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Class Vi Intermediate Filament Protein Nestin Is Induced During Activation of Rat Hepatic Stellate Cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Oxford Textbook of Clinical Hepatology
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Gene expression and synthesis of fibronectin isoforms in rat hepatic stellate cells. comparison with liver parenchymal cells and skin fibroblasts
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Immunocytochemical Detection of Desmin in Fat-Storing Cells (Ito Cells)
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Tissue distribution, quantitation and proliferation kinetics of fat-storing cells in carbon tetrachloride-injured rat liver
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Comparison of Glial Fibrillary Acidic Protein and Desmin Staining in Normal and Ccl4–Induced Fibrotic Rat Livers
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Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
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Myogenesis and the Intermediate Filament Protein, Nestin
inferredcites →https://doi.org/10.1006/excr.1994.1281openalex-snapshot
Colocalization of Nestin and Vimentin/Desmin in Skeletal Muscle Cells Demonstrated by Three-Dimensional Fluorescence Digital Imaging Microscopy
inferredcites →https://doi.org/10.1007/bf00194608openalex-snapshot
Immunohistochemical identification of Ito cells and their myofibroblastic transformation in adult human liver
inferredcites →https://doi.org/10.1007/bf02890000openalex-snapshot
Desmin and actin in the identification of Ito cells and in monitoring their evolution to myofibroblasts in experimental liver fibrosis
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/s002580050190openalex-snapshot
The intermediate filament protein nestin occurs transiently in differentiating testis of rat and mouse
inferredcites →https://doi.org/10.1007/s004410050524openalex-snapshot
Expression of neural cell adhesion molecule (N-CAM) in perisinusoidal stellate cells of the human liver
inferredcites →https://doi.org/10.1016/0003-2697(87)90021-2openalex-snapshot
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
inferredcites →https://doi.org/10.1016/0092-8674(90)90662-xopenalex-snapshot
CNS stem cells express a new class of intermediate filament protein
inferredcites →https://doi.org/10.1016/0959-437x(94)90135-popenalex-snapshot
Genetic and epigenetic control in neural crest development
inferredcites →https://doi.org/10.1016/s0092-8674(00)81112-5openalex-snapshot
Alternative Neural Crest Cell Fates Are Instructively Promoted by TGFβ Superfamily Members
inferredcites →https://doi.org/10.1016/s0165-5728(85)80073-4openalex-snapshot
Extra-neural glial fibrillary acidic protein (GFAP) immunoreactivity in perisinusoidal stellate cells of rat liver
inferredcites →https://doi.org/10.1016/s0168-8278(96)80269-8openalex-snapshot
Glial fibrillary acidic protein - a cell type specific marker for Ito cells in vivo and in vitro
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)80245-6openalex-snapshot
Cells of the hepatic sinusoid
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Oxford textbook of clinical hepatology
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
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Book Review Ethical Problems in Dialysis and Transplantation (Developments in Nephrology. Vol. 33.) Edited by Carl M. Kjellstrand and John B. Dossetor. 235 pp., illustrated. Boston, Kluwer Academic, 1992. $108.50. 0-7923-1625-8
inferredcites →https://doi.org/10.1056/nejm199306243282508openalex-snapshot
The Cellular Basis of Hepatic Fibrosis -- Mechanisms and Treatment Strategies
inferredcites →https://doi.org/10.1073/pnas.74.12.5463openalex-snapshot
DNA sequencing with chain-terminating inhibitors
inferredcites →https://doi.org/10.1083/jcb.126.2.445openalex-snapshot
Differential organization of desmin and vimentin in muscle is due to differences in their head domains.
inferredcites →https://doi.org/10.1083/jcb.131.2.453openalex-snapshot
Rapid, widespread, and longlasting induction of nestin contributes to the generation of glial scar tissue after CNS injury.
inferredcites →https://doi.org/10.1097/00001756-199410000-00011openalex-snapshot
Reactive astrocytes express the embryonic intermediate neurofilament nestin
inferredcites →https://doi.org/10.1111/j.1750-3639.1994.tb00838.xopenalex-snapshot
GFAP and Astrogliosis
inferredcites →https://doi.org/10.1161/01.cir.82.2.332openalex-snapshot
Role of neural crest in congenital heart disease.
