU; Hsieh F.-J.
臺大學術典藏 2021-01-27T01:38:19Z 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.;Chia-Li Yu;Hsieh W.-S.;Lin W.-L.;Hsu S.-M.; Su Y.-N.; Hung C.-C.; Li H.; Lee C.-N.; Cheng W.-F.; Tsao P.-N.; Chang M.-C.; CHIA-LI YU; Hsieh W.-S.; Lin W.-L.; Hsu S.-M.
臺大學術典藏 2021-01-27T01:38:18Z Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1. Lee M.J.; 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.; CHIA-LI YU
臺大學術典藏 2021-01-21T02:05:10Z Excess soluble fms-like tyrosine kinase 1 and low platelet counts in premature neonates of preeclamptic mothers Tsao P.-N.;Wei S.-C.;Su Y.-N.;Chou H.-C.;Chien-Yi Chen;Hsieh W.-S.; Tsao P.-N.; Wei S.-C.; Su Y.-N.; Chou H.-C.; CHIEN-YI CHEN; Hsieh W.-S.
臺大學術典藏 2021-01-21T02:05:10Z Vascular endothelial growth factor in preterm infants with respiratory distress syndrome Tsao P.-N.;Wei S.-C.;Chou H.-C.;Su Y.-N.;Chien-Yi Chen;Hsieh F.-J.;Hsieh W.-S.; Tsao P.-N.; Wei S.-C.; Chou H.-C.; Su Y.-N.; CHIEN-YI CHEN; Hsieh F.-J.; Hsieh W.-S.
臺大學術典藏 2021-01-21T02:05:07Z 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.;Chien-Yi Chen;Chang Y.-H.;Hsieh W.-S.; Chen L.-R.; Tsao P.-N.; Su Y.-N.; Fan P.-C.; Chou H.-C.; CHIEN-YI CHEN; Chang Y.-H.; Hsieh W.-S.
臺大學術典藏 2021-01-21T02:05:06Z Holt-Oram syndrome with right lung agenesis caused by a de novo mutation in the TBX5 gene [2] Tseng Y.-R.;Su Y.-N.;Lu F.L.;Jeng S.-F.;Hsieh W.-S.;Chien-Yi Chen;Chou H.-C.;Peng S.S.-F.; Tseng Y.-R.; Su Y.-N.; Lu F.L.; Jeng S.-F.; Hsieh W.-S.; CHIEN-YI CHEN; Chou H.-C.; Peng S.S.-F.
臺大學術典藏 2021-01-21T02:05:06Z 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.;Chien-Yi Chen;Hsu W.-M.;Hsieh F.-J.;Hsu S.-M.; Tsao P.-N.; Chan F.-T.; Wei S.-C.; Hsieh W.-S.; Chou H.-C.; Su Y.-N.; CHIEN-YI CHEN; Hsu W.-M.; Hsieh F.-J.; Hsu S.-M.
臺大學術典藏 2021-01-21T02:05:05Z 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.; CHIEN-YI CHEN; Chou H.-C.; Tsao P.-N.; Hsieh W.-S.
臺大學術典藏 2021-01-21T02:05:02Z 211 G to A variation of UDP-glucuronosyl transferase 1A1 gene and neonatal Breastfeeding jaundice Chou H.-C.;Chen M.-H.;Yang H.-I.;Su Y.-N.;Hsieh W.-S.;Chien-Yi Chen;Chen H.-L.;Chang M.-H.;Tsao P.-N.; Chou H.-C.; Chen M.-H.; Yang H.-I.; Su Y.-N.; Hsieh W.-S.; CHIEN-YI CHEN; Chen H.-L.; Chang M.-H.; Tsao P.-N.
臺大學術典藏 2021-01-21T02:05:01Z Novel heterozygous tissue-nonspecific alkaline phosphatase (TNAP) gene mutations causing lethal perinatal hypophosphatasia Chang K.-C.; Lin P.-H.; Su Y.-N.; Peng S.S.-F.; Lee N.-C.; Chou H.-C.; CHIEN-YI CHEN; Hsieh W.-S.; Tsao P.-N.
臺大學術典藏 2021-01-21T02:04:51Z The sFlt-1/PlGF ratio as a predictor for poor pregnancy and neonatal outcomes Chang Y.-S.;Chen C.-N.;Jeng S.-F.;Su Y.-N.;Chien-Yi Chen;Chou H.-C.;Tsao P.-N.;Hsieh W.-S.; Chang Y.-S.; Chen C.-N.; Jeng S.-F.; Su Y.-N.; CHIEN-YI CHEN; Chou H.-C.; Tsao P.-N.; Hsieh W.-S.
臺大學術典藏 2021-01-15T02:46:30Z Neonatal and Pregnancy Outcome in Primary Antiphospholipid Syndrome: A 10-year Experience in One Medical Center Chou A.-K.; SONG-CHOU HSIEH; Su Y.-N.; Jeng S.-F.; Chen C.-Y.; Chou H.-C.; Tsao P.-N.; Hsieh W.-S.
臺大學術典藏 2021-01-15T02:46:26Z A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity Lin S.-Y.; SONG-CHOU HSIEH; Lin Y.-C.; Lee C.-N.; Tsai M.-H.; Lai L.-C.; Chuang E.Y.; Chen P.-C.; Hung C.-C.; Chen L.-Y.; Hsieh W.S.; Niu D.-M.; Su Y.-N.; Ho H.-N.
