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Hepatic Stellate Cells and Liver Fibrosis
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0185(199804)250:4<430::aid-ar6>3.0.co;2-0openalex-snapshot
Morphology of sites of adhesion between hepatic stellate cells (vitamin A-storing cells) and a three-dimensional extracellular matrix
inferredcites →https://doi.org/10.1002/1097-4652(2001)9999:9999<00::aid-jcp1059>3.0.co;2-sopenalex-snapshot
Constitutive phosphorylation and nuclear localization of Smad3 are correlated with increased collagen gene transcription in activated hepatic stellate cells
inferredcites →https://doi.org/10.1002/aja.1001320404openalex-snapshot
“Sternzellen” in the liver: Perisinusoidal cells with special reference to storage of vitamin A
inferredcites →https://doi.org/10.1002/ar.a.20096openalex-snapshot
Neuroregulation of the neuroendocrine compartment of the liver
inferredcites →https://doi.org/10.1002/cbf.2838openalex-snapshot
HSCs play a distinct role in different phases of oval cell‐mediated liver regeneration
inferredcites →https://doi.org/10.1002/hep.1840040307openalex-snapshot
Purified Rat Liver Fat-Storing Cells in Culture Divide and Contain Collagen
inferredcites →https://doi.org/10.1002/hep.1840070609openalex-snapshot
Biochemical characteristics of isolated rat liver stellate cells
inferredcites →https://doi.org/10.1002/hep.1840130628openalex-snapshot
Tissue distribution, quantitation and proliferation kinetics of fat-storing cells in carbon tetrachloride-injured rat liver
inferredcites →https://doi.org/10.1002/hep.1840150103openalex-snapshot
Hepatocyte growth factor/hepatopoietin A is expressed in fat-storing cells from rat liver but not myofibroblast-like cells derived from fat-storing cells
inferredcites →https://doi.org/10.1002/hep.1840190224openalex-snapshot
Ito cell heterogeneity: Desmin-negative Ito cells in normal rat liver
inferredcites →https://doi.org/10.1002/hep.1840210335openalex-snapshot
Expression of SPARC in normal and fibrotic livers
inferredcites →https://doi.org/10.1002/hep.1840220230openalex-snapshot
Regulation of the α2(I) collagen gene transcription in fat-storing cells derived from a cirrhotic liver
inferredcites →https://doi.org/10.1002/hep.1840380415openalex-snapshot
Interferon Alfa Down–Regulates Collagen Gene Transcription and Suppresses Experimental Hepatic Fibrosis in Mice
inferredcites →https://doi.org/10.1002/hep.1840380418openalex-snapshot
Human Hepatic Stellate Cells Show Features of Antigen–Presenting Cells and Stimulate Lymphocyte Proliferation
inferredcites →https://doi.org/10.1002/hep.20015openalex-snapshot
Differential modulation of rat hepatic stellate phenotype by natural and synthetic retinoids
inferredcites →https://doi.org/10.1002/hep.20427openalex-snapshot
A dual reporter gene transgenic mouse demonstrates heterogeneity in hepatic fibrogenic cell populations
inferredcites →https://doi.org/10.1002/hep.20974openalex-snapshot
Reversal of Hepatic Fibrosis — Fact or Fantasy?
inferredcites →https://doi.org/10.1002/hep.21564openalex-snapshot
Sinusoidal remodeling and angiogenesis: A new function for the liver-specific pericyte?
inferredcites →https://doi.org/10.1002/hep.21606openalex-snapshot
Hepatic stellate cell protrusions couple platelet-derived growth factor-BB to chemotaxis
inferredcites →https://doi.org/10.1002/hep.22413openalex-snapshot
Activation of hepatic stellate cells after phagocytosis of lymphocytes: A novel pathway of fibrogenesis
inferredcites →https://doi.org/10.1002/hep.22589openalex-snapshot
Adenosine induces loss of actin stress fibers and inhibits contraction in hepatic stellate cells via Rho inhibition†
inferredcites →https://doi.org/10.1002/hep.22697openalex-snapshot
Functional linkage of cirrhosis‐predictive single nucleotide polymorphisms of toll‐like receptor 4 to hepatic stellate cell responses†‡
inferredcites →https://doi.org/10.1002/hep.22701openalex-snapshot
p75 neurotrophin receptor signaling regulates hepatic myofibroblast proliferation and apoptosis in recovery from rodent liver fibrosis†
inferredcites →https://doi.org/10.1002/hep.22721openalex-snapshot
Mesenchymal origin of hepatic stellate cells, submesothelial cells, and perivascular mesenchymal cells during mouse liver development†
inferredcites →https://doi.org/10.1002/hep.22890openalex-snapshot
Hepatic stellate cells express functional CXCR4
inferredcites →https://doi.org/10.1002/hep.22952openalex-snapshot
CCR2 promotes hepatic fibrosis in mice #
inferredcites →https://doi.org/10.1002/hep.23184openalex-snapshot
The niche of stellate cells within rat liver #
inferredcites →https://doi.org/10.1002/hep.23279openalex-snapshot
Increased Caffeine Consumption Is Associated With Reduced Hepatic Fibrosis
inferredcites →https://doi.org/10.1002/hep.23829openalex-snapshot
Paracrine Signals from Mesenchymal Cell Populations Govern the Expansion and Differentiation of Human Hepatic Stem Cells to Adult Liver Fates
inferredcites →https://doi.org/10.1002/hep.23922openalex-snapshot
Micro-RNA profiling reveals a role for miR-29 in human and murine liver fibrosis
inferredcites →https://doi.org/10.1002/hep.24047openalex-snapshot
Combination of retinoic acid and ursodeoxycholic acid attenuates liver injury in bile duct-ligated rats and human hepatic cells
inferredcites →https://doi.org/10.1002/hep.24119openalex-snapshot
Septum Transversum-Derived Mesothelium Gives Rise to Hepatic Stellate Cells and Perivascular Mesenchymal Cells in Developing Mouse Liver §Δ
inferredcites →https://doi.org/10.1002/hep.24281openalex-snapshot
The nicotinamide adenine dinucleotide phosphate oxidase (NOX) homologues NOX1 and NOX2/gp91phox mediate hepatic fibrosis in mice
inferredcites →https://doi.org/10.1002/hep.24352openalex-snapshot
Murine hepatic stellate cells veto CD8 T cell activation by a CD54-dependent mechanism
inferredcites →https://doi.org/10.1002/hep.24384openalex-snapshot
Hepatic stellate cells: Partners in crime for liver metastases?
inferredcites →https://doi.org/10.1002/hep.24388openalex-snapshot
Critical role of tumor necrosis factor receptor 1, but not 2, in hepatic stellate cell proliferation, extracellular matrix remodeling, and liver fibrogenesis
inferredcites →https://doi.org/10.1002/hep.24427openalex-snapshot
Complementary vascular and matrix regulatory pathways underlie the beneficial mechanism of action of sorafenib in liver fibrosis
inferredcites →https://doi.org/10.1002/hep.24598openalex-snapshot
Protease profiling of liver fibrosis reveals the ADAM metallopeptidase with thrombospondin type 1 motif, 1 as a central activator of transforming growth factor beta
inferredcites →https://doi.org/10.1002/hep.24621openalex-snapshot
Dendritic Cell Regulation of Carbon Tetrachloride–Induced Murine Liver Fibrosis Regression
inferredcites →https://doi.org/10.1002/hep.24701openalex-snapshot
Osteopontin, an Oxidant Stress Sensitive Cytokine, Up-regulates Collagen-I via Integrin αVβ3 Engagement and PI3K/pAkt/NFκB Signaling
inferredcites →https://doi.org/10.1002/hep.25650openalex-snapshot
Comparative proteomic analysis of rat hepatic stellate cell activation: A comprehensive view and suppressed immune response
inferredcites →https://doi.org/10.1002/hep.25754openalex-snapshot
Histone methyltransferase ASH1 orchestrates fibrogenic gene transcription during myofibroblast transdifferentiation
inferredcites →https://doi.org/10.1002/hep.25757openalex-snapshot
The basic helix-loop-helix transcription factor, heart and neural crest derivatives expressed transcript 2, marks hepatic stellate cells in zebrafish: Analysis of stellate cell entry into the developing liver
inferredcites →https://doi.org/10.1002/hep.25780openalex-snapshot
Antagonism of sphingosine 1-phosphate receptor 2 causes a selective reduction of portal vein pressure in bile duct-ligated rodents
