Accès gratuit
Med Sci (Paris)
Volume 24, Numéro 2, Février 2008
Page(s) 157 - 162
Section M/S revues
Publié en ligne 15 février 2008
  1. Hall A. Rho GTPases and the actin cytoskeleton. Science 1998; 279 : 509–14. [Google Scholar]
  2. Burridge K, Wennerberg K. Rho and Rac take center stage. Cell 2004; 116 : 167–79. [Google Scholar]
  3. Vetter IR, Wittinghofer A. The guanine nucleotide-binding switch in three dimensions. Science 2001; 294 : 1299–304. [Google Scholar]
  4. Valencia A, Chardin P, Wittinghofer A, Sander C. The ras protein family: evolutionary tree and role of conserved amino acids. Biochemistry 1991; 30 : 4637–48. [Google Scholar]
  5. Williams CL. The polybasic region of Ras and Rho family small GTPases: a regulator of protein interactions and membrane association and a site of nuclear localization signal sequences. Cell Signal 2003; 15 : 1071–80. [Google Scholar]
  6. Armstrong SA, Hannah VC, Goldstein JL, Brown MS. CAAX geranylgeranyl transferase transfers farnesyl as efficiently as geranylgeranyl to RhoB. J Biol Chem 1995; 270 : 7864–8. [Google Scholar]
  7. Sahai E, Marshall CJ. RHO-GTPases and cancer. Nat Rev Cancer 2002; 2 : 133–42. [Google Scholar]
  8. Olson MF, Paterson HF, Marshall CJ. Signals from Ras and Rho GTPases interact to regulate expression of p21Waf1/Cip1. Nature 1998; 394 : 295–9. [Google Scholar]
  9. Adnane J, Muro-Cacho C, Mathews L, Sebti SM, Munoz-Antonia T. Suppression of rho B expression in invasive carcinoma from head and neck cancer patients. Clin Cancer Res 2002; 8 : 2225–32. [Google Scholar]
  10. Zalcman G, Closson V, Linares-Cruz G, et al. Regulation of Ras-related RhoB protein expression during the cell cycle. Oncogene 1995; 10 : 1935–45. [Google Scholar]
  11. Knaus UG, Wang Y, Reilly AM, Warnock D, Jackson JH. Structural requirements for PAK activation by Rac GTPases. J Biol Chem 1998; 273 : 21512–8. [Google Scholar]
  12. Haataja L, Groffen J, Heisterkamp N. Characterization of RAC3, a novel member of the Rho family. J Biol Chem 1997; 272 : 20384–8. [Google Scholar]
  13. Roberts AW, Kim C, Zhen L, et al. Deficiency of the hematopoietic cell-specific Rho family GTPase Rac2 is characterized by abnormalities in neutrophil function and host defense. Immunity 1999; 10 : 183–96. [Google Scholar]
  14. Katoh H, Negishi M. RhoG activates Rac1 by direct interaction with the Dock180-binding protein Elmo. Nature 2003; 424 : 461–4. [Google Scholar]
  15. Nakaya M, Tanaka M, Okabe Y, Hanayama R, Nagata S. Opposite effects of rho family GTPases on engulfment of apoptotic cells by macrophages. J Biol Chem 2006; 281 : 8836–42. [Google Scholar]
  16. Michaelson D, Silletti J, Murphy G, et al. Differential localization of Rho GTPases in live cells: regulation by hypervariable regions and RhoGDI binding. J Cell Biol 2001; 152 : 111–26. [Google Scholar]
  17. Tanabe K, Tachibana T, Yamashita T, et al. The small GTP-binding protein TC10 promotes nerve elongation in neuronal cells, and its expression is induced during nerve regeneration in rats. J Neurosci 2000; 20 : 4138–44. [Google Scholar]
  18. Erschbamer MK, Hofstetter CP, Olson L. RhoA, RhoB, RhoC, Rac1, Cdc42, and Tc10 mRNA levels in spinal cord, sensory ganglia, and corticospinal tract neurons and long-lasting specific changes following spinal cord injury. J Comp Neurol 2005; 484 : 224–33. [Google Scholar]
