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显示项目 485221-485230 / 2348570 (共234857页)
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| 臺大學術典藏 |
2018-09-10T14:53:38Z |
Identification of novel loci for bipolar I disorder in a multi-stage genome-wide association study
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Kuo, P.H. ; Chuang, L.C. ; Liu, J.R. ; Liu, C.M. ; Huang, M.C. ; Lin, S.K. ; Sunny Sun, H. ; Hsieh, M.H. ; Hung, H. ; Lu, R.B.; CHIH-MIN LIU; HUNG HUNG; PO-HSIU KUO |
| 臺北醫學大學 |
2014 |
Identification of novel loci for bipolar I disorder in multi-stage genome-wide association study
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PH, Kuo;LC, Chuang;JR, Liu;CM, Liu;MC, Huang;SK, Lin;Sunny, Sunny Sun H;MH, Hsieh;Hung, Hung H;RB, Lu |
| 臺北醫學大學 |
2014 |
Identification of novel loci for bipolar I disorder in multi-stage genome-wide association study
|
Kuo, PH;Chuang, LC;Liu, JR;Liu, CM;Huang, MC;Lin, SK;Sunny Sun, H;Hsieh, MH;Hung, H;Lu, RB |
| 中國醫藥大學 |
2012-05 |
Identification of novel mechanisms of silymarin on the carbon tetrachloride-induced liver fibrosis in mice by nuclear factor-κB bioluminescent imaging-guided transcriptomic analysis
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李佳橙(Chia-Cheng Li);項千芸(Chien-Yun Hsiang);吳世祿(Shih-Lu Wu);侯庭鏞(Tin-Yun Ho)* |
| 輔英科技大學 |
2015-09-19 |
Identification of novel molecular markers
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陳琮棋 |
| 國家衛生研究院 |
2018-09-10 |
Identification of novel mouse and rat CB1R isoforms and in silico modeling of human CB1R for peripheral cannabinoid therapeutics
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Liu, QR;Huang, NS;Qu, H;O’Connell, JF;Gonzalez-Mariscal, I;Santa-Cruz-Calvo, S;Doyle, ME;Xi, ZX;Wang, Y;Onaivi, ES;Egan, JM |
| 國立交通大學 |
2018-08-21T05:54:00Z |
Identification of novel mutations in endometrial cancer patients by whole-exome sequencing
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Chang, Ya-Sian; Huang, Hsien-Da; Yeh, Kun-Tu; Chang, Jan-Gowth |
| 中山醫學大學 |
2007 |
Identification of Novel Mutations in the KCNQ4 Gene of Patients with Nonsyndromic Deafness from Taiwan
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Ching-Chyuan Su;Jiann-Jou Yang;Jia-Ching Shieh;Mao-Chang Su;Shuan-Yow Li |
| 中山醫學大學 |
2006-07-26 |
Identification of Novel Mutations in the KCNQ4 Gene of Patients with Nonsyndromic Deafness from Taiwan
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Su, Ching-Chyuan; Yang, Jiann-Jou; Shieh, Jia-Ching; Su, Mao-Chang; Li, Shuan-Yow |
| 臺大學術典藏 |
2009 |
Identification of novel mutations in the SLC25A15 Gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study
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Palmieri F.; Santorelli F.M.; Pierri C.L.; Hernandez J.M.; Martinez-Hernandez E.; Walter J.; Besley G.; Aldamiz-Echevarria L.; Scarano G.; Melone M.A.B.; Tessa A.; Fiermonte G.; Dionisi-Vici C.; Paradies E.; Baumgartner M.R.; YIN-HSIU CHIEN; Loguercio C.; De Baulny H.O.; Nassogne M.-C.; Schiff M.; Deodato F.; Parenti G.; Rutledge S.L.; Antonia Vilaseca M. |
显示项目 485221-485230 / 2348570 (共234857页)
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每页显示[10|25|50]项目
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