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Showing items 41-65 of 156 (7 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-07-06T02:04:12Z	A fault-tolerant method for HLA typing with PacBio data	Chang C.-J.; PEI-LUNG CHEN; Yang W.-S.; Chao K.-M.
臺大學術典藏	2021-07-06T02:04:11Z	An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report	Yu T.-Y.; Lin H.-S.; PEI-LUNG CHEN; Huang T.-S.
臺大學術典藏	2021-07-06T02:04:11Z	Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing	Lin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:11Z	STAT3 mediates regorafenib-induced apoptosis in hepatocellular carcinoma	Tai W.-T.; Chu P.-Y.; Shiau C.-W.; Chen Y.-L.; Li Y.-S.; Hung M.-H.; Chen L.-J.; PEI-LUNG CHEN; Su J.-C.; Lin P.-Y.; Yu H.-C.; Chen K.-F.
臺大學術典藏	2021-07-06T02:04:10Z	Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling	Liu Y.; Pham X.; Zhang L.; PEI-LUNG CHEN; Burzynski G.; McGaughey D.M.; He S.; McGrath J.A.; Wolyniec P.; Fallin M.D.; Pierce M.S.; McCallion A.S.; Pulver A.E.; Avramopoulos D.; Valle D.
臺大學術典藏	2021-07-06T02:04:09Z	Identifying children with poor cochlear implantation outcomes using massively parallel sequencing	Wu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-M.
臺大學術典藏	2021-07-06T02:04:09Z	Association between serum levels of adipocyte fatty acid-binding protein and free thyroxine	Tseng F.-Y.; PEI-LUNG CHEN; Chen Y.-T.; Chi Y.-C.; Shih S.-R.; Wang C.-Y.; Chen C.-L.; Yang W.-S.
臺大學術典藏	2021-07-06T02:04:08Z	Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study	PEI-LUNG CHEN; Shih S.-R.; Wang P.-W.; Lin Y.-C.; Chu C.-C.; Lin J.-H.; Chen S.-C.; Chang C.-C.; Huang T.-S.; Tsai K.S.; Tseng F.-Y.; Wang C.-Y.; Lu J.-Y.; Chiu W.-Y.; Chang C.-C.; Chen Y.-H.; Chen Y.-T.; Fann C.S.-J.; Yang W.-S.; Chang T.-C.
臺大學術典藏	2021-07-06T02:04:08Z	Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-K?ster-Hauser syndrome	Chen M.-J.; Wei S.-Y.; Yang W.-S.; Wu T.-T.; Li H.-Y.; Ho H.-N.; Yang Y.-S.; PEI-LUNG CHEN
臺大學術典藏	2021-07-06T02:04:07Z	Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer	Lin P.-H.;Kuo W.-H.;Huang A.-C.;Lu Y.-S.;Lin C.-H.;Kuo S.-H.;Wang M.-Y.;Liu C.-Y.;Cheng F.T.-F.;Yeh M.-H.;Li H.-Y.;Yang Y.-H.;Hsu Y.-H.;Fan S.-C.;Li L.-Y.;Yu S.-L.;Chang K.-J.;Pei-Lung Chen;Ni Y.-H.;Huang C.-S.; Lin P.-H.; Kuo W.-H.; Huang A.-C.; Lu Y.-S.; Lin C.-H.; Kuo S.-H.; Wang M.-Y.; Liu C.-Y.; Cheng F.T.-F.; Yeh M.-H.; Li H.-Y.; Yang Y.-H.; Hsu Y.-H.; Fan S.-C.; Li L.-Y.; Yu S.-L.; Chang K.-J.; PEI-LUNG CHEN; Ni Y.-H.; Huang C.-S.
臺大學術典藏	2021-07-06T02:04:07Z	Long-term cochlear implant outcomes in children with GJB2 and SLC26A4 mutations	Wu C.-M.; Ko H.-C.; Tsou Y.-T.; Lin Y.-H.; Lin J.-L.; Chen C.-K.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏	2021-07-06T02:04:06Z	Follicular thyroid carcinoma with NRAS Q61K and GNAS R201H mutations that had a good 131I treatment response	Lu J.-Y.;Hung P.-J.;Pei-Lung Chen;Yen R.-F.;Kuo K.-T.;Yang T.-L.;Wang C.-Y.;Chang T.-C.;Huang T.-S.;Chang C.-C.; Lu J.-Y.; Hung P.-J.; PEI-LUNG CHEN; Yen R.-F.; Kuo K.-T.; Yang T.-L.; Wang C.-Y.; Chang T.-C.; Huang T.-S.; Chang C.-C.
臺大學術典藏	2021-07-06T02:04:06Z	Serum Spot 14 concentration is negatively associated with thyroid-stimulating hormone level	Chen Y.-T.;Tseng F.-Y.;Pei-Lung Chen;Chi Y.-C.;Han D.-S.;Yang W.-S.; Chen Y.-T.; Tseng F.-Y.; PEI-LUNG CHEN; Chi Y.-C.; Han D.-S.; Yang W.-S.
