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Nrf2 promotes the development of fibrosis and tumorigenesis in mice with defective hepatic autophagy
Authors:Hong-Min Ni  Benjamin L. Woolbright  Jessica Williams  Bryan Copple  Wei Cui  James P. Luyendyk  Hartmut Jaeschke  Wen-Xing Ding
Affiliation:1 Department of Pharmacology, Toxicology and Therapeutics, The University of Kansas Medical Center, Kansas City, KS 66160, United States;2 Department of Pathology & Laboratory Medicine, The University of Kansas Medical Center, Kansas City, KS 66160, United States;3 Department of Pathobiology and Diagnostic Investigation, Michigan State University, East Lansing, MI 48824, United States
Abstract:
Keywords:Alb, albumin   ALT, alanine aminotransferase   α-SMA, α-smooth muscle actin   CTGF, connective tissue growth factor   CK 19, cytokeratin 19   ECM, extracellular matrix   EM, electron microscopy   FLIP, FLICE-like protein (FLIP) protein   GCLC, glutamate-cysteine ligase catalytic subunit   GCLM, glutamate-cysteine ligase modifier subunit   HCC, hepatocellular carcinoma   HSC, hepatic stellate cells   ICAM-1, Intercellular adhesion molecule 1   IL-6, interleukin 6   KC, C-X-C motif ligand 1   Keap1, Kelch-like ECH-associated protein 1   KO, knockout   LC3, microtubule light chain 3   LD, lipid droplets   Ly6B, lymphocyte antigen B superfamily   MIP1α, macrophage inflammatory protein 1α   NQO1, NAD(P)H quinone oxidoreductase   Nrf2, nuclear factor (erythroid-derived 2)-like 2   PCNA, proliferating cell nuclear antigen   ROS, reactive oxygen species   TGF-β1, transforming growth factor beta 1   TNF-α, tumor necrosis factor alpha   WT, wild type
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