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Ligand-dependent corepressor acts as a novel corepressor of thyroid hormone receptor and represses hepatic lipogenesis in mice
Authors:Song Yiyun  Shan Shifang  Zhang Ying  Liu Wei  Ding Weiqiao  Ren Wenxia  Xia Hongfeng  Li Xiaojun  Zhang Qin  Zhao Lei  Li Xihua  Yan Jun  Ying Hao
Affiliation:1 Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Graduate School of the Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200031, China
2 Nanjing Maternity and Child Health Care Hospital, Nanjing 210004, China
3 Department of Neuromuscular Disease, Xinhua Hospital, Shanghai Institute for Pediatric Research, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China
4 Department of Neuromuscular Disease, Children’s Hospital of Fudan University, Shanghai 201102, China
5 Model Animal Research Center and MOE Key Laboratory of Model Animals for Disease Study, Nanjing University, Nanjing 210061, China
6 Zhejiang Provincial Key Lab for Technology and Application of Model Organisms, School of Life Sciences, Wenzhou Medical College, Wenzhou 325035, China
Abstract:
Keywords:LCOR, ligand-dependent corepressor   ob/ob, leptin-deficient   TR, thyroid hormone receptor   TH, thyroid hormone   SRC, steroid receptor coactivators   PGC-1, peroxisome proliferator-activated receptor gamma coactivator-1   NCOR, nuclear receptor corepressor   SMRT, silencing mediator for retinoic acid receptor and thyroid hormone receptor   RIP140, nuclear receptor co-repressor nrip1   HDAC, histone deacetylases   CtBP, C-terminal binding protein   ME, malic enzyme   FAS, fatty acid synthase   ACC, acetyl-CoA carboxylase   SP14, thyroid hormone responsive SPOT14   T3, Triiodothyronine   TRE, thyroid hormone response elements   LFD, low-fat diet   HFD, high-fat diet   TG, triglyceride   MMI, methimazole   ChIP, chromatin immunoprecipitation   DIO1, deiodinase I   LBD, ligand-binding domain   Td, T3 deficient
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