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Showing items 739526-739550 of 2347236  (93890 Page(s) Totally)
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Institution Date Title Author
國立臺灣大學 2013 Runs of Homozygosity Associated with Speech Delay in Autism in a Taiwanese Han Population: Evidence for the Recessive Model Lin, Ping-I; Kuo, Po-Hsiu; Chen, Chia-Hsiang; Wu, Jer-Yuarn; Gau, Susan S-F.; Wu, Yu-Yu; Liu, Shih-Kai; 高淑芬; 郭柏秀
臺大學術典藏 2018-09-10T09:49:49Z Runs of Homozygosity Associated with Speech Delay in Autism in a Taiwanese Han Population: Evidence for the Recessive Model Lin, Ping-I; Kuo, Po-Hsiu; Chen, Chia-Hsiang; Wu, Jer-Yuarn; Gau, Susan S-F.; Wu, Yu-Yu; Liu, Shih-Kai; Mittal, Balraj; Lin, P.-I. and Kuo, P.-H. and Chen, C.-H. and Wu, J.-Y. and Gau, S.S.-F. and Wu, Y.-Y. and Liu, S.-K.; 高淑芬 ;郭柏秀; Lin, Ping-I; Lin, Ping-I; SUSAN SHUR-FEN GAU; PO-HSIU KUO; Kuo, Po-Hsiu; Chen, Chia-Hsiang; Wu, Jer-Yuarn; Wu, Jer-Yuarn; Gau, Susan S-F.; Gau, Susan S-F.; Wu, Yu-Yu; Liu, Shih-Kai; Mittal, Balraj; Mittal, Balraj
臺大學術典藏 2020-03-02T03:11:09Z Runs of Homozygosity Associated with Speech Delay in Autism in a Taiwanese Han Population: Evidence for the Recessive Model Lin P.-I.; Kuo P.-H.; Chen C.-H.; Wu J.-Y.; SUSAN SHUR-FEN GAU; Wu Y.-Y.; Liu S.-K.
國立臺灣大學 1998-06 Runs rules for bivariate Shewhart chart Chen, Argon; Guo, Ruey-Shan; Lee, Chun-Lin
臺大學術典藏 2018-09-10T07:10:39Z Runs Rules for Bivariate Shewhart Chart RUEY-SHAN GUO; RUEY-SHAN GUO; RUEY-SHAN GUO
國立臺灣科技大學 2001 Runtime and Compiler Support for Irregular Computations Raja Das;Hwang, Yuan-Shin;Saltz, Joel ;Sussman, Alan
國立臺灣科技大學 1995 Runtime and Language Support for Compiling Adaptive Irregular Programs Hwang, Yuan-Shin;Bongki Moon;Shamik D. Sharma;Ravi Ponnusamy;Raja Das;Joel H. Saltz
臺大學術典藏 2020-05-04T07:53:51Z Runtime monitoring for safety of intelligent vehicles. CHUNG-WEI LIN; Shiraishi, Shinichi; Watanabe, Kosuke; Kang, Eunsuk; Lin, Chung-Wei
臺大學術典藏 2018-09-10T14:57:47Z Runtime service recovery for open information gateway Chen, L.-Y.;Chen, H.-Y.;Shih, C.-S.;Chen, L.-J.;Lin, K.C.-J.;Chung, W.-H.; Chen, L.-Y.; Chen, H.-Y.; Shih, C.-S.; Chen, L.-J.; Lin, K.C.-J.; Chung, W.-H.; CHI-SHENG SHIH
臺大學術典藏 2020-05-04T07:44:24Z Runtime service recovery for open information gateway. Shih, Chi-Sheng; Chen, Ling-Jyh; Lin, Kate Ching-Ju; Chung, Wei-Ho; CHI-SHENG SHIH; Chen, Hsin-Yi; Chen, Liang-Yu; Chen, Liang-Yu;Chen, Hsin-Yi;Shih, Chi-Sheng;Chen, Ling-Jyh;Lin, Kate Ching-Ju;Chung, Wei-Ho
臺大學術典藏 2018-09-10T15:23:05Z Runtime techniques for efficient Ray-Tracing on heterogeneous systems Kao, C.-C.;Hsu, W.-C.; Kao, C.-C.; Hsu, W.-C.; WEI-CHUNG HSU
臺大學術典藏 2020-05-04T08:08:37Z Runtime techniques for efficient Ray-Tracing on heterogeneous systems. Kao, Chih-Chen;Hsu, Wei-Chung; Kao, Chih-Chen; Hsu, Wei-Chung; WEI-CHUNG HSU
