English | 繁體

Search in the results

UM

Browse/Search Results:  1-3 of 3 Help

Selected(0)Clear Items/Page:    Sort:
SiO2 stimulates macrophage stress to induce the transformation of lung fibroblasts into myofibroblasts and its relationship with the sphingomyelin metabolic pathway Journal article
Liu, Jing, Guan, Lan, Wang, Erjin, Schuchman, Edward H., He, Xingxuan, Zeng, Ming. SiO2 stimulates macrophage stress to induce the transformation of lung fibroblasts into myofibroblasts and its relationship with the sphingomyelin metabolic pathway[J]. Journal of Applied Toxicology, 2021, 41(10), 1584-1597.
Authors:  Liu, Jing;  Guan, Lan;  Wang, Erjin;  Schuchman, Edward H.;  He, Xingxuan; et al.
Favorite | TC[WOS]:7 TC[Scopus]:7  IF:2.7/3.2 | Submit date：2021/12/08
Fibrosis  Hfl-1 Cells  Rac  Silica  Sphingomyelin Signaling Pathway  Thp-1 Cells  
Exosomal miR-221 derived from hydroquinone-transformed malignant human bronchial epithelial cells is involved in cell viability of recipient cells Journal article
Jiang,Ran, Huang,Haoyu, Lian,Zhenwei, Hu,Zuqing, Lloyd,R. Stephen, Fang,Daokui, Li,Yanfeng, Xian,Hongyi, Yuan,Jianhui, Sha,Yan, Wang,Sanming, Hu,Dalin. Exosomal miR-221 derived from hydroquinone-transformed malignant human bronchial epithelial cells is involved in cell viability of recipient cells[J]. Journal of Applied Toxicology, 2019, 40(2), 224-233.
Authors:  Jiang,Ran;  Huang,Haoyu;  Lian,Zhenwei;  Hu,Zuqing;  Lloyd,R. Stephen; et al.
Favorite | TC[WOS]:18 TC[Scopus]:18  IF:2.7/3.2 | Submit date：2021/03/02
Benzene  Cell Viability  Exosomes  Intercellular Communications  Mir-221  Toxic Mechanism  
Exosomal miR‐221 derived from hydroquinone‐transformed malignant human bronchial epithelial cells is involved in cell viability of recipient cells Journal article
Jian, R, Wang, S. M., Lian,Zhenwei, Hu,Zuqing, Lloyd,R. Stephen, Fang,Daokui, Li,Yanfeng, Xian,Hongyi, Yuan,Jianhui, Sha,Yan, Wang,Sanming, Hu,Dalin. Exosomal miR‐221 derived from hydroquinone‐transformed malignant human bronchial epithelial cells is involved in cell viability of recipient cells[J]. Journal of Applied Toxicology, 2019, 40(2), 224-233.
Authors:  Jian, R;  Wang, S. M.;  Lian,Zhenwei;  Hu,Zuqing;  Lloyd,R. Stephen; et al.
Favorite | TC[WOS]:18 TC[Scopus]:18  IF:2.7/3.2 | Submit date：2022/07/27
Benzene  Cell Viability  Exosomes  Intercellular Communications  Mir‐221  Toxic Mechanism