1. Wang, Meilin, Liu, Hongliang, Liu, Zhensheng, Amos, Christopher I, Wei, Qingyi. 2016. Genetic variant in DNA repair gene GTF2H4 is associated with lung cancer risk: a large-scale analysis of six published GWAS datasets in the TRICL consortium. In Carcinogenesis, 37, 888-896. doi:10.1093/carcin/bgw070. https://pubmed.ncbi.nlm.nih.gov/27288692/
2. Seifert, Bryce A, Dejosez, Marion, Zwaka, Thomas P. 2017. Ronin influences the DNA damage response in pluripotent stem cells. In Stem cell research, 23, 98-104. doi:10.1016/j.scr.2017.06.014. https://pubmed.ncbi.nlm.nih.gov/28715716/
3. Liu, Hongying, Xu, Danping, Zhong, Xin, Ge, Junbo, Li, Hua. 2019. LncRNA-mRNA competing endogenous RNA network depicts transcriptional regulation in ischaemia reperfusion injury. In Journal of cellular and molecular medicine, 23, 2272-2276. doi:10.1111/jcmm.14163. https://pubmed.ncbi.nlm.nih.gov/30657634/
4. Porter, Louise F, Saptarshi, Neil, Fang, Yongxiang, Chavali, Venkata R M, Paraoan, Luminita. 2019. Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes. In Clinical epigenetics, 11, 6. doi:10.1186/s13148-019-0608-2. https://pubmed.ncbi.nlm.nih.gov/30642396/
5. Kim, J Y, Kim, J-H, Bae, J S, Park, C-S, Shin, H D. 2012. Lack of association between GTF2H4 genetic variants and AERD development and FEV1 decline by aspirin provocation. In International journal of immunogenetics, 39, 486-91. doi:10.1111/j.1744-313X.2012.01118.x. https://pubmed.ncbi.nlm.nih.gov/22524621/
智鼠故事 
