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Fig. 4 | Cilia

Fig. 4

From: Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia

Fig. 4

IFT43 mutations induce ciliogenesis defects. a, b ARL13B (green) and Ac-Tub (red) staining of the cilia in control and R03-121A fibroblasts. Pericentrin (green) staining was used to mark the centrosome. Nuclei were stained in blue. R03-121A fibroblasts did not show cilia staining with ARL13B or Ac-Tub, only pericentrin centriole staining

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