PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 12689941-3 2003 It is also known that FN production is greatly enhanced by adhesion of HCs to hyaluronan (HA) via CD44. Hyaluronic Acid 78-88 fibronectin 1 Homo sapiens 22-24 17929131-0 2007 Inhibition of nuclear factor-kappaB by hyaluronan in rheumatoid chondrocytes stimulated with COOH-terminal heparin-binding fibronectin fragment. Hyaluronic Acid 39-49 fibronectin 1 Homo sapiens 123-134 17929131-1 2007 The aim of this study was to examine the inhibitory effect of high molecular weight hyaluronan (HA) on nuclear factor (NF)-kappaB activation by COOH-terminal heparin-binding fibronectin fragment (HBFN-f) in rheumatoid arthritis (RA) chondrocytes. Hyaluronic Acid 84-94 fibronectin 1 Homo sapiens 174-185 16579693-0 2006 Fibronectin functional domains coupled to hyaluronan stimulate adult human dermal fibroblast responses critical for wound healing. Hyaluronic Acid 42-52 fibronectin 1 Homo sapiens 0-11 15762624-0 2005 Fibroblast cell behavior on bound and adsorbed fibronectin onto hyaluronan and sulfated hyaluronan substrates. Hyaluronic Acid 64-74 fibronectin 1 Homo sapiens 47-58 15762624-0 2005 Fibroblast cell behavior on bound and adsorbed fibronectin onto hyaluronan and sulfated hyaluronan substrates. Hyaluronic Acid 88-98 fibronectin 1 Homo sapiens 47-58 15762624-1 2005 The effect of fibronectin protein (Fn) coating onto polysaccharide layers of hyaluronic acid (Hyal) and its sulfated derivative (HyalS) on fibroblast cell adhesion was analyzed. Hyaluronic Acid 77-92 fibronectin 1 Homo sapiens 14-25 16101041-6 2005 Moreover, fibronectin and tenascin-c are present within the hyaluronan matrix at fertilization during the tubal sojourn of the ovum and the embryo. Hyaluronic Acid 60-70 fibronectin 1 Homo sapiens 10-21 15368267-5 2004 Hyaluronic acid (HA) is a highly elastic polysaccharide that is involved in natural valve morphogenesis and possesses binding interactions with FN. Hyaluronic Acid 0-15 fibronectin 1 Homo sapiens 144-146 15368267-5 2004 Hyaluronic acid (HA) is a highly elastic polysaccharide that is involved in natural valve morphogenesis and possesses binding interactions with FN. Hyaluronic Acid 17-19 fibronectin 1 Homo sapiens 144-146 12689941-3 2003 It is also known that FN production is greatly enhanced by adhesion of HCs to hyaluronan (HA) via CD44. Hyaluronic Acid 90-92 fibronectin 1 Homo sapiens 22-24 1632660-7 1992 Synovial tissue extension over fibronectin coated surfaces was inhibited when hyaluronic acid and chondroitin-4-sulphate, major components of cartilage proteoglycans, were present on the cartilage surface. Hyaluronic Acid 78-93 fibronectin 1 Homo sapiens 31-42 11049998-0 2000 Involvement of CD44-hyaluronan interaction in malignant cell homing and fibronectin synthesis in hairy cell leukemia. Hyaluronic Acid 20-30 fibronectin 1 Homo sapiens 72-83 10632453-0 1999 Hyaluronan suppresses fibronectin fragment-mediated damage to human cartilage explant cultures by enhancing proteoglycan synthesis. Hyaluronic Acid 0-10 fibronectin 1 Homo sapiens 22-33 10632453-5 1999 We found that 1 mg/ml hyaluronan completely blocked fibronectin fragment-mediated decreases in proteoglycan content in five of five specimens of cartilage from the human knee. Hyaluronic Acid 22-32 fibronectin 1 Homo sapiens 52-63 10632453-8 1999 The addition of hyaluronan to cartilage previously damaged by the fibronectin fragments or to osteoarthritic cartilage fully restored the proteoglycan content to control levels. Hyaluronic Acid 16-26 fibronectin 1 Homo sapiens 66-77 10632453-9 1999 We conclude that