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Epidermal growth factor (EGF)-like repeats of human tenascin-C as ligands for EGF receptor
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0029(19981201)43:5<395::aid-jemt6>3.0.co;2-topenalex-snapshot
Epidermal growth factor receptor-mediated motility in fibroblasts
inferredcites →https://doi.org/10.1002/(sici)1097-0290(19980305)57:5<571::aid-bit9>3.0.co;2-dopenalex-snapshot
Escape of autocrine ligands into extracellular medium: Experimental test of theoretical model predictions
inferredcites →https://doi.org/10.1002/(sici)1097-4636(20000605)50:3<331::aid-jbm6>3.0.co;2-topenalex-snapshot
Polymer latexes for cell-resistant and cell-interactive surfaces
inferredcites →https://doi.org/10.1002/(sici)1097-4652(199603)166:3<512::aid-jcp6>3.0.co;2-sopenalex-snapshot
Receptor-mediated effects on ligand availability influence relative mitogenic potencies of epidermal growth factor and transforming growth factor α
inferredcites →https://doi.org/10.1002/(sici)1521-3773(19981102)37:20<2754::aid-anie2754>3.0.co;2-3openalex-snapshot
Polyvalent Interactions in Biological Systems: Implications for Design and Use of Multivalent Ligands and Inhibitors
inferredcites →https://doi.org/10.1002/jbm.820270816openalex-snapshot
Effect of the conformation and orientation of adsorbed fibronectin on endothelial cell spreading and the strength of adhesion
inferredcites →https://doi.org/10.1007/bf00118180openalex-snapshot
In vitro invasiveness of DU-145 human prostate carcinoma cells is modulated by EGF receptor-mediated signals
inferredcites →https://doi.org/10.1007/bf00123400openalex-snapshot
EGF receptor signaling enhances in vivo invasiveness of DU-145 human prostate carcinoma cells
inferredcites →https://doi.org/10.1007/bf00132207openalex-snapshot
Expression of antisense epidermal growth factor receptor RNA downmodulates the malignant behavior of human colon cancer cells
inferredcites →https://doi.org/10.1007/bf00665957openalex-snapshot
EGF receptor in neoplasia and metastasis
inferredcites →https://doi.org/10.1007/bf01921736openalex-snapshot
Tenascins, a growing family of extracellular matrix proteins
inferredcites →https://doi.org/10.1016/0014-5793(89)81417-6openalex-snapshot
EGF‐like domains in extracellular matrix proteins: Localized signals for growth and differentiation?
inferredcites →https://doi.org/10.1016/0092-8674(87)90592-7openalex-snapshot
Overexpression of the human EGF receptor confers an EGF-dependent transformed phenotype to NIH 3T3 cells
inferredcites →https://doi.org/10.1016/0092-8674(89)90591-6openalex-snapshot
Transmembrane TGF-α precursors activate EGF/TGF-α receptors
inferredcites →https://doi.org/10.1016/0092-8674(89)90987-2openalex-snapshot
Domains of laminin with growth-factor activity
inferredcites →https://doi.org/10.1016/0304-3835(93)90164-5openalex-snapshot
Development of a novel human extracellular matrix for quantitation of the invasiveness of human cells
inferredcites →https://doi.org/10.1016/0955-0674(93)90037-qopenalex-snapshot
Tenascin-C, tenascin-R and tenascin-X: a family of talented proteins in search of functions
inferredcites →https://doi.org/10.1016/s0021-9258(18)37767-6openalex-snapshot
Cloning of authentic human epidermal growth factor as a bacterial secretory protein and its initial structure-function analysis by site-directed mutagenesis.
inferredcites →https://doi.org/10.1016/s0021-9258(18)45376-8openalex-snapshot
Influence of stereochemistry of the sequence Arg-Gly-Asp-Xaa on binding specificity in cell adhesion.
inferredcites →https://doi.org/10.1016/s0021-9258(18)48406-2openalex-snapshot
Mechanism of desensitization of the epidermal growth factor receptor protein-tyrosine kinase.
inferredcites →https://doi.org/10.1016/s0021-9258(18)82179-2openalex-snapshot
The functional importance of hydrophobicity of the tyrosine at position 13 of human epidermal growth factor in receptor binding
inferredcites →https://doi.org/10.1016/s0021-9258(18)89291-2openalex-snapshot
The interaction of plasma fibronectin with fibroblastic cells in suspension.
inferredcites →https://doi.org/10.1016/s0021-9258(18)99956-4openalex-snapshot
Regulation of postendocytic trafficking of the epidermal growth factor receptor through endosomal retention.
inferredcites →https://doi.org/10.1016/s0021-9258(19)85096-2openalex-snapshot
Synthetic peptides competitively inhibit both direct binding to fibroblasts and functional biological assays for the purified cell-binding domain of fibronectin.