inferredcites →https://doi.org/10.1002/hep.25975openalex-snapshot
Disparate profiles of dys-regulated miRNAs in activated hepatic stellate cells
inferredcites →https://doi.org/10.1002/hep.26056openalex-snapshot
Reduced Hepatic Stellate Cell Expression of Kruppel-Like Factor 6 Tumor Suppressor Isoforms Amplifies Fibrosis During Acute and Chronic Rodent Liver Injury
inferredcites →https://doi.org/10.1002/hep.510230634openalex-snapshot
Comparison of Glial Fibrillary Acidic Protein and Desmin Staining in Normal and Ccl4–Induced Fibrotic Rat Livers
inferredcites →https://doi.org/10.1002/hep.510260417openalex-snapshot
Retinoids exacerbate rat liver fibrosis by inducing the activation of latent TGF-β in liver stellate cells
inferredcites →https://doi.org/10.1002/hep.510270222openalex-snapshot
Cellular localization of endothelin-1 and increased production in liver injury in the rat: Potential for autocrine and paracrine effects on stellate cells
inferredcites →https://doi.org/10.1002/hep.510290107openalex-snapshot
Monocyte Chemotactic Protein–1 As A Chemoattractant for Human Hepatic Stellate Cells
inferredcites →https://doi.org/10.1002/hep.510290640openalex-snapshot
In Vitro Migratory Potential of Rat Quiescent Hepatic Stellate Cells and Its Augmentation by Cell Activation
inferredcites →https://doi.org/10.1002/hep.510300144openalex-snapshot
Transforming growth factor β and tumor necrosis factor α inhibit both apoptosis and proliferation of activated rat hepatic stellate cells
inferredcites →https://doi.org/10.1002/jcp.22063openalex-snapshot
Downregulation of hepatic stellate cell activation by retinol and palmitate mediated by adipose differentiation‐related protein (ADRP)
inferredcites →https://doi.org/10.1002/jcp.22598openalex-snapshot
Down‐regulation of cyclin E1 expression by microrna‐195 accounts for interferon‐β‐induced inhibition of hepatic stellate cell proliferation
inferredcites →https://doi.org/10.1002/jemt.1060140306openalex-snapshot
Ultrastructure and function of hepatic fat‐storing and pit cells
inferredcites →https://doi.org/10.1002/path.3005openalex-snapshot
The biphasic nature of hypoxia‐induced directional migration of activated human hepatic stellate cells
inferredcites →https://doi.org/10.1006/bbrc.1998.9984openalex-snapshot
Expressions of Vascular Endothelial Growth Factor in Nonparenchymal as Well as Parenchymal Cells in Rat Liver after Necrosis
inferredcites →https://doi.org/10.1006/bbrc.1999.0372openalex-snapshot
Expression of Osteopontin in Kupffer Cells and Hepatic Macrophages and Stellate Cells in Rat Liver after Carbon Tetrachloride Intoxication: A Possible Factor for Macrophage Migration into Hepatic Necrotic Areas
inferredcites →https://doi.org/10.1006/cbir.1998.0234openalex-snapshot
INDUCTION OF CELLULAR PROCESSES CONTAINING COLLAGENASE AND RETINOID BY INTEGRIN‐BINDING TO INTERSTITIAL COLLAGEN IN HEPATIC STELLATE CELL CULTURE
inferredcites →https://doi.org/10.1007/978-1-59745-518-3_10openalex-snapshot
The Role of Inflammation and Immunity in the Pathogenesis of Liver Fibrosis
inferredcites →https://doi.org/10.1007/978-4-431-67935-6_18openalex-snapshot
Morphological Aspects of Hepatic Fibrosis and Ito Cells (Hepatic Stellate Cells), with Special Reference to Their Myofibroblastic Transformation
inferredcites →https://doi.org/10.1007/bf00193944openalex-snapshot
Heterogeneity of myofibroblast phenotypic features: an example of fibroblastic cell plasticity
inferredcites →https://doi.org/10.1007/bf00312824openalex-snapshot
Intralobular heterogeneity of perisinusoidal stellate cells in porcine liver
inferredcites →https://doi.org/10.1007/bf02899424openalex-snapshot
Expression of the gene of the α-smooth muscle-actin isoform in rat liver and in rat fat-storing (ITO) cells
inferredcites →https://doi.org/10.1007/s004180050273openalex-snapshot
Hepatic stellate cells (vitamin A-storing cells) change their cytoskeleton structure by extracellular matrix components through a signal transduction system
inferredcites →https://doi.org/10.1007/s004410051073openalex-snapshot
The cell biology of liver fibrogenesis - an imbalance of proliferation, growth arrest and apoptosis of myofibroblasts
inferredcites →https://doi.org/10.1007/s10495-005-1055-4openalex-snapshot
The role and regulation of hepatic stellate cell apoptosis in reversal of liver fibrosis
inferredcites →https://doi.org/10.1007/s10620-010-1296-0openalex-snapshot
Loss of Matrix Metalloproteinase-2 Amplifies Murine Toxin-Induced Liver Fibrosis by Upregulating Collagen I Expression
inferredcites →https://doi.org/10.1007/s11010-011-1016-xopenalex-snapshot
Hepatic stellate cells produce vascular endothelial growth factor via phospho-p44/42 mitogen–activated protein kinase/cyclooxygenase-2 pathway
inferredcites →https://doi.org/10.1007/s12016-012-8323-1openalex-snapshot
Immunological Orchestration of Liver Fibrosis
inferredcites →https://doi.org/10.1007/s13105-011-0101-7openalex-snapshot
Vitamin A and lipid metabolism: relationship between hepatic stellate cells (HSCs) and adipocytes
inferredcites →https://doi.org/10.1016/0006-291x(90)90801-sopenalex-snapshot
Modulation of hepatic lipocyte proteoglycan synthesis and proliferation by Kupffer cell-derived transforming growth factors type β1 and type α
inferredcites →https://doi.org/10.1016/0006-291x(92)90545-vopenalex-snapshot
The gene of hepatocyte growth factor is expressed in fat-storing cells of rat liver and is downregulated during cell growth and by transforming growth factor-β
inferredcites →https://doi.org/10.1016/0014-4827(85)90243-5openalex-snapshot
Perisinusoidal fat-storing cells are the main vitamin A storage sites in rat liver
inferredcites →https://doi.org/10.1016/0016-5085(89)91431-5openalex-snapshot
Fat-storing (Ito) cells of rat liver synthesize and secrete apolipoproteins: comparison with hepatocytes
inferredcites →https://doi.org/10.1016/0016-5085(95)90399-2openalex-snapshot
Rat hepatic lipocytes synthesize and secrete transin (Stromelysin) in early primary culture
inferredcites →https://doi.org/10.1016/0016-5085(95)90767-xopenalex-snapshot
Fibroblast growth factor 2 and transforming growth factor β1 interactions in human liver myofibroblasts
inferredcites →https://doi.org/10.1016/0168-8278(89)90076-7openalex-snapshot
In vitro differentiation of fat-storing cells parallels marked increase of collagen synthesis and secretion
inferredcites →https://doi.org/10.1016/0168-8278(90)90080-bopenalex-snapshot
Nerves and perisinusoidal cells in human liver
inferredcites →https://doi.org/10.1016/0168-8278(92)90127-bopenalex-snapshot
Expression of insulin-like growth factor II (IGF-II) and IGF-II, IGF-I and insulin receptors mRNAs in isolated non-parenchymal rat liver cells
inferredcites →https://doi.org/10.1016/0270-9139(95)90327-5openalex-snapshot
Induction of ?-platelet-derived growth factor receptor in rat hepatic lipocytes during cellular activation in vivo and in culture Wong L, Yamasaki G, Johnson RL, Friedman SL. J Clin Invest 1994;94:1563?1569
inferredcites →https://doi.org/10.1016/j.addr.2009.03.011openalex-snapshot
Transcriptional regulation of hepatic stellate cells
inferredcites →https://doi.org/10.1016/j.ajpath.2011.09.002openalex-snapshot
Loss of Discoidin Domain Receptor 2 Promotes Hepatic Fibrosis after Chronic Carbon Tetrachloride through Altered Paracrine Interactions between Hepatic Stellate Cells and Liver-Associated Macrophages
inferredcites →https://doi.org/10.1016/j.bbadis.2012.09.008openalex-snapshot
Natural killer and natural killer T cells in liver fibrosis
inferredcites →https://doi.org/10.1016/j.bbadis.2013.02.019openalex-snapshot
Origins and functions of liver myofibroblasts
inferredcites →https://doi.org/10.1016/j.bbrc.2003.09.225openalex-snapshot