hyaluronan blocked damage at least partly by blocking penetration of the fibronectin fragments and slowing matrix metalloproteinase expression. Hyaluronic Acid 17-27 fibronectin 1 Homo sapiens 90-101 8838671-6 1996 Addition of heparin and heparan sulfate reversed the collagen IV mRNA induction whereas hyaluronic acid and chondroitin sulfate enhanced fibronectin and collagenase transcripts. Hyaluronic Acid 88-103 fibronectin 1 Homo sapiens 137-148 7752124-0 1995 Effects of hyaluronic acid on the release of cartilage matrix proteoglycan and fibronectin from the cell matrix layer of chondrocyte cultures: interactions between hyaluronic acid and chondroitin sulfate glycosaminoglycan. Hyaluronic Acid 11-26 fibronectin 1 Homo sapiens 79-90 7752124-1 1995 Hyaluronic acid (HA) of large sizes suppressed the release of cartilage matrix proteoglycan, fibronectin, and other macromolecules from the cell matrix layer of chondrocyte cultures, perhaps because HA of large sizes formed a viscous barrier in the matrix by its interactions with other extracellular matrix macromolecules. Hyaluronic Acid 0-15 fibronectin 1 Homo sapiens 93-104 8188759-12 1994 We conclude that hyaluronan binds to a fibrin- and heparin-binding domain at the N-terminal of plasma fibronectin and facilitates the attachment of epithelial cells. Hyaluronic Acid 17-27 fibronectin 1 Homo sapiens 102-113 8165568-8 1993 MSF stimulates the synthesis of a high molecular weight species of hyaluronic acid (HA). Hyaluronic Acid 67-82 fibronectin 1 Homo sapiens 0-3 8165568-8 1993 MSF stimulates the synthesis of a high molecular weight species of hyaluronic acid (HA). Hyaluronic Acid 84-86 fibronectin 1 Homo sapiens 0-3 1506427-0 1992 Antagonistic effects of TGF-beta 1 and MSF on fibroblast migration and hyaluronic acid synthesis. Hyaluronic Acid 71-86 fibronectin 1 Homo sapiens 39-42 1506427-4 1992 We have previously reported that this difference in behaviour results from the secretion by fetal fibroblasts of a "migration stimulating factor" (MSF) which is not made by their normal adult counterparts, and that MSF appears to act by stimulating the synthesis of hyaluronic acid (HA). Hyaluronic Acid 266-281 fibronectin 1 Homo sapiens 147-150 1506427-4 1992 We have previously reported that this difference in behaviour results from the secretion by fetal fibroblasts of a "migration stimulating factor" (MSF) which is not made by their normal adult counterparts, and that MSF appears to act by stimulating the synthesis of hyaluronic acid (HA). Hyaluronic Acid 266-281 fibronectin 1 Homo sapiens 215-218 1506427-4 1992 We have previously reported that this difference in behaviour results from the secretion by fetal fibroblasts of a "migration stimulating factor" (MSF) which is not made by their normal adult counterparts, and that MSF appears to act by stimulating the synthesis of hyaluronic acid (HA). Hyaluronic Acid 283-285 fibronectin 1 Homo sapiens 147-150 1506427-4 1992 We have previously reported that this difference in behaviour results from the secretion by fetal fibroblasts of a "migration stimulating factor" (MSF) which is not made by their normal adult counterparts, and that MSF appears to act by stimulating the synthesis of hyaluronic acid (HA). Hyaluronic Acid 283-285 fibronectin 1 Homo sapiens 215-218 10401858-0 1999 Hyaluronic acid (with fibronectin) as a bioimplant for the vocal fold mucosa. Hyaluronic Acid 0-15 fibronectin 1 Homo sapiens 22-33 9850161-1 1998 During human thymic differentiation, interactions between fibronectin (Fn)/beta1 integrins and hyaluronan (HA)/RHAMM control motility and Fn/beta1 