1. Hancock, Melissa L, Meyer, Rebecca C, Mistry, Meeta, Näär, Anders M, Flanagan, John G. 2019. Insulin Receptor Associates with Promoters Genome-wide and Regulates Gene Expression. In Cell, 177, 722-736.e22. doi:10.1016/j.cell.2019.02.030. https://pubmed.ncbi.nlm.nih.gov/30955890/
2. Minocha, Shilpi, Sung, Tzu-Ling, Villeneuve, Dominic, Lammers, Fabienne, Herr, Winship. 2016. Compensatory embryonic response to allele-specific inactivation of the murine X-linked gene Hcfc1. In Developmental biology, 412, 1-17. doi:10.1016/j.ydbio.2016.02.019. https://pubmed.ncbi.nlm.nih.gov/26921005/
3. Feng, Shenglei, Gui, Yiqian, Yin, Shi, Jiang, Xiaohua, Yuan, Shuiqiao. 2024. Histone demethylase KDM2A recruits HCFC1 and E2F1 to orchestrate male germ cell meiotic entry and progression. In The EMBO journal, 43, 4197-4227. doi:10.1038/s44318-024-00203-4. https://pubmed.ncbi.nlm.nih.gov/39160277/
4. He, Na, Guan, Bao-Zhu, Wang, Jie, Yi, Yong-Hong, Liao, Wei-Ping. . HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism. In Clinical and translational medicine, 13, e1289. doi:10.1002/ctm2.1289. https://pubmed.ncbi.nlm.nih.gov/37264743/
5. Hollstein, Ronja, Reiz, Benedikt, Kötter, Lucas, Lohmann, Katja, Kaiser, Frank J. . Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expression. In Human molecular genetics, 26, 2975-2983. doi:10.1093/hmg/ddx187. https://pubmed.ncbi.nlm.nih.gov/28486698/
6. Castro, Victoria L, Quintana, Anita M. 2020. The role of HCFC1 in syndromic and non-syndromic intellectual disability. In Medical research archives, 8, . doi:10.18103/mra.v8i6.2122. https://pubmed.ncbi.nlm.nih.gov/34164576/
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