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. 2025 Mar 14;36(4):ar50. doi: 10.1091/mbc.E24-12-0534

FIGURE 1:

FIGURE 1:

Expression patterns of MYC, miR-92, cRobo1 mRNA, and cRobo1 in the developing chicken spinal cord. (A, B) Immunostaining of MYC on transverse sections of developing chicken spinal cords at HH 15-17 (A) and HH 23-25 (B). (C–F) In situ hybridization of miR-92 (C–D) and cRobo1 mRNA (E–F) on transverse sections of developing chicken spinal cords at HH 15-17 (C and E) and HH 23-25 (D and F), respectively. (G–H) Immunostaining of cRobo1 on transverse sections of developing chicken spinal cords at HH 15-17 (G) and HH 23-25 (H). LF, the lateral funiculus; VF, the ventral funiculus. Arrowheads and arrows in A–F indicate the location of CN cell bodies and CA trajectories, respectively. White arrows in H indicate the LF and VF. Scale bar, 50 µm. (I) MYC expression (green) in a developing chicken CN and CA. An antibody against Axonin-1 was used to identify the CNs (red). A total of 100 cells were randomly analyzed. Scale bar, 10 µm.