inferredcites →https://doi.org/10.1016/s0065-230x(08)61023-4openalex-snapshot
Tumor Invasion: Role of Growth Factor-Induced Cell Motility
inferredcites →https://doi.org/10.1016/s0962-8924(99)01667-0openalex-snapshot
Cell adhesion: old and new questions
inferredcites →https://doi.org/10.1016/s0968-0004(99)01479-6openalex-snapshot
Cell adhesion: old and new questions
inferredcites →https://doi.org/10.1016/s1097-2765(00)80003-9openalex-snapshot
The Discoidin Domain Receptor Tyrosine Kinases Are Activated by Collagen
inferredcites →https://doi.org/10.1016/s1097-2765(00)80004-0openalex-snapshot
An Orphan Receptor Tyrosine Kinase Family Whose Members Serve as Nonintegrin Collagen Receptors
inferredcites →https://doi.org/10.1038/309030a0openalex-snapshot
Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule
inferredcites →https://doi.org/10.1038/36369openalex-snapshot
Tyrosine phosphorylation of the EGF receptor by the kinase Jak2 is induced by growth hormone
inferredcites →https://doi.org/10.1038/376337a0openalex-snapshot
Epithelial immaturity and multiorgan failure in mice lacking epidermal growth factor receptor
inferredcites →https://doi.org/10.1038/379557a0openalex-snapshot
Role of transactivation of the EGF receptor in signalling by G-protein-coupled receptors
inferredcites →https://doi.org/10.1038/47260openalex-snapshot
EGF receptor transactivation by G-protein-coupled receptors requires metalloproteinase cleavage of proHB-EGF
inferredcites →https://doi.org/10.1038/nbt1296-1696openalex-snapshot
Engineering epidermal growth factor for enhanced mitogenic potency
inferredcites →https://doi.org/10.1038/nm0996-1022openalex-snapshot
Tethered epidermal growth factor as a paradigm for growth factor–induced stimulation from the solid phase
inferredcites →https://doi.org/10.1073/pnas.74.9.3918openalex-snapshot
Variants of 3T3 cells lacking mitogenic response to epidermal growth factor.
inferredcites →https://doi.org/10.1073/pnas.83.11.3825openalex-snapshot
Monoclonal antibody against epidermal growth factor receptor is internalized without stimulating receptor phosphorylation.
inferredcites →https://doi.org/10.1073/pnas.84.15.5226openalex-snapshot
Solution structure of murine epidermal growth factor: determination of the polypeptide backbone chain-fold by nuclear magnetic resonance and distance geometry.
inferredcites →https://doi.org/10.1073/pnas.87.9.3289openalex-snapshot
Cell-cell adhesion mediated by binding of membrane-anchored transforming growth factor alpha to epidermal growth factor receptors promotes cell proliferation.
inferredcites →https://doi.org/10.1073/pnas.90.16.7691openalex-snapshot
Epidermal growth factor stimulates substrate-selective protein-tyrosine-phosphatase activity.
inferredcites →https://doi.org/10.1074/jbc.271.30.18224openalex-snapshot
Insulin and Epidermal Growth Factor Receptors Regulate Distinct Pools of Grb2-SOS in the Control of Ras Activation
inferredcites →https://doi.org/10.1074/jbc.274.13.8958openalex-snapshot
Effect of Epidermal Growth Factor Receptor Internalization on Regulation of the Phospholipase C-γ1 Signaling Pathway
inferredcites →https://doi.org/10.1074/jbc.274.16.11209openalex-snapshot
Integrin-mediated Migration of Murine B82L Fibroblasts Is Dependent on the Expression of an Intact Epidermal Growth Factor Receptor
inferredcites →https://doi.org/10.1083/jcb.114.3.533openalex-snapshot
A negative feedback loop attenuates EGF-induced morphological changes.
inferredcites →https://doi.org/10.1083/jcb.119.3.663openalex-snapshot
Characterization of multiple adhesive and counteradhesive domains in the extracellular matrix protein cytotactin.
inferredcites →https://doi.org/10.1083/jcb.124.4.547openalex-snapshot
Cell movement elicited by epidermal growth factor receptor requires kinase and autophosphorylation but is separable from mitogenesis
inferredcites →https://doi.org/10.1083/jcb.139.1.279openalex-snapshot
Regulation of Tenascin-C, a Vascular Smooth Muscle Cell Survival Factor that Interacts with the αvβ3 Integrin to Promote Epidermal Growth Factor Receptor Phosphorylation and Growth
inferredcites →https://doi.org/10.1091/mbc.2.8.599openalex-snapshot
Epidermal growth factor and transforming growth factor-alpha: differential intracellular routing and processing of ligand-receptor complexes.
inferredcites →https://doi.org/10.1091/mbc.7.6.871openalex-snapshot
Mitogenic signaling from the egf receptor is attenuated by a phospholipase C-gamma/protein kinase C feedback mechanism.