  19. Chiang SH, Baumann CA, Kanzaki M, et al. Insulin-stimulated GLUT4 translocation requires the CAP-dependent activation of TC10. Nature 2001; 410 : 944–8. [Google Scholar]
  20. De Toledo M, Senic-Matuglia F, Salamero J, et al. The GTP/GDP cycling of rho GTPase TCL is an essential regulator of the early endocytic pathway. Mol Biol Cell 2003; 14 : 4846–56. [Google Scholar]
  21. Tao W, Pennica D, Xu L, et al. Wrch-1, a novel member of the Rho gene family that is regulated by Wnt-1. Genes Dev 2001; 15 : 1796–807. [Google Scholar]
  22. Chenette EJ, Abo A, Der CJ. Critical and distinct roles of amino- and carboxyl-terminal sequences in regulation of the biological activity of the Chp atypical Rho GTPase. J Biol Chem 2005; 280 : 13784–92. [Google Scholar]
  23. Shutes A, Berzat AC, Cox AD, Der CJ. Atypical mechanism of regulation of the Wrch-1 Rho family small GTPase. Curr Biol 2004; 14 : 2052–6. [Google Scholar]
  24. Chardin P. Function and regulation of Rnd proteins. Nat Rev Mol Cell Biol 2006; 7 : 54–62. [Google Scholar]
  25. Foster R, Hu KQ, Lu Y, et al. Identification of a novel human Rho protein with unusual properties: GTPase deficiency and in vivo farnesylation. Mol Cell Biol 1996; 16 : 2689–99. [Google Scholar]
  26. Nobes CD, Lauritzen I, Mattei MG, et al. A new member of the Rho family, Rnd1, promotes disassembly of actin filament structures and loss of cell adhesion. J Cell Biol 1998; 141 : 187–97. [Google Scholar]
  27. Wennerberg K, Forget MA, Ellerbroek SM, et al. Rnd proteins function as RhoA antagonists by activating p190 RhoGAP. Curr Biol 2003; 13 : 1106–15. [Google Scholar]
  28. Oinuma I, Ishikawa Y, Katoh H, Negishi M. The Semaphorin 4D receptor Plexin-B1 is a GTPase activating protein for R-Ras. Science 2004; 305 : 862–5. [Google Scholar]
  29. Aspenstrom P, Fransson A, Saras J. Rho GTPases have diverse effects on the organization of the actin filament system. Biochem J 2004; 377 : 327–37. [Google Scholar]
  30. Gasman S, Kalaidzidis Y, Zerial M. RhoD regulates endosome dynamics through diaphanous-related formin and Src tyrosine kinase. Nat Cell Biol 2003; 5 : 195–204. [Google Scholar]
  31. Ellis S, Mellor H. The novel Rho-family GTPase rif regulates coordinated actin-based membrane rearrangements. Curr Biol 2000; 10 : 1387–90. [Google Scholar]
  32. Rivero F, Dislich H, Glockner G, Noegel AA. The Dictyostelium discoideum family of Rho-related proteins. Nucleic Acids Res 2001; 29 : 1068–79. [Google Scholar]
  33. Siripurapu V, Meth J, Kobayashi N, Hamaguchi M. DBC2 significantly influences cell-cycle, apoptosis, cytoskeleton and membrane-trafficking pathways. J Mol Biol 2005; 346 : 83–9. [Google Scholar]
  34. St-Pierre B, Jiang Z, Egan SE, Zacksenhaus E. High expression during neurogenesis but not mammogenesis of a murine homologue of the deleted in breast cancer2/Rhobtb2 tumor suppressor. Gene Expr Patterns 2004; 5 : 245–51. [Google Scholar]
  35. Cherry LK, Li X, Schwab P, et al. RhoH is required to maintain the integrin LFA-1 in a nonadhesive state on lymphocytes. Nat Immunol 2004; 5 : 961–7. [Google Scholar]

Les statistiques affichées correspondent au cumul d'une part des vues des résumés de l'article et d'autre part des vues et téléchargements de l'article plein-texte (PDF, Full-HTML, ePub... selon les formats disponibles) sur la platefome Vision4Press.

Les statistiques sont disponibles avec un délai de 48 à 96 heures et sont mises à jour quotidiennement en semaine.

Le chargement des statistiques peut être long.