1. Guidi, Riccardo, Wedeles, Christopher, Xu, Daqi, Hackney, Jason A, Wilson, Mark S. 2023. Argonaute3-SF3B3 complex controls pre-mRNA splicing to restrain type 2 immunity. In Cell reports, 42, 113515. doi:10.1016/j.celrep.2023.113515. https://pubmed.ncbi.nlm.nih.gov/38096048/
2. Chen, Tanxiu, Yang, Hao, Liu, Penghui, Lu, Shuaiyao, Peng, Xiaozhong. 2022. Splicing factor SF3B3, a NS5-binding protein, restricts ZIKV infection by targeting GCH1. In Virologica Sinica, 38, 222-232. doi:10.1016/j.virs.2022.12.005. https://pubmed.ncbi.nlm.nih.gov/36572150/
3. Wang, Junxiang, Weng, Yali, Li, Yinhan, Wu, Siying, Li, Huangyuan. 2023. The interplay between lncRNA NR_030777 and SF3B3 in neuronal damage caused by paraquat. In Ecotoxicology and environmental safety, 255, 114804. doi:10.1016/j.ecoenv.2023.114804. https://pubmed.ncbi.nlm.nih.gov/36948007/
4. Chang, Chun-Chi, Chang, Ya-Sian, Chan, Wen-Ling, Wei, Ren-Jeng, Chang, Jan-Gowth. . Detection of SF3B3 gene mutations in oral cancer by high resolution melting analysis. In Clinical laboratory, 60, 2023-9. doi:. https://pubmed.ncbi.nlm.nih.gov/25651737/
5. Zhang, Shouyue, Zhang, Jin, An, Yang, Xu, Heng, Liu, Bo. 2020. Multi-omics approaches identify SF3B3 and SIRT3 as candidate autophagic regulators and druggable targets in invasive breast carcinoma. In Acta pharmaceutica Sinica. B, 11, 1227-1245. doi:10.1016/j.apsb.2020.12.013. https://pubmed.ncbi.nlm.nih.gov/34094830/
6. Gökmen-Polar, Yesim, Neelamraju, Yaseswini, Goswami, Chirayu P, Janga, Sarath Chandra, Badve, Sunil. 2014. Expression levels of SF3B3 correlate with prognosis and endocrine resistance in estrogen receptor-positive breast cancer. In Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 28, 677-85. doi:10.1038/modpathol.2014.146. https://pubmed.ncbi.nlm.nih.gov/25431237/
7. Chen, Chaoqun, Huang, Fang, Li, Xiaojie, Qi, Yangfan, Wang, Yang. 2024. Identification of splicing factors signature predicting prognosis risk and the mechanistic roles of novel oncogenes in HNSCC. In Biochimica et biophysica acta. Molecular basis of disease, 1870, 167115. doi:10.1016/j.bbadis.2024.167115. https://pubmed.ncbi.nlm.nih.gov/38458543/
8. Li, Hao, Ding, Zhan, Fang, Zhuo-Ya, Fan, Yu-Jie, Xu, Yong-Zhen. . Conserved intronic secondary structures with concealed branch sites regulate alternative splicing of poison exons. In Nucleic acids research, 52, 6002-6016. doi:10.1093/nar/gkae185. https://pubmed.ncbi.nlm.nih.gov/38499485/