integrins mediate spontaneous Fn-dependent adhesion. Hyaluronic Acid 95-105 fibronectin 1 Homo sapiens 58-69 8807570-0 1996 Production of hyaluronan by glomerular mesangial cells in response to fibronectin and platelet-derived growth factor. Hyaluronic Acid 14-24 fibronectin 1 Homo sapiens 70-81 8807570-2 1996 We describe an increased production of hyaluronan from mesangial cell-enriched glomerular cores from diabetic animals, and further show that increased hyaluronan production follows the exposure of non-diabetic and diabetic preparations to fibronectin and to platelet-derived growth factor in vitro. Hyaluronic Acid 151-161 fibronectin 1 Homo sapiens 239-250 8188759-0 1994 Binding of hyaluronan to plasma fibronectin increases the attachment of corneal epithelial cells to a fibronectin matrix. Hyaluronic Acid 11-21 fibronectin 1 Homo sapiens 32-43 8188759-0 1994 Binding of hyaluronan to plasma fibronectin increases the attachment of corneal epithelial cells to a fibronectin matrix. Hyaluronic Acid 11-21 fibronectin 1 Homo sapiens 102-113 8188759-5 1994 Preincubation of the matrix proteins with hyaluronan (0.1-1.0 mg/ml) significantly increased the number of cells attached to the fibronectin matrix, but it did not increase the numbers of cells attached to laminin or collagen type IV. Hyaluronic Acid 42-52 fibronectin 1 Homo sapiens 129-140 8188759-11 1994 Further studies demonstrated that monoclonal antibody against the fibrin- and heparin-binding domain at the N-terminal of plasma fibronectin prevented radiolabeled hyaluronan from binding to fibronectin; likewise, the isolated N-terminal fragment, coupled with Sepharose 4B, bound to hyaluronan in columns. Hyaluronic Acid 164-174 fibronectin 1 Homo sapiens 129-140 8188759-11 1994 Further studies demonstrated that monoclonal antibody against the fibrin- and heparin-binding domain at the N-terminal of plasma fibronectin prevented radiolabeled hyaluronan from binding to fibronectin; likewise, the isolated N-terminal fragment, coupled with Sepharose 4B, bound to hyaluronan in columns. Hyaluronic Acid 164-174 fibronectin 1 Homo sapiens 191-202 8188759-11 1994 Further studies demonstrated that monoclonal antibody against the fibrin- and heparin-binding domain at the N-terminal of plasma fibronectin prevented radiolabeled hyaluronan from binding to fibronectin; likewise, the isolated N-terminal fragment, coupled with Sepharose 4B, bound to hyaluronan in columns. Hyaluronic Acid 284-294 fibronectin 1 Homo sapiens 129-140 1397194-3 1992 We have previously reported that MSF stimulates hyaluronic acid (HA) synthesis by adult skin fibroblasts and that this effect on matrix deposition appears to be responsible for the observed increase in cell motility. Hyaluronic Acid 48-63 fibronectin 1 Homo sapiens 33-36 1397194-3 1992 We have previously reported that MSF stimulates hyaluronic acid (HA) synthesis by adult skin fibroblasts and that this effect on matrix deposition appears to be responsible for the observed increase in cell motility. Hyaluronic Acid 65-67 fibronectin 1 Homo sapiens 33-36 1783088-7 1991 A significant correlation was found between lavage fibronectin levels and hyaluronan (r = 0.81, p less than 0.001). Hyaluronic Acid 74-84 fibronectin 1 Homo sapiens 51-62 1703972-2 1991 Our previous in vitro studies, comparing DA cells with those from the aorta (Ao), have shown, even in early gestation, a 10-fold increase in DA endothelial incorporation of hyaluronan into the subendothelial matrix, a 2-fold increase in smooth muscle fibronectin synthesis and, in response to endothelial conditioned medium, a 