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Tenascins: regulation and putative functions during pathological stress
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inferredcites →https://doi.org/10.1002/(sici)1096-9098(199702)64:2<98::aid-jso2>3.0.co;2-jopenalex-snapshot
Morphologic pattern of tenascin as a diagnostic biomarker in colon cancer
inferredcites →https://doi.org/10.1002/(sici)1096-9896(199912)189:4<475::aid-path462>3.0.co;2-vopenalex-snapshot
Synthesis and protein distribution of the unspliced large tenascin-C isoform in oral squamous cell carcinoma
inferredcites →https://doi.org/10.1002/(sici)1097-0177(200006)218:2<235::aid-dvdy2>3.0.co;2-gopenalex-snapshot
The tenascin family of ECM glycoproteins: Structure, function, and regulation during embryonic development and tissue remodeling
inferredcites →https://doi.org/10.1002/(sici)1097-0215(19961220)69:6<445::aid-ijc4>3.0.co;2-4openalex-snapshot
Expression of tenascin in invasion border of early breast cancer correlates with higher risk of distant metastasis
inferredcites →https://doi.org/10.1002/(sici)1097-0215(19970529)71:5<810::aid-ijc19>3.0.co;2-bopenalex-snapshot
Biodistribution of 111In‐labelled SCN‐bz‐DTPA‐BC‐2 MAb following loco‐regional injection into glioblastomas
inferredcites →https://doi.org/10.1002/(sici)1097-0215(19970717)72:2<217::aid-ijc3>3.0.co;2-uopenalex-snapshot
Distribution pattern of tenascin-C in normal and neoplastic mesenchymal tissues
inferredcites →https://doi.org/10.1002/(sici)1097-0215(19970717)72:2<236::aid-ijc6>3.0.co;2-sopenalex-snapshot
Human tenascin-C: Identification of a novel type III repeat in oral cancer and of novel splice variants in normal, malignant and reactive oral mucosae
inferredcites →https://doi.org/10.1002/(sici)1097-0215(19970926)73:1<10::aid-ijc2>3.0.co;2-4openalex-snapshot
Expression of fibronectin and tenascin-C mRNA by myofibroblasts, vascular cells and epithelial cells in human colon adenomas and carcinomas
inferredcites →https://doi.org/10.1002/(sici)1097-0215(19990812)82:4<477::aid-ijc2>3.0.co;2-5openalex-snapshot
Detection of tenascin-C isoforms in colorectal mucosa, ulcerative colitis, carcinomas and liver metastases
inferredcites →https://doi.org/10.1002/(sici)1097-4695(199804)35:1<1::aid-neu1>3.0.co;2-9openalex-snapshot
Zebrafish tenascin-W, a new member of the tenascin family
inferredcites →https://doi.org/10.1002/1096-9896(2000)9999:9999<::aid-path752>3.0.co;2-vopenalex-snapshot
Co-expression of tenascin-C and vimentin in human breast cancer cells indicates phenotypic transdifferentiation during tumour progression: correlation with histopathological parameters, hormone receptors, and oncoproteins
inferredcites →https://doi.org/10.1002/1097-0142(20010915)92:6<1419::aid-cncr1465>3.0.co;2-jopenalex-snapshot
Annexin II overexpression correlates with stromal tenascin-C overexpression
inferredcites →https://doi.org/10.1002/aja.1002030411openalex-snapshot
Embryonic expression of tenascin‐X suggests a role in limb, muscle, and heart development
inferredcites →https://doi.org/10.1002/art.1780351011openalex-snapshot
Expression of human tenascin in synovitis and its regulation by interleukin‐1
inferredcites →https://doi.org/10.1002/hep.510240525openalex-snapshot
Fibrolamellar Carcinoma of the Liver: Composition of the Extracellular Matrix and Expression of Cell–Matrix and Cell–Cell Adhesion Molecules
inferredcites →https://doi.org/10.1002/ijc.10233openalex-snapshot
Clinical impact and functional aspects of tenascin‐C expression during glioma progression
inferredcites →https://doi.org/10.1002/ijc.10546openalex-snapshot
Value of Tenascin‐C content and association with clinicopathological parameters in uterine cervical lesions
inferredcites →https://doi.org/10.1002/ijc.2910520504openalex-snapshot
Expression of different tenascin isoforms in normal, hyperplastic and neoplastic human breast tissues
inferredcites →https://doi.org/10.1002/ijc.2910610402openalex-snapshot
Tenascin‐C in serum: A questionable tumor marker
inferredcites →https://doi.org/10.1002/ijc.2910630324openalex-snapshot
Tenascin and fibronectin isoforms in human renal cell carcinomas, renal cell carcinoma cell lines and xenografts in nude mice
inferredcites →https://doi.org/10.1002/j.1460-2075.1988.tb03160.xopenalex-snapshot
Tenascin: cDNA cloning and induction by TGF‐beta.
inferredcites →https://doi.org/10.1002/jnr.1055openalex-snapshot
Tenascin‐R is expressed by Schwann cells in the peripheral nervous system
inferredcites →https://doi.org/10.1002/jor.1100180312openalex-snapshot
Mechanical modulation of tenascin‐C and collagen‐XII expression during avian synovial joint formation
inferredcites →https://doi.org/10.1002/path.1131openalex-snapshot
Tenascin‐C is a useful marker for disease activity in myocarditis
inferredcites →https://doi.org/10.1002/path.1214openalex-snapshot
Towards defining roles and relationships for tenascin‐C and TGFβ‐1 in the normal and neoplastic urinary bladder
inferredcites →https://doi.org/10.1002/path.1258openalex-snapshot
Markers for the development of early prostate cancer
inferredcites →https://doi.org/10.1006/dbio.1996.0266openalex-snapshot
Local Delivery of TGF β2 Can Substitute for Placode Epithelium to Induce Mesenchymal Condensation during Skin Appendage Morphogenesis
inferredcites →https://doi.org/10.1006/excr.1996.0014openalex-snapshot
Differential Regulation of Fibulin, Tenascin-C, and Nidogen Expression during Wound Healing of Normal and Glucocorticoid-Treated Mice
inferredcites →https://doi.org/10.1006/excr.1998.4363openalex-snapshot
Rapid and Reversible Regulation of Collagen XII Expression by Changes in Tensile Stress
inferredcites →https://doi.org/10.1006/excr.1999.4658openalex-snapshot
Tenascin-Y, a Component of Distinctive Connective Tissues, Supports Muscle Cell Growth
inferredcites →https://doi.org/10.1006/excr.2000.5041openalex-snapshot
Adhesion Modulation by Antiadhesive Molecules of the Extracellular Matrix
inferredcites →https://doi.org/10.1006/gyno.1999.5405openalex-snapshot
Expression of Tenascin in Human Cervical Cancer—Association of Tenascin Expression with Clinicopathological Parameters
inferredcites →https://doi.org/10.1007/bf01052668openalex-snapshot
Phase I studies of treatment of malignant gliomas and neoplastic meningitis with131I-radiolabeled monoclonal antibodies anti-tenascin 81C6 and anti-chondroitin proteoglycan sulfate Me1-14 F (ab?)2-a preliminary report
inferredcites →https://doi.org/10.1007/bf01921736openalex-snapshot
Tenascins, a growing family of extracellular matrix proteins
inferredcites →https://doi.org/10.1007/bf03032361openalex-snapshot
The distribution of extracellular matrix proteins and CD44S expression in human astrocytomas
inferredcites →https://doi.org/10.1007/s002590050397openalex-snapshot
Antibody-guided three-step therapy for high grade glioma with yttrium-90 biotin
inferredcites →https://doi.org/10.1007/s003840100312openalex-snapshot
Serum tenascin-C is an indicator of inflammatory bowel disease activity
inferredcites →https://doi.org/10.1007/s004030050200openalex-snapshot
Epicutaneous application of leukotriene B 4 induces patterns of tenascin and a heparan sulfate proteoglycan epitope that are typical for psoriatic lesions
inferredcites →https://doi.org/10.1016/0003-9969(95)00071-vopenalex-snapshot