inferredcites →https://doi.org/10.1177/29.6.7252134openalex-snapshot
Heavy metal intensification of DAB-based HRP reaction product.
inferredcites →https://doi.org/10.1177/43.8.7542682openalex-snapshot
Intermediate filaments in cardiac myogenesis: nestin in the developing mouse heart.
inferredcites →https://doi.org/10.1242/dev.34.1.125openalex-snapshot
Mesenchymal derivatives of the neural crest: analysis of chimaeric quail and chick embryos
inferredcites →https://doi.org/10.1242/jcs.106.4.1291openalex-snapshot
Transient expression of the intermediate filament nestin during skeletal muscle development
inferredcites →https://doi.org/10.1523/jneurosci.05-12-03310.1985openalex-snapshot
Identification of major cell classes in the developing mammalian nervous system
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Role Of Nestin Protein In Prognosis Of Breast Cancer
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Activation of rat hepatic stellate cells leads to loss of glutathion S -transferases and their enzymatic activity against products of oxidative stress
inferred← citeshttps://doi.org/10.1002/jcp.22794openalex-snapshot
Nestin expression is lost in ventricular fibroblasts during postnatal development of the rat heart and re‐expressed in scar myofibroblasts
inferred← citeshttps://doi.org/10.1002/jcp.25496openalex-snapshot
Nestin Expressed by Pre‐Existing Cardiomyocytes Recapitulated in Part an Embryonic Phenotype; Suppressive Role of p38 MAPK
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RETRACTED: Nestin Regulates Autophagy‐Dependent Ferroptosis Mediated Skeletal Muscle Atrophy by Ubiquitinating MAP 1LC3B
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Glial fibrillary acidic protein as an early marker of hepatic stellate cell activation in chronic and posttransplant recurrent hepatitis C
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Identifying activated hepatic stellate cells in chronic and posttransplant recurrent hepatitis C
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Advancements of non‐invasive imaging technologies for the diagnosis and staging of liver fibrosis: Present and future
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Adult Bone Marrow Stromal Cells Differentiate into Neural Cells in Vitro
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Reversibility of Liver Fibrosis
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Hepatic stellate cells and astrocytes: similarities and differences
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Activation of Hepatic Stellate Cells: Anti-Adipogenic Differentiation?
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Heterogeneity of Liver Cancer Stem Cells
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Stellate Cells and the Microcirculation
inferred← citeshttps://doi.org/10.1007/978-1-59259-885-4_2openalex-snapshot
Anatomy and Vascular Biology of the Cells in the Portal Circulation
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Morphology and Properties of Pericytes
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What’s New in Pancreatic Stellate Cell Biology?
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Development of the Neuroendocrine Leydig Cells
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Analysis of Proteins and Genes Dominantly Expressed in Stellate Cells of Activated Phenotype: the Molecular Approach to Liver Fibrosis
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Islet morphogenesis and stem cell markers
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Vimentin in cancer and its potential as a molecular target for cancer therapy
inferred← citeshttps://doi.org/10.1007/s00109-005-0680-2openalex-snapshot
Transcriptome analysis of human hepatic and pancreatic stellate cells: organ-specific variations of a common transcriptional phenotype
inferred← citeshttps://doi.org/10.1007/s00401-006-0031-6openalex-snapshot
Immunohistochemical expression of nestin in the non-tumorous hypophysis and in pituitary neoplasms
inferred← citeshttps://doi.org/10.1007/s00418-002-0412-4openalex-snapshot
Nestin expression in pancreatic stellate cells and angiogenic endothelial cells
inferred← citeshttps://doi.org/10.1007/s00418-002-0436-9openalex-snapshot
Modulation of cytokeratin expression during in vitro cultivation of human hepatic stellate cells: evidence of transdifferentiation from epithelial to mesenchymal phenotype
inferred← citeshttps://doi.org/10.1007/s00418-006-0204-3openalex-snapshot
Zonal hierarchy of differentiation markers and nestin expression during oval cell mediated rat liver regeneration
inferred← citeshttps://doi.org/10.1007/s00418-008-0544-2openalex-snapshot
Vinculin and cellular retinol-binding protein-1 are markers for quiescent and activated hepatic stellate cells in formalin-fixed paraffin embedded human liver
