FIGURE

Fig. 5

ID

ZDB-FIG-150320-21

Publication

Lu et al., 2015 - A function for the Joubert syndrome protein Arl13b in ciliary membrane extension and ciliary length regulation

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Fig. 5

Arl13b is sufficient to restore ciliary length in FoxJ1 deficient zebrafish embryos.(A) Overexpression of Arl13b in embryos deficient in FoxJ1 is sufficient to restore the length of motile cilia. Embryos were analyzed at 24 hpf. (B) Quantitation of ciliary length in different groups of embryos. 10 embryos were analyzed for each group, 50 cilia from each embryo.

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	WT + MO2-foxj1a
Knockdown Reagent:	MO2-foxj1a
Observed In:	pronephric duct motile cilium
Stage:	Prim-5

Phenotype Detail

Acknowledgments

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Reprinted from Developmental Biology, 397(2), Lu, H., Toh, M.T., Narasimhan, V., Thamilselvam, S.K., Choksi, S.P., Roy, S., A function for the Joubert syndrome protein Arl13b in ciliary membrane extension and ciliary length regulation, 225-36, Copyright (2015) with permission from Elsevier. Full text @ Dev. Biol.