L
Liping Xiang
Researcher at Fudan University
Publications - 6
Citations - 118
Liping Xiang is an academic researcher from Fudan University. The author has contributed to research in topics: Nonalcoholic fatty liver disease & Fatty liver. The author has an hindex of 3, co-authored 6 publications receiving 17 citations.
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Journal ArticleDOI
Transferrin receptor 1 ablation in satellite cells impedes skeletal muscle regeneration through activation of ferroptosis.
Hongrong Ding,Shujie Chen,Shujie Chen,Xiaohan Pan,Xiaoshuang Dai,Guihua Pan,Ze Li,Ze Li,Xudong Mai,Xudong Mai,Ye Tian,Ye Tian,Susu Zhang,Susu Zhang,Bingdong Liu,Guangchao Cao,Zhicheng Yao,Xiangping Yao,Xiangping Yao,Liang Gao,Li Yang,Xiaoyan Chen,Jia Sun,Hong Chen,Mulan Han,Yulong Yin,Guohuan Xu,Huijun Li,Weidong Wu,Zheng Chen,Jingchao Lin,Liping Xiang,Jun Hu,Yan Lu,Xiao Zhu,Liwei Xie,Liwei Xie,Liwei Xie +37 more
TL;DR: Transferrin receptor 1 (Tfr1) is associated with muscular dysfunction as muscle-specific deletion of Tfr1 results in growth retardation, metabolic disorder, and lethality as mentioned in this paper.
Journal ArticleDOI
Sparcl1 promotes nonalcoholic steatohepatitis progression in mice through upregulation of CCL2
Bin Liu,Liping Xiang,Jing Ji,Wei Liu,Ying Chen,Mingfeng Xia,Yuejun Liu,Wen-Yue Liu,Peiwu Zhu,Yi Jin,Yu Han,Jieli Lu,Xiaoying Li,Ming-Hua Zheng,Yan Lu +14 more
TL;DR: In this article, the authors identified increased expression of Sparcl1, a secreted glycoprotein, in the WAT from NASH mice, and showed that both chronic injection and overexpression of SPARcl1 exaggerated hepatic inflammation and liver injury in mice.
Journal ArticleDOI
Obesity-induced excess of 17-hydroxyprogesterone promotes hyperglycemia through activation of glucocorticoid receptor.
Yan Lu,E. Wang,Ying Chen,Bing Zhou,Jiejie Zhao,Liping Xiang,Yiling Qian,Jingjing Jiang,Lin Zhao,Xuelian Xiong,Zhi-Qiang Lu,Duojiao Wu,Bin Liu,Jing Yan,Rong Zhang,Huijie Zhang,Cheng Hu,Cheng Hu,Xiaoying Li +18 more
TL;DR: It is shown that 17-hydroxyprogesterone (17-OHP), an intermediate steroid in the biosynthetic pathway that converts cholesterol to cortisol, binds to and stimulates the transcriptional activity of GR, suggesting that selectively targeting hepatic Cyp17A1 may provide a therapeutic avenue for treating T2DM.
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The Nuclear Orphan Receptor NR2F6 Promotes Hepatic Steatosis through Upregulation of Fatty Acid Transporter CD36.
Bing Zhou,Lijing Jia,Zhijian Zhang,Liping Xiang,Youwen Yuan,Peilin Zheng,Bin Liu,Xingxing Ren,Hua Bian,Liwei Xie,Yao Li,Jieli Lu,Huijie Zhang,Yan Lu +13 more
TL;DR: Results provide evidence for an unpredicted role of NR2F6 that contributes to liver steatosis and suggest that NR2f6 antagonists may present a therapeutic strategy for reversing or treating NAFLD/NASH pathogenesis.
Journal ArticleDOI
Comparison of hepatic gene expression profiles between three mouse models of Nonalcoholic Fatty Liver Disease
Liping Xiang,Djurabekova Aziza Takhirovna,S Krishna Kumari,Yang Jiao,Yiling Qian,Yao Li,Fei Mao,Yan Lu +7 more
TL;DR: The results suggest that NAFLD is a heterogeneous disease with highly variable molecular mechanisms, and both distinct and common pathways in the regulation of lipid metabolism from transcriptomes of three mouse models.