Epimorphin is involved in differentiation of rat hepatic stem-like cells through cell–cell contact
inferredcites →https://doi.org/10.1016/j.bbrc.2006.11.029openalex-snapshot
CD133+ hepatic stellate cells are progenitor cells
inferredcites →https://doi.org/10.1016/j.bbrc.2011.02.009openalex-snapshot
Silencing tissue inhibitors of metalloproteinases (TIMPs) with short interfering RNA reveals a role for TIMP-1 in hepatic stellate cell proliferation
inferredcites →https://doi.org/10.1016/j.bbrc.2011.07.041openalex-snapshot
Suppression of hepatic stellate cell activation by microRNA-29b
inferredcites →https://doi.org/10.1016/j.bbrc.2012.03.025openalex-snapshot
miR-181b Promotes hepatic stellate cells proliferation by targeting p27 and is elevated in the serum of cirrhosis patients
inferredcites →https://doi.org/10.1016/j.biocel.2009.11.006openalex-snapshot
The role of stem cells in liver repair and fibrosis
inferredcites →https://doi.org/10.1016/j.cca.2005.06.014openalex-snapshot
Mechanisms of liver fibrosis
inferredcites →https://doi.org/10.1016/j.ccr.2012.02.007openalex-snapshot
Promotion of Hepatocellular Carcinoma by the Intestinal Microbiota and TLR4
inferredcites →https://doi.org/10.1016/j.cell.2008.06.049openalex-snapshot
Senescence of Activated Stellate Cells Limits Liver Fibrosis
inferredcites →https://doi.org/10.1016/j.cell.2013.03.020openalex-snapshot
Non-Cell-Autonomous Tumor Suppression by p53
inferredcites →https://doi.org/10.1016/j.cellsig.2012.07.023openalex-snapshot
The potential of microRNAs in liver fibrosis
inferredcites →https://doi.org/10.1016/j.febslet.2009.01.034openalex-snapshot
Over‐expressed microRNA‐27a and 27b influence fat accumulation and cell proliferation during rat hepatic stellate cell activation
inferredcites →https://doi.org/10.1016/j.jhep.2003.10.012openalex-snapshot
Commitment of bone marrow cells to hepatic stellate cells in mouse
inferredcites →https://doi.org/10.1016/j.jhep.2005.09.023openalex-snapshot
Hepatic stellate cells do not derive from the neural crest
inferredcites →https://doi.org/10.1016/j.jhep.2006.05.002openalex-snapshot
Different types of liver progenitor cells and their niches
inferredcites →https://doi.org/10.1016/j.jhep.2006.11.002openalex-snapshot
Epigenetic mechanism of stellate cell trans-differentiation
inferredcites →https://doi.org/10.1016/j.jhep.2007.01.029openalex-snapshot
Pro-fibrogenic potential of PDGF-D in liver fibrosis
inferredcites →https://doi.org/10.1016/j.jhep.2007.11.021openalex-snapshot
Integrin αvβ6 is a marker of the progression of biliary and portal liver fibrosis and a novel target for antifibrotic therapies
inferredcites →https://doi.org/10.1016/j.jhep.2008.03.020openalex-snapshot
Hepatic expression of A Disintegrin And Metalloproteinase (ADAM) and ADAMs with thrombospondin motives (ADAM-TS) enzymes in patients with chronic liver diseases
inferredcites →https://doi.org/10.1016/j.jhep.2008.11.025openalex-snapshot
miR-15b and miR-16 are implicated in activation of the rat hepatic stellate cell: An essential role for apoptosis
inferredcites →https://doi.org/10.1016/j.jhep.2010.06.020openalex-snapshot
Distinct roles for non-muscle myosin II isoforms in mouse hepatic stellate cells
inferredcites →https://doi.org/10.1016/j.jhep.2010.08.027openalex-snapshot
Association of caffeine intake and histological features of chronic hepatitis C
inferredcites →https://doi.org/10.1016/j.jhep.2010.09.022openalex-snapshot
Intracellular reactive oxygen species are required for directional migration of resident and bone marrow-derived hepatic pro-fibrogenic cells
inferredcites →https://doi.org/10.1016/j.jhep.2011.10.026openalex-snapshot
Macrophages: Central regulators of hepatic fibrogenesis and fibrosis resolution
inferredcites →https://doi.org/10.1016/j.jhep.2011.11.013openalex-snapshot
Intestinal decontamination inhibits TLR4 dependent fibronectin-mediated cross-talk between stellate cells and endothelial cells in liver fibrosis in mice
inferredcites →https://doi.org/10.1016/j.jhep.2012.07.016openalex-snapshot
Increased number and function of endothelial progenitor cells stimulate angiogenesis by resident liver sinusoidal endothelial cells (SECs) in cirrhosis through paracrine factors
inferredcites →https://doi.org/10.1016/j.jhep.2012.09.016openalex-snapshot
Activation of toll-like receptor 3 attenuates alcoholic liver injury by stimulating Kupffer cells and stellate cells to produce interleukin-10 in mice
inferredcites →https://doi.org/10.1016/j.jhep.2012.09.024openalex-snapshot
Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cells
inferredcites →https://doi.org/10.1016/j.jhep.2012.11.011openalex-snapshot
miR-122 regulates collagen production via targeting hepatic stellate cells and suppressing P4HA1 expression
inferredcites →https://doi.org/10.1016/j.jhep.2012.11.022openalex-snapshot
miR-133a mediates TGF-β-dependent derepression of collagen synthesis in hepatic stellate cells during liver fibrosis
inferredcites →https://doi.org/10.1016/j.jhep.2013.02.016openalex-snapshot
Endoplasmic reticulum stress induces fibrogenic activity in hepatic stellate cells through autophagy
inferredcites →https://doi.org/10.1016/j.jmb.2007.06.006openalex-snapshot
RNA-binding Protein RBMS3 Is Expressed in Activated Hepatic Stellate Cells and Liver Fibrosis and Increases Expression of Transcription Factor Prx1
inferredcites →https://doi.org/10.1016/j.phrs.2011.03.005openalex-snapshot
Endothelin and hepatic wound healing
inferredcites →https://doi.org/10.1016/j.taap.2012.06.022openalex-snapshot
DNMT1-mediated PTEN hypermethylation confers hepatic stellate cell activation and liver fibrogenesis in rats
inferredcites →https://doi.org/10.1016/j.transproceed.2010.09.139openalex-snapshot
The Role of Liver Stromal Cells in Dendritic Cells Development in Mice
inferredcites →https://doi.org/10.1016/j.transproceed.2011.11.049openalex-snapshot
Hepatic Stellate Cells Attenuate the Immune Response in Renal Transplant Recipients With Chronic Hepatitis
inferredcites →https://doi.org/10.1016/j.transproceed.2012.03.029openalex-snapshot
Inhibition of Allogenic T-Cell Cytotoxicity by Hepatic Stellate Cell via CD4+ CD25+ Foxp3+ Regulatory T Cells In Vitro
inferredcites →https://doi.org/10.1016/j.ydbio.2008.04.021openalex-snapshot
Wnt9a secreted from the walls of hepatic sinusoids is essential for morphogenesis, proliferation, and glycogen accumulation of chick hepatic epithelium
inferredcites →https://doi.org/10.1016/s0002-9440(10)61167-4openalex-snapshot
Pleiotrophin/Heparin-Binding Growth-Associated Molecule as a Mitogen of Rat Hepatocytes and Its Role in Regeneration and Development of Liver
inferredcites →https://doi.org/10.1016/s0002-9440(10)63383-4openalex-snapshot
Activated Hepatic Stellate Cells Express Keratinocyte Growth Factor in Chronic Liver Disease
inferredcites →https://doi.org/10.1016/s0002-9440(10)63522-5openalex-snapshot
Role of Fibroblast Growth Factor Type 1 and 2 in Carbon Tetrachloride-Induced Hepatic Injury and Fibrogenesis
inferredcites →https://doi.org/10.1016/s0002-9440(10)63544-4openalex-snapshot
Hepatocytes Express Nerve Growth Factor during Liver Injury
inferredcites →https://doi.org/10.1016/s0016-5085(03)01194-6openalex-snapshot
The chemokine CCL21 modulates lymphocyte recruitment and fibrosis in chronic hepatitis C1 1The authors thank Wanda Delogu and Nadia Navari for skillful technical help, Dr. Roberto G. Romanelli for help in collecting liver biopsy specimens, and Dr. Mario Strazzabosco (Ospedali Riuniti di Bergamo,…
inferredcites →https://doi.org/10.1016/s0016-5085(79)80170-5openalex-snapshot
Collagen Types in Normal and Cirrhotic Liver
inferredcites →https://doi.org/10.1016/s0021-9258(17)32069-0openalex-snapshot
Liver expression of epidermal growth factor RNA. Rapid increases in immediate-early phase of liver regeneration.
