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  1. 1.   The Wnt3a/beta-catenin target gene Mesogenin1 controls the segmentation clock by activating a Notch signalling program
  2. Chalamalasetty, R. B.; Dunty, W. C.; Biris, K. K.; Ajima, R.; Iacovino, M.; Beisaw, A.; Feigenbaum, L.; Chapman, D. L.; Yoon, J. K.; Kyba, M.; Yamaguchi, T. P.
  3. Nature Communications. 2011, Jul; 2: 12.
  1. 2.   The microRNA-processing enzyme Dicer is dispensable for somite segmentation but essential for limb bud positioning
  2. Zhang, Z.; O'Rourke, J. R.; McManus, M. T.; Lewandoski, M.; Harfe, B. D.; Sun, X.
  3. Developmental Biology. 2011, Mar; 351(2): 254-265.
  1. 3.   FGF4 and FGF8 comprise the wavefront activity that controls somitogenesis
  2. Naiche, L. A.; Holder, N.; Lewandoski, M.
  3. Proceedings of the National Academy of Sciences of the United States of America. 2011, Mar; 108(10): 4018-4023.
  1. 4.   A beta-catenin gradient links the clock and wavefront systems in mouse embryo segmentation
  2. Aulehla, A.; Wiegraebe, W.; Baubet, V.; Wahl, M. B.; Deng, C. X.; Taketo, M.; Lewandoski, M.; Pourquie, O.
  3. Nature Cell Biology. 2008 10(2): 186-193.
  1. 5.   Wnt3a/beta-catenin signaling controls posterior body development by coordinating mesoderm formation and segmentation
  2. Dunty, W. C.; Biris, K. K.; Chalamalasetty, R. B.; Taketo, M. M.; Lewandoski, M.; Yamaguchi, T. P.
  3. Development. 2008 135(1): 85-94.
  1. 6.   FGF signaling acts upstream of the NOTCH and WNT signaling pathways to control segmentation clock oscillations in mouse somitogenesis
  2. Wahl, M. B.; Deng, C.; Lewandoski, M.; Pourquie, O.
  3. Development. 2007, Nov; 134(22): 4033-4041.
  1. 7.   Mouse Ripply2 is downstream of Wnt3a and is dynamically expressed during somitogenesis
  2. Biris, K. K.; Dunty, W. C.; Yamaguchi, T. P.
  3. Developmental Dynamics. 2007, Nov; 236(11): 3167-3172.
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