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1

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

Опубліковано 2000

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Artigo

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2

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

Опубліковано 2001

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Artigo

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3

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

Опубліковано 1996

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Artigo

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4

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

Опубліковано 2009

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Artigo

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5

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

Опубліковано 2002

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Artigo

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6

Human Mitochondrial Leucyl-tRNA Synthetase Corrects Mitochondrial Dysfunctions Due to the tRNALeu(UUR) A3243G Mutation, Associated with Mitochondrial Encephalomyopathy,... за авторством Ronghua Li, Min‐Xin Guan

Опубліковано 2010

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Artigo

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7

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

Опубліковано 2009

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Artigo

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8

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

Опубліковано 2015

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Revisão

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9

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

Опубліковано 2017

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Revisão

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10

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

Опубліковано 2002

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Artigo

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11

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

Опубліковано 2016

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Artigo

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12

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

Опубліковано 2017

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Revisão

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13

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

Опубліковано 1999

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Artigo

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14

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

Опубліковано 2022

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Revisão

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15

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 Fam... за авторством Ronghua Li, Yuqi Liu, Zongbin Li, Li Yang, Shiwen Wang, Min‐Xin Guan

Опубліковано 2009

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Artigo

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16

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

Опубліковано 2014

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17

Mitochondrial Transfer RNA Met 4435A>G Mutation Is Associated With Maternally Inherited Hypertension in a Chinese Pedigree за авторством Yuqi Liu, Ronghua Li, Zongbin Li, Xinjian Wang, Li Yang, Shiwen Wang, Min‐Xin Guan

Опубліковано 2009

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18

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

Опубліковано 2018

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19

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

Опубліковано 1998

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20

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

Опубліковано 2017

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Artigo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Результати пошуку - Min‐Xin Guan

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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... за авторством Ronghua Li, Yuqi Liu, Zongbin Li, Li Yang, Shiwen Wang, Min‐Xin Guan

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

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

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

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

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

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

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