inferredcites →https://doi.org/10.1016/s0021-9258(18)81686-6openalex-snapshot
Maintenance of Differentiated Phenotype of Cultured Rat Hepatic Lipocytes by Basement Membrane Matrix
inferredcites →https://doi.org/10.1016/s0022-2275(20)38430-3openalex-snapshot
Effects of dietary retinoid and triglyceride on the lipid composition of rat liver stellate cells and stellate cell lipid droplets
inferredcites →https://doi.org/10.1016/s0024-3205(97)00372-xopenalex-snapshot
Expression of cytochrome P450 isoforms in rat hepatic stellate cells
inferredcites →https://doi.org/10.1016/s0046-8177(97)90011-3openalex-snapshot
Hepatic stellate cells and intralobular innervation in human liver cirrhosis
inferredcites →https://doi.org/10.1016/s0074-7696(08)61977-4openalex-snapshot
Perisinusoidal Stellate Cells (Fat-Storing Cells, Interstitial Cells, Lipocytes), Their Related Structure in and around the Liver Sinusoids, and Vitamin A-Storing Cells in Extrahepatic Organs
inferredcites →https://doi.org/10.1016/s0168-8278(00)00016-7openalex-snapshot
Human hepatic stellate cells secrete adrenomedullin: potential autocrine factor in the regulation of cell contractility
inferredcites →https://doi.org/10.1016/s0168-8278(03)00360-xopenalex-snapshot
Oxidative stress, KLF6 and transforming growth factor-β up-regulation differentiate non-alcoholic steatohepatitis progressing to fibrosis from uncomplicated steatosis in rats
inferredcites →https://doi.org/10.1016/s0168-8278(97)80257-7openalex-snapshot
Transforming growth factor-β gene expression in normal and fibrotic rat liver
inferredcites →https://doi.org/10.1016/s0168-8278(98)80200-6openalex-snapshot
Human hepatic stellate cells express class I alcohol dehydrogenase and aldehyde dehydrogenase but not cytochrome P4502E1
inferredcites →https://doi.org/10.1016/s0168-8278(99)80007-5openalex-snapshot
Expression patterns of matrix metalloproteinases and their inhibitors in parenchymal and non-parenchymal cells of rat liver: regulation by TNF-α and TGF-β1
inferredcites →https://doi.org/10.1016/s0168-8278(99)80011-7openalex-snapshot
Differential expression of monocyte chemotactic protein-1 (MCP-1) in transforming rat hepatic stellate cells
inferredcites →https://doi.org/10.1016/s0891-5849(01)00470-1openalex-snapshot
Aldehydes potentiate α2(I) collagen gene activity by JNK in hepatic stellate cells
inferredcites →https://doi.org/10.1021/pr3000927openalex-snapshot
Proteomic analysis of extracellular matrix from the hepatic stellate cell line LX-2 identifies CYR61 and Wnt-5a as novel constituents of fibrotic liver
inferredcites →https://doi.org/10.1034/j.1600-0528.2002.017408.xopenalex-snapshot
Local control of the immune response in the liver
inferredcites →https://doi.org/10.1038/332411a0openalex-snapshot
A novel potent vasoconstrictor peptide produced by vascular endothelial cells
inferredcites →https://doi.org/10.1038/labinvest.2010.48openalex-snapshot
Thyroid hormones induce activation of rat hepatic stellate cells through increased expression of p75 neurotrophin receptor and direct activation of Rho
inferredcites →https://doi.org/10.1038/labinvest.2010.88openalex-snapshot
Hepatic stellate cells’ involvement in progenitor-mediated liver regeneration
inferredcites →https://doi.org/10.1038/labinvest.2011.155openalex-snapshot
The function of integrin-linked kinase in normal and activated stellate cells: implications for fibrogenesis in wound healing
inferredcites →https://doi.org/10.1038/labinvest.3780073openalex-snapshot
PDGF-Mediated Chemoattraction of Hepatic Stellate Cells by Bile Duct Segments in Cholestatic Liver Injury
inferredcites →https://doi.org/10.1038/nature04723openalex-snapshot
Loss of autophagy in the central nervous system causes neurodegeneration in mice
inferredcites →https://doi.org/10.1038/nature07976openalex-snapshot
Autophagy regulates lipid metabolism
inferredcites →https://doi.org/10.1038/nature10152openalex-snapshot
Latent TGF-β structure and activation
inferredcites →https://doi.org/10.1038/nm.2490openalex-snapshot
Stimulating healthy tissue regeneration by targeting the 5-HT2B receptor in chronic liver disease
inferredcites →https://doi.org/10.1038/nm1663openalex-snapshot
TLR4 enhances TGF-β signaling and hepatic fibrosis
inferredcites →https://doi.org/10.1038/nrgastro.2010.168openalex-snapshot
Functional role of chemokines in liver disease models
inferredcites →https://doi.org/10.1038/sj.bjp.0706812openalex-snapshot
Adenosine A 2A receptors play a role in the pathogenesis of hepatic cirrhosis
inferredcites →https://doi.org/10.1038/sj.cdd.4401979openalex-snapshot
Regulation of myofibroblast transdifferentiation by DNA methylation and MeCP2: implications for wound healing and fibrogenesis
inferredcites →https://doi.org/10.1042/bj2870701openalex-snapshot
Secretion of 72 kDa type IV collagenase/gelatinase by cultured human lipocytes. Analysis of gene expression, protein synthesis and proteinase activity
inferredcites →https://doi.org/10.1042/bj2990079openalex-snapshot
Cellular sources of glutathione S-transferase P in primary cultured rat hepatocytes: localization by in situ hybridization
inferredcites →https://doi.org/10.1042/cbi20100321openalex-snapshot
Hepatic stellate cell (vitamin A‐storing cell) and its relative – past, present and future
inferredcites →https://doi.org/10.1046/j.0106-9543.2002.01674.xopenalex-snapshot
The correlation between portal myofibroblasts and development of intrahepatic bile ducts and arterial branches in human liver
inferredcites →https://doi.org/10.1053/gast.1996.v110.pm8566602openalex-snapshot
Endothelin 1 is overexpressed in human cirrhotic liver and exerts multiple effects on activated hepatic stellate cells
inferredcites →https://doi.org/10.1053/gast.2002.35384openalex-snapshot
Caspase 9–dependent killing of hepatic stellate cells by activated Kupffer cells
inferredcites →https://doi.org/10.1053/gast.2002.35953openalex-snapshot
Fas enhances fibrogenesis in the bile duct ligated mouse: A link between apoptosis and fibrosis
inferredcites →https://doi.org/10.1053/gast.2003.50012openalex-snapshot
Liver fibrosis: Insights into migration of hepatic stellate cells in response to extracellular matrix and growth factors
inferredcites →https://doi.org/10.1053/he.2000.6126openalex-snapshot
Modulation of transforming growth factor β response and signaling during transdifferentiation of rat hepatic stellate cells to myofibroblasts
inferredcites →https://doi.org/10.1053/j.gastro.2004.03.009openalex-snapshot
Spontaneous recovery from micronodular cirrhosis: Evidence for incomplete resolution associated with matrix cross-linking☆
inferredcites →https://doi.org/10.1053/j.gastro.2004.10.003openalex-snapshot
Inhibition of inhibitor of κB kinases stimulates hepatic stellate cell apoptosis and accelerated recovery from rat liver fibrosis
inferredcites →https://doi.org/10.1053/j.gastro.2005.03.088openalex-snapshot
Cell Type-Specific Intervention of Transforming Growth Factor β/Smad Signaling Suppresses Collagen Gene Expression and Hepatic Fibrosis in Mice
inferredcites →https://doi.org/10.1053/j.gastro.2005.10.055openalex-snapshot
Natural Killer Cells Ameliorate Liver Fibrosis by Killing Activated Stellate Cells in NKG2D-Dependent and Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand–Dependent Manners
inferredcites →https://doi.org/10.1053/j.gastro.2008.03.003openalex-snapshot
Mechanisms of Hepatic Fibrogenesis
inferredcites →https://doi.org/10.1053/j.gastro.2008.03.075openalex-snapshot
p75 Neurotrophin Receptor Is a Marker for Precursors of Stellate Cells and Portal Fibroblasts in Mouse Fetal Liver
inferredcites →https://doi.org/10.1053/j.gastro.2008.07.065openalex-snapshot
Hepatic Stellate Cells Secrete Angiopoietin 1 That Induces Angiogenesis in Liver Fibrosis
inferredcites →https://doi.org/10.1053/j.gastro.2008.10.020openalex-snapshot
Liver Myofibroblasts Regulate Infiltration and Positioning of Lymphocytes in Human Liver
inferredcites →https://doi.org/10.1053/j.gastro.2009.04.011openalex-snapshot
Kupffer Cells Mediate Leptin-Induced Liver Fibrosis
inferredcites →https://doi.org/10.1053/j.gastro.2009.10.002openalex-snapshot
MeCP2 Controls an Epigenetic Pathway That Promotes Myofibroblast Transdifferentiation and Fibrosis
inferredcites →https://doi.org/10.1053/j.gastro.2010.02.054openalex-snapshot
Thrombocytopenia Exacerbates Cholestasis-Induced Liver Fibrosis in Mice
inferredcites →https://doi.org/10.1053/j.gastro.2011.12.017openalex-snapshot
Role of Differentiation of Liver Sinusoidal Endothelial Cells in Progression and Regression of Hepatic Fibrosis in Rats
inferredcites →https://doi.org/10.1053/j.gastro.2011.12.038openalex-snapshot
Fibronectin Extra Domain-A Promotes Hepatic Stellate Cell Motility but Not Differentiation Into Myofibroblasts
inferredcites →https://doi.org/10.1053/j.gastro.2011.12.044openalex-snapshot
Autophagy Releases Lipid That Promotes Fibrogenesis by Activated Hepatic Stellate Cells in Mice and in Human Tissues
inferredcites →https://doi.org/10.1053/j.gastro.2012.05.049openalex-snapshot
Interleukin-17 Signaling in Inflammatory, Kupffer Cells, and Hepatic Stellate Cells Exacerbates Liver Fibrosis in Mice
inferredcites →https://doi.org/10.1053/j.gastro.2012.06.036openalex-snapshot
Deactivation of Hepatic Stellate Cells During Liver Fibrosis Resolution in Mice
inferredcites →https://doi.org/10.1053/j.gastro.2012.08.008openalex-snapshot
Hepatic Vascular Endothelial Growth Factor Regulates Recruitment of Rat Liver Sinusoidal Endothelial Cell Progenitor Cells
inferredcites →https://doi.org/10.1053/jhep.1997.v26.pm0009328313openalex-snapshot
Retinoids exacerbate rat liver fibrosis by inducing the activation of latent TGF-beta in liver stellate cells
inferredcites →https://doi.org/10.1053/jhep.2000.9322openalex-snapshot