2-fold increase in chondroitin sulfate. Hyaluronic Acid 173-183 fibronectin 1 Homo sapiens 251-262 2776119-4 1989 Form I hyaluronic acid exhibits greater binding to preparations of cellular fibronectin and to both normal and transformed cells than does form II. Hyaluronic Acid 7-22 fibronectin 1 Homo sapiens 76-87 1833226-5 1991 Studies concerned with the mechanism of action of MSF indicate that it stimulates the production of a high molecular weight class of hyaluronic acid (HA). Hyaluronic Acid 133-148 fibronectin 1 Homo sapiens 50-53 1833226-5 1991 Studies concerned with the mechanism of action of MSF indicate that it stimulates the production of a high molecular weight class of hyaluronic acid (HA). Hyaluronic Acid 150-152 fibronectin 1 Homo sapiens 50-53 1688536-1 1990 We have recently shown that the large hyaluronan-aggregating chondroitin sulfate proteoglycan from cartilage (PG-LA) is unfavorable as a substrate for neural crest cell migration in vitro and that this macromolecule inhibits cell dispersion on fibronectin substrates when included in the medium (R. Perris and S. Johansson, 1987, J. Hyaluronic Acid 38-48 fibronectin 1 Homo sapiens 244-255 2768134-6 1989 Data are presented indicating that a) hyaluronic acid is required for the elevated migratory activity displayed by confluent fetal and breast cancer patient skin fibroblast; b) adult fibroblasts exhibit a bell-shaped dose-response to MSF, with maximal stimulation of migration observed at a concentration of 10 ng/ml; c) the migratory activity of adult fibroblasts pre-incubated with MSF remains high in the absence of additional factor: and d) MSF affects both the quantity and size class distribution of hyaluronic acid synthesized by adult fibroblasts. Hyaluronic Acid 506-521 fibronectin 1 Homo sapiens 234-237 2768134-8 1989 The observations reported here suggest that MSF-induced alterations in hyaluronic acid synthesis may contribute to the molecular basis of such perturbations. Hyaluronic Acid 71-86 fibronectin 1 Homo sapiens 44-47 2313677-3 1990 Aggregation of cartilage proteoglycan by addition of hyaluronic acid also aggregated the endogenous fibronectin. Hyaluronic Acid 53-68 fibronectin 1 Homo sapiens 100-111 2768134-6 1989 Data are presented indicating that a) hyaluronic acid is required for the elevated migratory activity displayed by confluent fetal and breast cancer patient skin fibroblast; b) adult fibroblasts exhibit a bell-shaped dose-response to MSF, with maximal stimulation of migration observed at a concentration of 10 ng/ml; c) the migratory activity of adult fibroblasts pre-incubated with MSF remains high in the absence of additional factor: and d) MSF affects both the quantity and size class distribution of hyaluronic acid synthesized by adult fibroblasts. Hyaluronic Acid 38-53 fibronectin 1 Homo sapiens 234-237 2768134-6 1989 Data are presented indicating that a) hyaluronic acid is required for the elevated migratory activity displayed by confluent fetal and breast cancer patient skin fibroblast; b) adult fibroblasts exhibit a bell-shaped dose-response to MSF, with maximal stimulation of migration observed at a concentration of 10 ng/ml; c) the migratory activity of adult fibroblasts pre-incubated with MSF remains high in the absence of additional factor: and d) MSF affects both the quantity and size class distribution of hyaluronic acid synthesized by adult fibroblasts. Hyaluronic Acid 38-53 fibronectin 1 Homo sapiens 384-387 2768134-6 1989 Data are presented indicating that a) hyaluronic acid is required for the elevated migratory activity displayed by confluent