臺大學術典藏	2021-07-06T02:04:06Z	Serum levels of follistatin are positively associated with serum-free thyroxine levels in patients with hyperthyroidism or euthyroidism	Tseng F.-Y.;Chen Y.-T.;Chi Y.-C.;Pei-Lung Chen;Yang W.-S.; Tseng F.-Y.; Chen Y.-T.; Chi Y.-C.; PEI-LUNG CHEN; Yang W.-S.
臺大學術典藏	2021-07-06T02:04:05Z	First step towards precision medicine for antithyroid drug-induced agranulocytosis	Pei-Lung Chen;Fann C.S.-J.;Shih S.-R.;Yang W.-S.;Chang T.-C.; PEI-LUNG CHEN; Fann C.S.-J.; Shih S.-R.; Yang W.-S.; Chang T.-C.
臺大學術典藏	2021-07-06T02:04:05Z	Next generation sequencing yields the complete mitochondrial genome of the flathead mullet, Mugil cephalus cryptic species NWP2 (Teleostei: Mugilidae)	Shen K.-N.;Yen T.-C.;Chen C.-H.;Li H.-Y.;Pei-Lung Chen;Hsiao C.-D.; Shen K.-N.; Yen T.-C.; Chen C.-H.; Li H.-Y.; PEI-LUNG CHEN; Hsiao C.-D.
臺大學術典藏	2021-07-06T02:04:04Z	Intrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: A case report and literature review	Lin H.-C.; Lin C.-H.; PEI-LUNG CHEN; Cheng S.-J.; Chen P.-H.
臺大學術典藏	2021-07-06T02:04:04Z	Identification of a novel HLA-B allele, HLA-B*40:238, in a Taiwanese individual	Lee H.-L.; Lai S.-K.; PEI-LUNG CHEN; Chu C.-C.
臺大學術典藏	2021-07-06T02:04:04Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S.;Wu R.-M.;Pei-Lung Chen;Chen T.-F.;Li H.-Y.;Lin Y.-H.;Chen C.-Y.;Chen M.-L.;Tai C.-H.;Lin H.-I.;Lin C.-H.; Fan T.-S.; Wu R.-M.; PEI-LUNG CHEN; Chen T.-F.; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; Tai C.-H.; Lin H.-I.; Lin C.-H.
臺大學術典藏	2021-07-06T02:04:04Z	KCNN2 polymorphisms and cardiac tachyarrhythmias	Yu C.-C.;Chia-Ti T.;Pei-Lung Chen;Wu C.-K.;Chiu F.-C.;Chiang F.-T.;Chen P.-S.;Chen C.-L.;Lin L.-Y.;Juang J.-M.;Ho L.-T.;La L.-P.;Yang W.-S.;Lin J.-L.; Yu C.-C.; Chia-Ti T.; PEI-LUNG CHEN; Wu C.-K.; Chiu F.-C.; Chiang F.-T.; Chen P.-S.; Chen C.-L.; Lin L.-Y.; Juang J.-M.; Ho L.-T.; La L.-P.; Yang W.-S.; Lin J.-L.
臺大學術典藏	2021-07-06T02:04:03Z	Early measurement of IL-10 predicts the outcomes of patients with acute respiratory distress syndrome receiving extracorporeal membrane oxygenation /631/250/127 /692/53/2422 /13 /13/21 /13/31 /45/23 article	Liu C.-H.; Kuo S.-W.; Ko W.-J.; Tsai P.-R.; Wu S.-W.; Lai C.-H.; Wang C.-H.; Chen Y.-S.; PEI-LUNG CHEN; Liu T.-T.; Huang S.-C.; Jou T.-S.
臺大學術典藏	2021-07-06T02:04:03Z	Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: A case report and literature review	Chen Y.-F.; Chang Y.-Y.; Lan M.-Y.; PEI-LUNG CHEN; Lin C.-H.
臺大學術典藏	2021-07-06T02:04:02Z	A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss	Lin Y.-H.; Lin Y.-H.; Lu Y.-C.; Liu T.-C.; Chen C.-Y.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏	2021-07-06T02:04:02Z	Prediction Model for Audiological Outcomes in Patients with GJB2 Mutations	Chen P.-Y.; Lin Y.-H.; Liu T.-C.; Lin Y.-H.; Tseng L.-H.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Hsu C.-J.
臺大學術典藏	2021-07-06T02:04:02Z	A 1204-single nucleotide polymorphism and insertion–deletion polymorphism panel for massively parallel sequencing analysis of DNA mixtures	Hwa H.-L.; Chung W.-C.; PEI-LUNG CHEN; Lin C.-P.; Li H.-Y.; Yin H.-I.; Lee J.C.-I.

Showing items 41-65 of 156 (7 Page(s) Totally)
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