Risultati della ricerca - Guan, Min-xin

A Human Mitochondrial GTP Binding Protein Related to tRNA Modification May Modulate Phenotypic Expression of the Deafness-Associated Mitochondrial 12S rRNA Mutation di Li, Xiaoming, Guan, Min-Xin

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Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated Mutation di Qian, Yaping, Guan, Min-Xin

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Human Mitochondrial Leucyl-tRNA Synthetase Corrects Mitochondrial Dysfunctions Due to the tRNA(Leu(UUR)) A3243G Mutation, Associated with Mitochondrial Encephalomyopathy, Lactic Ac... di Li, Ronghua, Guan, Min-Xin

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Correction for Li and Guan, “Human Mitochondrial Leucyl-tRNA Synthetase Corrects Mitochondrial Dysfunctions Due to the tRNA(Leu(UUR)) A3243G Mutation, Associated with Mitochondrial... di Li, Ronghua, Guan, Min-Xin

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Combination of the loss of cmnm(5)U34 with the lack of s(2)U(34) modifications of tRNA(Lys), tRNA(Glu) and tRNA(Gln) altered mitochondrial biogenesis and respiration di Wang, Xinjian, Yan, Qingfeng, Guan, Min-Xin

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Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae di Wang, Xinjian, Yan, Qingfeng, Guan, Min-Xin

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Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity di Gao, Zewen, Chen, Ye, Guan, Min-Xin

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Mutations in MTO2 Related to tRNA Modification Impair Mitochondrial Gene Expression and Protein Synthesis in the Presence of a Paromomycin Resistance Mutation in Mitochondrial 15 S... di Yan, Qingfeng, Li, Xiaoming, Faye, Gèrard, Guan, Min-Xin

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The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells di Li, Qianqian, Gao, Zewen, Chen, Ye, Guan, Min-Xin

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In vitro culture of mammalian inner ear hair cells di Zhang, Lu-wen, Cang, Xiao-hui, Chen, Ye, Guan, Min-xin

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Investigating the Broad Matrix-Gate Network in the Mitochondrial ADP/ATP Carrier through Molecular Dynamics Simulations di Yao, Shihao, Ma, Boyuan, Yi, Qiuzi, Guan, Min-Xin, Cang, Xiaohui

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Failures in Mitochondrial tRNA(Met) and tRNA(Gln) Metabolism Caused by the Novel 4401A>G Mutation Are Involved in Essential Hypertension in a Han Chinese Family di Li, Ronghua, Liu, Yuqi, Li, Zongbin, Yang, Li, Wang, Shiwen, Guan, Min-Xin

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Frequency and spectrum of MT-TT variants associated with Leber’s hereditary optic neuropathy in a Chinese cohort of subjects di Lyu, Yuanyuan, Xu, Man, Chen, Jie, Ji, YanChun, Guan, Min-Xin, Zhang, Juanjuan

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Biochemical characterization of the mitochondrial tRNA(Ser(UCN)) T7511C mutation associated with nonsyndromic deafness di Li, Xiaoming, Fischel-Ghodsian, Nathan, Schwartz, Faina, Yan, Qingfeng, Friedman, Rick A., Guan, Min-Xin

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Species identification through mitochondrial rRNA genetic analysis di Yang, Li, Tan, Zongqing, Wang, Daren, Xue, Ling, Guan, Min-xin, Huang, Taosheng, Li, Ronghua

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Mechanistic insights into multiple-step transport of mitochondrial ADP/ATP carrier di Yao, Shihao, Yi, Qiuzi, Ma, Boyuan, Mao, Xiaoting, Chen, Ye, Guan, Min-Xin, Cang, Xiaohui

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Mitochondrial Transfer RNA(Met) 4435A>G Mutation Is Associated With Maternally Inherited Hypertension in a Chinese Pedigree di Liu, Yuqi, Li, Ronghua, Li, Zongbin, Wang, Xin-Jian, Yang, Li, Wang, Shiwen, Guan, Min-Xin

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Overexpression of human mitochondrial alanyl-tRNA synthetase suppresses biochemical defects of the mt-tRNA(Ala) mutation in cybrids di Zhao, Xiaoxu, Han, Jiamin, Zhu, Ling, Xiao, Yun, Wang, Chenghui, Hong, Fang, Jiang, Pingping, Guan, Min-Xin

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Deletion of Mtu1 (Trmu) in zebrafish revealed the essential role of tRNA modification in mitochondrial biogenesis and hearing function di Zhang, Qinghai, Zhang, Luwen, Chen, Danni, He, Xiao, Yao, Shihao, Zhang, Zengming, Chen, Ye, Guan, Min-Xin

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Association of MTHFR C677T polymorphism and type 2 diabetes mellitus (T2DM) susceptibility di Meng, Yanzi, Liu, Xiaoling, Ma, Kai, Zhang, Lili, Lu, Mao, Zhao, Minsu, Guan, Min‐Xin, Qin, Guijun

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