Tenascin expression in mucocutaneous diseases and related lesions of human oral mucosa
inferredcites →https://doi.org/10.1016/0007-1226(91)90008-8openalex-snapshot
The effect of mechanical stress on healing skin wounds: an experimental study in rabbits using tissue expansion
inferredcites →https://doi.org/10.1016/0012-1606(88)90252-7openalex-snapshot
The 140-kDa fibronectin receptor complex is required for mesodermal cell adhesion during gastrulation in the amphibian Pleurodeles waltlii
inferredcites →https://doi.org/10.1016/0012-1606(90)90256-iopenalex-snapshot
Exogenous tenascin inhibits mesodermal cell migration during amphibian gastrulation
inferredcites →https://doi.org/10.1016/0014-5793(93)80006-gopenalex-snapshot
Downregulation of collagen synthesis in fibroblasts within three‐dimensional collagen lattices involves transcriptional and posttranscriptional mechanisms
inferredcites →https://doi.org/10.1016/0046-8177(95)90004-7openalex-snapshot
Differentiation and proliferative activity in benign and malignant cartilage tumors of bone
inferredcites →https://doi.org/10.1016/0092-8674(86)90374-0openalex-snapshot
Tenascin: an extracellular matrix protein involved in tissue interactions during fetal development and oncogenesis
inferredcites →https://doi.org/10.1016/0092-8674(88)90158-4openalex-snapshot
Tenascin interferes with fibronectin action
inferredcites →https://doi.org/10.1016/s0002-9440(10)65388-6openalex-snapshot
Identification of a Glioblastoma-Associated Tenascin-C Isoform by a High Affinity Recombinant Antibody
inferredcites →https://doi.org/10.1016/s0002-9440(10)65482-xopenalex-snapshot
Mechanical Forces Induce Scar Remodeling
inferredcites →https://doi.org/10.1016/s0014-5793(00)01936-0openalex-snapshot
Tenascin‐C induced stimulation of chondrogenesis is dependent on the presence of the C‐terminal fibrinogen‐like globular domain
inferredcites →https://doi.org/10.1016/s0014-5793(01)02361-4openalex-snapshot
Binding of tenascin‐X to decorin
inferredcites →https://doi.org/10.1016/s0021-9258(18)98545-5openalex-snapshot
Extracellular proteins that modulate cell-matrix interactions. SPARC, tenascin, and thrombospondin
inferredcites →https://doi.org/10.1016/s0021-9258(20)89510-6openalex-snapshot
Syndecan from embryonic tooth mesenchyme binds tenascin.
inferredcites →https://doi.org/10.1016/s0022-510x(00)00347-6openalex-snapshot
Immunohistochemical markers for intracranial ependymoma recurrence
inferredcites →https://doi.org/10.1016/s0079-6123(01)32069-1openalex-snapshot
Tenascin-R as a regulator of CNS glial cell function
inferredcites →https://doi.org/10.1016/s0090-3019(00)00307-4openalex-snapshot
Expression of tenascin-C in astrocytic tumors: its relevance to proliferation and angiogenesis
inferredcites →https://doi.org/10.1016/s0344-0338(99)80113-7openalex-snapshot
Enhanced Tenascin Expression Correlates with Inflammation in Primary Sclerosing Cholangitis
inferredcites →https://doi.org/10.1016/s0923-1811(96)00570-1openalex-snapshot
Recruitment of cycling epidermal cells and expression of filaggrin, involucrin and tenascin in the margin of the active psoriatic plaque, in the uninvolved skin of psoriatic patients and in the normal healthy skin
inferredcites →https://doi.org/10.1016/s0945-053x(00)00106-2openalex-snapshot
Tenascin-C in development and disease: gene regulation and cell function
inferredcites →https://doi.org/10.1016/s0945-053x(00)00136-0openalex-snapshot
The structure and function of tenascins in the nervous system
inferredcites →https://doi.org/10.1016/s0945-053x(03)00004-0openalex-snapshot
How do fibroblasts translate mechanical signals into changes in extracellular matrix production?
inferredcites →https://doi.org/10.1016/s0945-053x(98)90083-xopenalex-snapshot
Tenascin-C expression in human epidermal keratinocytes is regulated by inflammatory cytokines and a stress response pathway
inferredcites →https://doi.org/10.1016/s0945-053x(99)00039-6openalex-snapshot
Regulation of extracellular matrix gene expression by mechanical stress
inferredcites →https://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
inferredcites →https://doi.org/10.1016/s0959-8049(98)00215-9openalex-snapshot
Expression of Tenascin-C in intraductal carcinoma of human breast: relationship to invasion
inferredcites →https://doi.org/10.1016/s1359-6101(02)00026-6openalex-snapshot
Regulation of cytokine signaling and inflammation
inferredcites →https://doi.org/10.1016/s1368-8375(01)00062-8openalex-snapshot
Tenascin and β6 integrin are overexpressed in floor of mouth in situ carcinomas and invasive squamous cell carcinomas
inferredcites →https://doi.org/10.1016/s8756-3282(97)00297-4openalex-snapshot
Regulation of Tenascin-C Expression in Bone Cells by Transforming Growth Factor-β
inferredcites →https://doi.org/10.1034/j.1600-0781.2000.160401.xopenalex-snapshot
A full‐UV spectrum absorbing daily use cream protects human skin against biological changes occurring in photoaging
inferredcites →https://doi.org/10.1038/307364a0openalex-snapshot
Prevention of gastrulation but not neurulation by antibodies to fibronectin in amphibian embryos
inferredcites →https://doi.org/10.1038/bjc.1996.480openalex-snapshot
Expression of the extracellular matrix protein tenascin in malignant and benign ovarian tumours
inferredcites →https://doi.org/10.1038/bjc.1998.15openalex-snapshot
Expression and degeneration of tenascin-C in human lung cancers
inferredcites →https://doi.org/10.1038/ng0997-104openalex-snapshot
Tenascin–X deficiency is associated with Ehlers–Danlos syndrome
inferredcites →https://doi.org/10.1038/ng850openalex-snapshot
Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition
inferredcites →https://doi.org/10.1038/sj.onc.1203360openalex-snapshot
Ets transcription factors cooperate with Sp1 to activate the human Tenascin-C promoter
inferredcites →https://doi.org/10.1038/sj.onc.1205726openalex-snapshot
Identification of differentially expressed genes in pulmonary adenocarcinoma by using cDNA array
inferredcites →https://doi.org/10.1046/j.1365-2133.1999.02920.xopenalex-snapshot
Increased expression of tenascin C by keloids in vivo and in vitro
inferredcites →https://doi.org/10.1046/j.1432-0436.1997.6220071.xopenalex-snapshot
The expression of tenascin-C with the AD1 variable repeat in embryonic tissues, cell lines and tumors in various vertebrate species
inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00563.xopenalex-snapshot
Cell adhesion to tenascin‐X
inferredcites →https://doi.org/10.1046/j.1523-1747.1998.00401.xopenalex-snapshot
Effect of Tenascin-C Deficiency on Chemically Induced Dermatitis in the Mouse
inferredcites →https://doi.org/10.1046/j.1523-1747.1999.00802.xopenalex-snapshot
Spatiotemporal Changes of Fibronectin, Tenascin-C, Fibulin-1, and Fibulin-2 in the Skin During the Development of Chronic Contact Dermatitis
inferredcites →https://doi.org/10.1056/nejmoa002939openalex-snapshot
A Recessive Form of the Ehlers–Danlos Syndrome Caused by Tenascin-X Deficiency
inferredcites →https://doi.org/10.1073/pnas.86.17.6582openalex-snapshot
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus.
inferredcites →https://doi.org/10.1073/pnas.86.19.7437openalex-snapshot
Tenascin, an extracellular matrix protein, exerts immunomodulatory activities.
