Toole BP, Munaim SF, Welles S, Knudson CB: Hyaluronate-cell interactions and growth factor regulation of hyaluronate synthesis during embryo development. In: Evered D, Whelan J (eds) Biology of Hyaluronan. John Wiley and Sons, Chichester, 1989, vol. 143, pp 146–159 Google Scholar
Balazs EA, Hogberg B, Laurent TC: The biological activity of Hyaluron sulfuric acid. Acta Physiol Scand 23: 168–178, 1951 Google Scholar
Turley EA: Proteoglycans and cell adhesion: their putative role during tumorigenesis. Cancer Met Rev 3: 325–339, 1984 Google Scholar
Biology of Hyaluronan: CIBA Foundation (eds), Evered D, Whelan J (eds) John Wiley and Sons, Chichester, 1989, vol. 143
Kvist, Finnegan C: J Exp Zool 1965
Derby MA, Pintar JE: The histochemical specificity of Streptomyces hyaluronidase and chrondroitinase ABC. Histochem J 10: 529–547, 1978 Google Scholar
Toole BP: Developmental role of hyaluronate. 10: 93–100, 1982 Google Scholar
Markwald RR, Fitzharris TP, Bank H, Bernanke DH: Structural analyses on the matrical organization of glycosaminoglycan in developing endocardial cushions. Devel Biol 62: 292–316, 1978 Google Scholar
Boudreau N, Rabinovitch M: Developmentally regulated changes in extracellular matrix in endothelial and smooth muscle cells in the ductus arteriosus may be related to intimal proliferation. Lab Invest 64: 187–199, 1991 Google Scholar
Bray BA, Sampson PM, Osman M, Giondomenico A, Turimo GM: Early changes in lung tissue hyaluronan and hyaluronidase in bleomycin-induced alveolitis in hamsters. Am Rev Respir Dis 143: 284–288, 1991 Google Scholar
Nettlbladt O, Bergh J, Schenholm M, Tengblad A, Halgreen R: Accumulation of hyaluronic acid in the alveolar interstitial tissue in bleomycin-induced alveolitis. Am Rev Resp Dis 139: 759–762, 1989 Google Scholar
Laurent C, Soederberg O, Amiko M, Hartwig S: Repair of chronic tympanic membrane pertorations using applications of hyaluronan or rice paper protheses. J Ort Relat Spec 53: 37–40, 1991 Google Scholar
Iozzo RV: Porteoglycans: structure, function and role in neoplasia. Lab Invest 53: 373–396, 1985 Google Scholar
Turley EA, Austen L, Vandelight K, Clary C: Hyaluronan and a cell-associated Hyaluronan binding protein regulate the locomotion of _ras_-transformed cells. J Cell Biol 112: 1041–1047, 1991 Google Scholar
Bernanke DH, Markwald RR: Effects of hyaluronic acid on cardiac cushion tissue cells in collagen matrix cultures. Texas Rep Biol Med 39: 271–285, 1979 Google Scholar
Hadden CM, Lewis JH: Hyaluronan as a propellant for epithelial movement: the development of semicircular canals in the inner ear of Xenopus. Development 112: 541–550, 1991 Google Scholar
Hakansson L, Hallgren R, Venge P: Regulation of granulocyte function by hyaluronic acid. J Clin Invest 66: 298–305, 1980 Google Scholar
Hakansson L, Hallgren R, Venge P, Artursson G, Vedung S: Hyaluronic acid stimulates neutrophil function in vitro and in vivo. Scand J Infect Dis Suppl 24: 54–56, 1980 Google Scholar
Stamenkovic I, Aruffo A, Amist M, Seed B: The hematopoietic and epithelial forms of CD44 are distinct polypeptides with different adhesion potentials for hyaluronanbearing cells. Embo J 10: 343–348, 1991 Google Scholar
Turley EA, Karnovsky B, Hall C, Cripps V: Manuscript in review, 1991
Boudreaux N, Turley EA, Rabinovitch M: Fibronectin hyaluronan and a hyaluronan binding protein contribute to increased ductus ateriosus smooth muscle cell migration. Devel Biol 143: 235–247, 1991 Google Scholar
Huszar G, Willetts M, Corrales M: Hyaluronic acid (sperm select) improves retention of sperm motility and velocity in normospermic and oligospermic specimens. Fert Steril 54: 1127–1134, 1990 Google Scholar
West DC, Kumar S: Hyaluronan and angiogenesis. In: CIBA FDN sympos. Evered D, Whelan J (eds) Biology of Hyaluron. J. Wiley and Sons, Chichester 143: 157–207, 1989 Google Scholar
Schor SL, Schor AM, Grey AM, Chen J, Rushton G, Grant NE, Eins I: Mechanisms of action of the migration stimulating fractor produced by fetal and cancer patient fibroblasts: effect on hyaluronic acid synthesis. In Vitro Cell Devel Biol 25: 737–745, 1989 Google Scholar
Trimble WS, Johnson PW, Hozumi N, Roder JC: Inducible cellular transformation by a metallothionein-ras hybrid oncogene leads to natural killer cell susceptibility. Nature 321: 782–785, 1986 Google Scholar
Partin AW, Isaacs JT, Trieger B, Coffey DS: Early cell motility changes associated with an increase in metastic ability in rat prostatic cancer cells transfected with the Harvey ras oncogene. Cancer Res 48: 6050–6053, 1988 Google Scholar
Goetnick PF, Stirpe NS, Tsonis PA, Carlome D: The tandomly repeated sequences of cartilage link protein contain the sites for interaction with hyaluronic acid. J Cell Biol 105: 2403–2408, 1987 Google Scholar
Doege K, Sasaki M, Horigan E, Hassell JR, Yamada Y: Complete primary structure of the rat cartilage proteoglycan core protein deduced from cDNA clones. J Biol Chem 262: 17757–17767, 1987 Google Scholar
