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Home All issues Volume 18 / No 10 (Octobre 2002) Med Sci (Paris), 18 10 (2002) 982-988 References
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Issue
Med Sci (Paris)
Volume 18, Number 10, Octobre 2002
Page(s) 982 - 988
Section M/S Revues : Articles de Synthèse
DOI https://doi.org/10.1051/medsci/20021810982
Published online 15 October 2002
  1. Jones FS, Jones PL. The tenascin family of ECM glycoproteins : structure, function and regulation during embryonnic development and tissue remodeling. Dev Dyn 2000; 218 : 235–59. [Google Scholar]
  2. Erickson HP, Inglesias JL. A six-armed oligomer isolated from cell surface fibronectin preparations. Nature 1984; 311 : 267–9. [Google Scholar]
  3. Joester A, Faissner A. Evidence for combinatorial variability of tenascin-C isoforms and developmental regulation in the mouse central nervous system. J Biol Chem 1999; 274 : 17144–51. [Google Scholar]
  4. Joester A, Faissner A. The structure and function of tenascins in the nervous system. Matrix Biol 2001; 20 : 13–22. [Google Scholar]
  5. Jones PL, Jones FS. Tenascin-C in development and disease : gene regulation and cell function. Matrix Biol 2001; 19 : 581–96. [Google Scholar]
  6. Crossin KL, Hoffman S, Grumet M, Thiery JP, Edelman GM. Site restricted expression of cytotactin during development of the chicken embryo. J Cell Biol 1986; 102 : 1917–30. [Google Scholar]
  7. Kawano H, Ohyama K, Kawamura K, Nagatsu I. Migration of dopaminergic neurons in the embryonic mesencephalon of mice. Brain Res Dev Brain Res 1986; 86 : 101–13. [Google Scholar]
  8. Kiernan BW, Götz B, Faissner A, ffrench-Constant C. Tenascin-C inhibits oligodendrocyte precursor cell migration by both adhesion-dependent and adhesion-independent mechanisms. Mol Cell Neurosci 1996; 7 : 322–35. [Google Scholar]
  9. Faissner A, Kruse J. J1/tenascin is a repulsive substrate for central nervous system neurons. Neuron 1990; 5 : 627–37. [Google Scholar]
  10. Götz M, Scholze A, Clement A, et al. Tenascin-C contains distinct adhesive, anti-adhesive, and neurite outgrowth promoting sites for neurons. J Cell Biol 1996; 132 : 681–99. [Google Scholar]
  11. Chuong CM, Crossin KL, Edelman GM. Sequential expression and differential function of multiple adhesion molecules during the formation of cerebellar cortical layers. J Cell Biol 1987; 104 : 331–42. [Google Scholar]
  12. Götz M, Bolz J, Joester A, Faissner A. Tenascin-C synthesis and influence on axonal growth during rat cortical development. Eur J Neurosci 1997; 9 : 496–506. [Google Scholar]
  13. Saga Y, Yagi T, Ikawa Y, Sakakura T, Aizawa S. Mice develop normally without tenascin. Genes Dev 1992; 6 : 1821–31. [Google Scholar]
  14. Forsberg E, Hirsch E, Frohlich L, et al. Skin wounds and severe nerves heal normally in mice lacking tenascin-C. Proc Natl Acad Sci USA 1996; 93 : 6594–9. [Google Scholar]
  15. Kiernan BW, Garcion E, Ferguson J, et al.. Myelination and behavior of tenascin-C null transgenic mice. Eur J Neurosci 1999; 11 : 3082–92. [Google Scholar]
  16. Mackie EJ, Tucker RP. The tenascin-C knockout revisited. J Cell Sci 1999; 112 : 3847–53. [Google Scholar]
  17. Mège RM, Nicolet M, Pincon-Raymond M, Murawsky M, Rieger F. Cytotactin is involved in synaptogenesis during regeneration of the frog neuromuscular system. Dev Biol 1992; 149 : 381–94. [Google Scholar]
  18. Schachner M. Neural recognition molecules and synaptic plasticity. Curr Opin Cell Biol 1997; 9 : 627–34. [Google Scholar]
  19. Cifuentes-Diaz C, Velasco E, Meunier FA, et al. The peripheral nerve and the neuromuscular junction are affected in the tenascin-C-deficient mouse. Cell Mol Biol 1998; 44 : 357–79. [Google Scholar]
  20. Cifuentes-Diaz C, Faille L, Goudou D, Schachner M, Rieger F, Angaut-Petit D. Abnormal reinnervation of skeletal muscle in a tenascin-C-deficient mouse. J Neurosci Res 2002; 67 : 93–9. [Google Scholar]
  21. Bartsch U. The extracellular matrix molecule tenascin-C : expression in vivo and functional characterization in vitro. Prog Neurobiol 1996; 49 : 145–68. [Google Scholar]
  22. Garcion E, Faissner A, ffrench-Constant C. Knockout mice reveal a contribution of the extracellular matrix molecule tenascin-C to neural precursor proliferation and migration. Development 2001; 126 : 2485–96. [Google Scholar]
  23. Frost E, Kiernan BW, Faissner A, ffrench-Constant C. Regulation of oligodendrocyte precursor migration by extracellular matrix : evidence for substrate-specific inhibition of migration by tenascin-C. Dev Neurosci 1996; 18 : 266–73. [Google Scholar]

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