1. Zhao, Xueying, Chen, Jin, Yin, Shangqi, Yuan, Zhengrong, Wang, Yajie. 2022. The expression of cuproptosis-related genes in hepatocellular carcinoma and their relationships with prognosis. In Frontiers in oncology, 12, 992468. doi:10.3389/fonc.2022.992468. https://pubmed.ncbi.nlm.nih.gov/36313717/
2. Dreishpoon, Margaret B, Bick, Nolan R, Petrova, Boryana, Golub, Todd R, Tsvetkov, Peter. 2023. FDX1 regulates cellular protein lipoylation through direct binding to LIAS. In The Journal of biological chemistry, 299, 105046. doi:10.1016/j.jbc.2023.105046. https://pubmed.ncbi.nlm.nih.gov/37453661/
3. Gkiourtzis, Nikolaos, Tramma, Despoina, Papadopoulou-Legbelou, Kyriaki, Moutafi, Maria, Evangeliou, Athanasios. 2023. Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin-2 (FDX2) gene. In American journal of medical genetics. Part A, 191, 2843-2849. doi:10.1002/ajmg.a.63368. https://pubmed.ncbi.nlm.nih.gov/37565517/
4. Aggarwal, Anjali, Pillai, Nishitha R, Billington, Charles J, Schema, Lynn, Berry, Susan A. 2021. Rare presentation of FDX2-related disorder and untargeted global metabolomics findings. In American journal of medical genetics. Part A, 188, 1239-1244. doi:10.1002/ajmg.a.62608. https://pubmed.ncbi.nlm.nih.gov/34905296/
5. Joshi, Pallavi R, Sadre, Shayan, Guo, Xiaoyan A, McCoy, Jason G, Mootha, Vamsi K. 2023. Lipoylation is dependent on the ferredoxin FDX1 and dispensable under hypoxia in human cells. In The Journal of biological chemistry, 299, 105075. doi:10.1016/j.jbc.2023.105075. https://pubmed.ncbi.nlm.nih.gov/37481209/
6. Miyahara, Shuko, Ohuchi, Mai, Nomura, Miyuki, Yamada, Hidekazu, Tanuma, Nobuhiro. 2024. FDX2, an iron-sulfur cluster assembly factor, is essential to prevent cellular senescence, apoptosis or ferroptosis of ovarian cancer cells. In The Journal of biological chemistry, 300, 107678. doi:10.1016/j.jbc.2024.107678. https://pubmed.ncbi.nlm.nih.gov/39151727/
7. Gurgel-Giannetti, Juliana, Lynch, David S, Paiva, Anderson Rodrigues Brandão de, Houlden, Henry, Kok, Fernando. . A novel complex neurological phenotype due to a homozygous mutation in FDX2. In Brain : a journal of neurology, 141, 2289-2298. doi:10.1093/brain/awy172. https://pubmed.ncbi.nlm.nih.gov/30010796/
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