inferredcites →https://doi.org/10.1126/science.2305263openalex-snapshot
Ligand-Induced Transformation by a Noninternalizing Epidermal Growth Factor Receptor
inferredcites →https://doi.org/10.1126/science.274.5295.2086openalex-snapshot
Control of EGF Receptor Signaling by Clathrin-Mediated Endocytosis
inferredcites →https://doi.org/10.1126/science.283.5400.381openalex-snapshot
Emergent Properties of Networks of Biological Signaling Pathways
inferredcites →https://doi.org/10.1126/science.7618084openalex-snapshot
Targeted Disruption of Mouse EGF receptor: Effect of Genetic Background on Mutant Phenotype
inferredcites →https://doi.org/10.1126/science.7618085openalex-snapshot
Strain-Dependent Epithelial Defects in Mice Lacking the EGF Receptor
inferredcites →https://doi.org/10.1126/science.7973638openalex-snapshot
Ligands for EPH-Related Receptor Tyrosine Kinases that Require Membrane Attachment or Clustering for Activity
inferredcites →https://doi.org/10.1242/jcs.111.5.615openalex-snapshot
EGF receptor regulation of cell motility: EGF induces disassembly of focal adhesions independently of the motility-associated PLCγ signaling pathway
inferredcites →https://doi.org/10.1242/jcs.113.10.1677openalex-snapshot
Cell adhesion and motility depend on nanoscale RGD clustering
inferredcites →https://doi.org/10.1242/jcs.99.3.583openalex-snapshot
Rapid epithelialisation of fetal wounds is associated with the early deposition of tenascin
inferredcites →https://doi.org/10.14670/hh-14.1175openalex-snapshot
EGF receptor signaling in prostate morphogenesis and tumorigenesis.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Role of Tenascin C in Central Nervous System Diseases
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Targeted Radiotherapy of Central Nervous System Malignancies
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Granulation Tissue Formation and Remodeling
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Interference with anoikis‐induced cell death of dopamine neurons: Implications for augmenting embryonic graft survival in a rat model of Parkinson's disease
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Integrin β1 is involved in the signaling of glial cell line‐derived neurotrophic factor
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Myocardial Cell Signaling During the Transition to Heart Failure
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Fetal oxygen tension promotes tenascin‐C–dependent lung branching morphogenesis
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Integrated genomic and transcriptional analysis of the in vitro evolution of telomerase‐immortalized urothelial cells (TERT‐NHUC)
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Lysophosphatidic acid‐regulated mitogenic ERK signaling in androgen‐insensitive prostate cancer PC‐3 cells
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Tenascin‐C upregulates matrix metalloproteinase‐9 in breast cancer cells: Direct and synergistic effects with transforming growth factor β1
inferred← citeshttps://doi.org/10.1002/ijc.23417openalex-snapshot
Tenascin‐W, a new marker of cancer stroma, is elevated in sera of colon and breast cancer patients
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2019.tb00057.xopenalex-snapshot
Myocardial Cell Signaling During the Transition to Heart Failure
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From Cell–ECM interactions to tissue engineering
inferred← citeshttps://doi.org/10.1002/jcp.20986openalex-snapshot
Tenascin cytotactin epidermal growth factor‐like repeat binds epidermal growth factor receptor with low affinity
inferred← citeshttps://doi.org/10.1002/jcp.21232openalex-snapshot
Cell surface restriction of EGFR by a tenascin cytotactin‐encoded EGF‐like repeat is preferential for motility‐related signaling
inferred← citeshttps://doi.org/10.1002/jcp.21635openalex-snapshot
The epidermal growth factor receptor ligands at a glance
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The hematopoietic stem cell niche: what are we trying to replicate?
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Activation of epidermal growth factor receptors in astrocytes: From development to neural injury
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Tenascin C deletion impairs tendon healing and functional recovery after rotator cuff repair
inferred← citeshttps://doi.org/10.1002/path.1642openalex-snapshot
Frequent overexpression of multiple ErbB receptors by head and neck squamous cell carcinoma contrasts with rare antibody immunity in patients
inferred← citeshttps://doi.org/10.1002/pros.20667openalex-snapshot
Downregulation of several fibulin genes in prostate cancer
inferred← citeshttps://doi.org/10.1002/term.3367openalex-snapshot
Matricellular protein Tenascin‐C enhances mesenchymal stem cell angiogenic and wound healing efficacy under ischemic conditions
inferred← citeshttps://doi.org/10.1002/wdev.340openalex-snapshot
Understanding the marvels behind liver regeneration
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Pro-Invasive Molecular Cross-Signaling between Cancer Cells and Myofibroblasts
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Motility in Tumor Invasion and Metastasis — An Overview
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Cell Motility in Prostate Tumor Invasion and Metastasis
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1.4.6 The baryon octet and (Omega-)
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EGFR Signaling Pathways in Pancreatic Cancer Pathogenesis
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CHANGING EXTRACELLULAR MATRIX LIGANDS DURING METASTASIS
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The Epidermal Growth Factor Receptor in Normal and Neoplastic Epithelia
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Hypoxia and Lung Branching Morphogenesis
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EGFR (ErbB) Signaling Pathways in Pancreatic Cancer Pathogenesis
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EGFR (ErbB) Signaling Pathways in Pancreatic Cancer Pathogenesis
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Tenascin-C Function in Glioma: Immunomodulation and Beyond
inferred← citeshttps://doi.org/10.1007/978-3-319-51890-9_1openalex-snapshot
Pathogenesis of Human ACP
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Epidermal Growth Factor (EGF) in Wound Repair
