Dahkkiohcama bohtosat

1

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

Almmustuhtton 2000

Viečča ollesdeavstta
Artigo

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Furkejuvvon:
2

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

Almmustuhtton 2001

Viečča ollesdeavstta
Artigo

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Furkejuvvon:
3

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

Almmustuhtton 1996

Viečča ollesdeavstta
Artigo

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Furkejuvvon:
4

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

Almmustuhtton 2009

Viečča ollesdeavstta
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 Dahkki Xiaoming Li, Min‐Xin Guan

Almmustuhtton 2002

Viečča ollesdeavstta
Artigo

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Furkejuvvon:
6

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

Almmustuhtton 2010

Viečča ollesdeavstta
Artigo

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Furkejuvvon:
7

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

Almmustuhtton 2009

Viečča ollesdeavstta
Artigo

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8

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

Almmustuhtton 2015

Viečča ollesdeavstta Viečča ollesdeavstta
Revisão

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9

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

Almmustuhtton 2017

Viečča ollesdeavstta
Revisão

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Furkejuvvon:
10

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

Almmustuhtton 2002

Viečča ollesdeavstta Viečča ollesdeavstta
Artigo

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Furkejuvvon:
11

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

Almmustuhtton 2016

Viečča ollesdeavstta Viečča ollesdeavstta
Artigo

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12

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

Almmustuhtton 2017

Viečča ollesdeavstta Viečča ollesdeavstta
Revisão

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Furkejuvvon:
13

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

Almmustuhtton 1999

Viečča ollesdeavstta Viečča ollesdeavstta
Artigo

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14

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

Almmustuhtton 2022

Viečča ollesdeavstta Viečča ollesdeavstta
Revisão

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Furkejuvvon:
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... Dahkki Ronghua Li, Yuqi Liu, Zongbin Li, Li Yang, Shiwen Wang, Min‐Xin Guan

Almmustuhtton 2009

Viečča ollesdeavstta Viečča ollesdeavstta
Artigo

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Furkejuvvon:
16

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

Almmustuhtton 2014

Viečča ollesdeavstta Viečča ollesdeavstta
Artigo

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17

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

Almmustuhtton 2009

Viečča ollesdeavstta Viečča ollesdeavstta
Artigo

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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 Dahkki Juanjuan Zhang, Yanchun Ji, Yuanyuan Lu, Runing Fu, Man Xu, Xiaoling Liu, Min‐Xin Guan

Almmustuhtton 2018

Viečča ollesdeavstta Viečča ollesdeavstta
Artigo

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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... Dahkki Min‐Xin Guan, José Antonio Enrı́quez, Nathan Fischel‐Ghodsian, Ram S. Puranam, Catherine Lin, Marion A. Maw, Giuseppe Attardi

Almmustuhtton 1998

Viečča ollesdeavstta
Artigo

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Furkejuvvon:
20

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

Almmustuhtton 2017

Viečča ollesdeavstta Viečča ollesdeavstta
Artigo

Lasit oiddohiidda

Furkejuvvon:

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

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

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

Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated Mutation Dahkki 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 Dahkki 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,... Dahkki 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 Dahkki Xinjian Wang, Qingfeng Yan, Min‐Xin Guan

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

Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity Dahkki 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 Dahkki Xiaoming Li, Ronghua Li, Xinhua Lin, Min‐Xin Guan

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

The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells Dahkki 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 Dahkki Junzhuan Qiu, Ying Qian, Victoria Chen, Min‐Xin Guan, Binghui Shen

Emerging functions of mitochondria-encoded noncoding RNAs Dahkki 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... Dahkki Ronghua Li, Yuqi Liu, Zongbin Li, Li Yang, Shiwen Wang, Min‐Xin Guan

Species identification through mitochondrial rRNA genetic analysis Dahkki 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 Dahkki 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 Dahkki 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 Dahkki Mi Zhou, Ling Xue, Yaru Chen, Haiying Li, Qiufen He, Bibin Wang, Feilong Meng, Meng Wang, Min‐Xin Guan

Ohcanbohtosat - Min‐Xin Guan

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

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

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

Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated Mutation Dahkki 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 Dahkki 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,... Dahkki 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 Dahkki Xinjian Wang, Qingfeng Yan, Min‐Xin Guan

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

Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity Dahkki 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 Dahkki Xiaoming Li, Ronghua Li, Xinhua Lin, Min‐Xin Guan

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

The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells Dahkki 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 Dahkki Junzhuan Qiu, Ying Qian, Victoria Chen, Min‐Xin Guan, Binghui Shen

Emerging functions of mitochondria-encoded noncoding RNAs Dahkki 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... Dahkki Ronghua Li, Yuqi Liu, Zongbin Li, Li Yang, Shiwen Wang, Min‐Xin Guan

Species identification through mitochondrial rRNA genetic analysis Dahkki 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 Dahkki 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 Dahkki 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 Dahkki Mi Zhou, Ling Xue, Yaru Chen, Haiying Li, Qiufen He, Bibin Wang, Feilong Meng, Meng Wang, Min‐Xin Guan

Ohcanreaiddut:

Laktáseaddji fáttát

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... Dahkki 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 Dahkki 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 Dahkki Juanjuan Zhang, Yanchun Ji, Yuanyuan Lu, Runing Fu, Man Xu, Xiaoling Liu, Min‐Xin Guan