inferred← citeshttps://doi.org/10.1007/s00418-013-1142-5openalex-snapshot
Syncoilin is an intermediate filament protein in activated hepatic stellate cells
inferred← citeshttps://doi.org/10.1007/s00428-002-0631-zopenalex-snapshot
Expression of SPARC by activated hepatic stellate cells and its correlation with the stages of fibrogenesis in human chronic hepatitis
inferred← citeshttps://doi.org/10.1007/s00428-003-0804-4openalex-snapshot
Vinculin: a novel marker for quiescent and activated hepatic stellate cells in human and rat livers
inferred← citeshttps://doi.org/10.1007/s00441-002-0590-3openalex-snapshot
Distribution of the intermediate filament nestin in the muscularis propria of the human gastrointestinal tract
inferred← citeshttps://doi.org/10.1007/s00535-017-1404-4openalex-snapshot
Human hepatic stellate cell isolation and characterization
inferred← citeshttps://doi.org/10.1007/s00701-003-0023-4openalex-snapshot
Intermediate filament nestin expressions in human cord blood monocytes (HCMNCs)
inferred← citeshttps://doi.org/10.1007/s00795-018-0183-1openalex-snapshot
Hepatic stellate cells derived from the nestin-positive cells in septum transversum during rat liver development
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Potential neural progenitor cells in fetal liver and regenerating liver
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Co-localization of nestin and PDX-1 in small evaginations of the main pancreatic duct in adult rats
inferred← citeshttps://doi.org/10.1007/s10735-007-9078-5openalex-snapshot
The diffuse stellate cell system
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Fibrotic Disease: from Signaling Pathways and Biomarkers to Molecular Imaging
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The stellate cell system (vitamin A-storing cell system)
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Myoepithelial Cells: Their Origin and Function in Lacrimal Gland Morphogenesis, Homeostasis, and Repair
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Cirrhosis in the Era of Genomic Medicine
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Genomics in Pathogenesis of Cirrhosis
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Bile Acid Metabolism During Development
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Bile Formation and Cholestasis
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Different Hepatic Cell Populations of the Fibroblast Lineage with Fibrogenic Potential
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Stem Cells Expressing Matrix Metalloproteinase-13 mRNA Appear during Regression Reversal of Hepatic Cirrhosis
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Bile Formation and Cholestasis
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Crucial role of fibrogenesis in pancreatic diseases
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Nestin-positive microglia in adult rat cerebral cortex
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Relationships Among Stellate Cell Activation, Progenitor Cells, and Hepatic Regeneration
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Feline bone marrow-derived mesenchymal stromal cells (MSCs) show similar phenotype and functions with regards to neuronal differentiation as human MSCs
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The blockade of endothelin A receptor protects astrocytes against hypoxic injury: Common effects of BQ-123 and erythropoietin on the rejuvenation of the astrocyte population
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Characterization of glial fibrillary acidic protein (GFAP)-expressing hepatic stellate cells and myofibroblasts in thioacetamide (TAA)-induced rat liver injury
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Immunohistochemical characterization of glial fibrillary acidic protein (GFAP)-expressing cells in a rat liver cirrhosis model induced by repeated injections of thioacetamide (TAA)
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Astrocyte growth effects of vascular endothelial growth factor (VEGF) application to perinatal neocortical explants: receptor mediation and signal transduction pathways
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Synemin expression is widespread in liver fibrosis and is induced in proliferating and malignant biliary epithelial cells
inferred← citeshttps://doi.org/10.1016/j.humpath.2008.02.022openalex-snapshot
Nestin expression correlates with nerve and retroperitoneal tissue invasion in pancreatic cancer
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2004.03.023openalex-snapshot
Stem cells and pancreatic differentiation in vitro
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On the origin of stellate cells: mesodermal, endodermal or neuro-ectodermal?