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Cell Motility in Cancer Invasion and Metastasis
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A matricellular protein and EGF-like repeat signalling in the social amoebozoan Dictyostelium discoideum
inferred← citeshttps://doi.org/10.1007/s00018-022-04259-5openalex-snapshot
The extracellular matrix molecule tenascin-C modulates cell cycle progression and motility of adult neural stem/progenitor cells from the subependymal zone
inferred← citeshttps://doi.org/10.1007/s00066-006-1459-2openalex-snapshot
Early Effects of Rhenium-188 Treatment on Proliferation, Migration, and Matrix Synthesis of Cultured Human Aortic Smooth Muscle Cells
inferred← citeshttps://doi.org/10.1007/s00418-008-0485-9openalex-snapshot
Extracellular matrix of the central nervous system: from neglect to challenge
inferred← citeshttps://doi.org/10.1007/s00441-008-0715-4openalex-snapshot
Effects of tenascin-W on osteoblasts in vitro
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Tenascin-C is expressed by human glioma in vivo and shows a strong association with tumor blood vessels
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The remarkable legacy of the K6/ODC mouse: mechanisms of polyamine-promoted tumorigenesis revealed
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Extracellular Matrix in Neural Plasticity and Regeneration
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Neural Differentiation of Human-Induced Pluripotent Stem Cells (hiPSc) on Surface-Modified Nanofibrous Scaffolds Coated with Platelet-Rich Plasma
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The role of tenascin-C in tissue injury and tumorigenesis
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Brevican, Neurocan, Tenascin-C and Versican are Mainly Responsible for the Invasiveness of Low-Grade Astrocytoma
inferred← citeshttps://doi.org/10.1007/s13277-015-4160-1openalex-snapshot
DCN deficiency promotes renal cell carcinoma growth and metastasis through downregulation of P21 and E-cadherin
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The Pro-reparative Engine: Stem Cells Aid Healing by Dampening Inflammation
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Recent advances of FAPI PET tracers in the diagnosis of liver cancer
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Cell-ECM Interactions in Repair and Regeneration
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Cell–ECM Interactions in Repair and Regeneration
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The Dynamics of Cell-ECM Interactions, with Implications for Tissue Engineering
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Structural Proteins | Major Proteins of the Extracellular Matrix
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The dynamics of cell–extracellular matrix interactions, with implications for tissue engineering
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Cell–ECM Interactions in Repair and Regeneration
inferred← citeshttps://doi.org/10.1016/b978-012370615-7/50011-1openalex-snapshot
The Dynamics of Cell–ECM Interactions
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Some Background Concepts
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Extracellular Matrix Remodeling in Intestinal Homeostasis and Disease
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Growth factor binding to the pericellular matrix and its importance in tissue engineering☆
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Matrikines as mediators of tissue remodelling
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Tenascin C Induces Epithelial-Mesenchymal Transition–Like Change Accompanied by SRC Activation and Focal Adhesion Kinase Phosphorylation in Human Breast Cancer Cells
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Cleavage of extracellular matrix in periodontitis: Gingipains differentially affect cell adhesion activities of fibronectin and tenascin-C
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Tenascin-C affects invasiveness of EGFR-mutated lung adenocarcinoma through a putative paracrine loop
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Tenascin C regulates multiple microglial functions involving TLR4 signaling and HDAC1
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.12.081openalex-snapshot
An EGF-like peptide sequence from Dictyostelium enhances cell motility and chemotaxis
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Staphylococcal superantigen-like protein 8 (SSL8) binds to tenascin C and inhibits tenascin C–fibronectin interaction and cell motility of keratinocytes
inferred← citeshttps://doi.org/10.1016/j.biocel.2004.01.007openalex-snapshot
Connective tissues: signalling by tenascins
inferred← citeshttps://doi.org/10.1016/j.biocel.2004.12.002openalex-snapshot
Potential oncogenic action of tenascin-C in tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2009.05.061openalex-snapshot
The influence of tethered epidermal growth factor on connective tissue progenitor colony formation
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2010.01.138openalex-snapshot
Synergistic effects of tethered growth factors and adhesion ligands on DNA synthesis and function of primary hepatocytes cultured on soft synthetic hydrogels
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Epidermal growth factor-like repeats of tenascin-C-induced constriction of cerebral arteries via activation of epidermal growth factor receptors in rats
inferred← citeshttps://doi.org/10.1016/j.canlet.2006.02.017openalex-snapshot
Tenascin-C induced signaling in cancer
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EGFR family and Src family kinase interactions: mechanics matters?
inferred← citeshttps://doi.org/10.1016/j.cellsig.2011.03.008openalex-snapshot
An extracellular matrix, calmodulin-binding protein from Dictyostelium with EGF-like repeats that enhance cell motility
inferred← citeshttps://doi.org/10.1016/j.cellsig.2012.05.004openalex-snapshot
EGF-like peptide-enhanced cell movement in Dictyostelium is mediated by protein kinases and the activity of several cytoskeletal proteins
inferred← citeshttps://doi.org/10.1016/j.clindermatol.2009.05.013openalex-snapshot
Cosmeceuticals and peptides
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Polymers to direct cell fate by controlling the microenvironment