Angello JC, Haushka SD: Hyaluronic acid synthesis and turnover by myotubes in culture. Devel Biol 73: 322–337, 1979 Google Scholar
Underhill CB, Toole BP: Receptors for hyaluronate on the surface of parent and virus transformed cell lines. Binding and aggregation studies. Exp Cell Res 131: 419–423, 1981 Google Scholar
Turley EA: Hyaluronan binding proteins and receptors. Adv Drug Del 7: 257–264, 1991 Google Scholar
Toole BP: Hyaluronan and its binding proteins the hyaladherins. Curr Opin Cell Biol 2: 839–844, 1990 Google Scholar
Neame PJ, Christner JE, Baker JR: The primary structure of link protein from rat chondrosarcoma proteoglycan aggregate. J Biol Chem 261: 3519–3535, 1986 Google Scholar
Krusius T, Gehlsen KR, Ruoslatti E: A fibroblast chrondroitin sulfate proteoglycan core protein contains lectin-like and growth factor-like sequences. J Biol Chem 262: 13120–13125, 1987 Google Scholar
Delpech B, Halavent C: Characterization and purification from Human Brain of a hyaluronic acid binding glycoprotein, Hyaluronectin. J Neurochem 36: 855–859, 1981 Google Scholar
Perides G, Lane WS, Andrew D, Dald D, Bignami A: Isolation and partial characterization of a glial Hyaluronate-binding protein. J Biol Chem 264: 5981–5987, 1989 Google Scholar
Hardwick C, Hoare K, Owens R, Hohn HP, Hook M, Moore D, Cripps V, Austen L, Turley EA: Molecular cloning of a novel hyaluronan receptor that mediates tumor cell motility. In revision
Turley EA: The role of cell associated hyaluronan-binding protein in fibroblast behaviour. In: Evered D, Whelan J (eds) Biology of Hyaluronan. John Wiley and Sons, Chichester, 1989, vol. 143, pp 121–137 Google Scholar
Barondes SH: Bifunctional properties of lectins: lectins redefined. Trends Biochem Sci 13: 480–482, 1988 Google Scholar
Rao CN, Castronova V, Schmitt MC, Wiwer UM, Claysmith AP, Liotta LA, Sobel ME: Evidence for a precursor of the high affinity metastasis-associated murine laminin receptor. Biochem 28: 7476–7486, 1989 Google Scholar
Yow HK, Wong JM, Chen HS, Lee CG, Steele GDJ, Chen LB: Increased mRNA expression of a laminin-binding protein in human colon carcinoma: complete sequence of full length cDNA encoding the protein. Proc Natl Acad Sci USA 85: 6394–6398, 1988 Google Scholar
Smedsrod B, Pertoft H, Eriksson S, Fraser JRE, Laurent TC: Studies on the uptake and degradation of sodium hyaluronate in rat liver endothelial cells. Biochem J 223: 617–626, 1984 Google Scholar
Raja RH, McCarthy CT, Weigel PH: Affinity and distribution of surface and intracellular hyalronic acid receptors in isolated rat liver endothelial cells. J Biol Chem 263: 16661–16668, 1988 Google Scholar
Forsberg N, Gustafson S: Characterization and purification of the hyaluronan-receptor on liver endothelial cells. BBA 48: 12–18, 1991 Google Scholar
Knudson W, Biswas C, Li X-Q, Nemec RE, Toole BP: The role and regulation of tumor associated hyaluronan. In: Evered D, Whelan J (eds) Biology of Hyaluronan. Wiley and Sons, Chichester 143: 150–169, 1989 Google Scholar
Prehm P, Mausolf A: Isolation of streptococcal hyaluronate synthase. Biochem J 235: 887–889, 1986 Google Scholar
Banerjee SD, Toole BP: Monoclonal antibody to chick embryo hyaluronan-binding protein: changes in distribution of binding protein during early brain development. Devel Biol 146: 186–197, 1991 Google Scholar
Turley EA, Moore D, Hayden LJ: Characterization of hyaluronate binding proteins isolated from 3T3 and murine sarcoma virus transformed 3T3 cells. Biochemistry 26: 2997–3005, 1987 Google Scholar
Turley EA, Auersperg N: A hyaluronate binding protein transiently codistributes with p21, k-ras in cultured cell lines. Exp Cell Res 181: 340–348, 1989 Google Scholar
Turley EA, Hoare K, Cripps V: Manuscript in review, 1991
Longaker MT, Chiu ES, Harrison MR, Crombleholme TM, Langer JC, Duncan BW, Adzick NS, Verrier ED, Stern R: Studies in fetal wound healing IV. Hyaluronic acid stimulating activity distinguishes fetal wound fluid from adult wound fluid. Ann Surg 210: 667–672, 1989 Google Scholar
Auspunk DH, Folkman J: Migration and proliferation of endothelial cells in preformed and newly formed blood vessels during angeogenesis. Microvasc Res 14: 53–65, 1977 Google Scholar
Turley EA, Hoare K, Cripps V: Manuscript in review
Gunthert U, Hotman M, Rudy W, Reber S, Zoller M, Haubman I, Matzku S, Wenzel A, Ponta H, Herrlich P: A new variant of glycoprotein CD44 confers metastatic potential to rat carcinoma cells. Cell 65: 13–24, 1991 Google Scholar
Culp LA: Molecular composition and origin of substrata-attached material from normal and virus-transformed cells. J Supramol Struct 5: 239, 1976 Google Scholar
Turley EA: Hyaluronic acid stimulates protein kinase activity in intact cells and is an isolated protein complex. J Biol Chem 264: 8951–8955, 1989 Google Scholar