inferredcites →https://doi.org/10.1073/pnas.96.6.2805openalex-snapshot
Syndecan-4 signals cooperatively with integrins in a Rhodependent manner in the assembly of focal adhesions and actin stress fibers
inferredcites →https://doi.org/10.1074/jbc.272.24.15501openalex-snapshot
The Fibrinogen-like Globe of Tenascin-C Mediates Its Interactions with Neurocan and Phosphacan/Protein-tyrosine Phosphatase-ζ/β
inferredcites →https://doi.org/10.1074/jbc.274.31.21840openalex-snapshot
Induction of Tenascin-C in Cardiac Myocytes by Mechanical Deformation
inferredcites →https://doi.org/10.1074/jbc.m010210200openalex-snapshot
Identification and Characterization of a Conformational Heparin-binding Site Involving Two Fibronectin Type III Modules of Bovine Tenascin-X
inferredcites →https://doi.org/10.1074/jbc.m104651200openalex-snapshot
Tenascin-C Aptamers Are Generated Using Tumor Cells and Purified Protein
inferredcites →https://doi.org/10.1078/0171-9335-00181openalex-snapshot
Coordinated regulation of procollagens I and III and their post-translational enzymes by dissipation of mechanical tension in human dermal fibroblasts
inferredcites →https://doi.org/10.1080/028418699431438openalex-snapshot
131I Radioconjugated Antibodies for the Locoregional Radioimmunotherapy of High-grade Malignant Glioma: Phase I and II Study
inferredcites →https://doi.org/10.1083/jcb.107.6.2757openalex-snapshot
Induction of tenascin in healing wounds.
inferredcites →https://doi.org/10.1083/jcb.109.4.1795openalex-snapshot
Cell adhesion to fibronectin and tenascin: quantitative measurements of initial binding and subsequent strengthening response.
inferredcites →https://doi.org/10.1083/jcb.115.4.1127openalex-snapshot
Focal adhesion integrity is downregulated by the alternatively spliced domain of human tenascin [published erratum appears in J Cell Biol 1992 Feb;116(3):833]
inferredcites →https://doi.org/10.1083/jcb.117.1.73openalex-snapshot
Isometric contraction by fibroblasts and endothelial cells in tissue culture: a quantitative study
inferredcites →https://doi.org/10.1083/jcb.122.1.265openalex-snapshot
Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B
inferredcites →https://doi.org/10.1083/jcb.124.4.401openalex-snapshot
Fibroblasts, myofibroblasts, and wound contraction
inferredcites →https://doi.org/10.1083/jcb.125.2.483openalex-snapshot
The distribution of tenascin-X is distinct and often reciprocal to that of tenascin-C.
inferredcites →https://doi.org/10.1083/jcb.127.6.2093openalex-snapshot
Tenascin-C expression by fibroblasts is elevated in stressed collagen gels.
inferredcites →https://doi.org/10.1083/jcb.134.6.1499openalex-snapshot
Tenascin-Y: a protein of novel domain structure is secreted by differentiated fibroblasts of muscle connective tissue.
inferredcites →https://doi.org/10.1083/jcb.200206109openalex-snapshot
Tenascin-C signaling through induction of 14-3-3 tau
inferredcites →https://doi.org/10.1083/jcb.98.6.1937openalex-snapshot
Chick myotendinous antigen. II. A novel extracellular glycoprotein complex consisting of large disulfide-linked subunits.
inferredcites →https://doi.org/10.1091/mbc.10.9.2933openalex-snapshot
The Fibrinogen Globe of Tenascin-C Promotes Basic Fibroblast Growth Factor-induced Endothelial Cell Elongation
inferredcites →https://doi.org/10.1091/mbc.e02-05-0292openalex-snapshot
Tenascin-C Modulates Matrix Contraction via Focal Adhesion Kinase– and Rho-mediated Signaling Pathways
inferredcites →https://doi.org/10.1093/ajcp/100.2.145openalex-snapshot
Tenascin Immunoreactivity in Lung Tumors
inferredcites →https://doi.org/10.1093/hmg/11.21.2581openalex-snapshot
Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB -TNXA hybrids in apparent large-scale gene conversions
inferredcites →https://doi.org/10.1093/nar/21.1.163openalex-snapshot
A novel tenascin type III repeat is part of a complex of tenascin mRNA alternative splices
inferredcites →https://doi.org/10.1097/00003086-199810001-00006openalex-snapshot
Mechanobiology of Skeletal Regeneration
inferredcites →https://doi.org/10.1097/00004424-199306000-00003openalex-snapshot
Distribution and Dosimetry of I-123-Labeled Monoclonal Antibody 81C6 in Patients with Anaplastic Glioma
inferredcites →https://doi.org/10.1097/00005537-200001000-00016openalex-snapshot
Characteristic Distribution Patterns of Tenascin in Laryngeal and Hypopharyngeal Cancers
inferredcites →https://doi.org/10.1097/00006123-199711000-00007openalex-snapshot
Tenascin-C Expression in the Cyst Wall and Fluid of Human Brain Tumors Correlates with Angiogenesis
inferredcites →https://doi.org/10.1097/00006123-200204000-00028openalex-snapshot
Occurrence of a Glioblastoma-associated Tenascin-C Isoform in Cerebral Cavernomas and Neighboring Vessels
inferredcites →https://doi.org/10.1111/1523-1747.ep12331160openalex-snapshot
IL-4 Upregulates Tenascin Synthesis in Scleroderma and Healthy Skin Fibroblasts
inferredcites →https://doi.org/10.1111/j.1365-2133.1991.tb03276.xopenalex-snapshot
Tenascin expression in hyperproliferative skin diseases
inferredcites →https://doi.org/10.1111/j.1365-2133.1994.tb13102.xopenalex-snapshot
Investigation of the expression of the extracellular matrix glycoproteins tenascin and fibronectin during acne vulgaris
inferredcites →https://doi.org/10.1111/j.1365-2133.1995.tb02486.xopenalex-snapshot
Dermo-epidermal separation is associated with induced tenascin expression in human skin
inferredcites →https://doi.org/10.1111/j.1365-2559.1994.tb01268.xopenalex-snapshot
The extracellular matrix in pigmented skin lesions: an immunohistochemical study
inferredcites →https://doi.org/10.1111/j.1600-0560.1994.tb00284.xopenalex-snapshot
Increased tenascin expression in melanocytic tumors
inferredcites →https://doi.org/10.1111/j.1749-6632.2001.tb03931.xopenalex-snapshot
Perivascular Responses after Angioplasty Which May Contribute to Postangioplasty Restenosis
inferredcites →https://doi.org/10.1128/mcb.12.5.2124openalex-snapshot
Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus.