Proteome analysis of rat hepatic stellate cells
inferredcites →https://doi.org/10.1053/jhep.2001.20793openalex-snapshot
Human and Rat Hepatic Stellate Cells Express Neurotrophins and Neurotrophin Receptors
inferredcites →https://doi.org/10.1053/jhep.2003.50005openalex-snapshot
Foxf1 +/− mice exhibit defective stellate cell activation and abnormal liver regeneration following CCl4 injury
inferredcites →https://doi.org/10.1053/jhep.2003.50044openalex-snapshot
Vascular mediators in the injured liver
inferredcites →https://doi.org/10.1053/jhep.2003.50068openalex-snapshot
Proangiogenic Role of Tumor–Activated Hepatic Stellate Cells in Experimental Melanoma Metastasis
inferredcites →https://doi.org/10.1053/jhep.2003.50097openalex-snapshot
Replicative Senescence of Activated Human Hepatic Stellate Cells Is Accompanied by A Pronounced Inflammatory But Less Fibrogenic Phenotype
inferredcites →https://doi.org/10.1053/jhep.2003.50176openalex-snapshot
The Normal Liver Harbors the Vitamin D Nuclear Receptor in Nonparenchymal and Biliary Epithelial Cells
inferredcites →https://doi.org/10.1053/jhep.2003.50182openalex-snapshot
Toll–Like Receptor 4 Mediates Inflammatory Signaling by Bacterial Lipopolysaccharide in Human Hepatic Stellate Cells
inferredcites →https://doi.org/10.1053/jhep.2003.50472openalex-snapshot
Kupffer Cell Engulfment of Apoptotic Bodies Stimulates Death Ligand and Cytokine Expression
inferredcites →https://doi.org/10.1055/s-2001-17550openalex-snapshot
History, Heterogeneity, Developmental Biology, and Functions of Quiescent Hepatic Stellate Cells
inferredcites →https://doi.org/10.1055/s-2001-17551openalex-snapshot
Hepatic Blood Flow Regulation by Stellate Cells in Normal and Injured Liver
inferredcites →https://doi.org/10.1055/s-2001-17557openalex-snapshot
Hepatic Stellate Cell Behavior during Resolution of Liver Injury
showing the first 200 of 327 · page through all 327
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Wuling Capsule Modulates Macrophage Polarization by Inhibiting the TLR4-NF-κB Signaling Pathway to Relieve Liver Fibrosis
inferred← citeshttps://doi.org/10.5281/zenodo.4744452openalex-extracted
LIVER FIBROSIS AND METHODS OF ASSESSMENT IN LIGHT OF CHRONIC HEPATITIS DELTA
inferred← citeshttps://doi.org/10.1002/1873-3468.12309openalex-snapshot
miR‐1273g‐3p modulates activation and apoptosis of hepatic stellate cells by directly targeting PTEN in HCV ‐related liver fibrosis
inferred← citeshttps://doi.org/10.1002/1873-3468.12448openalex-snapshot
Integrins and heparan sulfate proteoglycans on hepatic stellate cells (HSC) are novel receptors for HSC‐derived exosomes
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Synergistic MicroRNA Therapy in Liver Fibrotic Rat Using MRI‐Visible Nanocarrier Targeting Hepatic Stellate Cells
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Bisphenol A enhances apoptosis, fibrosis, and biochemical fluctuations in the liver of adult male rats with possible regression after recovery
inferred← citeshttps://doi.org/10.1002/cbf.3564openalex-snapshot
Retracted: Tormentic acid inhibits hepatic stellate cells activation via blocking PI3K /Akt/ mTOR and NF‐κB signalling pathways
inferred← citeshttps://doi.org/10.1002/cbin.10790openalex-snapshot
Molecular interplays in hepatic stellate cells: apoptosis, senescence, and phenotype reversion as cellular connections that modulate liver fibrosis
inferred← citeshttps://doi.org/10.1002/cphy.c140078openalex-snapshot
Liver Sinusoidal Endothelial Cells
inferred← citeshttps://doi.org/10.1002/edm2.105openalex-snapshot
Drug discovery and treatment paradigms in nonalcoholic steatohepatitis
inferred← citeshttps://doi.org/10.1002/fsn3.1046openalex-snapshot
Apoptotic effects of hsian‐tsao (Mesona procumbens Hemsley) on hepatic stellate cells mediated by reactive oxygen species and ERK, JNK, and caspase‐3 pathways
inferred← citeshttps://doi.org/10.1002/fsn3.1810openalex-snapshot
Malvidin induces hepatic stellate cell apoptosis via the endoplasmic reticulum stress pathway and mitochondrial pathway
inferred← citeshttps://doi.org/10.1002/hep.28130openalex-snapshot
Hepatic stellate cells regulate liver immunity to visceral leishmaniasis through P110δ‐dependent induction and expansion of regulatory T cells in mice
inferred← citeshttps://doi.org/10.1002/hep.28681openalex-snapshot
Five‐year histological and serological follow‐up of operationally tolerant pediatric liver transplant recipients enrolled in WISP‐R
inferred← citeshttps://doi.org/10.1002/hep.29523openalex-snapshot
NLRP3 inflammasome driven liver injury and fibrosis: Roles of IL‐17 and TNF in mice
inferred← citeshttps://doi.org/10.1002/hep.29627openalex-snapshot
MicroRNA‐21 and Dicer are dispensable for hepatic stellate cell activation and the development of liver fibrosis
inferred← citeshttps://doi.org/10.1002/hep.30799openalex-snapshot
High Risk of Fatty Liver Disease Amplifies the Alanine Transaminase–Lowering Effect of a HSD17B13 Variant
inferred← citeshttps://doi.org/10.1002/hep.32320openalex-snapshot
NOD‐like receptor protein 3 activation causes spontaneous inflammation and fibrosis that mimics human NASH
inferred← citeshttps://doi.org/10.1002/hep4.1290openalex-snapshot
Combatting Fibrosis: Exosome‐Based Therapies in the Regression of Liver Fibrosis
inferred← citeshttps://doi.org/10.1002/hep4.1298openalex-snapshot
An Inhibitor of Arginine‐Glycine‐Aspartate‐Binding Integrins Reverses Fibrosis in a Mouse Model of Nonalcoholic Steatohepatitis
inferred← citeshttps://doi.org/10.1002/hep4.1628openalex-snapshot
Hepatic Stellate Cell Regulation of Liver Regeneration and Repair
inferred← citeshttps://doi.org/10.1002/iub.1478openalex-snapshot
Dihydroartemisinin prevents liver fibrosis in bile duct ligated rats by inducing hepatic stellate cell apoptosis through modulating the PI 3 K / A kt pathway
inferred← citeshttps://doi.org/10.1002/jcb.28573openalex-snapshot
Human bone marrow‐derived mesenchymal stromal cells in combination with silymarin regulate hepatocyte growth factor expression and genotoxicity in carbon tetrachloride induced hepatotoxicity in Wistar rats
inferred← citeshttps://doi.org/10.1002/jcb.28756openalex-snapshot
Methyl helicterate inhibits hepatic stellate cell activation through downregulating the ERK1/2 signaling pathway
inferred← citeshttps://doi.org/10.1002/jcp.25055openalex-snapshot
Endotoxin‐stimulated Rat Hepatic Stellate Cells Induce Autophagy in Hepatocytes as a Survival Mechanism
inferred← citeshttps://doi.org/10.1002/jcp.29176openalex-snapshot
Autophagy inhibition via Becn1 downregulation improves the mesenchymal stem cells antifibrotic potential in experimental liver fibrosis
inferred← citeshttps://doi.org/10.1002/jcp.29545openalex-snapshot
Quiescent hepatic stellate cells induce toxicity and sensitivity to doxorubicin in cancer cells through a caspase‐independent cell death pathway: Central role of apoptosis‐inducing factor
inferred← citeshttps://doi.org/10.1002/lipd.12157openalex-snapshot
Comparison of Carotenoids for Their Antifibrogenic Effects in Hepatic Stellate Cells
inferred← citeshttps://doi.org/10.1002/mabi.201700064openalex-snapshot
Uptake of Retinoic Acid‐Modified PMMA Nanoparticles in LX‐2 and Liver Tissue by Raman Imaging and Intravital Microscopy
inferred← citeshttps://doi.org/10.1002/ptr.7001openalex-snapshot
Role of ellagic acid for the prevention and treatment of liver diseases
inferred← citeshttps://doi.org/10.1002/slct.202500446openalex-snapshot
Nanoparticle: Pathogenesis, Innovative Diagnosis, and Therapy of Liver Fibrosis
inferred← citeshttps://doi.org/10.1002/stem.3038openalex-snapshot
c-Met Signaling Is Essential for Mouse Adult Liver Progenitor Cells Expansion After Transforming Growth Factor-β-Induced Epithelial–Mesenchymal Transition and Regulates Cell Phenotypic Switch
inferred← citeshttps://doi.org/10.1007/978-1-0716-3207-9_2openalex-snapshot
Differentiation of Hepatic Stellate Cells from Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1007/978-1-0716-3207-9_7openalex-snapshot
Isolation of Hepatic Stellate Cells and Lymphocytes for Co-culture Systems
inferred← citeshttps://doi.org/10.1007/978-1-4614-9005-0_2openalex-snapshot
Normal Functional Biology of the Liver
inferred← citeshttps://doi.org/10.1007/978-3-030-34521-1_27openalex-snapshot
Impact of Heparanse on Organ Fibrosis
inferred← citeshttps://doi.org/10.1007/978-3-030-44518-8_6openalex-snapshot
Stellate Cells in the Tumor Microenvironment
inferred← citeshttps://doi.org/10.1007/978-3-030-68844-8_4openalex-snapshot
Non-coding RNAs Related to Lipid Metabolism and Non-alcoholic Fatty Liver Disease
inferred← citeshttps://doi.org/10.1007/978-3-032-10997-2_1openalex-snapshot
Mechanisms of Liver Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-20538-0_3openalex-snapshot
Pathogenesis of Alcoholic Liver Disease
inferred← citeshttps://doi.org/10.1007/978-3-319-95828-6_6openalex-snapshot
Mechanisms of Fibrogenesis in NASH
inferred← citeshttps://doi.org/10.1007/978-3-319-98143-7_3openalex-snapshot
Macrophage Plasticity in Skin Fibrosis
inferred← citeshttps://doi.org/10.1007/978-981-15-0391-7_2openalex-snapshot
Nanomedicine for Hepatic Fibrosis
inferred← citeshttps://doi.org/10.1007/978-981-19-0063-1_14openalex-snapshot
Magnetic Resonance Elastography (MRE) to Assess Hepatic Fibrosis
inferred← citeshttps://doi.org/10.1007/s00011-013-0698-9openalex-snapshot
The significance of YKL-40 protein in liver fibrosis
inferred← citeshttps://doi.org/10.1007/s00018-016-2161-xopenalex-snapshot
Pathogenesis of nonalcoholic steatohepatitis
inferred← citeshttps://doi.org/10.1007/s00018-020-03457-3openalex-snapshot
Founder cells for hepatocytes during liver regeneration: from identification to application