fetal and breast cancer patient skin fibroblast; b) adult fibroblasts exhibit a bell-shaped dose-response to MSF, with maximal stimulation of migration observed at a concentration of 10 ng/ml; c) the migratory activity of adult fibroblasts pre-incubated with MSF remains high in the absence of additional factor: and d) MSF affects both the quantity and size class distribution of hyaluronic acid synthesized by adult fibroblasts. Hyaluronic Acid 38-53 fibronectin 1 Homo sapiens 384-387 3660729-0 1987 [Complex-formation with hyaluronic acid as a cause of fibronectin heterogeneity in the synovial fluid]. Hyaluronic Acid 24-39 fibronectin 1 Homo sapiens 54-65 3275431-10 1988 Alternatively, fibronectin, with its binding sites for hyaluronic acid and collagen, may act as a complex for boundary lubrication. Hyaluronic Acid 55-70 fibronectin 1 Homo sapiens 15-26 3394105-4 1988 Using cross-immunoelectrophoresis, the heterogeneity of synovial FN was revealed which was determined by complex formation with hyaluronic acid. Hyaluronic Acid 128-143 fibronectin 1 Homo sapiens 65-67 3660729-3 1987 The data obtained suggest that complexes of fibronectin and hyaluronic acid are responsible for physico-chemical heterogeneity of fibronectin in synovial fluid. Hyaluronic Acid 60-75 fibronectin 1 Homo sapiens 130-141 6292573-12 1982 Hyaluronic acid has an antagonistic function which, at higher concentrations, prevents the fibronectin fibrils from interacting with collagen and cell surfaces. Hyaluronic Acid 0-15 fibronectin 1 Homo sapiens 91-102 3332659-7 1987 MSF appears to promote fibroblast migration at high cell density by stimulating the deposition of hyaluronic acid in the extracellular matrix. Hyaluronic Acid 98-113 fibronectin 1 Homo sapiens 0-3 3524938-3 1986 The altered fibronectin distribution may be the result of altered interactions of fibronectin with extracellular matrix components, either due to abnormal fibronectin or to changes in other extracellular matrix molecules (e.g. collagens, hyaluronic acid). Hyaluronic Acid 238-253 fibronectin 1 Homo sapiens 12-23 6643486-3 1983 In low ionic strength buffer, intact fibronectin bound to heparin and high sulfated heparan sulfate, but not to low sulfated heparan sulfate, dermatan sulfate, chondroitin sulfates A and C, or hyaluronic acid. Hyaluronic Acid 193-208 fibronectin 1 Homo sapiens 37-48 222472-7 1979 Addition of fibronectin also affects binding of hyaluronic acid to the cells. Hyaluronic Acid 48-63 fibronectin 1 Homo sapiens 12-23 7068586-0 1982 Interaction of fibronectin and its proteolytic fragments with hyaluronic acid. Hyaluronic Acid 62-77 fibronectin 1 Homo sapiens 15-26 7068586-1 1982 The interaction of porcine plasma fibronectin and its proteolytic fragments with hyaluronic acid was investigated by affinity chromatography using hyaluronic acid-linked Sepharose 4B. Hyaluronic Acid 81-96 fibronectin 1 Homo sapiens 34-45 7068586-1 1982 The interaction of porcine plasma fibronectin and its proteolytic fragments with hyaluronic acid was investigated by affinity chromatography using hyaluronic acid-linked Sepharose 4B. Hyaluronic Acid 147-162 fibronectin 1 Homo sapiens 34-45 7068586-4 1982 This type of multiple interaction may account for the affinity for hyaluronic acid strong enough to prevent the elution of fibronectin from the hyaluronate-column with a buffer containing 2 M NaCl. Hyaluronic Acid 67-82 fibronectin 1 Homo sapiens 123-134 7068586-4 1982 This type of multiple interaction may account for the affinity for hyaluronic acid strong enough to prevent the elution of fibronectin from the hyaluronate-column