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Cellular retinol-binding protein-1 expression in normal and fibrotic/cirrhotic human liver: different patterns of expression in hepatic stellate cells and (myo)fibroblast subpopulations
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Generation of a monoclonal human single chain antibody fragment to hepatic stellate cells – a potential mechanism for targeting liver anti-fibrotic therapeutics
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Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cells
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Targeting Nestin+ hepatic stellate cells ameliorates liver fibrosis by facilitating TβRI degradation
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TGF-β1 signaling regulates mouse hepatic stellate cell differentiation via the Jagged1/Notch pathway
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Molecular aspects of medicine: from experimental to clinical hepatology
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The role of retinoic acid receptors in activated hepatic stellate cells
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Nestin expression in pancreatic exocrine cell lineages
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Local sympathetic signal enables the immune evasion of hepatic stellate cells
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A novel Golgi-Cox staining method for detecting and characterizing roles of the hepatic stellate cells in liver injury
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inferred← citeshttps://doi.org/10.1016/j.prp.2005.08.008openalex-snapshot
Neoplasm of hepatic stellate cells (spongiotic pericytoma): A new tumor entity in human liver
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Human hepatic stellate cell line (LX-2) exhibits characteristics of bone marrow-derived mesenchymal stem cells
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Pleiotrophin/Heparin-Binding Growth-Associated Molecule as a Mitogen of Rat Hepatocytes and Its Role in Regeneration and Development of Liver
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Hepatic Stellate Cells Express the Low Affinity Nerve Growth Factor Receptor p75 and Undergo Apoptosis in Response to Nerve Growth Factor Stimulation
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Synaptophysin: A Novel Marker for Human and Rat Hepatic Stellate Cells
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Acetylcholine promotes the proliferation and collagen gene expression of myofibroblastic hepatic stellate cells
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Increased expression of O-acetyl disialoganglioside synthase during rat liver fibrogenesis relates to stellate cell activation
inferred← citeshttps://doi.org/10.1016/s0016-5085(99)70413-0openalex-snapshot
The virtuosity of hepatic stellate cells
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Functional complexity of intermediate filament cytoskeletons: From structure to assembly to gene ablation
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Differentiation of Mouse Embryonic Stem Cells into Pancreatic and Hepatic Cells
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Alpha B-crystallin expression in human and rat hepatic stellate cells
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Hepatic stellate cell/myofibroblast subpopulations in fibrotic human and rat livers
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The origin of hepatic myofibroblastsMak KM, Leo MA, Lieber CS. Alcoholic liver injury in baboons: transformation of lipocytes to transitional cells [Gastroenterology 1984;87:188–200]
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Actin filament formation, reorganization and migration are impaired in hepatic stellate cells under influence of trichostatin A, a histone deacetylase inhibitor
inferred← citeshttps://doi.org/10.1016/s0168-8278(98)80269-9openalex-snapshot
Molecular regulation of hepatic fibrogenesis
inferred← citeshttps://doi.org/10.1016/s0271-5317(02)00542-0openalex-snapshot
Effects of high dose retinoic acid on adult rat liver: electron microscopic and immunohistochemical study
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On the track of a human circulating mesenchymal stem cell of neural crest origin