inferred← citeshttps://doi.org/10.1007/s00044-024-03267-3openalex-snapshot
Targeting cAMP signaling and phosphodiesterase 4 for liver disease treatment
inferred← citeshttps://doi.org/10.1007/s00204-015-1639-xopenalex-snapshot
Highlight report: overview of hepatoprotective compounds
inferred← citeshttps://doi.org/10.1007/s00204-025-04075-3openalex-snapshot
Hepatic stellate cell inhibition by angiotensin II receptor blocker mitigates liver injury and fibrosis via NF-κB-galectin-3 suppression in a rat nonalcoholic steatohepatitis model
inferred← citeshttps://doi.org/10.1007/s00210-016-1210-1openalex-snapshot
Gingerol protects against experimental liver fibrosis in rats via suppression of pro-inflammatory and profibrogenic mediators
inferred← citeshttps://doi.org/10.1007/s00210-018-1540-2openalex-snapshot
Glibenclamide protects against thioacetamide-induced hepatic damage in Wistar rat: investigation on NLRP3, MMP-2, and stellate cell activation
inferred← citeshttps://doi.org/10.1007/s00210-018-1577-2openalex-snapshot
2-Methoxyestradiol attenuates liver fibrosis in mice: implications for M2 macrophages
inferred← citeshttps://doi.org/10.1007/s00210-024-03666-8openalex-snapshot
Allopurinol abates hepatocellular carcinoma in rats via modulation of NLRP3 inflammasome and NF-κB pathway
inferred← citeshttps://doi.org/10.1007/s00210-025-04143-6openalex-snapshot
Pentadecanoic acid attenuates thioacetamide-induced liver fibrosis by modulating oxidative stress, inflammation, and ferroptosis pathways in rat
inferred← citeshttps://doi.org/10.1007/s00249-016-1176-4openalex-snapshot
Role of TRPC1 channels in pressure-mediated activation of murine pancreatic stellate cells
inferred← citeshttps://doi.org/10.1007/s00383-023-05593-wopenalex-snapshot
Potential mechanisms underlying the effect of hepatocyte growth factor on liver injury in short bowel syndrome model rats
inferred← citeshttps://doi.org/10.1007/s00394-024-03504-wopenalex-snapshot
EGCG suppressed activation of hepatic stellate cells by regulating the PLCE1/IP3/Ca2+ pathway
inferred← citeshttps://doi.org/10.1007/s00418-017-1581-5openalex-snapshot
Identification of markers for quiescent pancreatic stellate cells in the normal human pancreas
inferred← citeshttps://doi.org/10.1007/s00418-022-02123-yopenalex-snapshot
Characterization of focal adhesion proteins in rodent hepatic stellate cells
inferred← citeshttps://doi.org/10.1007/s00441-023-03835-wopenalex-snapshot
Long non-coding RNA HOX transcript antisense intergenic RNA depletion protects against alcoholic hepatitis through the microRNA-148a-3p/sphingosine 1-phosphate receptor 1 axis
inferred← citeshttps://doi.org/10.1007/s10517-016-3526-8openalex-snapshot
Effects of Melatonin on Differentiation Potential of Ito Cells in Mice with Induced Fibrosis of the Liver
inferred← citeshttps://doi.org/10.1007/s10534-021-00328-7openalex-snapshot
‘Magnesium’-the master cation-as a drug—possibilities and evidences
inferred← citeshttps://doi.org/10.1007/s10565-024-09956-4openalex-snapshot
Investigating the role of Wnt3a and Wnt5a as critical factors of hepatic stellate cell activation in acute toxicant-induced liver injury
inferred← citeshttps://doi.org/10.1007/s10620-020-06174-wopenalex-snapshot
MicroRNA-489-3p Represses Hepatic Stellate Cells Activation by Negatively Regulating the JAG1/Notch3 Signaling Pathway
inferred← citeshttps://doi.org/10.1007/s10620-020-06460-7openalex-snapshot
MicroRNA-503 Targets Mothers Against Decapentaplegic Homolog 7 Enhancing Hepatic Stellate Cell Activation and Hepatic Fibrosis
inferred← citeshttps://doi.org/10.1007/s10753-025-02304-6openalex-snapshot
CLICs Inhibitor IAA94 Alleviates Inflammation and Injury in Septic Liver by Preventing Pyroptosis in Macrophages
inferred← citeshttps://doi.org/10.1007/s10787-025-01759-1openalex-snapshot
Tetramethylpyrazine alleviates hepatic fibrosis induced by experimental mansonic schistosomiasis
inferred← citeshttps://doi.org/10.1007/s11010-020-03933-1openalex-snapshot
Resveratrol increases the activation markers and changes the release of inflammatory cytokines of hepatic stellate cells
inferred← citeshttps://doi.org/10.1007/s11010-022-04369-5openalex-snapshot
TGF-β activates NLRP3 inflammasome by an autocrine production of TGF-β in LX-2 human hepatic stellate cells
inferred← citeshttps://doi.org/10.1007/s11033-024-09307-wopenalex-snapshot
Search progress of pyruvate kinase M2 (PKM2) in organ fibrosis
inferred← citeshttps://doi.org/10.1007/s11302-014-9425-4openalex-snapshot
Expression of mediators of purinergic signaling in human liver cell lines
inferred← citeshttps://doi.org/10.1007/s11418-020-01394-wopenalex-snapshot
The effects of inhibiting the activation of hepatic stellate cells by lignan components from the fruits of Schisandra chinensis and the mechanism of schisanhenol
inferred← citeshttps://doi.org/10.1007/s11596-019-2104-5openalex-snapshot
Curcumin Recovers Intracellular Lipid Droplet Formation Through Increasing Perilipin 5 Gene Expression in Activated Hepatic Stellate Cells In Vitro
inferred← citeshttps://doi.org/10.1007/s11655-015-2430-9openalex-snapshot
Protective Effect of Ganshuang Granules (肝爽颗粒) on Liver Cirrhosis by Suppressing Regulatory T Cells in Mouse Model
inferred← citeshttps://doi.org/10.1007/s11686-025-01024-zopenalex-snapshot
The Effects of Extracellular Vesicles Derived from Hydatid Cyst Fluid on the Expression of microRNAs Involved in Liver Fibrosis
inferred← citeshttps://doi.org/10.1007/s11901-018-0406-xopenalex-snapshot
The Role of Anticoagulation in Treating Portal Hypertension
inferred← citeshttps://doi.org/10.1007/s12072-016-9758-xopenalex-snapshot
Hepatic stellate cells: fibrogenic, regenerative or both? Heterogeneity and context are key
inferred← citeshttps://doi.org/10.1007/s13105-015-0452-6openalex-snapshot
Inhibition of IRF3 expression reduces TGF-β1-induced proliferation of hepatic stellate cells
inferred← citeshttps://doi.org/10.1007/s13273-016-0031-0openalex-snapshot
Amygdalin inhibits HSC-T6 cell proliferation and fibrosis through the regulation of TGF-β/CTGF
inferred← citeshttps://doi.org/10.1007/s13273-021-00196-9openalex-snapshot
Jageum-Jung, the herbal pharmaceuticals, inhibits the hepatic fibrogenesis as mediated with TGF-β1/smad signaling
inferred← citeshttps://doi.org/10.1007/s13273-025-00521-6openalex-snapshot
Overview of the hazardous impacts of metabolism-disrupting chemicals on the progression of fatty liver diseases
inferred← citeshttps://doi.org/10.1007/s13577-022-00844-9openalex-snapshot
Induction of premature senescence and a less-fibrogenic phenotype by programmed cell death 4 knockdown in the human hepatic stellate cell line Lieming Xu-2
inferred← citeshttps://doi.org/10.1007/s13577-023-01017-yopenalex-snapshot
The miR-3074/BMP7 axis regulates TGF-β-caused activation of hepatic stellate cells in vitro and CCl4-caused murine liver fibrosis in vivo
inferred← citeshttps://doi.org/10.1007/s15010-018-1136-2openalex-snapshot
Serum YKL-40 as a biomarker for liver fibrosis in chronic hepatitis B patients with normal and mildly elevated ALT
inferred← citeshttps://doi.org/10.1007/s40124-014-0047-7openalex-snapshot
NASH and the Cross-Talk Between the Gut and Liver
inferred← citeshttps://doi.org/10.1007/s43152-021-00030-3openalex-snapshot
Extracellular Matrix Remodeling in Chronic Liver Disease
inferred← citeshttps://doi.org/10.1007/s43450-022-00252-yopenalex-snapshot
Therapeutic Potential of Plantamajoside
inferred← citeshttps://doi.org/10.1016/b978-0-12-420128-6.00010-5openalex-snapshot
Role of Developmental Morphogens in Liver Regeneration
inferred← citeshttps://doi.org/10.1016/b978-0-12-800134-9.00004-xopenalex-snapshot
Stellate Cells and Hepatic Fibrosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-800134-9.00005-1openalex-snapshot
Cytokine Production and Signaling in Stellate Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.65377-1openalex-snapshot
Hepatic Sinusoidal Cells and Liver-Associated Lymphocytes
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.95666-6openalex-snapshot
Ethanol-Induced Hepatotoxicity
inferred← citeshttps://doi.org/10.1016/b978-0-12-802389-1.00020-4openalex-snapshot
Chromatin Remodeling and Epigenetic Reprogramming in Chronic Disease and Cancer in the Liver and Pancreas
inferred← citeshttps://doi.org/10.1016/b978-0-12-803951-9.00026-4openalex-snapshot
Gallic Acid as a Putative Antioxidant in Usage Against Liver Disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-37591-7.00001-xopenalex-snapshot
Anatomy and Cellular Functions of the Liver
inferred← citeshttps://doi.org/10.1016/b978-0-323-37591-7.00005-7openalex-snapshot
The Liver's Response to Injury
inferred← citeshttps://doi.org/10.1016/b978-0-323-42873-6.00040-8openalex-snapshot
Regression of Liver Fibrosis
inferred← citeshttps://doi.org/10.1016/b978-0-323-95262-0.00001-2openalex-snapshot
The unique architecture of the hepatic sinusoid
inferred← citeshttps://doi.org/10.1016/b978-0-323-95262-0.00016-4openalex-snapshot
The liver sinusoid in acute-on-chronic liver failure
inferred← citeshttps://doi.org/10.1016/b978-0-443-15717-2.00124-4openalex-snapshot
Mesenchymal Stromal/Stem Cells and Their Interaction With Immune Cells
inferred← citeshttps://doi.org/10.1016/b978-0-443-26710-9.00001-8openalex-snapshot
Anatomy and histopathology of the liver
inferred← citeshttps://doi.org/10.1016/b978-0-444-63625-6.00005-7openalex-snapshot
Pathogenesis of Wilson disease
inferred← citeshttps://doi.org/10.1016/b978-0-7020-6697-9.00001-7openalex-snapshot
Structure, Function, and Responses to Injury
inferred← citeshttps://doi.org/10.1016/b978-0-7020-8228-3.00001-6openalex-snapshot
Structure, Function and Responses to Injury
inferred← citeshttps://doi.org/10.1016/b978-0-7020-8228-3.00006-5openalex-snapshot