臺大學術典藏 2021-01-11T07:19:40Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Lee C.-T.; Tung Y.-C.; Hwu W.-L.; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; Yang Y.-L.; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; SHIH-YAO LIU; Tsai W.-Y.; Lee N.-C.
臺大學術典藏 2021-01-08T07:28:12Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Cheng-Ting Lee;Tung Y.-C.;Hwu W.-L.;Shih J.-C.;Lin W.-H.;Wu M.-Z.;Kuo K.-T.;Yang Y.-L.;Chen H.-L.;Chen M.;Su Y.-N.;Jong Y.-J.;Liu S.-Y.;Tsai W.-Y.;Lee N.-C.; CHENG-TING LEE; Tung Y.-C.; Hwu W.-L.; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; Yang Y.-L.; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; Liu S.-Y.; Tsai W.-Y.; Lee N.-C.
臺大學術典藏 2021-01-08T06:17:24Z 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.;Yi-Ching Tung;Niu D.-M.;Hsu W.-M.;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.; YI-CHING TUNG; Niu D.-M.; Hsu W.-M.; 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 2021-01-08T06:17:19Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Lee C.-T.;Yi-Ching Tung;Hwu W.-L.;Shih J.-C.;Lin W.-H.;Wu M.-Z.;Kuo K.-T.;Yang Y.-L.;Chen H.-L.;Chen M.;Su Y.-N.;Jong Y.-J.;Liu S.-Y.;Tsai W.-Y.;Lee N.-C.; Lee C.-T.; YI-CHING TUNG; Hwu W.-L.; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; Yang Y.-L.; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; Liu S.-Y.; Tsai W.-Y.; Lee N.-C.
臺大學術典藏 2021-01-08T02:16:01Z Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan Lin Y.-H.; Ke Y.-Y.; Tsao P.-N.; CHUN-YI LU; Chun-Yi Lu;Tsao P.-N.;Ke Y.-Y.;Lin Y.-H.;Lin Y.-H.;Hung C.-C.;Su Y.-N.;Hsu W.-C.;Hsieh W.-S.;Huang L.-M.;Wu C.-C.;Hsu C.-J.; Hsu C.-J.; Lin Y.-H.; Hung C.-C.; Su Y.-N.; Hsu W.-C.; Hsieh W.-S.; Huang L.-M.; Wu C.-C.
臺大學術典藏 2021-01-06T05:46:48Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Jou-Kou Wang;Wu M.-H.;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; JOU-KOU WANG; Wu M.-H.; Hsieh F.-J.
臺大學術典藏 2021-01-06T03:39:08Z IKZF1 deletions predict a poor prognosis in children with B-cell progenitor acute lymphoblastic leukemia: A multicenter analysis in Taiwan 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.; Chang H.-H.; Lin S.-W.; Su Y.-N.; Lin D.-T.; YUNG-LI YANG; Hung C.-C.; Chen J.-S.; Lin K.-H.
臺大學術典藏 2021-01-06T03:38:55Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Lee C.-T.; Tung Y.-C.; Hwu W.-L.; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; YUNG-LI YANG; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; Liu S.-Y.; Tsai W.-Y.; Lee N.-C.
臺大學術典藏 2021-01-06T03:38:54Z TP53 alterations in relapsed childhood acute lymphoblastic leukemia Lin K.-H.; Lin C.-Y.; Lin T.-K.; Chang Y.-H.; Jou S.-T.; Chang W.-T.; Yu C.-H.; Lu M.-Y.; Chen S.-H.; Wu K.-H.; Wang S.-C.; Chang H.-H.; Su Y.-N.; Hung C.-C.; Lin D.-T.; Chen H.-Y.; YUNG-LI YANG
臺大學術典藏 2021-01-06T03:38:51Z MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia Lu M.-Y.; Chen S.-H.; Cheng C.-N.; Wu K.-H.; Wang S.-C.; Chang H.-H.; Li M.-J.; Ni Y.-L.; Su Y.-N.; Lin D.-T.; Chen H.-Y.; Harrison C.J.; Hung C.-C.; Lin S.-W.; YUNG-LI YANG; Yu C.-H.; Lin T.-K.; Jou S.-T.; Lin C.-Y.; Lin K.-H.
臺大學術典藏 2021-01-05T08:07:44Z 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 Lo H.-M.; Huang S.K.S.; Lin J.-L.; Lai L.-P.;Su Y.-N.;Chiang F.-T.;Juang J.-M.;Liu Y.-B.;Ho Y.-L.;Chen W.-J.;Yeh S.-J.;Wang C.-C.;Ko Y.-L.;Wu T.-J.;Ueng K.-C.;Lei M.-H.;Tsao H.-M.;Chen S.-A.;Lin T.-K.;Mei-Hwan Wu;Lo H.-M.;Huang S.K.S.;Lin J.-L.; Lai L.-P.; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; MEI-HWAN WU
臺大學術典藏 2021-01-05T08:07:39Z Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Mei-Hwan Wu;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; MEI-HWAN WU; Hsieh F.-J.

Showing items 131-180 of 715  (15 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 9 10 > >>
View [10|25|50] records per page