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Tenascin C: a multifaceted interplayer in the rheumatoid arthritis pathogenesis and progression - insights and implications
inferred← citeshttps://doi.org/10.1016/j.ejcb.2012.08.004openalex-snapshot
More than matrix: The multifaceted role of decorin in cancer
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Data-independent acquisition-based comparative analysis of whey proteomes in human colostrum, mature milk, and small ruminant milk for precision infant formula development
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.05.068openalex-snapshot
Recombinant mussel protein Pvfp5β enhances cell adhesion of poly(vinyl alcohol)/k-carrageenan hydrogel scaffolds
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.101096openalex-snapshot
Bidirectional epithelial–mesenchymal crosstalk provides self-sustaining profibrotic signals in pulmonary fibrosis
inferred← citeshttps://doi.org/10.1016/j.jdermsci.2005.05.001openalex-snapshot
Matrikines and matricryptins: Implications for cutaneous cancers and skin repair
inferred← citeshttps://doi.org/10.1016/j.jgg.2017.05.004openalex-snapshot
Multiple analyses indicate the specific association of NR1I3, C6 and TNN with low hip BMD risk
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2015.02.002openalex-snapshot
Glucocorticoids and the non-steroidal selective glucocorticoid receptor modulator, compound A, differentially affect colon cancer-derived myofibroblasts
inferred← citeshttps://doi.org/10.1016/j.jtos.2023.05.005openalex-snapshot
Tenascins and osteopontin in biological response in cornea
inferred← citeshttps://doi.org/10.1016/j.matbio.2011.02.001openalex-snapshot
SMOC1 is a tenascin-C interacting protein over-expressed in brain tumors
inferred← citeshttps://doi.org/10.1016/j.matbio.2012.02.003openalex-snapshot
CyrA, a matricellular protein that modulates cell motility in Dictyostelium discoideum
inferred← citeshttps://doi.org/10.1016/j.matbio.2014.07.005openalex-snapshot
Revisiting the matricellular concept
inferred← citeshttps://doi.org/10.1016/j.matbio.2015.08.001openalex-snapshot
Skin tissue repair: Matrix microenvironmental influences
inferred← citeshttps://doi.org/10.1016/j.matbio.2020.04.006openalex-snapshot
Extracellular matrix-derived peptides in tissue remodeling and fibrosis
inferred← citeshttps://doi.org/10.1016/j.mcn.2003.10.024openalex-snapshot
Hedgehog interacting protein in the mature brain: membrane-associated and soluble forms
inferred← citeshttps://doi.org/10.1016/j.mcn.2016.11.003openalex-snapshot
Tenascin-C in the matrisome of neural stem and progenitor cells
inferred← citeshttps://doi.org/10.1016/j.mlong.2009.10.008openalex-snapshot
Vieillissement et pathologies pulmonaires : régulation de l’inflammation par les peptides d’élastine
inferred← citeshttps://doi.org/10.1016/j.mvr.2008.08.008openalex-snapshot
The counteradhesive proteins, thrombospondin 1 and SPARC/osteonectin, open the tyrosine phosphorylation-responsive paracellular pathway in pulmonary vascular endothelia
inferred← citeshttps://doi.org/10.1016/j.patbio.2014.02.007openalex-snapshot
Extracellular matrix and wound healing
inferred← citeshttps://doi.org/10.1016/j.pccm.2024.02.001openalex-snapshot
Dysregulated bidirectional epithelial–mesenchymal crosstalk: A core determinant of lung fibrosis progression
inferred← citeshttps://doi.org/10.1016/j.peptides.2011.12.014openalex-snapshot
EGF-like peptide of Dictyostelium discoideum is not a chemoattractant but it does restore folate-mediated chemotaxis in the presence of signal transduction inhibitors
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2016.09.002openalex-snapshot
Matrix reloaded: CCN, tenascin and SIBLING group of matricellular proteins in orchestrating cancer hallmark capabilities
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2024.108682openalex-snapshot
Matrikines in the skin: Origin, effects, and therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.09.012openalex-snapshot
Tenascins in CNS lesions
inferred← citeshttps://doi.org/10.1016/j.tranon.2024.101888openalex-snapshot
Tenascin-C as a potential biomarker and therapeutic target for esophageal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.ucl.2005.02.004openalex-snapshot
Clinical Applications for Targeted Therapy in Bladder Cancer
inferred← citeshttps://doi.org/10.1016/j.ydbio.2004.06.006openalex-snapshot
Activation of epidermal growth factor receptors directs astrocytes to organize in a network surrounding axons in the developing rat optic nerve
inferred← citeshttps://doi.org/10.1016/j.yexcr.2006.01.015openalex-snapshot
Collagen XVII promotes integrin-mediated squamous cell carcinoma transmigration—A novel role for αIIb integrin and tirofiban
inferred← citeshttps://doi.org/10.1016/j.yexcr.2011.06.006openalex-snapshot
Tenascin-C in the extracellular matrix promotes the selection of highly proliferative and tubulogenesis-defective endothelial cells
inferred← citeshttps://doi.org/10.1016/j.yexcr.2017.11.034openalex-snapshot
Glucocorticoids indirectly decrease colon cancer cell proliferation and invasion via effects on cancer-associated fibroblasts
inferred← citeshttps://doi.org/10.1016/s0001-4079(19)30865-9openalex-snapshot
La matrice extracellulaire : un partenaire majeur de la cicatrisation des plaies
inferred← citeshttps://doi.org/10.1016/s0074-7696(03)30001-4openalex-snapshot
The Thrombospondin Type 1 Repeat (TSR) and Neuronal Differentiation: Roles of SCO-Spondin Oligopeptides on Neuronal Cell Types and Cell Lines∗
inferred← citeshttps://doi.org/10.1016/s0959-8049(02)00210-1openalex-snapshot
Immunohistochemical expression of extracellular matrix components tenascin, fibronectin, collagen type IV and laminin in breast cancer: their prognostic value and role in tumour invasion and progression
inferred← citeshttps://doi.org/10.1016/s0962-8924(03)00129-6openalex-snapshot
Tales from the crypt[ic] sites of the extracellular matrix
inferred← citeshttps://doi.org/10.1038/jid.2012.263openalex-snapshot
Melanoma Cell Invasiveness Is Promoted at Least in Part by the Epidermal Growth Factor–Like Repeats of Tenascin-C
inferred← citeshttps://doi.org/10.1038/labinvest.2013.132openalex-snapshot
Matrikine and matricellular regulators of EGF receptor signaling on cancer cell migration and invasion
inferred← citeshttps://doi.org/10.1038/nrm905openalex-snapshot
Signalling shortcuts: cell-surface receptors in the nucleus?
