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显示项目 455901-455925 / 2310171 (共92407页)
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机构 日期 题名 作者
中國醫藥大學 2001 Haplotype analysis in patients with velopharyngeal insufficiency (VPI) minimizes one VPI locus in 2.8Mb region of 22q11. Tsai, LP; Tsou, KS; Shi, YR; Wu, JY; Tsai, FJ
國立臺灣大學 2006 Haplotype Analysis of Endothelial Nitric Oxide Synthase (Nos3) Genetic Variants and Tardive Dyskinesia in Patients with Schizophrenia 白雅美; 林朝誠; 林知遠; BAI, YA-MEI; LIN, CHAO-CHENG; LIN, CHIH-YUAN
國立臺灣大學 2009 Haplotype Analysis of Lrrk2 R1441h Carriers with Parkinsonism 林靜嫻; 吳瑞美; LIN, CHIN-HSIEN; WU, RUEY-MEEI
臺大學術典藏 2018-09-10T07:22:49Z Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism Ross, O.A. and Spanaki, C. and Griffith, A. and Lin, C.-H. and Kachergus, J. and Haugarvoll, K. and Latsoudis, H. and Plaitakis, A. and Ferreira, J.J. and Sampaio, C. and Bonifati, V. and Wu, R.-M. and Zabetian, C.P. and Farrer, M.J.; Ruey-Meei Wu; Chin-Hsien Lin
臺大學術典藏 2009 Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism Ross O.A; Spanaki C; Griffith A; Lin C.-H; Kachergus J; Haugarvoll K; Latsoudis H; Plaitakis A; Ferreira J.J; Sampaio C; Bonifati V; RUEY-MEEI WU; Zabetian C.P; Farrer M.J.
臺大學術典藏 2020-03-04T07:45:27Z Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism Ross O.A.; Spanaki C.; Griffith A.; CHIN-HSIEN LIN; Kachergus J.; Haugarvoll K.; Latsoudis H.; Plaitakis A.; Ferreira J.J.; Sampaio C.; Bonifati V.; Wu R.-M.; Zabetian C.P.; Farrer M.J.
臺大學術典藏 2020-11-03T12:12:56Z Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism Ross O.A.;Spanaki C.;Griffith A.;Chin-Hsien Lin;Kachergus J.;Haugarvoll K.;Latsoudis H.;Plaitakis A.;Ferreira J.J.;Sampaio C.;Bonifati V.;Wu R.-M.;Zabetian C.P.;Farrer M.J.; Ross O.A.; Spanaki C.; Griffith A.; CHIN-HSIEN LIN; Kachergus J.; Haugarvoll K.; Latsoudis H.; Plaitakis A.; Ferreira J.J.; Farrer M.J.; Zabetian C.P.; Sampaio C.; Bonifati V.; Wu R.-M.
義守大學 2009-09 Haplotype analysis of single nucleotide polymorphisms in the vascular endothelial growth factor (VEGFA) gene and antidepressant treatment response in major depressive disorder Shih-Jen Tsai; Chen-Jee Hong; Ying-Jay Liou; Tai-Jui Chen; Mao-Liang Chen; Sheue-Jane Hou; Feng-Chang Yen;Younger W.-Y. Yu
亞洲大學 2022-01-01 Haplotype distribution of SARS-CoV-2 variants in low and high vaccination rate countries during ongoing global COVID-19 pandemic in early 2021 Bu, Ngoc-Niem;Bui, Ngoc-Niem;Lin, Yu-Tzu;Lin, Yu-Tzu;黃素華;Huang, Su-Hua;林振文
臺大學術典藏 2020-07-03T08:28:35Z Haplotype frequencies of nine Y-chromosome STR loci in the Taiwanese Han population Tsai L.-C.;Yuen T.-Y.;Hsieh H.-M.;Lin M.;Tzeng C.-H.;Huang N.-E.;Linacre A.;James Chun-I Lee; Tsai L.-C.; Yuen T.-Y.; Hsieh H.-M.; Lin M.; Tzeng C.-H.; Huang N.-E.; Linacre A.; JAMES CHUN-I LEE
國立臺灣大學 2013 Haplotype Kernel Association Test as a Powerful Method to Identify Chromosomal Regions Harboring Uncommon Causal Variants Lin, Wan-Yu; Yi, Nengjun; Lou, Xiang-Yang; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun; 林菀俞
臺大學術典藏 2018-09-10T09:41:02Z Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants Lin, Wan-Yu;Yi, Nengjun;Lou, Xiang-Yang;Zhi, Degui;Zhang, Kui;Gao, Guimin;Tiwari, Hemant K.;Liu, Nianjun; Lin, Wan-Yu; WAN-YU LIN; Yi, Nengjun; Lou, Xiang-Yang; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun
臺大學術典藏 2022-05-04T09:10:39Z Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants WAN-YU LIN; Yi N.; Lou X.-Y.; Zhi D.; Zhang K.; Gao G.; Tiwari H.K.; Liu N.
