Figure 4
- ID
- ZDB-FIG-201230-41
- Publication
- Epting et al., 2020 - Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome
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Reduced fraction of ciliated cells and increased primary cilia length in fibroblasts from patients. (a) Fibroblasts from two controls (images from one control shown) and from the individuals FA.II‐1, FA.II‐2, FB.II‐2 were fixed after 72 h of serum starvation and stained for ARL13B and CEP164 (Alexa488, green), CBY1 (Cy3, red), and nuclei (Hoechst, blue). The CBY1 signal was detected at the transition zone in the control, but not in cells from FA.II‐1, FA.II‐2, FB.II‐2. Scale bars are 10 µm in the left panel and 2 µm in the magnified pictures. (b) Fibroblasts from two controls and from the affected individuals FA.II‐1, FA.II‐2, FB.II‐2 were fixed after 72h serum starvation and stained for acetylated tubulin, CEP164, and nuclei (Hoechst). The numbers of ciliated fibroblasts were significantly reduced in FA.II‐1, FA.II‐2, and FB.II‐2 ( |