inferredcites →https://doi.org/10.1128/mcb.17.6.3202openalex-snapshot
The c-Jun-Induced Transformation Process Involves Complex Regulation of Tenascin-C Expression†
inferredcites →https://doi.org/10.1136/thorax.58.2.135openalex-snapshot
Relationship between inflammatory cells and structural changes in the lungs of asymptomatic and never smokers: a biopsy study
inferredcites →https://doi.org/10.1152/ajplung.1998.274.6.l1049openalex-snapshot
Induction of tenascin in rat lungs undergoing bleomycin-induced pulmonary fibrosis
inferredcites →https://doi.org/10.1152/ajpregu.00060.2002openalex-snapshot
Reloading of atrophied rat soleus muscle induces tenascin-C expression around damaged muscle fibers
inferredcites →https://doi.org/10.1159/000019099openalex-snapshot
An Unequal Crossover between the RCCX Modules of the Human MHC Leading to the Presence of a CYP21B Gene and a Tenascin TNXB/TNXA-RP2 Recombinant between C4A and C4B Genes in a Patient with Juvenile Rheumatoid Arthritis
inferredcites →https://doi.org/10.1159/000055338openalex-snapshot
The Clinical Significance of Tenascin-C Splice Variant Expression in Chondrosarcoma
inferredcites →https://doi.org/10.1159/000063713openalex-snapshot
Decorin Expression during Development of Bovine Skeletal Muscle and Its Role in Morphogenesis of the Intramuscular Connective Tissue
inferredcites →https://doi.org/10.1159/000211446openalex-snapshot
Effects of Calcipotriol and Clobetasol-17-Propionate on UVB-lrradiated Human Skin: An Immunohistochemical Study
inferredcites →https://doi.org/10.1161/01.cir.99.10.1284openalex-snapshot
Tenascin-C Is Expressed in Macrophage-Rich Human Coronary Atherosclerotic Plaque
inferredcites →https://doi.org/10.1161/hh1401.093582openalex-snapshot
Prx1 Controls Vascular Smooth Muscle Cell Proliferation and Tenascin-C Expression and Is Upregulated With Prx2 in Pulmonary Vascular Disease
inferredcites →https://doi.org/10.1164/ajrccm.154.2.8756830openalex-snapshot
Tenascin Immunoreactivity as a Prognostic Marker in Usual Interstitial Pneumonia
inferredcites →https://doi.org/10.1164/ajrccm.156.3.9610084openalex-snapshot
Tenascin Is Increased in Airway Basement Membrane of Asthmatics and Decreased by an Inhaled Steroid
inferredcites →https://doi.org/10.1164/ajrccm.161.6.9907025openalex-snapshot
Evidence of Airway Inflammation and Remodeling in Ski Athletes with and without Bronchial Hyperresponsiveness to Methacholine
inferredcites →https://doi.org/10.1164/ajrccm.162.6.9912001openalex-snapshot
Inflammation and Structural Changes in the Airways of Patients with Atopic and Nonatopic Asthma
inferredcites →https://doi.org/10.1172/jci12881openalex-snapshot
The Ehlers-Danlos syndrome: on beyond collagens
inferredcites →https://doi.org/10.1177/0006355x2003040001003045openalex-snapshot
The role of tenascin‐C in adaptation of tendons to compressive loading
inferredcites →https://doi.org/10.1186/1471-2121-3-13openalex-snapshot
The CXC chemokine cCAF stimulates precocious deposition of ECM molecules by wound fibroblasts, accelerating development of granulation tissue
inferredcites →https://doi.org/10.1200/jco.1998.16.6.2202openalex-snapshot
Iodine-131-labeled antitenascin monoclonal antibody 81C6 treatment of patients with recurrent malignant gliomas: phase I trial results.
inferredcites →https://doi.org/10.1200/jco.20.5.1389openalex-snapshot
Phase II Trial of Murine 131I-Labeled Antitenascin Monoclonal Antibody 81C6 Administered Into Surgically Created Resection Cavities of Patients With Newly Diagnosed Malignant Gliomas
inferredcites →https://doi.org/10.1200/jco.2002.20.5.1389openalex-snapshot
Phase II Trial of Murine 131I-Labeled Antitenascin Monoclonal Antibody 81C6 Administered Into Surgically Created Resection Cavities of Patients With Newly Diagnosed Malignant Gliomas
inferredcites →https://doi.org/10.1242/dev.128.13.2485openalex-snapshot
Knockout mice reveal a contribution of the extracellular matrix molecule tenascin-C to neural precursor proliferation and migration
inferredcites →https://doi.org/10.1242/jcs.106.2.597openalex-snapshot
Dual function of tenascin: simultaneous promotion of neurite growth and inhibition of glial migration
inferredcites →https://doi.org/10.1242/jcs.107.2.487openalex-snapshot
Induction of human tenascin (neuronectin) by growth factors and cytokines: cell type-specific signals and signalling pathways
inferredcites →https://doi.org/10.1242/jcs.110.13.1513openalex-snapshot
Concerted action of tenascin-C domains in cell adhesion, anti-adhesion and promotion of neurite outgrowth
inferredcites →https://doi.org/10.1242/jcs.112.18.3157openalex-snapshot
Mechanical loading regulates tenascin-C expression in the osteotendinous junction
inferredcites →https://doi.org/10.1242/jcs.113.20.3583openalex-snapshot
Rapid and reciprocal regulation of tenascin-C and tenascin-Y expression by loading of skeletal muscle
inferredcites →https://doi.org/10.1242/jcs.95.2.263openalex-snapshot
Binding of hexabrachion (tenascin) to the extracellular matrix and substratum and its effect on cell adhesion
inferredcites →https://doi.org/10.1359/jbmr.1997.12.1.52openalex-snapshot
Expression of Tenascin-C in Bones Responding to Mechanical Load
inferredcites →https://doi.org/10.1359/jbmr.2002.17.7.1180openalex-snapshot
Phenotypic Effects of Biglycan Deficiency Are Linked to Collagen Fibril Abnormalities, Are Synergized by Decorin Deficiency, and Mimic Ehlers-Danlos-Like Changes in Bone and Other Connective Tissues
inferredcites →https://doi.org/10.14670/hh-17.301openalex-snapshot
Angiogenesis in the central nervous system: a role for vascular endothelial growth factor/vascular permeability factor and tenascin-C. Common molecular effectors in cerebral neoplastic and non-neoplastic "angiogenic diseases".
inferredcites →https://doi.org/10.1523/jneurosci.18-16-06218.1998openalex-snapshot
Tenascin-R Is Antiadhesive for Activated Microglia that Induce Downregulation of the Protein after Peripheral Nerve Injury: a New Role in Neuronal Protection
inferredcites →https://doi.org/10.2174/1381612003399275openalex-snapshot
Astatine-211-Labeled Radiotherapeutics An Emerging Approach to Targeted Alpha-Particle Radiotherapy
inferredcites →https://doi.org/10.2174/1566524024605699openalex-snapshot
Function of Cytokines within the TGF-β Superfamily as Determined from Transgenic and Gene Knockout Studies in Mice
inferredcites →https://doi.org/10.2307/3579787openalex-snapshot
Unlike Tenascin-X, Tenascin-C Is Highly Up-Regulated in Pig Cutaneous and Underlying Muscle Tissue Developing Fibrosis after Necrosis Induced by Very High-Dose Gamma Radiation
inferredcites →https://doi.org/10.3109/10428199609054786openalex-snapshot
Expression of Tenascin is Related to Histologic Malignancy and Angiogenesis in B-Cell non-Hodgkin's Lymphomas
inferredcites →https://doi.org/10.3892/ijmm.5.5.505openalex-snapshot
Clinical significance of tenascin-C expression in osteosarcoma: tenascin-C promotes distant metastases of osteosarcoma.
