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The Journal of Neuroscience, April 1, 2003, ():

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Control of Growth Cone Motility and Morphology by LIM Kinase and Slingshot via Phosphorylation and Dephosphorylation of Cofilin
J. Neurosci. Endo et al. 23 (7): 2527.

Movies

Files in this Data Supplement:

  • Movie 2c - Axonal transport of LIMK1(WT)-YFP. Chick E7 DRG neurons were infected with HSV coding for YFP-fused chick LIMK1(WT), and recorded 12 h later by video fluorescence microscopy. Each frame is acquired every 5 seconds (area : 260 mm x 260 mm). Anterograde and retrograde movements of LIMK1(WT)-YFP-containing vesicles can be seen.
  • Movie 3a - Time-lapse fluorescence images of growth cones expressing YFP-actin. Each frame is acquired every 2 minutes (area : 100 mm x 100 mm). See legend to Figure 3A for details.
  • Movie 3b - Time-lapse fluorescence images of growth cones expressing YFP-actin plus LIMK1(WT)-CFP. Each frame is acquired every 2 minutes (area : 100 mm x 100 mm). See legend to Figure 3B for details.
  • Movie 3c - Time-lapse fluorescence images of growth cones expressing YFP-actin plus LIMK1(D467A)-CFP. Each frame is acquired every 2 minutes (area : 100 mm x 100 mm). See legend to Figure 3C for details.
  • Movie 4a - Time-lapse fluorescence images of growth cones expressing cof(WT)-YFP. Each frame is acquired every 2 minutes (area : 80 mm x 80 mm). See legend to Figure 4A for details.
  • Movie 4b - Time-lapse fluorescence images of growth cones expressing cof(S3A)-YFP. Each frame is acquired every 2 minutes (area : 80 mm x 80 mm). See legend to Figure 4B for details.
  • Movie 4c - Time-lapse fluorescence images of growth cones expressing SSH1(WT)-YFP. Each frame is acquired every 2 minutes (area : 80 mm x 80 mm). See legend to Figure 4C for details.
  • Movie 4d - Time-lapse fluorescence images of growth cones expressing SSH1(CS)-YFP. Each frame is acquired every 2 minutes (area : 80 mm x 80 mm). See legend to Figure 4D for details.




This Article
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