1. Wang, Pu, Yan, Feng, Li, Zhijun, Parnell, Scott E, Xiong, Yue. 2019. Impaired plasma membrane localization of ubiquitin ligase complex underlies 3-M syndrome development. In The Journal of clinical investigation, 129, 4393-4407. doi:10.1172/JCI129107. https://pubmed.ncbi.nlm.nih.gov/31343991/
2. Nie, Jianyun, Xu, Chao, Jin, Jing, Pawson, Tony, Yang, Xiang-Jiao. 2015. Ankyrin repeats of ANKRA2 recognize a PxLPxL motif on the 3M syndrome protein CCDC8. In Structure (London, England : 1993), 23, 700-12. doi:10.1016/j.str.2015.02.001. https://pubmed.ncbi.nlm.nih.gov/25752541/
3. Huang, Jungang, Li, Zexiong, Huang, Weipeng, Lin, Jun, Xu, Mingwei. 2024. Ablation of CCDC8 provides cardioprotection against cardiomyocyte apoptosis via TNF signaling pathway in myocardial ischemia reperfusion injury. In Life sciences, 358, 123151. doi:10.1016/j.lfs.2024.123151. https://pubmed.ncbi.nlm.nih.gov/39424266/
4. Li, Yunfen, Chen, Zhengting, Cao, Ke, Liu, Xiaoling, Li, Wenhui. 2021. G9a Regulates Cell Sensitivity to Radiotherapy via Histone H3 Lysine 9 Trimethylation and CCDC8 in Lung Cancer. In OncoTargets and therapy, 14, 3721-3728. doi:10.2147/OTT.S296937. https://pubmed.ncbi.nlm.nih.gov/34140780/
5. Jiang, Xiangxiang, Jia, Xiaopeng, Sun, Jinhuan, Zhang, Lei, Wei, Min. 2020. Overexpressed coiled-coil domain containing protein 8 (CCDC8) mediates newly synthesized HIV-1 Gag lysosomal degradation. In Scientific reports, 10, 11416. doi:10.1038/s41598-020-68341-3. https://pubmed.ncbi.nlm.nih.gov/32651437/
6. Yan, Jun, Yan, Feng, Li, Zhijun, Whitehurst, Angelique W, Xiong, Yue. 2014. The 3M complex maintains microtubule and genome integrity. In Molecular cell, 54, 791-804. doi:10.1016/j.molcel.2014.03.047. https://pubmed.ncbi.nlm.nih.gov/24793695/
7. Nakagawa, Tadahiko, Sato, Yasushi, Tanahashi, Toshihito, Bando, Yoshimi, Takayama, Tetsuji. 2019. JMJD2A sensitizes gastric cancer to chemotherapy by cooperating with CCDC8. In Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 23, 426-436. doi:10.1007/s10120-019-01024-9. https://pubmed.ncbi.nlm.nih.gov/31677131/
8. Hanson, Dan, Murray, Philip G, O'Sullivan, James, Clayton, Peter E, Black, Graeme C M. 2011. Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth. In American journal of human genetics, 89, 148-53. doi:10.1016/j.ajhg.2011.05.028. https://pubmed.ncbi.nlm.nih.gov/21737058/
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