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Showing items 739966-739975 of 2348487 (234849 Page(s) Totally) << < 73992 73993 73994 73995 73996 73997 73998 73999 74000 74001 > >> View [10|25|50] records per page
| 國立成功大學 |
2018-11-01 |
Runup of laboratory-generated breaking solitary and periodic waves on a uniform slope
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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
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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
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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
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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
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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
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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
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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.
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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
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(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
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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. |
Showing items 739966-739975 of 2348487 (234849 Page(s) Totally) << < 73992 73993 73994 73995 73996 73997 73998 73999 74000 74001 > >> View [10|25|50] records per page
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