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Mitochondrion|June 21, 2025
Novel mutations in MTERF3: First report of a new genetic cause in two Chinese patients with developmental delay, intermittent hypoglycemia and metabolic acidosisRuoyu Duan, Refiloe Laurentinah Mahlatsi, Ya Wang, et al.
Diabetes|November 23, 2021
GRP75 Regulates Mitochondrial-Supercomplex Turnover to Modulate Insulin SensitivityQiongya Zhao, Ting Luo, Feng Gao, et al.
Cell Reports|April 14, 2021
A membrane arm of mitochondrial complex I sufficient to promote respirasome formationHezhi Fang, Xianglai Ye, Jie Xie, et al.
Journal of Human Genetics|December 9, 2022
Novel biallelic mutations in TMEM126B cause splicing defects and lead to Leigh-like syndrome with severe complex I deficiencyXiyue Zhou, Xiaoting Lou, Yuwei Zhou, et al.
Gene|January 30, 2023
De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndromeXiaoting Lou, Yuwei Zhou, Zhimei Liu, et al.
Molecular & Cellular Proteomics : MCP|January 21, 2026
Multi-Omics Profiling Reveals Distinct Immunosuppression and Metabolic Dysregulation in Aggressive Subtypes of Thyroid CancerShanying Gui, Kate Huang, Jianling Qiang, et al.
Annals of Clinical and Translational Neurology|February 6, 2025
Novel pathogenic mtDNA variants in Chinese children with neurological mitochondrial disordersZhimei Liu, Kexin Pan, Mingzhao Wang, et al.
Cell Discovery|July 24, 2023
The Fe-S cluster assembly protein IscU2 increases α-ketoglutarate catabolism and DNA 5mC to promote tumor growthXiaojun Ren, Jimei Yan, Qiongya Zhao, et al.
Metabolism: Clinical and Experimental|June 27, 2022
Serine active site containing protein 1 depletion alters lipid metabolism and protects against high fat diet-induced obesity in miceMiaomiao Du, Xueyun Li, Fangyi Xiao, et al.
Science Translational Medicine|March 2, 2022
SERAC1 is a component of the mitochondrial serine transporter complex required for the maintenance of mitochondrial DNAHezhi Fang, Anran Xie, Miaomiao Du, et al.
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