inferredcites →https://doi.org/10.4049/jimmunol.166.12.7534openalex-snapshot
Blockade of α5β1 Integrins Reverses the Inhibitory Effect of Tenascin on Chemotaxis of Human Monocytes and Polymorphonuclear Leukocytes Through Three-Dimensional Gels of Extracellular Matrix Proteins
inferredcites →https://doi.org/10.4049/jimmunol.169.8.4604openalex-snapshot
The Relationship Between Allergen-Induced Tissue Eosinophilia and Markers of Repair and Remodeling in Human Atopic Skin
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4683475openalex-extracted
The Role of Tenascin C in Central Nervous System Diseases
inferred← citeshttps://doi.org/10.1001/archotol.134.5.539openalex-snapshot
Examination of Oral Cancer Biomarkers by Tissue Microarray Analysis
inferred← citeshttps://doi.org/10.1002/9781118704509.ch6openalex-snapshot
Granulation Tissue Formation and Remodeling
inferred← citeshttps://doi.org/10.1002/adbi.202300448openalex-snapshot
Comprehensive Matrisome Profiling of Human Adipose Tissue for Soft Tissue Reconstruction
inferred← citeshttps://doi.org/10.1002/art.20488openalex-snapshot
Joint hypermobility syndromes: The pathophysiologic role of tenascin‐X gene defects
inferred← citeshttps://doi.org/10.1002/cyto.a.21028openalex-snapshot
Cell cycle dependent TN‐C promoter activity determined by live cell imaging
inferred← citeshttps://doi.org/10.1002/dvdy.20731openalex-snapshot
Avian tenascin‐W: Expression in smooth muscle and bone, and effects on calvarial cell spreading and adhesion in vitro
inferred← citeshttps://doi.org/10.1002/eji.200636271openalex-snapshot
Deficiency of tenascin C attenuates allergen‐induced bronchial asthma in the mouse
inferred← citeshttps://doi.org/10.1002/glia.20721openalex-snapshot
A new in vitro model of the glial scar inhibits axon growth
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/jcb.21215openalex-snapshot
Mechanisms of metastasis: Epithelial‐to‐mesenchymal transition and contribution of tumor microenvironment
inferred← citeshttps://doi.org/10.1002/jcb.23265openalex-snapshot
Regulation of tenascin expression in bone
inferred← citeshttps://doi.org/10.1002/jmri.22869openalex-snapshot
Gadofluorine M enhanced MRI in experimental glioma: Superior and persistent intracellular tumor enhancement compared with conventional MRI
inferred← citeshttps://doi.org/10.1002/jnr.23773openalex-snapshot
A microglial hypothesis of globoid cell leukodystrophy pathology
inferred← citeshttps://doi.org/10.1002/jnr.24330openalex-snapshot
Tenascin‐C in brain injuries and edema after subarachnoid hemorrhage: Findings from basic and clinical studies
inferred← citeshttps://doi.org/10.1002/jor.20092openalex-snapshot
Achilles Tendon characterization in GDF-7 deficient mice
inferred← citeshttps://doi.org/10.1002/jor.21074openalex-snapshot
The effect of high‐energy extracorporeal shock waves on hyaline cartilage of adult rats in vivo
inferred← citeshttps://doi.org/10.1002/jor.21112openalex-snapshot
Role of myostatin (GDF‐8) signaling in the human anterior cruciate ligament
inferred← citeshttps://doi.org/10.1002/lt.25365openalex-snapshot
Overproduction of Tenascin‐C Driven by Lipid Accumulation in the Liver Aggravates Hepatic Ischemia/Reperfusion Injury in Steatotic Mice
inferred← citeshttps://doi.org/10.1002/path.1438openalex-snapshot
Preface to extracellular matrix and disease
inferred← citeshttps://doi.org/10.1002/path.1589openalex-snapshot
mRNA expression and protein distribution of the unspliced tenascin‐C isoform in prostatic adenocarcinoma
inferred← citeshttps://doi.org/10.1002/path.1730openalex-snapshot
Diagnostic utility of tenascin‐C for evaluation of the activity of human acute myocarditis
inferred← citeshttps://doi.org/10.1002/path.1935openalex-snapshot
Tenascin C and annexin II expression in the process of pancreatic carcinogenesis
inferred← citeshttps://doi.org/10.1002/path.2099openalex-snapshot
Deficiency of tenascin‐C attenuates liver fibrosis in immune‐mediated chronic hepatitis in mice
inferred← citeshttps://doi.org/10.1002/path.4104openalex-snapshot
The myofibroblast matrix: implications for tissue repair and fibrosis
inferred← citeshttps://doi.org/10.1002/pmic.201400088openalex-snapshot
MALDI imaging mass spectrometry: Discrimination of pathophysiological regions in traumatized skeletal muscle by characteristic peptide signatures
inferred← citeshttps://doi.org/10.1002/pmic.202300242openalex-snapshot
Proteomic profiling of ovarian clear cell carcinomas identifies prognostic biomarkers for chemotherapy
inferred← citeshttps://doi.org/10.1002/ppul.20252openalex-snapshot
Similarities and dissimilarities of branching and septation during lung development
inferred← citeshttps://doi.org/10.1002/pro.503openalex-snapshot
Phenotypic effects of Ehlers–Danlos syndrome‐associated mutation on the FnIII domain of tenascin‐X
inferred← citeshttps://doi.org/10.1007/0-387-31389-3_7openalex-snapshot
The Subventricular Zone Responds Dynamically to Mechanical Brain Injuries
inferred← citeshttps://doi.org/10.1007/0-387-33650-8_9openalex-snapshot
Pro-Invasive Molecular Cross-Signaling between Cancer Cells and Myofibroblasts
inferred← citeshttps://doi.org/10.1007/3-211-26392-6_129openalex-snapshot
Collagen and Elastic Fibres
inferred← citeshttps://doi.org/10.1007/3-211-30826-1_133openalex-snapshot
Kollagene und Elastische Fasern
inferred← citeshttps://doi.org/10.1007/978-0-387-32562-0_12openalex-snapshot
Extracellular Matrix Molecules and Formation of CNS Synapses
inferred← citeshttps://doi.org/10.1007/978-1-4614-6438-9_101622-1openalex-snapshot
Tenascin-C (TNC, Tnc)
inferred← citeshttps://doi.org/10.1007/978-3-030-40146-7_1openalex-snapshot
The Tumor Microenvironment: Focus on Extracellular Matrix
inferred← citeshttps://doi.org/10.1007/978-3-030-48457-6_9openalex-snapshot
Tenascin-C Function in Glioma: Immunomodulation and Beyond
inferred← citeshttps://doi.org/10.1007/978-3-030-80614-9_4openalex-snapshot
Basic Components of Connective Tissues and Extracellular Matrix: Fibronectin, Fibrinogen, Laminin, Elastin, Fibrillins, Fibulins, Matrilins, Tenascins and Thrombospondins
inferred← citeshttps://doi.org/10.1007/978-3-030-92090-6_1-1openalex-snapshot
Composition of the Extracellular Matrix
inferred← citeshttps://doi.org/10.1007/978-3-030-98950-7_5openalex-snapshot
Role of the Extracellular Matrix in Tumor Stroma: Barrier or Support?
inferred← citeshttps://doi.org/10.1007/978-3-031-48067-6_6openalex-snapshot
Carbon Monoxide Against Ischemia-Reperfusion Injury: A Tour into the Immune System
inferred← citeshttps://doi.org/10.1007/978-3-031-56363-8_1openalex-snapshot
Composition of the Extracellular Matrix
inferred← citeshttps://doi.org/10.1007/978-3-031-89844-0_2openalex-snapshot
Tenascin-C as a Target for Intervention in Delayed Cerebral Ischemia After Subarachnoid Hemorrhage
inferred← citeshttps://doi.org/10.1007/978-3-211-75718-5_35openalex-snapshot
Possible role of tenascin-C in cerebral vasospasm after aneurysmal subarachnoid haemorrhage
inferred← citeshttps://doi.org/10.1007/978-3-211-99390-3_143openalex-snapshot
Collagen and Elastic Fibres
inferred← citeshttps://doi.org/10.1007/978-3-319-04981-6_20openalex-snapshot
Tenascin-C Is a Possible Mediator Between Initial Brain Injury and Vasospasm-Related and -Unrelated Delayed Cerebral Ischemia After Aneurysmal Subarachnoid Hemorrhage
inferred← citeshttps://doi.org/10.1007/978-3-319-16724-4_5openalex-snapshot
Classification of Chronic Rhinosinusitis and Its Subsets
inferred← citeshttps://doi.org/10.1007/978-3-319-26594-0_124-1openalex-snapshot
Fibroblast Evaluation: Extracellular Matrix Synthesis
inferred← citeshttps://doi.org/10.1007/978-3-319-32383-1_124openalex-snapshot
Fibroblast Evaluation: Extracellular Matrix Synthesis
inferred← citeshttps://doi.org/10.1007/978-3-319-39147-2_4openalex-snapshot
Role of the Extracellular Matrix in Tumor Stroma: Barrier or Support?