Hepatitis Due to Hepatotropic Viruses
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2019.08.001openalex-snapshot
Liver DCs in health and disease
inferred← citeshttps://doi.org/10.1016/j.ab.2022.114842openalex-snapshot
A novel, simple and reliable method for the determination of hydronidone and its metabolites M3 and M4 in human plasma and urine by HPLC-MS/MS and its application to a pharmacokinetic study in health Chinese subjects
inferred← citeshttps://doi.org/10.1016/j.actbio.2022.08.065openalex-snapshot
Collagenase-I decorated co-delivery micelles potentiate extracellular matrix degradation and hepatic stellate cell targeting for liver fibrosis therapy
inferred← citeshttps://doi.org/10.1016/j.ajpath.2016.07.011openalex-snapshot
Fibrogenic Signaling Is Suppressed in Hepatic Stellate Cells through Targeting of Connective Tissue Growth Factor (CCN2) by Cellular or Exosomal MicroRNA-199a-5p
inferred← citeshttps://doi.org/10.1016/j.ajpath.2017.01.013openalex-snapshot
Transforming Growth Factors α and β Are Essential for Modeling Cholangiocarcinoma Desmoplasia and Progression in a Three-Dimensional Organotypic Culture Model
inferred← citeshttps://doi.org/10.1016/j.ajpath.2020.05.017openalex-snapshot
Perivascular Fibro-Adipogenic Progenitor Tracing during Post-Traumatic Osteoarthritis
inferred← citeshttps://doi.org/10.1016/j.ajpath.2020.08.002openalex-snapshot
Pyruvate Kinase M2 Tetramerization Protects against Hepatic Stellate Cell Activation and Liver Fibrosis
inferred← citeshttps://doi.org/10.1016/j.ajpath.2021.08.004openalex-snapshot
Inhibition of Hepatic Stellate Cell Activation Suppresses Tumorigenicity of Hepatocellular Carcinoma in Mice
inferred← citeshttps://doi.org/10.1016/j.ajpath.2024.07.009openalex-snapshot
Cancer-Associated Fibroblasts in Intrahepatic Cholangiocarcinoma
inferred← citeshttps://doi.org/10.1016/j.amjms.2023.04.024openalex-snapshot
Role of ferroptosis in fibrosis diseases
inferred← citeshttps://doi.org/10.1016/j.amjms.2023.08.016openalex-snapshot
Knockdown of TXNDC5 alleviates CCL4-induced hepatic fibrosis in mice by enhancing endoplasmic reticulum stress
inferred← citeshttps://doi.org/10.1016/j.bbadis.2015.05.015openalex-snapshot
Recent insights on the role of cholesterol in non-alcoholic fatty liver disease
inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.07.019openalex-snapshot
Lipid droplet proteins and metabolic diseases
inferred← citeshttps://doi.org/10.1016/j.bbagen.2020.129559openalex-snapshot
Liver-derived extracellular vesicles: A cell by cell overview to isolation and characterization practices
inferred← citeshttps://doi.org/10.1016/j.bbalip.2018.10.008openalex-snapshot
Of mice and men: The physiological role of adipose triglyceride lipase (ATGL)
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2014.11.029openalex-snapshot
Dipeptidyl peptidase 9 subcellular localization and a role in cell adhesion involving focal adhesion kinase and paxillin
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.11.029openalex-snapshot
Effect of acid-sensing ion channel 1a on the process of liver fibrosis under hyperglycemia
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.11.010openalex-snapshot
Dimethyl α-ketoglutarate reduces CCl4-induced liver fibrosis through inhibition of autophagy in hepatic stellate cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.01.148openalex-snapshot
Positive feedback loop of YB-1 interacting with Smad2 promotes liver fibrosis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.09.156openalex-snapshot
Thymosin β4 attenuates liver fibrosis via suppressing Notch signaling
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.10.110openalex-snapshot
Dihydroceramide is a key metabolite that regulates autophagy and promotes fibrosis in hepatic steatosis model
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.12.143openalex-snapshot
Metformin ameliorates activation of hepatic stellate cells and hepatic fibrosis by succinate and GPR91 inhibition
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.03.156openalex-snapshot
A novel STAT3 inhibitor, STX-0119, attenuates liver fibrosis by inactivating hepatic stellate cells in mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.12.039openalex-snapshot
Diethyldithiocarbamate inhibits the activation of hepatic stellate cells via PPARα/FABP1 in mice with non-alcoholic steatohepatitis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.149958openalex-snapshot
PFKFB3-mediated glycolysis in hepatic stellate cells promotes liver regeneration
inferred← citeshttps://doi.org/10.1016/j.bbrep.2016.09.010openalex-snapshot
Quantitative imaging of fibrotic and morphological changes in liver of non-alcoholic steatohepatitis (NASH) model mice by second harmonic generation (SHG) and auto-fluorescence (AF) imaging using two-photon excitation microscopy (TPEM)
inferred← citeshttps://doi.org/10.1016/j.bbrep.2019.100678openalex-snapshot
Antifibrotic effect of methylated quercetin derivatives on TGFβ-induced hepatic stellate cells
inferred← citeshttps://doi.org/10.1016/j.bcp.2025.116884openalex-snapshot
Macrophage-derived CCL1 targets CCR8 receptor in hepatic stellate cells to promote liver fibrosis through JAk/STAT pathway
inferred← citeshttps://doi.org/10.1016/j.biocel.2015.09.003openalex-snapshot
Mesenchymal stem cells: In vivo therapeutic application ameliorates carbon tetrachloride induced liver fibrosis in rats
inferred← citeshttps://doi.org/10.1016/j.biocel.2015.12.005openalex-snapshot
Myocardin-related transcription factor A (MRTF-A) plays an essential role in hepatic stellate cell activation by epigenetically modulating TGF-β signaling
inferred← citeshttps://doi.org/10.1016/j.biocel.2022.106170openalex-snapshot
Rab31 promotes activation of hepatic stellate cells by accelerating TGF-β receptor II complex endocytosis
inferred← citeshttps://doi.org/10.1016/j.biochi.2015.06.016openalex-snapshot
Epigenetic modifications by histone deacetylases: Biological implications and therapeutic potential in liver fibrosis
inferred← citeshttps://doi.org/10.1016/j.biochi.2020.12.022openalex-snapshot
Transcriptional regulation of alcohol induced liver fibrosis in a translational porcine hepatocellular carcinoma model
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2017.05.047openalex-snapshot
Functionality based method for simultaneous isolation of rodent hepatic sinusoidal cells
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.120538openalex-snapshot
Localized inhibition of platelets and platelet derived growth factor by a matrix targeted glycan mimetic significantly attenuates liver fibrosis
inferred← citeshttps://doi.org/10.1016/j.biopha.2018.06.134openalex-snapshot
Protective effects of Kangxian ruangan capsule against nonalcoholic fatty liver disease fibrosis in rats induced by MCD diet
inferred← citeshttps://doi.org/10.1016/j.biopha.2018.10.005openalex-snapshot
Carvedilol attenuates liver fibrosis by suppressing autophagy and promoting apoptosis in hepatic stellate cells
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.109932openalex-snapshot
Total phenolic extract of Euscaphis konishii hayata Pericarp attenuates carbon tetrachloride (CCl4)-induced liver fibrosis in mice
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110586openalex-snapshot
Polydatin attenuates hepatic stellate cell proliferation and liver fibrosis by suppressing sphingosine kinase 1
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110683openalex-snapshot
Protective effect of picroside I against hepatic fibrosis in mice via sphingolipid metabolism, bile acid biosynthesis, and PPAR signaling pathway
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112281openalex-snapshot
JQ-1 ameliorates schistosomiasis liver fibrosis by suppressing JAK2 and STAT3 activation
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116490openalex-snapshot
Lactoferrin as a therapeutic agent for attenuating hepatic stellate cell activation in thioacetamide-induced liver fibrosis
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117206openalex-snapshot
Interference with mitochondrial function as part of the antifibrogenic effect of Rilpivirine: A step towards novel targets in hepatic stellate cell activation
inferred← citeshttps://doi.org/10.1016/j.cbd.2022.101007openalex-snapshot
Proteomic analysis of hepatic fibrosis induced by a high starch diet in largemouth bass (Micropterus salmoides)
inferred← citeshttps://doi.org/10.1016/j.cbi.2018.08.016openalex-snapshot
Antioxidant and anti-inflammatory activities of berberine attenuate hepatic fibrosis induced by thioacetamide injection in rats
inferred← citeshttps://doi.org/10.1016/j.cbi.2018.10.015openalex-snapshot
Long-term diosbulbin B treatment induced liver fibrosis in mice
inferred← citeshttps://doi.org/10.1016/j.cbi.2019.01.019openalex-snapshot
Taurine protected As2O3-induced the activation of hepatic stellate cells through inhibiting PPARα-autophagy pathway
inferred← citeshttps://doi.org/10.1016/j.cell.2020.09.012openalex-snapshot
Single-Cell Transcriptomics Reveals Early Emergence of Liver Parenchymal and Non-Parenchymal Cell Lineages
inferred← citeshttps://doi.org/10.1016/j.cellsig.2022.110437openalex-snapshot
Arg-Gly-Asp-binding integrins activate hepatic stellate cells via the hippo signaling pathway
inferred← citeshttps://doi.org/10.1016/j.cellsig.2024.111302openalex-snapshot
m6A epitranscriptomic and epigenetic crosstalk in liver fibrosis: Special emphasis on DNA methylation and non-coding RNAs
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2023.139998openalex-snapshot
Adverse outcome pathway exploration of furan-induced liver fibrosis in rats: Genotoxicity pathway or oxidative stress pathway through CYP2E1 activation?
