1. Wu, Jihao, Chen, Xiong, Li, Ruijun, Li, Yanbing, Huang, Yinong. 2024. Identifying genetic determinants of sarcopenia-related traits: a Mendelian randomization study of druggable genes. In Metabolism: clinical and experimental, 160, 155994. doi:10.1016/j.metabol.2024.155994. https://pubmed.ncbi.nlm.nih.gov/39117060/
2. Richard, Daniel, Liu, Zun, Cao, Jiaxue, Roach, Neil, Capellini, Terence D. 2020. Evolutionary Selection and Constraint on Human Knee Chondrocyte Regulation Impacts Osteoarthritis Risk. In Cell, 181, 362-381.e28. doi:10.1016/j.cell.2020.02.057. https://pubmed.ncbi.nlm.nih.gov/32220312/
3. Gumus, Evren, Temiz, Ebru, Sarikaya, Baran, Sipahioglu, Serkan, Gonel, Ataman. 2020. The Association Between BMP-2, UQCC1 and CX3CR1 Polymorphisms and the Risk of Developmental Dysplasia of the Hip. In Indian journal of orthopaedics, 55, 169-175. doi:10.1007/s43465-020-00235-y. https://pubmed.ncbi.nlm.nih.gov/33569111/
4. Tucker, Elena J, Wanschers, Bas F J, Szklarczyk, Radek, Huynen, Martijn A, Thorburn, David R. 2013. Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression. In PLoS genetics, 9, e1004034. doi:10.1371/journal.pgen.1004034. https://pubmed.ncbi.nlm.nih.gov/24385928/
5. Yang, Aruhan, Zhu, Xiaoxue, Zhang, Lei, Ding, Yanhua, Lv, Guoyue. 2022. Non-invasive evaluation of NAFLD and the contribution of genes: an MRI-PDFF-based cross-sectional study. In Hepatology international, 16, 1035-1051. doi:10.1007/s12072-022-10355-2. https://pubmed.ncbi.nlm.nih.gov/35829866/
智鼠故事 