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Mécanismes de la fibrogénèse hépatique
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Intermediate-filament expression in ocular tissue
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Plasticity of adult bone marrow stem cells
inferred← citeshttps://doi.org/10.1021/acsnano.3c06107openalex-snapshot
Antioxidative Hyaluronic Acid–Bilirubin Nanomedicine Targeting Activated Hepatic Stellate Cells for Anti-Hepatic-Fibrosis Therapy
inferred← citeshttps://doi.org/10.1021/cbmi.5c00055openalex-snapshot
Molecular Imaging Probes for Early Detection and Staging of Liver Fibrosis
inferred← citeshttps://doi.org/10.1034/j.1600-0676.2002.01503.xopenalex-snapshot
Intrahepatic expression of the hepatic stellate cell marker fibroblast activation protein correlates with the degree of fibrosis in hepatitis C virus infection
inferred← citeshttps://doi.org/10.1038/emm.2001.31openalex-snapshot
Chronic liver injury, TGF-β, and cancer
inferred← citeshttps://doi.org/10.1038/labinvest.2010.88openalex-snapshot
Hepatic stellate cells’ involvement in progenitor-mediated liver regeneration
inferred← citeshttps://doi.org/10.1038/labinvest.3700349openalex-snapshot
Role for Hedgehog signaling in hepatic stellate cell activation and viability
inferred← citeshttps://doi.org/10.1038/labinvest.3700537openalex-snapshot
Hedgehog-mediated mesenchymal–epithelial interactions modulate hepatic response to bile duct ligation
inferred← citeshttps://doi.org/10.1038/s41388-019-0705-xopenalex-snapshot
Src and SHP2 coordinately regulate the dynamics and organization of vimentin filaments during cell migration
inferred← citeshttps://doi.org/10.1038/s41598-024-53089-xopenalex-snapshot
Knockdown of Hyaluronan synthase 2 suppresses liver fibrosis in mice via induction of transcriptomic changes similar to 4MU treatment
inferred← citeshttps://doi.org/10.1038/sj.bjp.0706298openalex-snapshot
Somatostatin at nanomolar concentration reduces collagen I and III synthesis by, but not proliferation of activated rat hepatic stellate cells
inferred← citeshttps://doi.org/10.1038/sj.ki.5002277openalex-snapshot
Nestin expression in the kidney with an obstructed ureter
inferred← citeshttps://doi.org/10.1038/srep13320openalex-snapshot
Bile acids induce hepatic differentiation of mesenchymal stem cells
inferred← citeshttps://doi.org/10.1042/cbi20100321openalex-snapshot
Hepatic stellate cell (vitamin A‐storing cell) and its relative – past, present and future
inferred← citeshttps://doi.org/10.1046/j.1469-7580.2000.19740635.xopenalex-snapshot
Immunohistochemical analysis of development of desmin‐positive hepatic stellate cells in mouse liver
inferred← citeshttps://doi.org/10.1053/gast.2001.27971openalex-snapshot
Somatostatin suppresses endothelin-1–induced rat hepatic stellate cell contraction via somatostatin receptor subtype 1
inferred← citeshttps://doi.org/10.1053/gast.2003.50015openalex-snapshot
Peroxisome proliferator-activated receptor-β signaling contributes to enhanced proliferation of hepatic stellate cells
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1053/jhep.2000.18658openalex-snapshot
Inhibition of Hepatic Stellate Cell Proliferation and Activation by the Semisynthetic Analogue of Fumagillin Tnp–470 in Rats
inferred← citeshttps://doi.org/10.1053/jhep.2000.20243openalex-snapshot
Mechanisms and Therapy of Hepatic Fibrosis: Report of the Aasld Single Topic Basic Research Conference
inferred← citeshttps://doi.org/10.1053/jhep.2001.20793openalex-snapshot
Human and Rat Hepatic Stellate Cells Express Neurotrophins and Neurotrophin Receptors
inferred← citeshttps://doi.org/10.1053/jhep.2001.21045openalex-snapshot
Formation of Normal Desmin Intermediate Filaments in Mouse Hepatic Stellate Cells Requires Vimentin
inferred← citeshttps://doi.org/10.1053/jhep.2001.23500openalex-snapshot
In Vitro And In Vivo Activation of Rat Hepatic Stellate Cells Results In De Novo Expression of L–Type Voltage–Operated Calcium Channels
inferred← citeshttps://doi.org/10.1053/jhep.2002.31165openalex-snapshot
Keratins: Guardians of the liver
inferred← citeshttps://doi.org/10.1053/jhep.2002.31166openalex-snapshot
Inhibition of rat liver fibrogenesis through noradrenergic antagonism
inferred← citeshttps://doi.org/10.1053/jhep.2003.50005openalex-snapshot
Foxf1 +/− mice exhibit defective stellate cell activation and abnormal liver regeneration following CCl4 injury
