Risultati della ricerca - Min‐Xin Guan

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  1. 1
    A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

    A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity di Min‐Xin Guan

    Pubblicazione 2000
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  2. 2
    Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

    Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation di Min‐Xin Guan

    Pubblicazione 2001
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  3. 3
    Biochemical evidence for nuclear gene involvement in phenotype of non- syndromic deafness associated with mitochondrial 12S rRNA mutation

    Biochemical evidence for nuclear gene involvement in phenotype of non- syndromic deafness associated with mitochondrial 12S rRNA mutation di Min‐Xin Guan

    Pubblicazione 1996
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  4. 4
    Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated Mutation

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

    Pubblicazione 2009
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  5. 5
    A Human Mitochondrial GTP Binding Protein Related to tRNA Modification May Modulate Phenotypic Expression of the Deafness-Associated Mitochondrial 12S rRNA Mutation

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

    Pubblicazione 2002
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  6. 6
    Human Mitochondrial Leucyl-tRNA Synthetase Corrects Mitochondrial Dysfunctions Due to the tRNA<sup>Leu(UUR)</sup> A3243G Mutation, Associated with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Symptoms and Diabetes

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

    Pubblicazione 2010
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  7. 7
    Combination of the Loss of cmnm5U34 with the Lack of s2U34 Modifications of tRNALys, tRNAGlu, and tRNAGln Altered Mitochondrial Biogenesis and Respiration

    Combination of the Loss of cmnm5U34 with the Lack of s2U34 Modifications of tRNALys, tRNAGlu, and tRNAGln Altered Mitochondrial Biogenesis and Respiration di Xinjian Wang, Qingfeng Yan, Min‐Xin Guan

    Pubblicazione 2009
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  8. 8
    A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation

    A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation di Chao Chen, Ye Chen, Min‐Xin Guan

    Pubblicazione 2015
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  9. 9
    Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity

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

    Pubblicazione 2017
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  10. 10
    Isolation and Characterization of the Putative Nuclear Modifier Gene MTO1 Involved in the Pathogenesis of Deafness-associated Mitochondrial 12 S rRNA A1555G Mutation

    Isolation and Characterization of the Putative Nuclear Modifier Gene MTO1 Involved in the Pathogenesis of Deafness-associated Mitochondrial 12 S rRNA A1555G Mutation di Xiaoming Li, Ronghua Li, Xinhua Lin, Min‐Xin Guan

    Pubblicazione 2002
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  11. 11
    Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets

    Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets di Jing Chen, Hamidreza Riazifar, Min‐Xin Guan, Taosheng Huang

    Pubblicazione 2016
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  12. 12
    The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells

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

    Pubblicazione 2017
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  13. 13
    Human Exonuclease 1 Functionally Complements Its Yeast Homologues in DNA Recombination, RNA Primer Removal, and Mutation Avoidance

    Human Exonuclease 1 Functionally Complements Its Yeast Homologues in DNA Recombination, RNA Primer Removal, and Mutation Avoidance di Junzhuan Qiu, Ying Qian, Victoria Chen, Min‐Xin Guan, Binghui Shen

    Pubblicazione 1999
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  14. 14
    Emerging functions of mitochondria-encoded noncoding RNAs

    Emerging functions of mitochondria-encoded noncoding RNAs di Bingbing Ren, Min‐Xin Guan, Tianhua Zhou, Xiujun Cai, Ge Shan

    Pubblicazione 2022
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  15. 15
    Failures in Mitochondrial tRNA <sup>Met</sup> and tRNA <sup>Gln</sup> Metabolism Caused by the Novel 4401A&gt;G Mutation Are Involved in Essential Hypertension in a Han Chinese Family

    Failures in Mitochondrial tRNA <sup>Met</sup> and tRNA <sup>Gln</sup> Metabolism Caused by the Novel 4401A&gt;G Mutation Are Involved in Essential Hypertension in a Han Chinese Fam... di Ronghua Li, Yuqi Liu, Zongbin Li, Li Yang, Shiwen Wang, Min‐Xin Guan

    Pubblicazione 2009
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  16. 16
    Species identification through mitochondrial rRNA genetic analysis

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

    Pubblicazione 2014
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  17. 17
    Mitochondrial Transfer RNA <sup>Met</sup> 4435A&gt;G Mutation Is Associated With Maternally Inherited Hypertension in a Chinese Pedigree

    Mitochondrial Transfer RNA <sup>Met</sup> 4435A&gt;G Mutation Is Associated With Maternally Inherited Hypertension in a Chinese Pedigree di Yuqi Liu, Ronghua Li, Zongbin Li, Xinjian Wang, Li Yang, Shiwen Wang, Min‐Xin Guan

    Pubblicazione 2009
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  18. 18
    Leber’s hereditary optic neuropathy (LHON)-associated ND5 12338T &gt; C mutation altered the assembly and function of complex I, apoptosis and mitophagy

    Leber’s hereditary optic neuropathy (LHON)-associated ND5 12338T &gt; C mutation altered the assembly and function of complex I, apoptosis and mitophagy di Juanjuan Zhang, Yanchun Ji, Yuanyuan Lu, Runing Fu, Man Xu, Xiaoling Liu, Min‐Xin Guan

    Pubblicazione 2018
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  19. 19
    The Deafness-Associated Mitochondrial DNA Mutation at Position 7445, Which Affects tRNA<sup>Ser(UCN)</sup> Precursor Processing, Has Long-Range Effects on NADH Dehydrogenase Subunit ND6 Gene Expression

    The Deafness-Associated Mitochondrial DNA Mutation at Position 7445, Which Affects tRNA<sup>Ser(UCN)</sup> Precursor Processing, Has Long-Range Effects on NADH Dehydrogenase Subuni... di Min‐Xin Guan, José Antonio Enrı́quez, Nathan Fischel‐Ghodsian, Ram S. Puranam, Catherine Lin, Marion A. Maw, Giuseppe Attardi

    Pubblicazione 1998
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  20. 20
    A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function

    A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function di Mi Zhou, Ling Xue, Yaru Chen, Haiying Li, Qiufen He, Bibin Wang, Feilong Meng, Meng Wang, Min‐Xin Guan

    Pubblicazione 2017
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