inferred← citeshttps://doi.org/10.1038/nrn2978openalex-snapshot
The stem cell potential of glia: lessons from reactive gliosis
inferred← citeshttps://doi.org/10.1038/onc.2015.131openalex-snapshot
IGFBP2 potentiates nuclear EGFR–STAT3 signaling
inferred← citeshttps://doi.org/10.1038/s41419-020-2438-8openalex-snapshot
Tumor-associated macrophages promote ovarian cancer cell migration by secreting transforming growth factor beta induced (TGFBI) and tenascin C
inferred← citeshttps://doi.org/10.1038/s41419-022-05496-zopenalex-snapshot
Matrix protein Tenascin-C promotes kidney fibrosis via STAT3 activation in response to tubular injury
inferred← citeshttps://doi.org/10.1038/sj.onc.1207403openalex-snapshot
Enhanced tenascin-C expression and matrix deposition during Ras/TGF-β-induced progression of mammary tumor cells
inferred← citeshttps://doi.org/10.1038/srep25326openalex-snapshot
Platelet lysate gel and endothelial progenitors stimulate microvascular network formation in vitro: tissue engineering implications
inferred← citeshttps://doi.org/10.1038/srep45181openalex-snapshot
Nephronectin plays critical roles in Sox2 expression and proliferation in dental epithelial stem cells via EGF-like repeat domains
inferred← citeshttps://doi.org/10.1039/9781839168956-00003openalex-snapshot
Matrix Biology: Extracellular Matrix – Building Function Through Complexity
inferred← citeshttps://doi.org/10.1039/c4ra05534aopenalex-snapshot
Recent progress in the research of biomaterials regulating cell behavior
inferred← citeshttps://doi.org/10.1042/bj20090341openalex-snapshot
Isolation and characterization of a secreted, cell-surface glycoprotein SCUBE2 from humans
inferred← citeshttps://doi.org/10.1042/cs20190893openalex-snapshot
Regulation of cellular senescence by extracellular matrix during chronic fibrotic diseases
inferred← citeshttps://doi.org/10.1042/ebc20180015openalex-snapshot
A systems perspective of heterocellular signaling
inferred← citeshttps://doi.org/10.1042/ebc20190025openalex-snapshot
Adhesion and growth factor receptor crosstalk mechanisms controlling cell migration
inferred← citeshttps://doi.org/10.1046/j.1432-0436.2002.700912.xopenalex-snapshot
Motility cues in the tumor microenvironment
inferred← citeshttps://doi.org/10.1055/s-0031-1272832openalex-snapshot
Epithelial-Mesenchymal Interactions in Biliary Diseases
inferred← citeshttps://doi.org/10.1074/jbc.m205317200openalex-snapshot
Decorin Binds to a Narrow Region of the Epidermal Growth Factor (EGF) Receptor, Partially Overlapping but Distinct from the EGF-binding Epitope
inferred← citeshttps://doi.org/10.1074/jbc.m400242200openalex-snapshot
Alternative Splicing in the Aggrecan G3 Domain Influences Binding Interactions with Tenascin-C and Other Extracellular Matrix Proteins
inferred← citeshttps://doi.org/10.1074/jbc.m500249200openalex-snapshot
Keratocan, a Cornea-specific Keratan Sulfate Proteoglycan, Is Regulatedby Lumican
inferred← citeshttps://doi.org/10.1074/jbc.m512980200openalex-snapshot
Versican G3 Domain Regulates Neurite Growth and Synaptic Transmission of Hippocampal Neurons by Activation of Epidermal Growth Factor Receptor
inferred← citeshttps://doi.org/10.1074/jbc.m809198200openalex-snapshot
Epidermal Growth Factor-like Repeats of Thrombospondins Activate Phospholipase Cγ and Increase Epithelial Cell Migration through Indirect Epidermal Growth Factor Receptor Activation
inferred← citeshttps://doi.org/10.1074/jbc.r500005200openalex-snapshot
Meet the Tenascins: Multifunctional and Mysterious
inferred← citeshttps://doi.org/10.1080/028418602753669481openalex-snapshot
Growth Factor-Induced Cell Motility in Tumor Invasion
inferred← citeshttps://doi.org/10.1080/09168451.2017.1362975openalex-snapshot
Comprehensive DNA microarray expression profiles of tumors in tenascin-C-knockout mice
inferred← citeshttps://doi.org/10.1080/19336918.2014.1000071openalex-snapshot
Role of tenascins in the ECM of gliomas
inferred← citeshttps://doi.org/10.1080/19336918.2015.1008331openalex-snapshot
Tenascin C in metastasis: A view from the invasive front
inferred← citeshttps://doi.org/10.1080/19336918.2015.1008332openalex-snapshot
Tenascin-C and integrins in cancer
inferred← citeshttps://doi.org/10.1080/19336918.2016.1259057openalex-snapshot
Hedgehog signaling stimulates Tenascin C to promote invasion of pancreatic ductal adenocarcinoma cells through Annexin A2
inferred← citeshttps://doi.org/10.1083/jcb.200208145openalex-snapshot
Binding to EGF receptor of a laminin-5 EGF-like fragment liberated during MMP-dependent mammary gland involution
inferred← citeshttps://doi.org/10.1089/ten.tea.2009.0720openalex-snapshot
Ligament-Derived Matrix Stimulates a Ligamentous Phenotype in Human Adipose-Derived Stem Cells
