1. Valente, Onofrio, Dobner, Jochen, Ramachandran, Haribaskar, Ventura, Natascia, Rossi, Andrea. 2022. Generation of an induced pluripotent stem cell line (IUFi002-A) from a Leigh syndrome patient carrying mutations in the NDUFS1 gene. In Stem cell research, 65, 102971. doi:10.1016/j.scr.2022.102971. https://pubmed.ncbi.nlm.nih.gov/36403546/
2. Zhu, Yunlong, Wang, Zhongliang, Ni, Jianliang, Zhang, Wen, Zhang, Chen. 2014. Genetic variant in NDUFS1 gene is associated with schizophrenia and negative symptoms in Han Chinese. In Journal of human genetics, 60, 11-6. doi:10.1038/jhg.2014.94. https://pubmed.ncbi.nlm.nih.gov/25354934/
3. Wu, Dong, He, Lin, Xu, Zhe, Qin, Jun, Li, Ling. 2023. The combination of NDUFS1 with CD4+ T cell infiltration predicts favorable prognosis in kidney renal clear cell carcinoma. In Frontiers in cell and developmental biology, 11, 1168462. doi:10.3389/fcell.2023.1168462. https://pubmed.ncbi.nlm.nih.gov/37469574/
4. Kashani, Alireza, Thiffault, Isabelle, Dilenge, Marie-Emmanuelle, Braverman, Nancy, Bernard, Geneviève. 2014. A homozygous mutation in the NDUFS1 gene presents with a mild cavitating leukoencephalopathy. In Neurogenetics, 15, 161-4. doi:10.1007/s10048-014-0412-2. https://pubmed.ncbi.nlm.nih.gov/24952175/
5. Elkholi, Rana, Abraham-Enachescu, Ioana, Trotta, Andrew P, Pfleger, Cathie M, Chipuk, Jerry Edward. 2019. MDM2 Integrates Cellular Respiration and Apoptotic Signaling through NDUFS1 and the Mitochondrial Network. In Molecular cell, 74, 452-465.e7. doi:10.1016/j.molcel.2019.02.012. https://pubmed.ncbi.nlm.nih.gov/30879903/
6. Peng, Li, Ma, Wei, Xie, Qing, Chen, Baihua. 2021. Identification and validation of hub genes for diabetic retinopathy. In PeerJ, 9, e12126. doi:10.7717/peerj.12126. https://pubmed.ncbi.nlm.nih.gov/34603851/
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