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. Author manuscript; available in PMC: 2015 May 13.
Published in final edited form as: Stem Cells. 2015 Jan;33(1):68–78. doi: 10.1002/stem.1854

Figure 7.

Figure 7

The impact of taxol on the morphology of parkin-deficient neurons. (A–H) Representative morphology of P001 (A, B) or P002 (C, D) TH+ neurons treated with vehicle (A, C) or taxol (1 nM for 14 days) (B, D) and quantification of their total neurite length (E), number of terminals (F), number of branch points (G) and Sholl analysis (H). (I–P) Representative morphology of P001 (I, J) or P002 (K, L) TH− neurons treated with vehicle (I, K) or taxol (1 nM for 14 days) (J, L) and quantification of their total neurite length (M), number of terminals (N), number of branch points (O) and Sholl analysis (P). *, p < 0.001, vs. vehicle-treated P001 or P002, n = 52 TH+ neurons and n = 54 TH− neurons for each condition of P001 or P002 neurons, all from three independent experiments.