inferred← citeshttps://doi.org/10.1089/ten.tea.2012.0568openalex-snapshot
The Matrikine Tenascin-C Protects Multipotential Stromal Cells/Mesenchymal Stem Cells from Death Cytokines Such as FasL
inferred← citeshttps://doi.org/10.1089/ten.tea.2013.0165openalex-snapshot
Multilayered Electrospun Scaffolds for Tendon Tissue Engineering
inferred← citeshttps://doi.org/10.1089/ten.tea.2013.0188openalex-snapshot
Different Forms of Tenascin-C with Tenascin-R Regulate Neural Differentiation in Bone Marrow-Derived Human Mesenchymal Stem Cells
inferred← citeshttps://doi.org/10.1089/wound.2012.0417openalex-snapshot
Interactions of the Extracellular Matrix and Progenitor Cells in Cutaneous Wound Healing
inferred← citeshttps://doi.org/10.1089/wound.2014.0599openalex-snapshot
Fibrinogen-Related Proteins in Tissue Repair: How a Unique Domain with a Common Structure Controls Diverse Aspects of Wound Healing
inferred← citeshttps://doi.org/10.1093/carcin/bgi336openalex-snapshot
Insulin-like growth factor 1 is a potent stimulator of cervical cancer cell invasiveness and proliferation that is modulated by α v β 3 integrin signaling
inferred← citeshttps://doi.org/10.1096/fasebj.23.1_supplement.741.12openalex-snapshot
Investigation of the Role of Glypican 3 in Liver Regeneration and Hepatocyte Proliferation
inferred← citeshttps://doi.org/10.1096/fj.03-1110fjeopenalex-snapshot
Tenascin‐C and SF/HGF produced by myofibroblasts in vitro provide convergent proinvasive signals to human colon cancer cells through RhoA and Rac
inferred← citeshttps://doi.org/10.1097/01.ico.0000247207.55520.a4openalex-snapshot
Ocular Surface Tissue Morphogenesis in Normal and Disease States Revealed by Genetically Modified Mice
inferred← citeshttps://doi.org/10.1097/01.mp.0000086860.65672.73openalex-snapshot
Tenascin Expression at the Invasive Front Is Associated with Poor Prognosis in Intrahepatic Cholangiocarcinoma
inferred← citeshttps://doi.org/10.1097/lvt.0000000000000122openalex-snapshot
An extensive evaluation of hepatic markers of damage and regeneration in controlled and uncontrolled donation after circulatory death
inferred← citeshttps://doi.org/10.1100/2012/765909openalex-snapshot
Identification of Proteins with Potential Osteogenic Activity Present in the Water-Soluble Matrix Proteins fromCrassostrea gigasNacre Using a Proteomic Approach
inferred← citeshttps://doi.org/10.1101/2020.09.08.20190280openalex-snapshot
Bioinformatical analysis identified significant genes in the PI3K-Akt signaling pathway relating with poor prognosis of skin cutaneous melanoma
inferred← citeshttps://doi.org/10.1101/2022.01.10.474416openalex-snapshot
Collagen XVIII promotes breast cancer through EGFR/ErbB signaling and its ablation improves the efficacy of ErbB-targeting inhibitors
inferred← citeshttps://doi.org/10.1101/2025.10.01.677488openalex-snapshot
Hippo/YAP1 Signaling Regulates the Oligodendrocyte–Astrocyte Fate Switch and Ependymal Gene Expression in Adult Spinal Cord Stem Cells
inferred← citeshttps://doi.org/10.1111/etp.12008openalex-snapshot
Granulation tissue formation and remodeling
inferred← citeshttps://doi.org/10.1111/exd.12435openalex-snapshot
Matricryptins and matrikines: biologically active fragments of the extracellular matrix
inferred← citeshttps://doi.org/10.1111/j.0022-202x.2005.23620.xopenalex-snapshot
Suprabasal Induction of Ornithine Decarboxylase in Adult Mouse Skin Is Sufficient to Activate Keratinocytes
inferred← citeshttps://doi.org/10.1111/j.1067-1927.2004.012111.xopenalex-snapshot
Keloid fibroblast responsiveness to epidermal growth factor and activation of downstream intracellular signaling pathways
inferred← citeshttps://doi.org/10.1111/j.1067-1927.2004.012302.xopenalex-snapshot
Extracellular matrix signaling through growth factor receptors during wound healing
inferred← citeshttps://doi.org/10.1111/j.1365-2591.2012.02089.xopenalex-snapshot
Tenascin‐ C promotes differentiation of rat dental pulp cells in vitro
inferred← citeshttps://doi.org/10.1111/j.1432-1033.2004.04363.xopenalex-snapshot
Folding of epidermal growth factor‐like repeats from human tenascin studied through a sequence frame‐shift approach
inferred← citeshttps://doi.org/10.1111/j.1524-475x.2009.00466.xopenalex-snapshot
Interactions between extracellular matrix and growth factors in wound healing
inferred← citeshttps://doi.org/10.1111/j.1524-475x.2010.00662.xopenalex-snapshot
Cellular/extracellular matrix cross‐talk in scar evolution and control
inferred← citeshttps://doi.org/10.1111/j.1582-4934.2007.00015.xopenalex-snapshot
Constitutive and ligand‐induced nuclear localization of oxytocin receptor
inferred← citeshttps://doi.org/10.1111/j.1582-4934.2011.01360.xopenalex-snapshot
How do tenascins influence the birth and life of a malignant cell?
