1. Wang, Xin, Liu, Qian, Yu, Hai-Tao, Yang, Ying, Wang, Jian-Zhi. 2024. A positive feedback inhibition of isocitrate dehydrogenase 3β on paired-box gene 6 promotes Alzheimer-like pathology. In Signal transduction and targeted therapy, 9, 105. doi:10.1038/s41392-024-01812-5. https://pubmed.ncbi.nlm.nih.gov/38679634/
2. Bizjak, Tina, Gorenjak, Mario, Potočnik, Uroš, But, Igor. 2020. Polymorphism on chromosome 20p13 near the IDH3B gene is associated with uterine prolapse. In European journal of obstetrics, gynecology, and reproductive biology, 252, 155-159. doi:10.1016/j.ejogrb.2020.06.047. https://pubmed.ncbi.nlm.nih.gov/32619879/
3. Lin, Wenhao, Ye, Changchun, Sun, Liangzhang, Kong, Ranran, Xu, Zhengshui. 2024. A novel mitochondrial metabolism-related gene signature for predicting the prognosis of oesophageal squamous cell carcinoma. In Aging, 16, 9649-9679. doi:10.18632/aging.205892. https://pubmed.ncbi.nlm.nih.gov/38843392/
4. Ren, Zhuqing, Liu, Wanghong, Zheng, Rong, Ni, Debin, Xiong, Yuanzhu. 2011. A 304 bp insertion/deletion mutation in promoter region induces the increase of porcine IDH3β gene expression. In Molecular biology reports, 39, 1419-26. doi:10.1007/s11033-011-0876-1. https://pubmed.ncbi.nlm.nih.gov/21617947/
5. Duncan, Dianne M, Kiefel, Paula, Duncan, Ian. 2017. Mutants for Drosophila Isocitrate Dehydrogenase 3b Are Defective in Mitochondrial Function and Larval Cell Death. In G3 (Bethesda, Md.), 7, 789-799. doi:10.1534/g3.116.037366. https://pubmed.ncbi.nlm.nih.gov/28104670/
6. Yoshimi, N, Futamura, T, Bergen, S E, Landén, M, Hashimoto, K. 2016. Cerebrospinal fluid metabolomics identifies a key role of isocitrate dehydrogenase in bipolar disorder: evidence in support of mitochondrial dysfunction hypothesis. In Molecular psychiatry, 21, 1504-1510. doi:10.1038/mp.2015.217. https://pubmed.ncbi.nlm.nih.gov/26782057/
7. Bianco, Lorenzo, Navarro, Julien, Michiels, Christelle, Audo, Isabelle, Zeitz, Christina. 2025. Identification of IDH3G, encoding the gamma subunit of mitochondrial isocitrate dehydrogenase, as a novel candidate gene for X-linked retinitis pigmentosa. In Genetics in medicine : official journal of the American College of Medical Genetics, , 101418. doi:10.1016/j.gim.2025.101418. https://pubmed.ncbi.nlm.nih.gov/40119724/
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