Danmin Shen

Capital University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index474citations30works5.22yr avg
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Research Topics

Mitochondrial Function and Pathology(13), Metabolism and Genetic Disorders(9), Ferroptosis and cancer prognosis(6), Metalloenzymes and iron-sulfur proteins(4), ATP Synthase and ATPases Research(4)

Publications30 total

RNA sequencing resolves cryptic pathogenic variants in mitochondrial disease
2026Open Access
Complex de novo tetrasomy and trisomy of 2p22.2 involving EIF2AK2 in a child with global developmental delay: a case report and literature review
Frontiers in Pediatrics·2026Open Access
Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Orphanet Journal of Rare Diseases·2026Open Access
Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Figshare·2026Open Access
Additional file 1 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Figshare·2026Open Access
Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Figshare·2026Open Access
Additional file 3 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Figshare·2026Open Access
Additional file 2 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Figshare·2026Open Access
Additional file 3 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Figshare·2026Open Access
Additional file 1 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Figshare·2026Open Access
Additional file 2 of Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease
Figshare·2026Open Access
Clinical, metabolic, and genetic characteristics of 42 children with mitochondrial short-chain enoyl-CoA hydratase 1 deficiency in China
Molecular Genetics and Metabolism·2025· 1 cited
A novel m.5906G > a variant in MT-CO1 causes MELAS/Leigh overlap syndrome
Molecular Genetics and Genomics·2024
Itaconate protects ferroptotic neurons by alkylating GPx4 post stroke
Cell Death and Differentiation·2024· 33 cited
Targeted macrophage phagocytosis by Irg1/itaconate axis improves the prognosis of intracerebral hemorrhagic stroke and peritonitis
EBioMedicine·2024· 44 citedOpen Access
IL-10 protects against OPC ferroptosis by regulating lipid reactive oxygen species levels post stroke
Redox Biology·2023· 41 citedOpen Access
H3K9 trimethylation dictates neuronal ferroptosis through repressing <i>Tfr1</i>
Journal of Cerebral Blood Flow & Metabolism·2023· 18 citedOpen Access
Detection of Ferroptosis in Models of Brain Diseases
Methods in molecular biology·2023· 2 cited
Inhibition of the LRRC8A channel promotes microglia/macrophage phagocytosis and improves outcomes after intracerebral hemorrhagic stroke
iScience·2022· 17 citedOpen Access
The contribution of spinal dorsal horn astrocytes in neuropathic pain at the early stage of EAE
Neurobiology of Disease·2022· 13 citedOpen Access
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Frequent Co-authors

Qian Li(11), Minhan Song(11), Ruoyu Duan(11), Zhimei Liu(10), Huafang Jiang(10), Liye Hu(9), Zhongnan Xiao(8), Ting Lan(8), Zhaoli Luo(8), Fei Yang(8), Zhimei Liu(8), Jiuwei Li(8), Chunqiang Xu(8), Weihua Zhang(8), Ji Zhou(8), Zixuan Zhang(8), Tongyue Li(8), Ying Zou(8), Junling Wang(8), Fang Fang(8)