1. Tsai, Jhih-Jie, Hsu, Wen-Bin, Liu, Jia-Hua, Chang, Ching-Wen, Tang, Tang K. 2019. CEP120 interacts with C2CD3 and Talpid3 and is required for centriole appendage assembly and ciliogenesis. In Scientific reports, 9, 6037. doi:10.1038/s41598-019-42577-0. https://pubmed.ncbi.nlm.nih.gov/30988386/
2. Sharma, Ashwani, Gerard, Samuel F, Olieric, Natacha, Steinmetz, Michel O. 2018. Cep120 promotes microtubule formation through a unique tubulin binding C2 domain. In Journal of structural biology, 203, 62-70. doi:10.1016/j.jsb.2018.01.009. https://pubmed.ncbi.nlm.nih.gov/29398280/
3. Langner, Ewa, Cheng, Tao, Kefaloyianni, Eirini, Wang, Baolin, Mahjoub, Moe R. 2023. Cep120 is essential for kidney stromal progenitor cell growth and differentiation. In EMBO reports, 25, 428-454. doi:10.1038/s44319-023-00019-z. https://pubmed.ncbi.nlm.nih.gov/38177914/
4. Chang, Chia-Hsiang, Chen, Ting-Yu, Lu, I-Ling, Lin, Pin-Yeh, Tang, Tang K. 2021. CEP120-mediated KIAA0753 recruitment onto centrioles is required for timely neuronal differentiation and germinal zone exit in the developing cerebellum. In Genes & development, 35, 1445-1460. doi:10.1101/gad.348636.121. https://pubmed.ncbi.nlm.nih.gov/34711653/
5. Dong, Yan, Zhang, Ke, Yao, He, Zhao, Shichao, Shi, Xiaoyi. 2023. Clinical and genetic characteristics of 36 children with Joubert syndrome. In Frontiers in pediatrics, 11, 1102639. doi:10.3389/fped.2023.1102639. https://pubmed.ncbi.nlm.nih.gov/37547106/
6. Roosing, Susanne, Romani, Marta, Isrie, Mala, Gleeson, Joseph G, Valente, Enza Maria. 2016. Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes. In Journal of medical genetics, 53, 608-15. doi:10.1136/jmedgenet-2016-103832. https://pubmed.ncbi.nlm.nih.gov/27208211/
7. Powell, L, Barroso-Gil, M, Clowry, G J, Miles, C G, Sayer, J A. 2020. Expression patterns of ciliopathy genes ARL3 and CEP120 reveal roles in multisystem development. In BMC developmental biology, 20, 26. doi:10.1186/s12861-020-00231-3. https://pubmed.ncbi.nlm.nih.gov/33297941/