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机构 日期 题名 作者
臺大學術典藏 2021-09-23T08:02:10Z A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples Cohen O.S.; Weickert T.W.; Hess J.L.; Paish L.M.; McCoy S.Y.; Rothmond D.A.; Galletly C.; Liu D.; Weinberg D.D.; Huang X.-F.; Xu Q.; Shen Y.; Zhang D.; Yue W.; Yan J.; Wang L.; Lu T.; He L.; Shi Y.; Xu M.; Che R.; Tang W.; Chen C.-H.; Chang W.-H.; Hwu H.-G.; CHIH-MIN LIU; Liu Y.-L.; Wen C.-C.; Fann C.S.-J.; Chang C.-C.; Kanazawa T.; Middleton F.A.; Duncan T.M.; Faraone S.V.; Weickert C.S.; Tsuang M.T.; Glatt S.J.
臺大學術典藏 2021-09-23T08:02:07Z Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia CHIH-MIN LIU; Liu Y.-L.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Hsu P.-C.; Chang C.-C.; Chen W.J.; Hwang T.-J.; Hsieh M.H.; Liu C.-C.; Chien Y.-L.; Lin Y.-T.; Tsuang M.T.
臺大學術典藏 2021-08-31T06:42:25Z Genetic polymorphisms and tissue expression of interleukin-22 associated with risk and therapeutic response of gastric mucosa-associated lymphoid tissue lymphoma Liao F.; Hsu Y.-C.; Kuo S.-H.; Yang Y.-C.; Chen J.-P.; Hsu P.-N.; Lin C.-W.; Chen L.-T.; ANN-LII CHENG; Fann C.S.J.; Lin J.-T.; Wu M.-S.
臺大學術典藏 2021-08-13T03:35:17Z ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function Liu C.-M.; Fann C.S.-J.; Chen C.-Y.; Liu Y.-L.; Oyang Y.-J.; Yang W.-C.; Chang C.-C.; Wen C.-C.; Chen W.J.; Hwang T.-J.; Hsieh M.H.; CHEN-CHUNG LIU; Faraone S.V.; Tsuang M.T.; Hwu H.-G.
臺大學術典藏 2021-08-13T03:35:09Z Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits Liu Y.-L.; Wang S.-C.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Yang W.-C.; Hsu P.-C.; Chang C.-C.; Wen C.-C.; Tsai-Wu J.-J.; Hwang T.-J.; Hsieh M.H.; CHEN-CHUNG LIU; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; Chen W.J.; Liu C.-M.
臺大學術典藏 2021-08-13T03:35:05Z Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia Liu C.-M.; Liu Y.-L.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Hsu P.-C.; Chang C.-C.; Chen W.J.; Hwang T.-J.; Hsieh M.H.; CHEN-CHUNG LIU; Chien Y.-L.; Lin Y.-T.; Tsuang M.T.
臺大學術典藏 2021-07-06T08:49:47Z Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactions LIN-CHAU CHANG; Chang C.-C.; Chen P.-L.; Wang S.-H.; Chen Y.-H.; Tsai Y.-H.; Shih S.-R.; Chiu W.-Y.; Fann C.S.-J.; Yang W.-S.; Chang T.-C.
臺大學術典藏 2021-07-06T02:04:18Z Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in Taiwan PEI-LUNG CHEN; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; Yang W.-S.; Chang T.-C.
臺大學術典藏 2021-07-06T02:04:18Z Family-based association study of cytotoxic T-lymphocyte antigen-4 with susceptibility to Graves' disease in Han population of Taiwan PEI-LUNG CHEN; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; Yang W.-S.; Chang T.-C.
臺大學術典藏 2021-07-06T02:04:16Z Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles PEI-LUNG CHEN; Fann C.-S.-J.; Chu C.-C.; Chang C.-C.; Chang S.-W.; Hsieh H.-Y.; Lin M.; Yang W.-S.; Chang T.-C.

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