with a buffer containing 2 M NaCl. Hyaluronic Acid 144-155 fibronectin 1 Homo sapiens 123-134 7407251-5 1980 Heparin as well as highly sulfate heparan sulfate and hyaluronic acid brought about agglutination of plastic beads coated with gelatin when fibronectin was present. Hyaluronic Acid 54-69 fibronectin 1 Homo sapiens 140-151 437704-10 1979 Hyaluronic acid and putrescine prevented the insolubilization of native collagen type III, by fibronectin and heparin. Hyaluronic Acid 0-15 fibronectin 1 Homo sapiens 94-105 30485523-9 2018 The effects of sulfated hyaluronic acid were predominantly linked to an alteration in the composition of the extracellular matrix, affecting the synthesis, secretion, and/or activity of fibrillary (fibronectin and thrombospondin-2) and nonfibrillary (transglutaminase-2, periostin, and lysyloxidase) extracellular matrix components, including proteases and their inhibitors (matrix metalloproteinase-2, tissue inhibitor of metalloproteinase-3). Hyaluronic Acid 24-39 fibronectin 1 Homo sapiens 198-209 33002348-0 2020 Engineered Full-Length Fibronectin-Hyaluronic Acid Hydrogels for Stem Cell Engineering. Hyaluronic Acid 35-50 fibronectin 1 Homo sapiens 23-34 33710248-0 2021 Hyaluronic acid drives mesenchymal stromal cell-derived extracellular matrix assembly by promoting fibronectin fibrillogenesis. Hyaluronic Acid 0-15 fibronectin 1 Homo sapiens 99-110 22467423-4 2013 Nevertheless, current studies suggest that laminin, collagen type III, collagen type IV and hyaluronic acid help to maintain the undifferentiated phenotype of LPCs and promote their proliferation when cultured in media supplemented with growth factors chosen for LPC expansion, whereas collagen type I and fibronectin are generally associated with a differentiated phenotype under the same conditions. Hyaluronic Acid 92-107 fibronectin 1 Homo sapiens 286-317 27808176-0 2016 Sulfated hyaluronan alters fibronectin matrix assembly and promotes osteogenic differentiation of human bone marrow stromal cells. Hyaluronic Acid 9-19 fibronectin 1 Homo sapiens 27-38 27808176-4 2016 Synthetically sulfated hyaluronan derivatives (sHA) can serve as model molecules with a well characterized sulfation pattern to study sGAG-FN interaction. Hyaluronic Acid 23-33 fibronectin 1 Homo sapiens 139-141 26221979-2 2015 In this work, we have investigated the molecular interactions between FN and various components of the synovial fluid such as lubricin (LUB), hyaluronan (HA), and serum albumin (SA), which are all believed to contribute to joint lubrication. Hyaluronic Acid 142-152 fibronectin 1 Homo sapiens 70-72 26221979-2 2015 In this work, we have investigated the molecular interactions between FN and various components of the synovial fluid such as lubricin (LUB), hyaluronan (HA), and serum albumin (SA), which are all believed to contribute to joint lubrication. Hyaluronic Acid 154-156 fibronectin 1 Homo sapiens 70-72 25549589-0 2015 Hyaluronan Controls the Deposition of Fibronectin and Collagen and Modulates TGF-beta1 Induction of Lung Myofibroblasts. Hyaluronic Acid 0-10 fibronectin 1 Homo sapiens 38-49 25549589-8 2015 Inhibition of hyaluronan synthesis in TGF-beta1-induced lung myofibroblasts over a 4day period with 4-methyl umbelliferone (4-MU) further enhanced myofibroblast morphology, caused increased deposition of fibronectin and type I collagen in the ECM, and increased expression of alpha-smooth muscle actin and hyaluronan synthase 2 (HAS2) mRNA. Hyaluronic Acid 14-24 fibronectin 1 Homo sapiens 204-215 25549589-12 2015 Time-lapse imaging of the immediate effects of hyaluronidase