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机构 日期 题名 作者
亞洲大學 2009-02 Interleukin-18 gene 105A/C genetic polymorphism is associated with the susceptibility of Kawasaki disease. ;Chen, SY;萬磊;Wan, Lei;Huang, YC;Sheu, JJ;Lan, YC;Lai, CH;Lin, CW;Chang, JS;Tsai, Y;Liu, SP;Lin, YJ;Tsai, FJ
亞洲大學 2008-10 Short-Term versus Long-Term Intermittent Hypobaric Hypoxia on Cardiac Fibrosis and Fas Death Receptor Dependent Apoptotic Pathway in Rat Hearts Lin, YM;Lin, Yueh-Min;Huang, SK;Huang, Shu-Kuei;Wang, HF;Wang, Hsuch Fang;Chen, LM;Chen, Li-Mien;Tsai, FJ;Tsai, Fuu-Jen;Hsu, HH;Hsu, Hsi-Hsien;Kuo, CH;Kuo, Chia-Hua;Wang, PS;Wang, Paulus S.;Huang, CY;Huang, Chih-Yang;Lee, SD;Lee, Shin-Da
亞洲大學 2008-10 Collagen type 3 alpha 1 polymorphism and risk of pelvic organ prolapse Chen, HY;Chen, Huey-Yi;Chung, YW;Chung, Ya-Wen;Lin, WY;Lin, Wei-Yong;Wang, JC;Wang, Jiunn-Chin;Tsai, FJ;Tsai, Fuu-Jen;Tsai, CH;Tsai, Chang-Hai
國立臺灣大學 2008-10 Risk factors for suicide in Taiwanese college students Gau, Susan SF; Chen, YY; Tsai, FJ; Lee, MB; Chiu, YN; Soong, WT; Hwu, HG
亞洲大學 2008-07 Cytokine (IL-6) and chemokine (IL-8) gene polymorphisms among rheumatoid arthritis patients in Taiwan Lo, SF;Lo, S. -F.; Huang, CM ;Huang, C. -M.; Lin, HC ;Lin, H. -C.; Chen, WC ;Chen, W. -C.; Tsai, CH ;Tsai, C. -H.; Tsai, FJ ;Tsai, F. -J.
國立臺灣大學 2008-07 Early detection of Pompe disease by newborn screening is feasible: results from the Taiwan screening program. Chien, YH; Chiang, SC; Zhang, XK; Keutzer, J; Lee, NC; Huang, AC; Chen, CA; Wu, MH; Huang, PH; Tsai, FJ; Chen, YT; Hwu, WL
國立臺灣大學 2008-05 Identification of eight novel mutations of the acid alpha-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II. Wan, L; Lee, CC; Hsu, CM; Hwu, WL; Yang, CC; Tsai, CH; Tsai, FJ
中山醫學大學 2008 IGF-II/mannose 6-phosphate receptor activation induces metalloproteinase-9 matrix activity and increases plasminogen activator expression in H9c2 cardiomyoblast cells. Chang, MH; Kuo, WW; Chen, RJ; Lu, MC; Tsai, FJ; Kuo, WH; Chen, LY; Wu, WJ; Huang, CY; Chu, CH
高雄醫學大學 2008 第一型干擾素可以藉由著活化與形成STAT2:STAT6雙體而誘發肝細胞表現IL-1受器? 萬磊;陳炳宏;蔡輔仁; Wan L;Lin CW;Lin YJ;Sheu JJ;Chen BH;Liao CC;Tsai Y;Lin WY;Lai CH;Tsai FJ
國立臺灣大學 2008 Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation Chen, CP; Lin, SP; Su, YN; Chien, SC; Tsai, FJ; Wang, W

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