Free Access
Issue
Math. Model. Nat. Phenom.
Volume 7, Number 6, 2012
Biological oscillations
Page(s) 95 - 106
DOI https://doi.org/10.1051/mmnp/20127605
Published online 12 December 2012
  1. A. Aulehla, O. Pourquié. Signaling gradients during paraxial mesoderm development. Cold Spring Harb. Perspect. Biol., 2 (2010), a000869. [CrossRef] [PubMed] [Google Scholar]
  2. A. Aulehla, C. Wehrle, B. Brand-Saberi, R. Kemler, A. Gossler, B. Kanzler, B. G. Herrman. Wnt3a plays a major role in the segmentation clock controlling somitogenesis. Dev. Cell., 4 (2003), 395-406. [CrossRef] [PubMed] [Google Scholar]
  3. A. Aulehla, W. Wiegrabe, V. Baubet, M. B. Wahl, X. Deng, M. Taketo, M. Lewandoski, O. Pourquié. A β-catenin gradient links the clock and wavefront systems in mouse embryo segmentation. Nat. Cell. Biol., 10 (2008), 186-193. [CrossRef] [PubMed] [Google Scholar]
  4. M. Campanelli, T. Gedeon. Somitogenesis clock-wave initiation requires differential decay and multiple binding sites for clock protein. PLoS Comp. Biol., 6 (2010), e1000728. [CrossRef] [Google Scholar]
  5. M. Campanelli. Multicellular mathematical models of somitogenesis. PhD thesis Montana State University (2009), ISBN 9781109317299. [Google Scholar]
  6. B. Christ, C. P. Ordahl. Early stages of chick somite development. Anat. Embryol., 191 (1995), 381-396. [CrossRef] [PubMed] [Google Scholar]
  7. O. Cinquin. Understanding the somitogenesis clock: what’s missing ? Mech. Dev., 124 (2007), 501-517. [CrossRef] [PubMed] [Google Scholar]
  8. J. Cooke, E. C. Zeeman. A clock and wavefront model for control of the number of repeated structures during animal morphogenesis. J. Theor. Biol., 58 (1976), 455-476. [CrossRef] [PubMed] [Google Scholar]
  9. M. L. Dequéant, E. Glynn, K. Gaudenz, M. Wahl, J. Chen, A. Mushegian, O. Pourquié. A complex oscillating network of signaling genes underlies the mouse segmentation clock. Science, 314 (2006), 1595-1598. [CrossRef] [PubMed] [Google Scholar]
  10. M. L. Dequéant, O. Pourquié. Segmental patterning of the vertebrate embryonic axis. Nat. Rev. Gen., 9 (2008), 370-382. [CrossRef] [PubMed] [Google Scholar]
  11. R. Diez del Corral, I. Olivera-Martínez, A. Goriely, E. Gale, M. Maden, K. Storey. Opposing FGF and retinoid pathways control ventral neural pattern, neuronal differentiation, and segmentation during body axis extension. Neuron, 40 (2003), 65-79. [CrossRef] [PubMed] [Google Scholar]
  12. J. Dubrulle, O. Pourquié. Coupling segmentation to axis formation. Dev., 131 (2004), 5783-5793. [CrossRef] [Google Scholar]
  13. J. Dubrulle, O. Pourquié. fgf8 mRNA decay establishes a gradient that couples axial elongation to patterning in the vertebrate embryo. Nature, 427 (2004), 419-422. [CrossRef] [PubMed] [Google Scholar]
  14. B. Ermentrout. Simulating, analyzing, and animating dynamical systems: a guide to XPPAUT for researchers and students. 1st Ed. Society for Industrial Mathematics. Philadelphia (2002). [Google Scholar]
  15. S. Gibb, M. Maroto, J. K. Dale. The segmentation clock mechanism moves up a notch. Trends Cell Biol., 20 (2010), 593-600. [CrossRef] [PubMed] [Google Scholar]