inferred← citeshttps://doi.org/10.1111/j.1600-0463.2006.apm_249.xopenalex-snapshot
Tenascin‐C expression in Merkel cell carcinoma lymph node metastasis
inferred← citeshttps://doi.org/10.1111/j.1749-6632.2002.tb03056.xopenalex-snapshot
Emerging Design Principles in Biomaterials and Scaffolds for Tissue Engineering
inferred← citeshttps://doi.org/10.1111/nep.14031openalex-snapshot
Mesangial cell‐derived tenascin‐C contributes to mesangial cell proliferation and matrix protein production in IgA nephropathy
inferred← citeshttps://doi.org/10.1116/1.5045231openalex-snapshot
Engineered systems to study the synergistic signaling between integrin-mediated mechanotransduction and growth factors (Review)
inferred← citeshttps://doi.org/10.1126/sciadv.add9275openalex-snapshot
How the mechanobiology orchestrates the iterative and reciprocal ECM-cell cross-talk that drives microtissue growth
inferred← citeshttps://doi.org/10.1126/science.1069210openalex-snapshot
Tissue Engineering--Current Challenges and Expanding Opportunities
inferred← citeshttps://doi.org/10.1126/science.1106587openalex-snapshot
Exploring and Engineering the Cell Surface Interface
inferred← citeshttps://doi.org/10.1134/s1607672910040149openalex-snapshot
Biodegradable matrices from regenerated silk of Bombix mori
inferred← citeshttps://doi.org/10.1152/ajpcell.00260.2001openalex-snapshot
Autocrine loops with positive feedback enable context-dependent cell signaling
inferred← citeshttps://doi.org/10.1152/ajpcell.00333.2022openalex-snapshot
A virological view of tenascin-C in infection
inferred← citeshttps://doi.org/10.1155/2010/795385openalex-snapshot
Epidermal Growth Factor (EGF) Treatment on Multipotential Stromal Cells (MSCs). Possible Enhancement of Therapeutic Potential of MSC
inferred← citeshttps://doi.org/10.1158/0008-5472.can-06-3348openalex-snapshot
Endothelin Receptor Type B Counteracts Tenascin-C–Induced Endothelin Receptor Type A–Dependent Focal Adhesion and Actin Stress Fiber Disorganization
inferred← citeshttps://doi.org/10.1158/0008-5472.can-20-1264openalex-snapshot
EpCAM Signaling Promotes Tumor Progression and Protein Stability of PD-L1 through the EGFR Pathway
inferred← citeshttps://doi.org/10.1158/1078-0432.c.6517087openalex-snapshot
Data from Association of an Extracellular Matrix Gene Cluster with Breast Cancer Prognosis and Endocrine Therapy Response
inferred← citeshttps://doi.org/10.1158/1078-0432.c.6517087.v1openalex-snapshot
Data from Association of an Extracellular Matrix Gene Cluster with Breast Cancer Prognosis and Endocrine Therapy Response
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-06-0182openalex-snapshot
Microarray-Based Identification of Tenascin C and Tenascin XB , Genes Possibly Involved in Tumorigenesis Associated with Neurofibromatosis Type 1
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-08-0555openalex-snapshot
Association of an Extracellular Matrix Gene Cluster with Breast Cancer Prognosis and Endocrine Therapy Response
inferred← citeshttps://doi.org/10.1159/000112848openalex-snapshot
Tenascin C in Stem Cell Niches: Redundant, Permissive or Instructive?
inferred← citeshttps://doi.org/10.11606/t.42.2008.tde-30052008-123952openalex-snapshot
Análise comparativa das distribuições espaciais de moléculas envolvidas na migração e invasão de um tumor cerebral de rato in vivo.
inferred← citeshttps://doi.org/10.1161/strokeaha.122.041977openalex-snapshot
Epidermal Growth Factor Receptor Mediates Neuronal Apoptosis After Subarachnoid Hemorrhage in Mice
inferred← citeshttps://doi.org/10.1172/jci.insight.130751openalex-snapshot
Fibroblast subtypes define a metastatic matrisome in breast cancer
inferred← citeshttps://doi.org/10.1172/jci.insight.181935openalex-snapshot
Granzyme B cleaves tenascin-C to release its C-terminal domain in rheumatoid arthritis
inferred← citeshttps://doi.org/10.1177/1535370216658144openalex-snapshot
Liver metastases: Microenvironments and ex-vivo models
inferred← citeshttps://doi.org/10.1186/1471-2164-13-615openalex-snapshot
Transcriptome analysis of the spalax hypoxia survival response includes suppression of apoptosis and tight control of angiogenesis
inferred← citeshttps://doi.org/10.1186/1471-2407-10-443openalex-snapshot
The activation of Proteinase-Activated Receptor-1 (PAR1) mediates gastric cancer cell proliferation and invasion
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