Arl13b-KO 基因敲除小鼠

1. Cantagrel, Vincent, Silhavy, Jennifer L, Bielas, Stephanie L, Woods, C Geoffrey, Gleeson, Joseph G. . Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. In American journal of human genetics, 83, 170-9. doi:10.1016/j.ajhg.2008.06.023. https://pubmed.ncbi.nlm.nih.gov/18674751/

2. Barral, Duarte C, Garg, Salil, Casalou, Cristina, Hsu, Victor W, Brenner, Michael B. 2012. Arl13b regulates endocytic recycling traffic. In Proceedings of the National Academy of Sciences of the United States of America, 109, 21354-9. doi:10.1073/pnas.1218272110. https://pubmed.ncbi.nlm.nih.gov/23223633/

3. Dilan, Tanya L, Moye, Abigail R, Salido, Ezequiel M, Goldberg, Andrew F X, Ramamurthy, Visvanathan. 2018. ARL13B, a Joubert Syndrome-Associated Protein, Is Critical for Retinogenesis and Elaboration of Mouse Photoreceptor Outer Segments. In The Journal of neuroscience : the official journal of the Society for Neuroscience, 39, 1347-1364. doi:10.1523/JNEUROSCI.1761-18.2018. https://pubmed.ncbi.nlm.nih.gov/30573647/