中國醫藥大學 2010-06 Haplotype of BAK1 (BCL2 antagonist killer 1) polymorphisms associated with the risk of developing Kawasaki disease in Taiwanese children 黃毓銓(Yu-Chuen Huang);林應如(Ying-Ju Lin);張正成(Jeng-Sheng Chang);陳世殷(Shih-Yin, Chen);萬磊(Lei Wan);許晉銓(Jinn-Chyuan Sheu);賴志河(Chih-Ho Lai);林振文(Lin Cheng Wen);劉詩平(Shih-Ping Liu);蔡輔仁(Fuu-Jen Tsai)*
高雄醫學大學 2007 Haplotype Tag SNP Selection using Hybrid Algorithms  Yang, Cheng-Hong;Ho, Chang-Hsuan;谷德倫;張學偉 
高雄醫學大學 2008 Haplotype Tagging SNPs Selection Using Particle Swarm Optimization  Yang, Cheng-Hong;Ho, Chang-Hsuan;張學偉;Chuang , Li-Yeh
國立臺灣大學 2012 Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs Lin, Wan-Yu; Yi, Nengjun; Zhi, Degui; Zhang, Kui; Gao, Guimin; Tiwari, Hemant K.; Liu, Nianjun; 林菀俞
臺大學術典藏 2022-05-04T09:10:40Z Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs WAN-YU LIN; Yi N.; Zhi D.; Zhang K.; Gao G.; Tiwari H.K.; Liu N.
國家衛生研究院 2019-07 Haplotypes constructed by Whole exome sequencing to map and identify a novel disease-causing RP2 gene variant from a recessive X linked Retinities Pigmentosa family Ching, Y;Fan, W;Lin, W;Tsai, W;Hu, L;Huang, S;Chung, R
國家衛生研究院 2011-11 Haplotypes of DNA repair and cell cycle control genes, X-ray exposure, and risk of childhood acute lymphoblastic leukemia Chokkalingam, AP;Bartley, K;Wiemels, JL;Metayer, C;Barcellos, LF;Hansen, HM;Aldrich, MC;Guha, N;Urayama, KY;Scelo, G;Chang, JS;Month, SR;Wiencke, JK;Buffler, PA
臺大學術典藏 2020-03-17T06:22:39Z Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits Liu C.-M.; Chen W.J.; Tsuang M.T.; Faraone S.V.; Fang C.-P.; Liu C.-C.; Chien Y.-L.; MING-HSIEN HSIEH; Hwang T.-J.; Tsai-Wu J.-J.; Wen C.-C.; Chang C.-C.; Liu Y.-L.; Wang S.-C.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Yang W.-C.; Hsu P.-C.
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 2021-10-22T07:39:45Z Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits Liu Y.-L.; Wang S.-C.; HAI-GWO HWU; 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.; Liu C.-C.; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; Chen W.J.; Liu C.-M.
臺大學術典藏 2021-09-23T08:02:11Z 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.; Liu C.-C.; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; Chen W.J.; CHIH-MIN LIU
臺大學術典藏 2022-05-05T05:15:47Z 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.; Liu C.-C.; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; WEI J. CHEN; Liu C.-M.

显示项目 455901-455925 / 2310171 (共92407页)
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每页显示[10|25|50]项目