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"tsai tf"的相關文件
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| 國家衛生研究院 |
2025-10-01 |
Synthesis and biological evaluation of indoline derivatives as CDGSH iron sulfur domain 2 activators
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Yao, CH;Wang, LY;Shen, ZQ;Huang, YW;Tsai, CH;Song, JS;Chen, CH;Chen, YC;Tsai, TF;Lee, JC |
| 國家衛生研究院 |
2025-10 |
Activation of CISD2 as a protective strategy against doxorubicin-induced cardiotoxicity
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Chou, YJ;Yeh, CH;Chen, CF;Lo, CJ;Yang, JH;Chiu, WT;Kao, CH;Tzeng, TY;Shen, ZQ;Tung, CY;Lu, CK;Cheng, ML;Hsieh, PCH;Fu, SL;Tsai, TF |
| 國家衛生研究院 |
2025-08-21 |
Cisd2 delays atrial aging via a modulation of calcium homeostasis that mitigates atrial myopathy
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Yeh, CH;Shen, ZQ;Chen, LH;Seah, C;Tzeng, TY;Tung, CY;Chiu, WT;Kao, CH;Tsai, TF |
| 國家衛生研究院 |
2025-08-20 |
Trans-omics analyses identify the biochemical network of LPCAT1 associated with coronary artery disease
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Hsu, PWC;Yeh, CH;Lo, CJ;Tsai, TH;Chan, YH;Chou, YJ;Yang, N;Cheng, ML;Sheu, WHH;Lai, CC;Sytwu, HK;Tsai, TF |
| 國家衛生研究院 |
2025-06 |
Wolfram syndrome 2 gene (CISD2) deficiency disrupts Ca2+-mediated insulin secretion in beta-cells
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Shen, ZQ;Chiu, WT;Kao, CH;Chen, YC;Chen, LH;Teng, TW;Hsiung, SY;Tzeng, TY;Tung, CY;Juan, CC;Tsai, TF |
| 國家衛生研究院 |
2025-05-08 |
Cisd1 synergizes with Cisd2 to modulate protein processing by maintaining mitochondrial and ER homeostasis
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Chen, YF;Teng, YC;Yang, JH;Kao, CH;Tsai, TF |
| 國家衛生研究院 |
2025-03-06 |
Machine-learning assisted discovery unveils novel interplay between gut microbiota and host metabolic disturbance in diabetic kidney disease
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Wu, IW;Liao, YC;Tsai, TH;Lin, CH;Shen, ZQ;Chan, YH;Tu, CW;Chou, YJ;Lo, CJ;Yeh, CH;Chen, CY;Pan, HC;Hsu, HJ;Lee, CC;Cheng, ML;Sheu, WH;Lai, CC;Sytwu, HK;Tsai, TF |
| 國家衛生研究院 |
2025-01-09 |
Artificial intelligence-enhanced electrocardiography improves the detection of coronary artery disease
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Yeh, CH;Tsai, TH;Chen, CH;Chou, YJ;Mao, CT;Su, TP;Yang, NI;Lai, CC;Chen, CT;Sytwu, HK;Tsai, TF |
| 國家衛生研究院 |
2025-01-03 |
Transcriptomic predictors of rapid progression from mild cognitive impairment to Alzheimer's disease
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Huang, YL;Tsai, TH;Shen, ZQ;Chan, YH;Tu, CW;Tung, CY;Wang, PN;Tsai, TF |
| 國家衛生研究院 |
2024-11-19 |
A dominant negative Kcnd3 F227del mutation in mice causes spinocerebellar ataxia type 22 (SCA22) by impairing ER and Golgi functioning
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Hung, HC;Lin, JH;Teng, YC;Kao, CH;Wang, PY;Soong, BW;Tsai, TF |
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