Transcriptome-Based Analysis Reveals Therapeutic Effects of Resveratrol on Endometriosis in aRat Model
Wang, Chunyan, Chen, Zhengyun, Zhao, Xianlei, Lin, Cuicui, Hong, Shenghui, Lou, Yuhan, Shi, Xiaomeng, Zhao, Mengdan, Yang, Xiaohang, Guan, Min-Xin, Xi, Yongmei
Published in Drug design, development and therapy (01.01.2021)
Published in Drug design, development and therapy (01.01.2021)
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Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family
Zhao, Hui, Li, Ronghua, Wang, Qiuju, Yan, Qingfeng, Deng, Jian-Hong, Han, Dongyi, Bai, Yidong, Young, Wie-Yen, Guan, Min-Xin
Published in American journal of human genetics (01.01.2004)
Published in American journal of human genetics (01.01.2004)
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Isolation and Characterization of the Putative Nuclear Modifier Gene MTO1 Involved in the Pathogenesis of Deafness-associated Mitochondrial 12 S rRNA A1555G Mutation
Li, Xiaoming, Li, Ronghua, Lin, Xinhua, Guan, Min-Xin
Published in The Journal of biological chemistry (26.07.2002)
Published in The Journal of biological chemistry (26.07.2002)
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Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss
ZHIYUAN LI, RONGHUA LI, GUAN, Min-Xin, JIANFU CHEN, ZHISU LIAO, YI ZHU, YAPING QIAN, SUDAO XIONG, HEMAN-ACKAH, Selena, JIANBO WU, CHOO, Daniel I
Published in Human genetics (01.06.2005)
Published in Human genetics (01.06.2005)
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The Novel A4435G Mutation in the Mitochondrial tRNAMet May Modulate the Phenotypic Expression of the LHON-Associated ND4 G11778A Mutation
Qu, Jia, Li, Ronghua, Zhou, Xiangtian, Tong, Yi, Lu, Fan, Qian, Yaping, Hu, Yongwu, Mo, Jun Qin, West, Constance E, Guan, Min-Xin
Published in Investigative ophthalmology & visual science (01.02.2006)
Published in Investigative ophthalmology & visual science (01.02.2006)
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Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
Zhao, Hui, Young, Wie-Yen, Yan, Qingfeng, Li, Ronghua, Cao, Juyang, Wang, Qiuju, Li, Xiaoming, Peters, Jennifer L., Han, Dongyi, Guan, Min-Xin
Published in Nucleic acids research (01.01.2005)
Published in Nucleic acids research (01.01.2005)
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Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation
Young, Wie-Yen, Zhao, Lidong, Qian, Yaping, Wang, Qiuju, Li, Ning, Greinwald, John H., Guan, Min-Xin
Published in Biochemical and biophysical research communications (25.03.2005)
Published in Biochemical and biophysical research communications (25.03.2005)
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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 rRNA
Yan, Qingfeng, Li, Xiaoming, Faye, Gèrard, Guan, Min-Xin
Published in The Journal of biological chemistry (12.08.2005)
Published in The Journal of biological chemistry (12.08.2005)
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Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss
Li, Ronghua, Xing, Guangqian, Yan, Ming, Cao, Xing, Liu, Xue-Zhong, Bu, Xingkuan, Guan, Min-Xin
Published in American journal of medical genetics. Part A (15.01.2004)
Published in American journal of medical genetics. Part A (15.01.2004)
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Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation
Zhao, Lidong, Young, Wie-Yen, Li, Roughua, Wang, Qiuju, Qian, Yaping, Guan, Min-Xin
Published in Biochemical and biophysical research communications (24.12.2004)
Published in Biochemical and biophysical research communications (24.12.2004)
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Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss
Yuan, Huijun, Qian, Yaping, Xu, Yanjun, Cao, Juyang, Bai, Linna, Shen, Weidong, Ji, Fei, Zhang, Xin, Kang, Dongyang, Mo, Jun Qin, Greinwald, John H, Han, Dongyi, Zhai, Suoqiang, Young, Wie-Yen, Guan, Min-Xin
Published in American journal of medical genetics. Part A (01.10.2005)
Published in American journal of medical genetics. Part A (01.10.2005)
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Journal Article
Leber’s hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families
Zhou, Xiangtian, Wei, Qiping, Yang, Li, Tong, Yi, Zhao, Fuxin, Lu, Chunjie, Qian, Yaping, Sun, Yanghong, Lu, Fan, Qu, Jia, Guan, Min-Xin
Published in Biochemical and biophysical research communications (03.02.2006)
Published in Biochemical and biophysical research communications (03.02.2006)
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Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber’s hereditary optic neuropathy
Qian, Yaping, Zhou, Xiangtian, Hu, Yongwu, Tong, Yi, Li, Ronghua, Lu, Fan, Yang, Huanming, Mo, Jun Qin, Qu, Jia, Guan, Min-Xin
Published in Biochemical and biophysical research communications (01.07.2005)
Published in Biochemical and biophysical research communications (01.07.2005)
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The effect of the mtDNA4834 deletion on hearing
Kong, Wei-Jia, Hu, Yu-Juan, Wang, Qiong, Wang, Ying, Han, Yue-Chen, Cheng, Hua-Mao, Kong, Wen, Guan, Min-Xin
Published in Biochemical and biophysical research communications (26.05.2006)
Published in Biochemical and biophysical research communications (26.05.2006)
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Journal Article
Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation
Wang, Qiuju, Li, Qing-Zhong, Han, Dongyi, Zhao, Yali, Zhao, Lidong, Qian, Yaping, Yuan, Hu, Li, Ronghua, Zhai, Suoqiang, Young, Wie-Yen, Guan, Min-Xin
Published in Biochemical and biophysical research communications (10.02.2006)
Published in Biochemical and biophysical research communications (10.02.2006)
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