1. Yang, Lin, Pang, Xinping, Guo, Wenbo, Wang, Kui, Pang, Chaoyang. 2023. An Exploration of the Coherent Effects between METTL3 and NDUFA10 on Alzheimer's Disease. In International journal of molecular sciences, 24, . doi:10.3390/ijms241210111. https://pubmed.ncbi.nlm.nih.gov/37373264/
2. Zhang, Haokun, Shao, Yuanhua, Chen, Weijun, Chen, Xin. 2021. Identifying Mitochondrial-Related Genes NDUFA10 and NDUFV2 as Prognostic Markers for Prostate Cancer through Biclustering. In BioMed research international, 2021, 5512624. doi:10.1155/2021/5512624. https://pubmed.ncbi.nlm.nih.gov/34124242/
3. Hoefs, Saskia J G, van Spronsen, Francjan J, Lenssen, Ellen W H, Smeitink, Jan A M, van den Heuvel, Lambert P. 2010. NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. In European journal of human genetics : EJHG, 19, 270-4. doi:10.1038/ejhg.2010.204. https://pubmed.ncbi.nlm.nih.gov/21150889/
4. Zhu, Yuhan, Song, Binyu, Yang, Ziyi, Chen, Lin, Song, Baoqiang. 2023. Integrative lactylation and tumor microenvironment signature as prognostic and therapeutic biomarkers in skin cutaneous melanoma. In Journal of cancer research and clinical oncology, 149, 17897-17919. doi:10.1007/s00432-023-05483-7. https://pubmed.ncbi.nlm.nih.gov/37955686/
5. Minoia, Francesca, Bertamino, Marta, Picco, Paolo, Santorelli, Filippo Maria, Di Rocco, Maja. 2017. Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation. In JIMD reports, 37, 37-43. doi:10.1007/8904_2017_9. https://pubmed.ncbi.nlm.nih.gov/28247337/
6. Yan, Li, Pan, Chun-Shui, Liu, Yu-Ying, He, Ke, Han, Jing-Yan. 2021. The Composite of 3, 4-Dihydroxyl-Phenyl Lactic Acid and Notoginsenoside R1 Attenuates Myocardial Ischemia and Reperfusion Injury Through Regulating Mitochondrial Respiratory Chain. In Frontiers in physiology, 12, 538962. doi:10.3389/fphys.2021.538962. https://pubmed.ncbi.nlm.nih.gov/34322032/
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