臺大學術典藏 2020-06-11T06:45:48Z Runtime temperature-based power estimation for optimizing throughput of thermal-constrained multi-core processors Oh, D.;Kim, N.S.;Chen, C.C.P.;Davoodi, A.;Hu, Y.H.; Oh, D.; Kim, N.S.; Chen, C.C.P.; Davoodi, A.; Hu, Y.H.; CHUNG-PING CHEN
國立成功大學 2022-02-1 Runup of breaking solitary waves on rough uniform slopes Wu;Yun-Ta;Huang;Kang-Wei;Kobayashi;Nobuhisa
國立成功大學 2018-11-01 Runup of laboratory-generated breaking solitary and periodic waves on a uniform slope 吳昀達; WU, YUN-TA; Yun Ta Wu, Philip Li Fan Liu, Kao Shu Hwang, Hwung Hweng Hwung
淡江大學 2018-08-30 Runup of laboratory-generated breaking solitary and periodic waves on a uniform slope Wu, Yun-Ta;Liu, Philip Li-Fan;Hwang, Kao-Shu;Hwung, Hwung-Hweng
臺大學術典藏 2007 RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome Tien H.-F.; Tseng M.-H.; SHANG-JU WU; Chen C.-Y.; Lin L.-I.; Tang J.-L.; Ko B.-S.; Tsay W.; Chou W.-C.; Yao M.
臺大學術典藏 2021-01-06T03:58:48Z RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome Chen C.-Y.; Lin L.-I.; JIH-LUH TANG; Ko B.-S.; Tsay W.; Chou W.-C.; Yao M.; Wu S.-J.; Tseng M.-H.; Tien H.-F.
臺大學術典藏 2021-02-05T06:29:46Z RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome Chen C.-Y.; Lin L.-I.; Tang J.-L.; Ko B.-S.; Tsay W.; WEN-CHIEN CHOU; Yao M.; Wu S.-J.; Tseng M.-H.; Tien H.-F.
臺大學術典藏 2007 RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome Lin L.-I.; Tang J.-L.; Chen C.-Y.; HWEI-FANG TIEN; Tseng M.-H.; Wu S.-J.; Yao M.; Chou W.-C.; Tsay W.; Ko B.-S.
臺大學術典藏 2007 RUNX1 gene mutation in primary myelodysplastic syndrome - The mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome Ko B.-S.; Tang J.-L.; Chen C.-Y.; Lin L.-I.; Tsay W.; Chou W.-C.; MING YAO; Wu S.-J.; Tseng M.-H.; Tien H.-F.
國立臺灣大學 2008-11 RUNX1 gene mutation in primary myelodysplastic syndrome--the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome. Chen, CY; Lin, LI; Tang, JL; Ko, BS; Tsay, W; Chou, WC; Yao, M; Wu, SJ; Tseng, MH; Tien, HF.
中國醫藥大學 2011-07-08 Runx2 and Osterix Gene Expression in Human Bone Marrow Stromal Cells Are Mediated by Far-Infrared Radiation (Ming-Tzu Tsai)*;(Yung-Sheng Lin);(Wan-Chi Chen);(Chien-Hua Ho);許瑞廷(Jui-Ting Hsu);黃恆立(Heng-Li Huang);(Ming-Tzu Tsai)
臺大學術典藏 2006 Runx2 inhibits chondrocyte proliferation and hypertrophy through its expression in the perichondrium Karsenty G.; Ornitz D.M.; Hinoi E.;Bialek P.;You-Tzung Chen;Rached M.-T.;Groner Y.;Behringer R.R.;Ornitz D.M.;Karsenty G.; Hinoi E.; Bialek P.; YOU-TZUNG CHEN; Rached M.-T.; Groner Y.; Behringer R.R.
國立臺灣大學 2006-11 Runx2 inhibits chondrocyte proliferation and hypertrophy through its expression in the perichondrium. Hinoi, Eiichi; Bialek, Peter; Chen, You-Tzung; Groner, Yoram; Behringer, Richard R.; Ornitz, David M.; Karsenty, Gerard

Showing items 739526-739550 of 2347236  (93890 Page(s) Totally)
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