1. Xu, Taojie, Yang, Minghua, Jian, Zonghui, Jia, Junjing, Zhao, Sumei. 2022. Cloning of FITM2 gene and investigating its expression levels in Banna miniature inbred pig (Sus scrofa) tissues. In Animal biotechnology, 34, 1566-1572. doi:10.1080/10495398.2022.2041024. https://pubmed.ncbi.nlm.nih.gov/35189068/
2. Lawson, Keith A, Sousa, Cristovão M, Zhang, Xiaoyu, Kung, Charles, Moffat, Jason. 2020. Functional genomic landscape of cancer-intrinsic evasion of killing by T cells. In Nature, 586, 120-126. doi:10.1038/s41586-020-2746-2. https://pubmed.ncbi.nlm.nih.gov/32968282/
3. Salazar-Villacorta, Ainara, Bond, Laura M, Kim, Leehyeon, Walther, Tobias C, Farese, Robert V. 2025. Partial loss of FITM2 function causes hereditary spastic paraplegia. In medRxiv : the preprint server for health sciences, , . doi:10.1101/2025.01.23.24319660. https://pubmed.ncbi.nlm.nih.gov/39974099/
4. Chen, Yan, Ji, Li-Juan, Wang, Yan, Guo, Xiang-Feng. 2021. High FITM2 expression promotes cell migration ability of hepatocellular carcinoma by regulating the formation of caveolae and indicates poor patient survival. In Histology and histopathology, 36, 1085-1092. doi:10.14670/HH-18-382. https://pubmed.ncbi.nlm.nih.gov/34672358/
5. Zazo Seco, Celia, Castells-Nobau, Anna, Joo, Seol-Hee, Kremer, Hannie, Siddiqi, Saima. 2016. A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. In Disease models & mechanisms, 10, 105-118. doi:10.1242/dmm.026476. https://pubmed.ncbi.nlm.nih.gov/28067622/
智鼠故事 
