Code Repository for Clinicomics Analysis
0 citationsZenodo (CERN European Organization for Nuclear Research)
Xiaoting Lou
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
24Publications signalées
148Citations signalées
3Affiliations récentes
Institutions déclarées
Domaines associés
Mitochondrial Function and PathologyATP Synthase and ATPases ResearchMetabolism and Genetic DisordersRNA modifications and cancerMetalloenzymes and iron-sulfur proteins
Publications récentes
Code Repository for Clinicomics Analysis
0 citationsZenodo (CERN European Organization for Nuclear Research)
COG5 deficiency disrupts cellular copper homeostasis and underlies the impaired mitochondrial OXPHOS function
Yuwei Zhou, Keyi Li, Ruowei Zhu, Xue Ma et autres
0 citationsPLoS Genetics
A Heteroplasmic MT-CO2 m.8024G > A Variant Is Associated with Mitochondrial Bioenergetic Deficiency and Optic Atrophy
Jing Wu, Cunhui Pan, Ruowei Zhu, Xi Huang et autres
1 citationMolecular Neurobiology
Biallelic FOXRED1 mutations cause infantile mitochondrial encephalopathy with complex I disassembly and basal ganglia degeneration
Ruowei Zhu, Xi‐Ping Huang, Haolin Duan, Tenghui Wu et autres
0 citationsMitochondrion
β-hydroxybutyrate dehydrogenase promotes pancreatic cancer cell proliferation through regulation of the NAD+/NADH balance and mitochondrial acetylation
Xiujuan Wei, Chengkai Zhang, Xiaoguang Zheng, Xiaojun Ren et autres
2 citationsJournal of Biological Chemistry
Expanding the phenotypic and genetic spectrum of GTPBP3 deficiency: findings from nine Chinese pedigrees
Yaojun Xie, Keyi Li, Li Yang, Xiaofei Zeng et autres
1 citationOrphanet Journal of Rare Diseases
Prestack true-amplitude angle-domain viscoelastic least squares reverse time migration
Yue Wang, Yang Luo, Peng Shen, Jingru Chen et autres
0 citations
Biallelic variants in the NDUFAF6 cause mitochondrial respiratory complex assembly defects associated with Leigh syndrome in probands
Yuwei Zhou, Xiaofei Zeng, Luyi Zhang, Yin Xiaojie et autres
4 citationsMolecular Genetics and Metabolism Reports
Expanding the phenotypic and genetic spectrum of GTPBP3 deficiency: findings from nine Chinese pedigrees
Yaojun Xie, Keyi Li, Yang Li, Xiaofei Zeng et autres
0 citationsResearch Square
Integrative multi-omics profiling reveals the molecular subtypes and circulating biomarkers for pediatric mitochondrial disease
Jianxin Lyu, Xiaoting Lou, Zhehui Chen, Qiongya Zhao et autres
0 citationsResearch Square
De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndrome
Xiaoting Lou, Yuwei Zhou, Zhimei Liu, Yaojun Xie et autres
15 citationsGene
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