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1

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

出版事項 2000

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Artigo

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2

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

出版事項 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 著者: Min‐Xin Guan

出版事項 1996

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Artigo

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4

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

出版事項 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 著者: Xiaoming Li, Min‐Xin Guan

出版事項 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,... 著者: Ronghua Li, Min‐Xin Guan

出版事項 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 著者: Xinjian Wang, Qingfeng Yan, Min‐Xin Guan

出版事項 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 著者: Chao Chen, Ye Chen, Min‐Xin Guan

出版事項 2015

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Revisão

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9

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

出版事項 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 著者: Xiaoming Li, Ronghua Li, Xinhua Lin, Min‐Xin Guan

出版事項 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 著者: Jing Chen, Hamidreza Riazifar, Min‐Xin Guan, Taosheng Huang

出版事項 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 著者: Qianqian Li, Zewen Gao, Ye Chen, Min‐Xin Guan

出版事項 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 著者: Junzhuan Qiu, Ying Qian, Victoria Chen, Min‐Xin Guan, Binghui Shen

出版事項 1999

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Artigo

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14

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

出版事項 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... 著者: Ronghua Li, Yuqi Liu, Zongbin Li, Li Yang, Shiwen Wang, Min‐Xin Guan

出版事項 2009

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Artigo

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16

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

出版事項 2014

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Artigo

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17

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

出版事項 2009

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

出版事項 2018

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

出版事項 1998

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Artigo

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20

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

出版事項 2017

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

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

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

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

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

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

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

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

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

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

検索結果 - Min‐Xin Guan

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

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

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

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

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

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

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

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

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

Species identification through mitochondrial rRNA genetic analysis 著者: 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 著者: 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 著者: 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 著者: 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... 著者: 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 著者: 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 著者: Juanjuan Zhang, Yanchun Ji, Yuanyuan Lu, Runing Fu, Man Xu, Xiaoling Liu, Min‐Xin Guan