inferred← citeshttps://doi.org/10.1055/s-2004-815564openalex-snapshot
Progenitor Cells in Diseased Human Liver
inferred← citeshttps://doi.org/10.1074/jbc.275.4.2247openalex-snapshot
Molecular Regulation of Hepatic Fibrosis, an Integrated Cellular Response to Tissue Injury
inferred← citeshttps://doi.org/10.1074/jbc.m310284200openalex-snapshot
Peroxisome Proliferator-activated Receptor γ Induces a Phenotypic Switch from Activated to Quiescent Hepatic Stellate Cells
inferred← citeshttps://doi.org/10.1080/019262302753559551openalex-snapshot
Review Article: Cystic Degeneration/Spongiosis Hepatis in Rats
inferred← citeshttps://doi.org/10.1080/08977190290023913openalex-snapshot
Expression of Pleiotrophin in Hepatic Nonparenchymal Cells and Preneoplastic Nodules in Carbon Tetrachloride-induced Fibrotic Rat Liver
inferred← citeshttps://doi.org/10.1089/scd.2010.0418openalex-snapshot
The Epigenetic Regulation of Stem Cell Factors in Hepatic Stellate Cells
inferred← citeshttps://doi.org/10.1089/scd.2017.0128openalex-snapshot
Combined Methylome and Transcriptome Analysis During Rat Hepatic Stellate Cell Activation
inferred← citeshttps://doi.org/10.1093/glycob/cwab038openalex-snapshot
Inhibition of hyaluronan secretion by novel coumarin compounds and chitin synthesis inhibitors
inferred← citeshttps://doi.org/10.1093/toxsci/kfi127openalex-snapshot
Precision-Cut Liver Slices as a New Model to Study Toxicity-Induced Hepatic Stellate Cell Activation in a Physiologic Milieu
inferred← citeshttps://doi.org/10.1097/00001756-200111160-00030openalex-snapshot
Neural phenotype expression of cultured human cord blood cells in vitro
inferred← citeshttps://doi.org/10.1097/00006676-200410000-00015openalex-snapshot
Redox-Mediated Enrichment of Self-Renewing Adult Human Pancreatic Cells That Possess Endocrine Differentiation Potential
inferred← citeshttps://doi.org/10.1097/00029330-200610020-00010openalex-snapshot
Effects of hepatotrophic factors on the liver after portacaval shunt in rats with portal hypertension
inferred← citeshttps://doi.org/10.1097/01.jnen.0000173892.24800.03openalex-snapshot
Transplantation of Human Umbilical Cord Blood-Derived Adherent Progenitors Into the Developing Rodent Brain
inferred← citeshttps://doi.org/10.1097/01.lab.0000024429.73158.deopenalex-snapshot
Dystroglycan Expression in Hepatic Stellate Cells: Role in Liver Fibrosis
inferred← citeshttps://doi.org/10.1097/01.lab.0000062890.40534.1copenalex-snapshot
Phenotypic Determination and Characterization of Nestin-Positive Precursors Derived from Human Fetal Pancreas
inferred← citeshttps://doi.org/10.1097/01.mpa.0000174939.97438.9fopenalex-snapshot
Are There Any Stem Cells in the Pancreas?
inferred← citeshttps://doi.org/10.1097/01.mpa.0000220860.01120.21openalex-snapshot
Defined Localization of Nestin-expressing Cells in l-arginine-induced Acute Pancreatitis
inferred← citeshttps://doi.org/10.1111/j.1440-1827.2010.02532.xopenalex-snapshot
Heterogeneous expression of nestin in myofibroblasts of various human tissues
inferred← citeshttps://doi.org/10.1111/j.1469-7580.2011.01404.xopenalex-snapshot
Phenotypes of articular disc cells in the rat temporomandibular joint as demonstrated by immunohistochemistry for nestin and GFAP
inferred← citeshttps://doi.org/10.1111/j.1469-7580.2012.01501.xopenalex-snapshot
Alterations in intermediate filaments expression in disc cells from the rat temporomandibular joint following exposure to continuous compressive force
inferred← citeshttps://doi.org/10.1111/j.1471-4159.2006.03922.xopenalex-snapshot
Mouse brains deficient in neuronal PDGF receptor‐β develop normally but are vulnerable to injury
inferred← citeshttps://doi.org/10.1111/j.1478-3231.2010.02229.xopenalex-snapshot
The hepatic vagus nerve stimulates hepatic stellate cell proliferation in rat acute hepatitis via muscarinic receptor type 2
inferred← citeshttps://doi.org/10.1111/j.1572-0241.2004.30110.xopenalex-snapshot
Evaluation of Liver Fibrosis: A Concise Review
inferred← citeshttps://doi.org/10.1111/j.1872-034x.2011.00804.xopenalex-snapshot
Epigenetic cell fate regulation of hepatic stellate cells
inferred← citeshttps://doi.org/10.1111/liv.12034openalex-snapshot
A histone deacetylase inhibitor, largazole, decreases liver fibrosis and angiogenesis by inhibiting transforming growth factor‐β and vascular endothelial growth factor signalling