inferred← citeshttps://doi.org/10.1007/978-3-319-67199-4_101622openalex-snapshot
Tenascin-C (TNC, Tnc)
inferred← citeshttps://doi.org/10.1007/978-3-319-77997-3_2openalex-snapshot
Staining Techniques and Microscopy
inferred← citeshttps://doi.org/10.1007/978-3-642-00475-9_10openalex-snapshot
Nanosystems for the Delivery of RNAi
inferred← citeshttps://doi.org/10.1007/978-3-642-00475-9_11openalex-snapshot
Interference RNA Intervention in Brain Tumors
inferred← citeshttps://doi.org/10.1007/978-3-642-16555-9_1openalex-snapshot
An Overview of Extracellular Matrix Structure and Function
inferred← citeshttps://doi.org/10.1007/978-3-642-20659-7_2openalex-snapshot
Staining Techniques and Microscopy
inferred← citeshttps://doi.org/10.1007/978-94-007-7893-1_3openalex-snapshot
Basic Components of Connective Tissues and Extracellular Matrix: Elastin, Fibrillin, Fibulins, Fibrinogen, Fibronectin, Laminin, Tenascins and Thrombospondins
inferred← citeshttps://doi.org/10.1007/978-981-19-1364-8_10openalex-snapshot
Congenital X-Linked Retinoschisis
inferred← citeshttps://doi.org/10.1007/978-981-32-9636-7_8openalex-snapshot
Under the ECM Dome: The Physiological Role of the Perinodal Extracellular Matrix as an Ion Diffusion Barrier
inferred← citeshttps://doi.org/10.1007/bf02893856openalex-snapshot
Distribution pattern of Tenascin-C in glioblastoma: Correlation with angiogenesis and tumor cell proliferation
inferred← citeshttps://doi.org/10.1007/s00018-007-6419-1openalex-snapshot
Sulfatide-tenascin interaction mediates binding to the extracellular matrix and endocytic uptake of liposomes in glioma cells
inferred← citeshttps://doi.org/10.1007/s00018-011-0783-6openalex-snapshot
Advances in tenascin-C biology
inferred← citeshttps://doi.org/10.1007/s00018-013-1356-7openalex-snapshot
Damage-associated molecular patterns and their receptors in upper airway pathologies
inferred← citeshttps://doi.org/10.1007/s00125-020-05108-5openalex-snapshot
Serum tenascin-C is independently associated with increased major adverse cardiovascular events and death in individuals with type 2 diabetes: a French prospective cohort
inferred← citeshttps://doi.org/10.1007/s00380-013-0341-2openalex-snapshot
Serum tenascin-C level is associated with coronary plaque rupture in patients with acute coronary syndrome
inferred← citeshttps://doi.org/10.1007/s00408-012-9400-1openalex-snapshot
Elevated Tenascin-C Levels in Bronchoalveolar Lavage Fluid of Patients with Sarcoidosis
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/s00418-026-02516-3openalex-snapshot
Longitudinal progression of tissue remodeling in experimental pulmonary hypertension is accompanied by a continuously increasing re-expression of extra domain A-containing fibronectin
inferred← citeshttps://doi.org/10.1007/s00428-011-1088-8openalex-snapshot
Immunohistochemical study of stromal and vascular components of tonsillar polyps: high endothelial venules as participants of the polyp’s lymphoid tissue
inferred← citeshttps://doi.org/10.1007/s00428-025-04088-4openalex-snapshot
Dermatofibrosarcoma protuberans with PDGFD rearrangements: a case series featuring a novel EMILIN1::PDGFD fusion and comprehensive literature review
inferred← citeshttps://doi.org/10.1007/s00441-008-0715-4openalex-snapshot
Effects of tenascin-W on osteoblasts in vitro
inferred← citeshttps://doi.org/10.1007/s00441-011-1313-4openalex-snapshot
The laser lesion of the mouse visual cortex as a model to study neural extracellular matrix remodeling during degeneration, regeneration and plasticity of the CNS
inferred← citeshttps://doi.org/10.1007/s00441-013-1704-9openalex-snapshot
Tenascin-C is expressed by human glioma in vivo and shows a strong association with tumor blood vessels
inferred← citeshttps://doi.org/10.1007/s00441-021-03416-9openalex-snapshot
Cyclically stretched ACL fibroblasts emigrating from spheroids adapt their cytoskeleton and ligament-related expression profile
inferred← citeshttps://doi.org/10.1007/s10059-012-0054-xopenalex-snapshot
Tenascin-C Produced by Oxidized LDL-Stimulated Macrophages Increases Foam Cell Formation through Toll-like Receptor-4
inferred← citeshttps://doi.org/10.1007/s10103-014-1691-4openalex-snapshot
Increased cell proliferation and differential protein expression induced by low-level Er:YAG laser irradiation in human gingival fibroblasts: proteomic analysis
inferred← citeshttps://doi.org/10.1007/s10237-005-0012-zopenalex-snapshot
An Introductory Review of Cell Mechanobiology
inferred← citeshttps://doi.org/10.1007/s10238-009-0057-xopenalex-snapshot
Differential expression of tenascin-C in the developing human lung: an immunohistochemical study
inferred← citeshttps://doi.org/10.1007/s10495-015-1106-4openalex-snapshot
Tenascin-C induces resistance to apoptosis in pancreatic cancer cell through activation of ERK/NF-κB pathway
inferred← citeshttps://doi.org/10.1007/s10555-010-9249-9openalex-snapshot
Expression of tenascin-C and its isoforms in the breast
inferred← citeshttps://doi.org/10.1007/s10571-011-9759-1openalex-snapshot
Existence of Tenascin-C Isoforms in Rat that Contain the Alternatively Spliced AD1 Domain are Developmentally Regulated During Hippocampal Development
inferred← citeshttps://doi.org/10.1007/s10571-015-0170-1openalex-snapshot
Extracellular Matrix Glycoprotein-Derived Synthetic Peptides Differentially Modulate Glioma and Sarcoma Cell Migration
inferred← citeshttps://doi.org/10.1007/s10911-010-9189-6openalex-snapshot
Extracellular Matrix Composition Reveals Complex and Dynamic Stromal-Epithelial Interactions in the Mammary Gland
inferred← citeshttps://doi.org/10.1007/s12020-022-03027-6openalex-snapshot
Assessment of circulating fibrotic proteins (periostin and tenascin -C) In Type 2 diabetes mellitus patients with and without retinopathy
inferred← citeshttps://doi.org/10.1007/s12035-015-9386-9openalex-snapshot
Anti-Vascular Endothelial Growth Factor Treatment Suppresses Early Brain Injury After Subarachnoid Hemorrhage in Mice
inferred← citeshttps://doi.org/10.1007/s12079-009-0075-1openalex-snapshot
The role of tenascin-C in tissue injury and tumorigenesis
inferred← citeshttps://doi.org/10.1007/s12079-017-0413-7openalex-snapshot
The role of α9β1 integrin and its ligands in the development of autoimmune diseases
inferred← citeshttps://doi.org/10.1007/s12105-011-0265-zopenalex-snapshot
Tenascin-C in Chronic Sclerosing Sialadenitis
inferred← citeshttps://doi.org/10.1007/s12975-014-0333-2openalex-snapshot
Tenascin-C Causes Neuronal Apoptosis After Subarachnoid Hemorrhage in Rats
inferred← citeshttps://doi.org/10.1007/s13277-016-5162-3openalex-snapshot
Proteomic analysis of differentially expressed proteins in vitreous humor of patients with retinoblastoma using iTRAQ-coupled ESI-MS/MS approach
inferred← citeshttps://doi.org/10.1007/s13402-022-00700-wopenalex-snapshot
Immunotherapy and immunoengineering for breast cancer; a comprehensive insight into CAR-T cell therapy advancements, challenges and prospects
inferred← citeshttps://doi.org/10.1007/s42485-022-00092-3openalex-snapshot
Mass spectrometric analysis of chondroitin sulfate-linked peptides
inferred← citeshttps://doi.org/10.1016/b0-12-370879-6/00148-4openalex-snapshot
EXTRACELLULAR MATRIX | Matricellular Proteins
inferred← citeshttps://doi.org/10.1016/b978-0-12-397157-9.00003-5openalex-snapshot
Extracellular Matrix (ECM) Molecules
inferred← citeshttps://doi.org/10.1016/b978-0-12-407696-9.00006-3openalex-snapshot
Prospective Potency of TGF-β1 on Maintenance and Regeneration of Periodontal Tissue
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.21353-8openalex-snapshot
Structural Proteins | Major Proteins of the Extracellular Matrix
inferred← citeshttps://doi.org/10.1016/b978-0-12-816193-7.00015-4openalex-snapshot
Genetics of musculoskeletal soft tissue injuries: Current status, challenges, and future directions
inferred← citeshttps://doi.org/10.1016/b978-0-443-15840-7.00013-0openalex-snapshot
