1. Fuhrmann, Dominik C, Wittig, Ilka, Brüne, Bernhard. 2018. TMEM126B deficiency reduces mitochondrial SDH oxidation by LPS, attenuating HIF-1α stabilization and IL-1β expression. In Redox biology, 20, 204-216. doi:10.1016/j.redox.2018.10.007. https://pubmed.ncbi.nlm.nih.gov/30368040/
2. Zhou, Xiyue, Lou, Xiaoting, Zhou, Yuwei, Yang, Yanling, Wang, Ya. 2022. Novel biallelic mutations in TMEM126B cause splicing defects and lead to Leigh-like syndrome with severe complex I deficiency. In Journal of human genetics, 68, 239-246. doi:10.1038/s10038-022-01102-4. https://pubmed.ncbi.nlm.nih.gov/36482121/
3. Wen, Shaodi, Zou, Renrui, Du, Xiaoyue, Wang, Xin, Shen, Bo. 2024. Identification of macrophage-related genes correlated with prognosis and immunotherapy efficacy in non-small cell lung cancer. In Heliyon, 10, e27170. doi:10.1016/j.heliyon.2024.e27170. https://pubmed.ncbi.nlm.nih.gov/38500993/
4. Wei, Lihong, Fan, Yun, Wei, Lingling, Yang, Jiaqing, Zheng, Xianzhao. 2020. Ablation of TMEM126B protects against oxygen-glucose deprivation/reoxygenation-induced injuries of PC12 cells via maintaining mitochondrial anti-apoptotic functions. In Archives of biochemistry and biophysics, 696, 108634. doi:10.1016/j.abb.2020.108634. https://pubmed.ncbi.nlm.nih.gov/33075301/
5. Alston, Charlotte L, Compton, Alison G, Formosa, Luke E, Thorburn, David R, Taylor, Robert W. 2016. Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype. In American journal of human genetics, 99, 217-27. doi:10.1016/j.ajhg.2016.05.021. https://pubmed.ncbi.nlm.nih.gov/27374774/
6. Andrews, Byron, Carroll, Joe, Ding, Shujing, Fearnley, Ian M, Walker, John E. 2013. Assembly factors for the membrane arm of human complex I. In Proceedings of the National Academy of Sciences of the United States of America, 110, 18934-9. doi:10.1073/pnas.1319247110. https://pubmed.ncbi.nlm.nih.gov/24191001/