  16. S. Gibb, A. Zagorska, K. Melton, G. Tenin, I. Vacca, P. Trainor, M. Maroto, J. K. Dale. Interfering with Wnt signalling alters the periodicity of the segmentation clock. Dev. Biol., 330 (2009), 21-31. [CrossRef] [PubMed] [Google Scholar]
  17. F. Giudicelli, E. M. Özbudak, G. J. Wright, J. Lewis. Setting the tempo in development: An investigation of the zebrafish somite clock mechanism. PLoS Biol., 5 (2007), 1309-1323. [CrossRef] [Google Scholar]
  18. A. Goldbeter, D. Gonze, O. Pourquié. Sharp developmental thresholds defined through bistability by antagonistic gradients of retinoic acid and FGF signaling. Dev. Dyn., 236 (2007), 1495-1508. [CrossRef] [PubMed] [Google Scholar]
  19. A. Goldbeter, O. Pourquié. Modeling the segmentation clock as a network of coupled oscillations in the Notch, Wnt and FGF signaling pathways. J. Theor. Biol., 252 (2008), 574-585. [CrossRef] [PubMed] [Google Scholar]
  20. C. Gomez, E. M. Özbudak, J. Wunderlich, D. Baumann, J. Lewis, O. Pourquié. Control of segment number in vertebrate embryos. Nat. Lett., 454 (2008), 335-339. [CrossRef] [Google Scholar]
  21. A. Ishikawa, S. Kitajima, Y. Takahashi, H. Kokub, J. Kanno, T. Inoue, Y. Saga. Mouse Nkd2, a Wnt antagonist, exhibits oscillatory gene expression in the PSM under the control of Notch signaling. Mech. Dev., 121 (2004), 1443-1453. [CrossRef] [PubMed] [Google Scholar]
  22. P. B. Jensen, L. Pedersen, S. Krishna, M. H. Jensen. A Wnt oscillator model for somitogenesis. Biophys. J., 98 (2010), 943-950. [CrossRef] [PubMed] [Google Scholar]
  23. J. Lewis. Autoinhibition with transcriptional delay: a simple mechanism for the zebrafish somitogenesis oscillator. Curr. Biol., 13 (2003), 1398-1408. [CrossRef] [PubMed] [Google Scholar]
  24. I. Palmeirim, D. Henrique, D. Ish-Horowicz, O. Pourquié. Avian hairy gene expression identifies a molecular clock linked to vertebrate segmentation and somitogenesis. Cell, 91 (1997), 639-648. [CrossRef] [PubMed] [Google Scholar]
  25. P. C. G. Rida, N. Le Minh, Y. J. Jiang. A Notch feeling of somite segmentation and beyond. Dev. Biol., 265 (2004), 2-22. [CrossRef] [PubMed] [Google Scholar]
  26. J. G. Rodríguez-González, M. Santillán, A. C. Fowler, M. C. Mackey. The segmentation clock in mice: interaction between the Wnt and Notch signalling pathways. J. Theor. Biol., 248 (2007), 37-47. [CrossRef] [PubMed] [Google Scholar]
  27. Y. Saga, H. Takeda. The making of the somite: Molecular events in vertebrate segmentation. Nat. Rev. Gen., 2 (2001), 835-845. [CrossRef] [Google Scholar]
  28. M. Santillán, M. C. Mackey. A proposed mechanism for the interaction of the segmentation clock and the determination front in somitogenesis. PLoS ONE, 3 (2008), e1561. [CrossRef] [PubMed] [Google Scholar]
  29. M. B. Wahl, C. Deng, M. Lewandoski, O. Pourquié. FGF signaling acts upstream of the NOTCH and WNT signaling pathways to control segmentation clock oscillations in mouse somitogenesis. Dev., 134 (2007), 4033-4041. [CrossRef] [Google Scholar]
  30. Y. Yasuhiko, S. Haraguchi, S. Kitajima, Y. Takahashi, J. Kanno, Y. Saga. Tbx6-mediated notch signaling controls somite-specific mesp2 expression. Proc. Natl. Acad. Sci. USA, 103 (2006), 3651-6. [CrossRef] [Google Scholar]

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