Toxicant-induced injury and tissue repair
inferred← citeshttps://doi.org/10.1016/b978-0-444-52137-8.00001-2openalex-snapshot
Development and maturation of the spinal cord
inferred← citeshttps://doi.org/10.1016/b978-0-444-63486-3.00003-7openalex-snapshot
Neural ECM molecules in synaptic plasticity, learning, and memory
inferred← citeshttps://doi.org/10.1016/j.actbio.2013.01.002openalex-snapshot
Towards constructing extracellular matrix-mimetic hydrogels: An elastic hydrogel constructed from tandem modular proteins containing tenascin FnIII domains
inferred← citeshttps://doi.org/10.1016/j.acthis.2014.05.007openalex-snapshot
Temporal expression of tenascin-C and type I collagen in response to gonadotropins in the immature rat ovary
inferred← citeshttps://doi.org/10.1016/j.acthis.2014.06.006openalex-snapshot
Infrared LED light therapy influences the expression of fibronectin and tenascin in skin wounds of malnourished rats—A preliminary study
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2010.11.038openalex-snapshot
High circulating levels of large splice variants of tenascin-C is associated with mortality and cardiovascular disease in chronic kidney disease patients
inferred← citeshttps://doi.org/10.1016/j.bbadis.2007.11.001openalex-snapshot
Tenascin C interacts with Ecto-5′-nucleotidase (eN) and regulates adenosine generation in cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbadis.2013.01.003openalex-snapshot
Cleavage of extracellular matrix in periodontitis: Gingipains differentially affect cell adhesion activities of fibronectin and tenascin-C
inferred← citeshttps://doi.org/10.1016/j.bbagen.2017.06.010openalex-snapshot
Formation and remodeling of the brain extracellular matrix in neural plasticity: Roles of chondroitin sulfate and hyaluronan
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2007.11.012openalex-snapshot
GATA-6 is a novel transcriptional repressor of the human Tenascin-C gene expression in fibroblasts
inferred← citeshttps://doi.org/10.1016/j.bbalip.2022.159207openalex-snapshot
Vascular and lymphatic regulation of gastrointestinal function and disease risk
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2004.08.001openalex-snapshot
Induction of tenascin-C by cyclic tensile strain versus growth factors: distinct contributions by Rho/ROCK and MAPK signaling pathways
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.01.013openalex-snapshot
Tenascin-C induction by cyclic strain requires integrin-linked kinase
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.12.012openalex-snapshot
The regulation of tenascin expression by tissue microenvironments
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2009.01.012openalex-snapshot
From mechanotransduction to extracellular matrix gene expression in fibroblasts
inferred← citeshttps://doi.org/10.1016/j.bbr.2017.05.047openalex-snapshot
Enriched environment alters the behavioral profile of tenascin-C deficient mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.05.013openalex-snapshot
Cardiac extracellular matrix tenascin-C deposition during fibronectin degradation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.03.021openalex-snapshot
Tenascin-C is a potential cancer-associated fibroblasts marker and predicts poor prognosis in prostate cancer
inferred← citeshttps://doi.org/10.1016/j.bcp.2022.115156openalex-snapshot
Carbon monoxide mechanism of protection against renal ischemia and reperfusion injury
inferred← citeshttps://doi.org/10.1016/j.biocel.2003.12.003openalex-snapshot
Tissue repair and the dynamics of the extracellular matrix
inferred← citeshttps://doi.org/10.1016/j.biocel.2003.12.006openalex-snapshot
Functional regulation of T lymphocytes by modulatory extracellular matrix proteins
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.biocel.2012.02.014openalex-snapshot
Tenascin-C and its functions in neuronal plasticity
inferred← citeshttps://doi.org/10.1016/j.biochi.2024.10.003openalex-snapshot
Structural extracellular matrix-mediated molecular signaling in wound repair and tissue regeneration
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2013.09.099openalex-snapshot
Rejuvenation of chondrogenic potential in a young stem cell microenvironment
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.06.036openalex-snapshot
The cell adhesion and proliferation activities of a peptide derived from human tenascin-C are dependent on two Ile residues
inferred← citeshttps://doi.org/10.1016/j.bpc.2022.106944openalex-snapshot
Characterisation of collagen type I matrices for pathophysiologically relevant spatial cancer cell cultures
inferred← citeshttps://doi.org/10.1016/j.bpj.2009.12.3238openalex-snapshot
Modulating the Mechanical Stability of Extracellular Matrix Protein Tenascin-C in a Controlled and Reversible Fashion
inferred← citeshttps://doi.org/10.1016/j.canlet.2006.02.017openalex-snapshot
Tenascin-C induced signaling in cancer
inferred← citeshttps://doi.org/10.1016/j.canlet.2011.10.007openalex-snapshot
Nanoencapsulated anti-CK2 small molecule drug or siRNA specifically targets malignant cancer but not benign cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2016.02.031openalex-snapshot
Hyaluronan: A modulator of the tumor microenvironment
inferred← citeshttps://doi.org/10.1016/j.cardiores.2004.06.006openalex-snapshot
Matricellular proteins in the heart: possible role during stress and remodeling
inferred← citeshttps://doi.org/10.1016/j.cardiores.2004.10.034openalex-snapshot
Tenascin-C is an essential factor for neointimal hyperplasia after aortotomy in mice
inferred← citeshttps://doi.org/10.1016/j.carpath.2006.12.001openalex-snapshot
Elevated expressions of osteopontin and tenascin C in ascending aortic aneurysms are associated with trileaflet aortic valves as compared with bicuspid aortic valves
inferred← citeshttps://doi.org/10.1016/j.carpath.2011.12.005openalex-snapshot
Deletion of tenascin-C gene exacerbates atherosclerosis and induces intraplaque hemorrhage in Apo-E-deficient mice
inferred← citeshttps://doi.org/10.1016/j.celrep.2012.09.005openalex-snapshot
Endogenous Control of Immunity against Infection: Tenascin-C Regulates TLR4-Mediated Inflammation via MicroRNA-155
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.08.062openalex-snapshot
Sterile Inflammation Enhances ECM Degradation in Integrin β1 KO Embryonic Skin
inferred← citeshttps://doi.org/10.1016/j.clineuro.2024.108634openalex-snapshot
Independent elevation of plasma fibulin-5 proceeding chronic hydrocephalus development after aneurysmal subarachnoid hemorrhage
inferred← citeshttps://doi.org/10.1016/j.contraception.2018.05.020openalex-snapshot
Molecular characterization of PRM-associated endometrial changes, PAEC, following mifepristone treatment
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2016.04.017openalex-snapshot
Clinical significance of immunohistochemically detected extracellular matrix proteins and their spatial distribution in primary cancer
inferred← citeshttps://doi.org/10.1016/j.ejogrb.2019.05.040openalex-snapshot
Autoantibodies common in patients with gastrointestinal diseases are not found in patients with endometriosis: A cross-sectional study
inferred← citeshttps://doi.org/10.1016/j.eplepsyres.2014.09.019openalex-snapshot
Role of TGF-β signaling pathway on Tenascin C protein upregulation in a pilocarpine seizure model
inferred← citeshttps://doi.org/10.1016/j.exer.2006.07.021openalex-snapshot
Cooperation of isoforms of laminin-332 and tenascin-CL during early adhesion and spreading of immortalized human corneal epithelial cells
inferred← citeshttps://doi.org/10.1016/j.exer.2008.01.013openalex-snapshot
Extracellular matrix in the trabecular meshwork
inferred← citeshttps://doi.org/10.1016/j.exer.2008.11.032openalex-snapshot
Matricellular proteins in the trabecular meshwork
inferred← citeshttps://doi.org/10.1016/j.expneurol.2010.04.019openalex-snapshot
