1. Gao, Kai, Deng, Xiong, Zheng, Wen, Xiu, Xiaofei, Deng, Hao. 2013. Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease. In BMC neurology, 13, 125. doi:10.1186/1471-2377-13-125. https://pubmed.ncbi.nlm.nih.gov/24063688/
2. Lü, YiQing, Cho, Tiffany, Mukherjee, Saptaparna, Durocher, Daniel, Schramek, Daniel. 2024. Genome-wide CRISPR screens identify novel regulators of wild-type and mutant p53 stability. In Molecular systems biology, 20, 719-740. doi:10.1038/s44320-024-00032-x. https://pubmed.ncbi.nlm.nih.gov/38580884/
3. Hoellerbauer, Pia, Kufeld, Megan, Arora, Sonali, Olson, James M, Paddison, Patrick J. 2024. FBXO42 activity is required to prevent mitotic arrest, spindle assembly checkpoint activation and lethality in glioblastoma and other cancers. In NAR cancer, 6, zcae021. doi:10.1093/narcan/zcae021. https://pubmed.ncbi.nlm.nih.gov/38774470/
4. Burdon, Kathryn P, Hattersley, Kathryn, Lachke, Salil A, Mackey, David A, Craig, Jamie E. 2008. Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract. In Molecular vision, 14, 1799-804. doi:. https://pubmed.ncbi.nlm.nih.gov/18843385/
智鼠故事 
