carbon tetrachloride has been researched along with artenimol in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Lu, C; Shao, J; Xu, W; Yao, S; Zhang, F; Zheng, S | 1 |
| Guo, M; Shao, J; Zhang, Z; Zhao, S; Zheng, S | 1 |
| Chen, AP; Cheng, XD; Kai, J; Shao, JJ; Tan, SZ; Wang, SJ; Wang, ZM; Wang, ZY; Xia, SW; Yang, X; Zhang, F; Zhang, T; Zhang, ZL; Zheng, SZ | 1 |
3 other study(ies) available for carbon tetrachloride and artenimol
| Article | Year |
|---|---|
Dihydroartemisinin counteracts fibrotic portal hypertension via farnesoid X receptor-dependent inhibition of hepatic stellate cell contraction.
Topics: Animals; Artemisinins; Carbon Tetrachloride; Cell Death; Chenodeoxycholic Acid; Gene Expression; Hepatic Stellate Cells; Hepatocytes; Humans; Hypertension, Portal; Liver; Liver Cirrhosis; Male; Mice; Mice, Inbred ICR; Mice, Transgenic; Portal Vein; Pregnenediones; Protective Agents; Rats; Rats, Sprague-Dawley; Receptors, Cytoplasmic and Nuclear | 2017 |
ROS-JNK1/2-dependent activation of autophagy is required for the induction of anti-inflammatory effect of dihydroartemisinin in liver fibrosis.
Topics: Acetylcysteine; Animals; Anthracenes; Anti-Inflammatory Agents; Antioxidants; Artemisinins; Autophagy; Carbon Tetrachloride; Gene Expression Regulation; Glutathione; Hepatic Stellate Cells; Humans; Liver; Liver Cirrhosis; Male; Mitogen-Activated Protein Kinase 8; Mitogen-Activated Protein Kinase 9; Primary Cell Culture; Rats; Rats, Sprague-Dawley; Reactive Oxygen Species; RNA, Small Interfering | 2016 |
LncRNA-H19 induces hepatic stellate cell activation via upregulating alcohol dehydrogenase III-mediated retinoic acid signals.
Topics: Aldehyde Oxidoreductases; Animals; Artemisinins; Carbon Tetrachloride; Cell Line; Gene Knockdown Techniques; Hepatic Stellate Cells; Lipid Metabolism; Liver; Liver Cirrhosis; Male; Mice; Mice, Inbred ICR; Receptors, Retinoic Acid; RNA, Long Noncoding; Signal Transduction; Tretinoin; Vitamin A | 2020 |