Combination of the loss of cmnm(5)U34 with the lack of s(2)U(34) modifications of tRNA(Lys), tRNA(Glu) and tRNA(Gln) altered mitochondrial biogenesis and respiration

por Wang, Xinjian, Yan, Qingfeng, Guan, Min-Xin
Publicado 2009

Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae

por Wang, Xinjian, Yan, Qingfeng, Guan, Min-Xin
Publicado 2009

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...

por Yan, Qingfeng, Li, Xiaoming, Faye, Gèrard, Guan, Min-Xin
Publicado 2005

Bile Acid Signaling and Liver Regeneration

por Fan, Mingjie, Wang, Xichun, Xu, Ganyu, Yan, Qingfeng, Huang, Wendong
Publicado en Biochim Biophys Acta (2014)

Nuclear Modifier MTO2 Modulates the Aminoglycoside-Sensitivity of Mitochondrial 15S rRNA C1477G Mutation in Saccharomyces cerevisiae

por He, Xiangyu, Zhu, Xiaoyu, Wang, Xuexiang, Wang, Wei, Dai, Yu, Yan, Qingfeng
Publicado 2013

Effects of luteolin on regulatory proteins and enzymes for myocyte calcium circulation in hypothermic preserved rat heart

por Yan, Qingfeng, Li, Yueping, Yan, Jia, Zhao, Ying, Liu, Yunzhong, Liu, Su
Publicado en Exp Ther Med (2018)

Luteolin improves heart preservation through inhibiting hypoxia-dependent L-type calcium channels in cardiomyocytes

por Yan, Qingfeng, Li, Yueping, Yan, Jia, Zhao, Ying, Liu, Yunzhong, Liu, Su
Publicado en Exp Ther Med (2019)

Biochemical characterization of the mitochondrial tRNA(Ser(UCN)) T7511C mutation associated with nonsyndromic deafness

por Li, Xiaoming, Fischel-Ghodsian, Nathan, Schwartz, Faina, Yan, Qingfeng, Friedman, Rick A., Guan, Min-Xin
Publicado 2004

The Effect of Peritoneal Fluid from Patients with Endometriosis on Mitochondrial Function and Development of Early Mouse Embryos

por Shu, Jing, Xing, Lili, Ding, Guolian, Luo, Qiong, Liu, Xinmei, Yan, Qingfeng, Sheng, Jianzhong, Huang, Hefeng
Publicado 2013

MTO1 Worked as a Modifier in the Aminoglycosides Sensitivity of Yeast Carrying a Mitochondrial 15S rRNA C1477G Mutation

por Zhu, Xiaoyu, He, Xiangyu, Wang, Wei, Zhou, Qiyin, Yu, Zhe, Dai, Yu, Zhu, Xufen, Yan, Qingfeng
Publicado en PLoS One (2015)

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

por Zhao, Hui, Li, Ronghua, Wang, Qiuju, Yan, Qingfeng, Deng, Jian-Hong, Han, Dongyi, Bai, Yidong, Young, Wie-Yen, Guan, Min-Xin
Publicado 2004

High-Performance Planar-Type Photodetector on (100) Facet of MAPbI(3) Single Crystal

por Lian, Zhipeng, Yan, Qingfeng, Lv, Qianrui, Wang, Ying, Liu, Lili, Zhang, Lijing, Pan, Shilie, Li, Qiang, Wang, Liduo, Sun, Jia-Lin
Publicado en Sci Rep (2015)

DNMT1 mediates chemosensitivity by reducing methylation of miRNA-20a promoter in glioma cells

por Zhou, Daoyang, Wan, Yingfeng, Xie, Dajiang, Wang, Yirong, Wei, Junhua, Yan, Qingfeng, Lu, Peng, Mo, Lianjie, Xie, Jixi, Yang, Shuxu, Qi, Xuchen
Publicado en Exp Mol Med (2015)

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

por Zhao, Hui, Young, Wie-Yen, Yan, Qingfeng, Li, Ronghua, Cao, Juyang, Wang, Qiuju, Li, Xiaoming, Peters, Jennifer L., Han, Dongyi, Guan, Min-Xin
Publicado 2005

A deafness-associated tRNA(His) mutation alters the mitochondrial function, ROS production and membrane potential

por Gong, Shasha, Peng, Yanyan, Jiang, Pingping, Wang, Meng, Fan, Mingjie, Wang, Xinjian, Zhou, Hong, Li, Huawei, Yan, Qingfeng, Huang, Taosheng, Guan, Min-Xin
Publicado 2014

A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase Deficiency

por Chen, Hong, Yuan, Ke, Zhang, Bingtao, Jia, Zexiao, Chen, Chun, Zhu, Yilin, Sun, Yaping, Zhou, Hui, Huang, Wendong, Liang, Li, Yan, Qingfeng, Wang, Chunlin
Publicado en Front Genet (2019)

Drosophila Prominin-like, a homolog of CD133, interacts with ND20 to maintain mitochondrial function

por Wang, Xuexiang, Zheng, Huimei, Jia, Zexiao, Lei, Zhaoying, Li, Mengyao, Zhuang, Qianqian, Zhou, Hui, Qiu, Yue, Fu, Yong, Yang, Xiaohang, Xi, Yongmei, Yan, Qingfeng
Publicado en Cell Biosci (2019)

Mechanistic Study on the Nuclear Modifier Gene MSS1 Mutation Suppressing Neomycin Sensitivity of the Mitochondrial 15S rRNA C1477G Mutation in Saccharomyces cerevisiae

por Zhou, Qiyin, Wang, Wei, He, Xiangyu, Zhu, Xiaoyu, Shen, Yaoyao, Yu, Zhe, Wang, Xuexiang, Qi, Xuchen, Zhang, Xuan, Fan, Mingjie, Dai, Yu, Yang, Shuxu, Yan, Qingfeng
Publicado 2014

The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathy

por Liu, Zhong, Song, Yanrui, Li, Dan, He, Xiangyu, Li, Shishi, Wu, Bifeng, Wang, Wei, Gu, Shulian, Zhu, Xiaoyu, Wang, Xuexiang, Zhou, Qiyin, Dai, Yu, Yan, Qingfeng
Publicado 2014

Mitochondrial Dysfunctions Contribute to Hypertrophic Cardiomyopathy in Patient iPSC-Derived Cardiomyocytes with MT-RNR2 Mutation

por Li, Shishi, Pan, Huaye, Tan, Chao, Sun, Yaping, Song, Yanrui, Zhang, Xuan, Yang, Wei, Wang, Xuexiang, Li, Dan, Dai, Yu, Ma, Qiang, Xu, Chenming, Zhu, Xufen, Kang, Lijun, Fu, Yong, Xu, Xuejun, Shu, Jing, Zhou, Naiming, Han, Feng, Qin, Dajiang, Huang, Wendong, Liu, Zhong, Yan, Qingfeng
Publicado en Stem Cell Reports (2018)