Analysis of combinatorial variability reveals selective accumulation of the fibronectin type III domains B and D of tenascin-C in injured brain
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2007.05.028openalex-snapshot
Tenascin is highly expressed in endometriosis and its expression is upregulated by estrogen
inferred← citeshttps://doi.org/10.1016/j.humpath.2008.12.017openalex-snapshot
High prevalence of chronic myocarditis in dilated cardiomyopathy referred for left ventriculoplasty: expression of tenascin C as a possible marker for inflammation
inferred← citeshttps://doi.org/10.1016/j.jacc.2006.03.033openalex-snapshot
Serum Tenascin-C Might Be a Novel Predictor of Left Ventricular Remodeling and Prognosis After Acute Myocardial Infarction
inferred← citeshttps://doi.org/10.1016/j.jacc.2017.07.789openalex-snapshot
Bone Marrow-Derived Tenascin-C Attenuates Cardiac Hypertrophy by Controlling Inflammation
inferred← citeshttps://doi.org/10.1016/j.jchemneu.2022.102147openalex-snapshot
The role of Tenascin C in intracerebral hemorrhage-induced secondary brain injury in rats via induction of neuronal cell death and neuroinflammation
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2018.12.002openalex-snapshot
The Intestinal Lymphatic System: Functions and Metabolic Implications
inferred← citeshttps://doi.org/10.1016/j.jconrel.2006.07.024openalex-snapshot
Intracellular drug delivery by sulfatide-mediated liposomes to gliomas
inferred← citeshttps://doi.org/10.1016/j.jdermsci.2005.06.001openalex-snapshot
Tenascin-C is upregulated in the skin lesions of patients with atopic dermatitis
inferred← citeshttps://doi.org/10.1016/j.jfma.2022.01.026openalex-snapshot
Tissue microenvironment dictates inflammation and disease activity in rheumatoid arthritis
inferred← citeshttps://doi.org/10.1016/j.jhep.2006.10.011openalex-snapshot
Expression of large tenascin-C splice variants by hepatic stellate cells/myofibroblasts in chronic hepatitis C
inferred← citeshttps://doi.org/10.1016/j.jid.2023.09.278openalex-snapshot
Extracellular Matrix Remodeling in Atopic Dermatitis Harnesses the Onset of an Asthmatic Phenotype and Is a Potential Contributor to the Atopic March
inferred← citeshttps://doi.org/10.1016/j.jmb.2009.01.019openalex-snapshot
Mechanical Design of the Third FnIII Domain of Tenascin-C
inferred← citeshttps://doi.org/10.1016/j.jmb.2009.05.057openalex-snapshot
Modulating the Mechanical Stability of Extracellular Matrix Protein Tenascin-C in a Controlled and Reversible Fashion
inferred← citeshttps://doi.org/10.1016/j.job.2024.05.005openalex-snapshot
Creating 3D constructs with cranial neural crest-derived cell lines using a bio-3D printer
inferred← citeshttps://doi.org/10.1016/j.job.2026.100738openalex-snapshot
The Runx2-SMOC axis in skeletal development: Expanding roles of Smoc1 and Smoc2 in development and disease
inferred← citeshttps://doi.org/10.1016/j.jss.2006.05.030openalex-snapshot
Adenoviral-Mediated Expression and Local Deposition of Recombinant Tenascin-C Perturbs Cell-Dependent Matrix Contraction
inferred← citeshttps://doi.org/10.1016/j.jstrokecerebrovasdis.2019.104485openalex-snapshot
Silencing of Tenascin-C Inhibited Inflammation and Apoptosis Via PI3K/Akt/NF-κB Signaling Pathway in Subarachnoid Hemorrhage Cell Model
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.jvs.2006.05.043openalex-snapshot
Gene expression changes evoked in a venous segment exposed to arterial flow
inferred← citeshttps://doi.org/10.1016/j.kint.2024.07.028openalex-snapshot
Transcription factor Twist1 drives fibroblast activation to promote kidney fibrosis via signaling proteins Prrx1/TNC
inferred← citeshttps://doi.org/10.1016/j.labinv.2025.104237openalex-snapshot
Tenascin-C Expression in Relation to Tumor-Stroma Interaction in Ameloblastoma
inferred← citeshttps://doi.org/10.1016/j.lfs.2014.03.006openalex-snapshot
Absence of feedback regulation in the synthesis of COL1A1
inferred← citeshttps://doi.org/10.1016/j.matbio.2005.07.005openalex-snapshot
Vascular smooth muscle cell response on thin films of collagen
inferred← citeshttps://doi.org/10.1016/j.matbio.2009.08.007openalex-snapshot
Specific processing of tenascin-C by the metalloprotease meprinβ neutralizes its inhibition of cell spreading
inferred← citeshttps://doi.org/10.1016/j.matbio.2010.08.003openalex-snapshot
Cryptic domains of tenascin-C differentially control fibronectin fibrillogenesis
inferred← citeshttps://doi.org/10.1016/j.matbio.2013.02.003openalex-snapshot
Interleukin-1 has opposing effects on connective tissue growth factor and tenascin-C expression in human cardiac fibroblasts
inferred← citeshttps://doi.org/10.1016/j.matbio.2014.01.007openalex-snapshot
Tenascins in stem cell niches
inferred← citeshttps://doi.org/10.1016/j.matbio.2014.05.005openalex-snapshot
Targeting the extracellular matrix: Matricellular proteins regulate cell–extracellular matrix communication within distinct niches of the intervertebral disc
inferred← citeshttps://doi.org/10.1016/j.matbio.2018.01.002openalex-snapshot
Extracellular matrix contribution to skin wound re-epithelialization
inferred← citeshttps://doi.org/10.1016/j.matbio.2018.04.003openalex-snapshot
Pulmonary immunity and extracellular matrix interactions
inferred← citeshttps://doi.org/10.1016/j.matbio.2023.04.003openalex-snapshot
Matricellular proteins in atherosclerosis development
inferred← citeshttps://doi.org/10.1016/j.matbio.2024.02.008openalex-snapshot
The role of fibrosis in cardiomyopathies: An opportunity to develop novel biomarkers of disease activity
inferred← citeshttps://doi.org/10.1016/j.matbio.2026.102051openalex-snapshot
Differences between astrocytes and fibroblasts in the effects of TGFβ on fibronectin matrix assembly
inferred← citeshttps://doi.org/10.1016/j.molbiopara.2016.12.002openalex-snapshot
Proteomic investigation of human cystic echinococcosis in the liver
inferred← citeshttps://doi.org/10.1016/j.molonc.2015.04.003openalex-snapshot
Mechanism of irradiation‐induced mammary cancer metastasis: A role for SAP‐dependent Mkl1 signaling
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.neurobiolaging.2013.04.013openalex-snapshot
Tenascin-C deficiency ameliorates Alzheimer's disease-related pathology in mice
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2004.06.078openalex-snapshot
Differential upregulation of extracellular matrix molecules associated with the appearance of granule cell dispersion and mossy fiber sprouting during epileptogenesis in a murine model of temporal lobe epilepsy
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2004.12.028openalex-snapshot
Tenascin-C regulates proliferation and migration of cultured astrocytes in a scratch wound assay
inferred← citeshttps://doi.org/10.1016/j.nutres.2020.12.001openalex-snapshot
A carbohydrate-restricted diet for patients with irritable bowel syndrome lowers serum C-peptide, insulin, and leptin without any correlation with symptom reduction
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2012.02.002openalex-snapshot
Matrikines and the lungs
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2004.03.003openalex-snapshot
The brain angiotensin system and extracellular matrix molecules in neural plasticity, learning, and memory
inferred← citeshttps://doi.org/10.1016/j.proghi.2006.02.003openalex-snapshot
Osteoarthritis: Cellular and molecular changes in degenerating cartilage
inferred← citeshttps://doi.org/10.1016/j.prp.2026.156468openalex-snapshot
ACE2 impairs epidermal regeneration by inhibiting TNC expression and PI3K/AKT/mTOR signaling
inferred← citeshttps://doi.org/10.1016/j.rmr.2015.08.004openalex-snapshot
Pneumopathie organisée cryptogénique
inferred← citeshttps://doi.org/10.1016/j.semcancer.2005.05.003openalex-snapshot
Stromagenesis: The changing face of fibroblastic microenvironments during tumor progression
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.09.012openalex-snapshot
Tenascins in CNS lesions
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