inferred← citeshttps://doi.org/10.1016/j.cmet.2016.09.016openalex-snapshot
Hepatocyte TAZ/WWTR1 Promotes Inflammation and Fibrosis in Nonalcoholic Steatohepatitis
inferred← citeshttps://doi.org/10.1016/j.cmet.2019.11.013openalex-snapshot
Macrophage MerTK Promotes Liver Fibrosis in Nonalcoholic Steatohepatitis
inferred← citeshttps://doi.org/10.1016/j.cmet.2020.03.010openalex-snapshot
Cholesterol Stabilizes TAZ in Hepatocytes to Promote Experimental Non-alcoholic Steatohepatitis
inferred← citeshttps://doi.org/10.1016/j.cyto.2018.09.004openalex-snapshot
Role of hepatic stellate cell (HSC)-derived cytokines in hepatic inflammation and immunity
inferred← citeshttps://doi.org/10.1016/j.cyto.2024.156587openalex-snapshot
Dual blockade of interleukin-17A and interleukin-17F as a therapeutic strategy for liver fibrosis: Investigating the potential effect and mechanism of brodalumab
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117250openalex-snapshot
Design, synthesis, and anti-liver fibrosis activity of novel non-steroidal vitamin D receptor agonists based on open-ring steroid scaffold
inferred← citeshttps://doi.org/10.1016/j.ejpb.2021.05.027openalex-snapshot
General sites of nanoparticle biodistribution as a novel opportunity for nanomedicine
inferred← citeshttps://doi.org/10.1016/j.ejphar.2020.173224openalex-snapshot
Role of linagliptin in preventing the pathological progression of hepatic fibrosis in high fat diet and streptozotocin-induced diabetic obese rats
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.173982openalex-snapshot
Carvacrol alleviates liver fibrosis by inhibiting TRPM7 and modulating the MAPK signaling pathway
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174604openalex-snapshot
Preventive and therapeutic role of betaine in liver disease: A review on molecular mechanisms
inferred← citeshttps://doi.org/10.1016/j.etap.2022.103928openalex-snapshot
Multiomics analysis of the impact of polychlorinated biphenyls on environmental liver disease in a mouse model
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.11.014openalex-snapshot
Nicotinamide mononucleotide inhibits hepatic stellate cell activation to prevent liver fibrosis via promoting PGE2 degradation
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.12.449openalex-snapshot
Role of necroptosis in chronic hepatic inflammation and fibrosis in a mouse model of increased oxidative stress
inferred← citeshttps://doi.org/10.1016/j.gene.2018.11.063openalex-snapshot
Insight into long noncoding competing endogenous RNA networks in hepatic fibrosis: The potential implications for mechanism and therapy
inferred← citeshttps://doi.org/10.1016/j.gene.2020.145284openalex-snapshot
Exploring the transcriptomic network of multi-ligand scavenger receptor Stabilin-1- and Stabilin-2-deficient liver sinusoidal endothelial cells
inferred← citeshttps://doi.org/10.1016/j.hbpd.2018.09.013openalex-snapshot
Histone deacetylase inhibitor suberoylanilide hydroxamic acid alleviates liver fibrosis by suppressing the transforming growth factor-β1 signal pathway
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e39892openalex-snapshot
Magnoflorine ameliorates hepatic fibrosis and hepatic stellate cell activation by regulating ferroptosis signaling pathway
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125540openalex-snapshot
A novel branched galacturonan from Gardenia jasminoides alleviates liver fibrosis linked to TLR4/NF-κB signaling
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125811openalex-snapshot
N6-methyladenosine-modified circIRF2, identified by YTHDF2, suppresses liver fibrosis via facilitating FOXO3 nuclear translocation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125906openalex-snapshot
Mesoporous polydopamine based biominetic nanodrug ameliorates liver fibrosis via antioxidation and TGF-β/SMADS pathway
inferred← citeshttps://doi.org/10.1016/j.intimp.2016.07.028openalex-snapshot
High-fat diet plus carbon tetrachloride-induced liver fibrosis is alleviated by betaine treatment in rats
inferred← citeshttps://doi.org/10.1016/j.intimp.2018.08.005openalex-snapshot
Octreotide attenuates hepatic fibrosis and hepatic stellate cells proliferation and activation by inhibiting Wnt/β-catenin signaling pathway, c-Myc and cyclin D1
inferred← citeshttps://doi.org/10.1016/j.intimp.2019.05.056openalex-snapshot
Wogonin attenuates liver fibrosis via regulating hepatic stellate cell activation and apoptosis
inferred← citeshttps://doi.org/10.1016/j.intimp.2020.107151openalex-snapshot
Amygdalin inhibits TGFβ1-induced activation of hepatic stellate cells (HSCs) in vitro and CCl4-induced hepatic fibrosis in rats in vivo
inferred← citeshttps://doi.org/10.1016/j.intimp.2022.108987openalex-snapshot
Igf2bp2 knockdown improves CCl4-induced liver fibrosis and TGF-β-activated mouse hepatic stellate cells by regulating Tgfbr1
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.109812openalex-snapshot
The emerging roles of ferroptosis in organ fibrosis and its potential therapeutic effect
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110180openalex-snapshot
A polysaccharide from Codonopsis pilosula roots attenuates carbon tetrachloride-induced liver fibrosis via modulation of TLR4/NF-κB and TGF-β1/Smad3 signaling pathway
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.111134openalex-snapshot
Human umbilical cord mesenchymal stem cells inhibit liver fibrosis via the microRNA-148a-5p/SLIT3 axis
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.111136openalex-snapshot
The impact of liver fibrosis on the progression of hepatocellular carcinoma via a hypoxia-immune-integrated prognostic model
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.111598openalex-snapshot
Wuling capsule modulates macrophage polarization by inhibiting the TLR4-NF-κB signaling pathway to relieve liver fibrosis
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112116openalex-snapshot
A comprehensive review of miR-21 in liver disease: Big impact of little things
inferred← citeshttps://doi.org/10.1016/j.isci.2021.103165openalex-snapshot
Extracellular PKM2 facilitates organ-tissue fibrosis progression
inferred← citeshttps://doi.org/10.1016/j.isci.2021.103233openalex-snapshot
Single-cell RNA transcriptome landscape of hepatocytes and non-parenchymal cells in healthy and NAFLD mouse liver
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108077openalex-snapshot
A liver digital twin for in silico testing of cellular and inter-cellular mechanisms in regeneration after drug-induced damage
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2023.06.013openalex-snapshot
Inflammatory liver tissue formation using oxygen permeable membrane based culture platform
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2022.01.015openalex-snapshot
Peroxidasin Deficiency Re-programs Macrophages Toward Pro-fibrolysis Function and Promotes Collagen Resolution in Liver
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2022.10.015openalex-snapshot
GLIS2 Prevents Hepatic Fibrosis by Competitively Binding HDAC3 to Inhibit Hepatic Stellate Cell Activation
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2024.01.002openalex-snapshot
“The Good, the Bad, and the Ugly” – About Diverse Phenotypes of Hepatic Stellate Cells in the Liver
inferred← citeshttps://doi.org/10.1016/j.jconrel.2021.03.016openalex-snapshot
Matrix metalloproteinase-1 decorated polymersomes, a surface-active extracellular matrix therapeutic, potentiates collagen degradation and attenuates early liver fibrosis
inferred← citeshttps://doi.org/10.1016/j.jconrel.2021.11.039openalex-snapshot
Nitric oxide facilitates the targeting Kupffer cells of a nano-antioxidant for the treatment of NASH
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