Related references
Note: Only part of the references are listed.Dihydroartemisinin protects against alcoholic liver injury through alleviating hepatocyte steatosis in a farnesoid X receptor-dependent manner
Wenxuan Xu et al.
TOXICOLOGY AND APPLIED PHARMACOLOGY (2017)
Autophagy regulates turnover of lipid droplets via ROS-dependent Rab25 activation in hepatic stellate cell
Zili Zhang et al.
REDOX BIOLOGY (2017)
Targeting molecules to medicine with mTOR, autophagy and neurodegenerative disorders
Kenneth Maiese
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY (2016)
Cellular senescence impact on immune cell fate and function
Rita Vicente et al.
AGING CELL (2016)
How autophagy both activates and inhibits cellular senescence
Chanhee Kang et al.
AUTOPHAGY (2016)
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J. Klionsky et al.
AUTOPHAGY (2016)
Bclaf1 is an important NF-κB signaling transducer and C/EBPβ regulator in DNA damage-induced senescence
A-w Shao et al.
CELL DEATH AND DIFFERENTIATION (2016)
Associations between autophagy, the ubiquitin-proteasome system and endoplasmic reticulum stress in hypoxia-deoxygenation or ischemia-reperfusion
Tao Fan et al.
EUROPEAN JOURNAL OF PHARMACOLOGY (2016)
The emerging role of GATA transcription factors in development and disease
Marjolein H. F. M. Lentjes et al.
EXPERT REVIEWS IN MOLECULAR MEDICINE (2016)
ROS-JNK1/2-dependent activation of autophagy is required for the induction of anti-inflammatory effect of dihydroartemisinin in liver fibrosis
Zili Zhang et al.
FREE RADICAL BIOLOGY AND MEDICINE (2016)
Dihydroartemisinin alleviates bile duct ligation-induced liver fibrosis and hepatic stellate cell activation by interfering with the PDGF-βR/ERK signaling pathway
Qin Chen et al.
INTERNATIONAL IMMUNOPHARMACOLOGY (2016)
Dihydroartemisinin Prevents Liver Fibrosis in Bile Duct Ligated Rats by Inducing Hepatic Stellate Cell Apoptosis through Modulating the PI3K/Akt Pathway
Qin Chen et al.
IUBMB LIFE (2016)
Dihydroartemisinin Restricts Hepatic Stellate Cell Contraction via an FXR-S1PR2-dependent Mechanism
Wenxuan Xu et al.
IUBMB LIFE (2016)
Autophagy maintains stemness by preventing senescence
Laura Garcia-Prat et al.
NATURE (2016)
The Degradation Pathway of the Mitophagy Receptor Atg32 Is Re-Routed by a Posttranslational Modification
Mariia Levchenko et al.
PLOS ONE (2016)
Autophagy and Immune Senescence
Hanlin Zhang et al.
TRENDS IN MOLECULAR MEDICINE (2016)
Activation of PPARγ/P53 signaling is required for curcumin to induce hepatic stellate cell senescence
H. Jin et al.
CELL DEATH & DISEASE (2016)
Hepatic Stellate Cells and microRNAs in Pathogenesis of Liver Fibrosis
Mio Kitano et al.
JOURNAL OF CLINICAL MEDICINE (2016)
Hepatic stellate cells: central modulators of hepatic carcinogenesis
Alexandra I. Thompson et al.
BMC GASTROENTEROLOGY (2015)
Acrylamide Induces Senescence in Macrophages through a Process Involving ATF3, ROS, p38/JNK, and a Telomerase-Independent Pathway
Kyung-Ho Kim et al.
CHEMICAL RESEARCH IN TOXICOLOGY (2015)
Pathobiology of liver fibrosis: a translational success story
Youngmin A. Lee et al.
GUT (2015)
GATA get a hold on senescence
Liam D. Cassidy et al.
SCIENCE (2015)
The DNA damage response induces inflammation and senescence by inhibiting autophagy of GATA4
Chanhee Kang et al.
SCIENCE (2015)
Isolation and Time Lapse Microscopy of Highly Pure Hepatic Stellate Cells
Matthias Bartneck et al.
ANALYTICAL CELLULAR PATHOLOGY (2015)
Rhus coriaria induces senescence and autophagic cell death in breast cancer cells through a mechanism involving p38 and ERK1/2 activation
Hussain El Hasasna et al.
SCIENTIFIC REPORTS (2015)
The role of miRNAs in stress-responsive hepatic stellate cells during liver fibrosis
Joeri Lambrecht et al.
FRONTIERS IN PHYSIOLOGY (2015)
Cellular senescence checkpoint function determines differential Notch1-dependent oncogenic and tumor-suppressor activities
S. Kagawa et al.
ONCOGENE (2015)
Autophagy suppresses melanoma tumorigenesis by inducing senescence
He Liu et al.
AUTOPHAGY (2014)
Tetramethylpyrazine reduces glucose and insulin-induced activation of hepatic stellate cells by inhibiting insulin receptor-mediated PI3K/AKT and ERK pathways
Feng Zhang et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2014)
Hepatic stellate cells and extracellular matrix in hepatocellular carcinoma: more complicated than ever
Vinicio Carloni et al.
LIVER INTERNATIONAL (2014)
A review of dihydroartemisinin as another gift from traditional Chinese medicine not only for malaria control but also for schistosomiasis control
Xu-Guang Zhang et al.
PARASITOLOGY RESEARCH (2014)
Curcumin modulates cannabinoid receptors in liver fibrosis in vivo and inhibits extracellular matrix expression in hepatic stellate cells by suppressing cannabinoid receptor type-1 in vitro
Zili Zhang et al.
EUROPEAN JOURNAL OF PHARMACOLOGY (2013)
Design, Synthesis and Evaluation of the Antibacterial Enhancement Activities of Amino Dihydroartemisinin Derivatives
Chong Wu et al.
MOLECULES (2013)
Senescence and aging: the critical roles of p53
A. Rufini et al.
ONCOGENE (2013)
CDK-Dependent Hsp70 Phosphorylation Controls G1 Cyclin Abundance and Cell-Cycle Progression
Andrew W. Truman et al.
CELL (2012)
Five dysfunctional telomeres predict onset of senescence in human cells
Zeenia Kaul et al.
EMBO REPORTS (2012)
Interleukin-22 induces hepatic stellate cell senescence and restricts liver fibrosis in mice
Xiaoni Kong et al.
HEPATOLOGY (2012)
Hepatic Stellate Cells: Partners in Crime for Liver Metastases?
Ningling Kang et al.
HEPATOLOGY (2011)
p16Ink4a overexpression in cancer: a tumor suppressor gene associated with senescence and high-grade tumors
C. Romagosa et al.
ONCOGENE (2011)
Senescence of activated stellate cells limits liver fibrosis
Valery Krizhanovsky et al.
CELL (2008)
PI3K is involved in PDGF-β receptor upregulation post-PDGF-BB treatment in mouse HSC
Carmen G. Lechuga et al.
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY (2006)