digestion showed that hyaluronan matrix primarily mediates attachment of membrane and cortical actin between focal contacts, suggesting that surface adhesion through hyaluronan and CD44 is distinct from focal adhesion through beta1 integrins and fibronectin. Hyaluronic Acid 83-93 fibronectin 1 Homo sapiens 307-318 27449338-4 2016 Polyethyleneglycole diacrylate/thiolated Hyaluronic Acid hydrogels (PEGDA/tHA) were coated with anti-Fibronectin aptamers. Hyaluronic Acid 41-56 fibronectin 1 Homo sapiens 101-112 25549589-13 2015 Fluorescein-labeled hyaluronan bound regularly along fibronectin fibers and co-localized more with beta1 integrin and less with CD44. Hyaluronic Acid 20-30 fibronectin 1 Homo sapiens 53-64 20552237-0 2010 Hyaluronan inhibits p38 mitogen-activated protein kinase via the receptors in rheumatoid arthritis chondrocytes stimulated with fibronectin fragment. Hyaluronic Acid 0-10 fibronectin 1 Homo sapiens 128-139 23531422-4 2013 FN adhesion on PPy/hyaluronic acid showed a significantly lower density of surface adhesion with the adhesion restricted to nodule structures, as opposed to their peripheries, of the polymer morphology. Hyaluronic Acid 19-34 fibronectin 1 Homo sapiens 0-2 23531422-7 2013 CONCLUSIONS: Given that the conductivity requires doping of the polymer, these findings suggest that FN adhesion is mediated by interactions with chondroitin sulfate and hyaluronic acid at the polymer surface and may be indicative of specific interactions due to contributions from electrostatic attraction between the FN and sulfate/anionic groups of the dopants. Hyaluronic Acid 170-185 fibronectin 1 Homo sapiens 101-103 21439409-0 2011 Fibronectin-hyaluronic acid composite hydrogels for three-dimensional endothelial cell culture. Hyaluronic Acid 12-27 fibronectin 1 Homo sapiens 0-11 23103154-0 2013 Improving the osteogenic potential of BMP-2 with hyaluronic acid hydrogel modified with integrin-specific fibronectin fragment. Hyaluronic Acid 49-64 fibronectin 1 Homo sapiens 106-117 20552237-1 2010 This study was aimed to examine the inhibitory mechanism of high molecular weight hyaluronan (HA) on nitric oxide (NO) production by NH2-terminal heparin-binding fibronectin fragment (FN-f) in rheumatoid arthritis (RA) chondrocytes. Hyaluronic Acid 82-92 fibronectin 1 Homo sapiens 162-173 19505400-4 2009 Results show that fibroblasts treated with hyaluronic acid plus aminoacid solution increased their proliferative activity, collagen I and III, and fibronectin synthesis. Hyaluronic Acid 43-58 fibronectin 1 Homo sapiens 147-158 20203421-0 2010 Comparison of hyaluronan effects among normal, osteoarthritis, and rheumatoid arthritis cartilages stimulated with fibronectin fragment. Hyaluronic Acid 14-24 fibronectin 1 Homo sapiens 115-126 20367505-0 2010 Increased maternal serum and cord blood fibronectin concentrations in preeclampsia are associated with higher placental hyaluronic acid and hydroxyproline content. Hyaluronic Acid 120-135 fibronectin 1 Homo sapiens 40-51 20367505-2 2010 The purpose of this study was to examine the relationship between maternal serum FN levels and the extracellular matrix molecule contents of placental tissue, such as FN, hyaluronic acid (HA) and hydroxyproline (HP) levels. Hyaluronic Acid 171-186 fibronectin 1 Homo sapiens 81-83 20367505-2 2010 The purpose of this study was to examine the relationship between maternal serum FN levels and the extracellular matrix molecule contents of placental tissue, such as FN, hyaluronic acid (HA) and hydroxyproline (HP) levels. Hyaluronic Acid 188-190 fibronectin 1 Homo sapiens 81-83