inferred← citeshttps://doi.org/10.1111/pin.12092openalex-snapshot
Phosphorylation of Thr1495 of nestin in a mouse model of cerebral ischemia and reperfusion damage
inferred← citeshttps://doi.org/10.1126/scitranslmed.add3949openalex-snapshot
An autocrine signaling circuit in hepatic stellate cells underlies advanced fibrosis in nonalcoholic steatohepatitis
inferred← citeshttps://doi.org/10.1134/s1990519x07020058openalex-snapshot
Expression of different liver cell markers during the early prenatal human development
inferred← citeshttps://doi.org/10.1136/gut.2003.026658openalex-snapshot
Hepatic fibrogenesis requires sympathetic neurotransmitters
inferred← citeshttps://doi.org/10.1136/gut.2003.036053openalex-snapshot
Expression of somatostatin receptors in normal and cirrhotic human liver and in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1136/gut.2005.085704openalex-snapshot
Targeted and regulable expression of transgenes in hepatic stellate cells and myofibroblasts in culture and in vivo using an adenoviral Cre/loxP system to antagonise hepatic fibrosis
inferred← citeshttps://doi.org/10.1136/gut.44.4.447openalex-snapshot
Helicobacter pylori resists arrest
inferred← citeshttps://doi.org/10.1136/gut.44.4.448openalex-snapshot
Omeprazole: Helicobacter pylori makes thee greater yet
inferred← citeshttps://doi.org/10.1136/gut.44.4.449openalex-snapshot
The hiatus hernia slides back into prominence
inferred← citeshttps://doi.org/10.1136/gut.44.4.451openalex-snapshot
New kids on the block: pancreatic stellate cells enter the fibrogenesis world
inferred← citeshttps://doi.org/10.1136/gut.49.4.565openalex-snapshot
Identification of novel molecules and pathogenic pathways in primary biliary cirrhosis: cDNA array analysis of intrahepatic differential gene expression
inferred← citeshttps://doi.org/10.1136/gutjnl-2011-301220openalex-snapshot
StellaTUM: current consensus and discussion on pancreatic stellate cell research
inferred← citeshttps://doi.org/10.1152/ajpcell.00403.2025openalex-snapshot
Pericytes in tissue fibrosis
inferred← citeshttps://doi.org/10.1152/ajpgi.00102.2006openalex-snapshot
Evidence for epithelial-mesenchymal transitions in adult liver cells
inferred← citeshttps://doi.org/10.1152/physiol.00002.2009openalex-snapshot
GABA’s Control of Stem and Cancer Cell Proliferation in Adult Neural and Peripheral Niches
inferred← citeshttps://doi.org/10.1152/physrev.00013.2007openalex-snapshot
Hepatic Stellate Cells: Protean, Multifunctional, and Enigmatic Cells of the Liver
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6496448openalex-snapshot
Data from Roles for the Stem Cell–Associated Intermediate Filament Nestin in Prostate Cancer Migration and Metastasis
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6496448.v1openalex-snapshot
Data from Roles for the Stem Cell–Associated Intermediate Filament Nestin in Prostate Cancer Migration and Metastasis
inferred← citeshttps://doi.org/10.1158/0008-5472.can-07-0806openalex-snapshot
Roles for the Stem Cell–Associated Intermediate Filament Nestin in Prostate Cancer Migration and Metastasis
inferred← citeshttps://doi.org/10.1159/000100278openalex-snapshot
Stem Cells in the Postnatal Pituitary?
inferred← citeshttps://doi.org/10.1159/000101322openalex-snapshot
Liver Fibrosis: Possible Involvement of EMT
inferred← citeshttps://doi.org/10.1159/000499750openalex-snapshot
Hepatic Stellate Cells Play a Functional Role in Exacerbating Ischemia-Reperfusion Injury in Rat Liver
inferred← citeshttps://doi.org/10.11606/d.74.2019.tde-04122019-114001openalex-snapshot
Efeito do emagrecimento nos parâmetros ultrassonográficos modo B e Doppler colorido do fígado e veia hepática direita de cadelas obesas
inferred← citeshttps://doi.org/10.11606/t.5.2014.tde-13082014-152043openalex-snapshot
Mapeamento de potencial nicho neurogênico no lobo temporal humano
inferred← citeshttps://doi.org/10.1172/jci200420997openalex-snapshot
Circulating fibrocytes traffic to the lungs in response to CXCL12 and mediate fibrosis
inferred← citeshttps://doi.org/10.1172/jci66024openalex-snapshot
Cancer stem cells in the development of liver cancer
inferred← citeshttps://doi.org/10.1177/002215540305100601openalex-snapshot
Nestin Is Expressed in Vascular Endothelial Cells in the Adult Human Pancreas
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