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Qingfeng Yan

Showing results (101-110 of 140) with videos related to

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Nucleic Acids Research|February 22, 2005
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing lossHui Zhao, Wie-Yen Young, Qingfeng Yan, et al.
Cell & Bioscience|January 1, 2020
<i>Drosophila</i> Prominin-like, a homolog of CD133, interacts with ND20 to maintain mitochondrial functionXuexiang Wang, Huimei Zheng, Zexiao Jia, et al.
Frontiers in Genetics|November 8, 2019
A Novel Compound Heterozygous <i>CYP17A1</i> Variant Causes 17α-Hydroxylase/17, 20-Lyase DeficiencyHong Chen, Ke Yuan, Bingtao Zhang, et al.
Plos One|March 6, 2014
Mechanistic study on the nuclear modifier gene MSS1 mutation suppressing neomycin sensitivity of the mitochondrial 15S rRNA C1477G mutation in Saccharomyces cerevisiaeQiyin Zhou, Wei Wang, Xiangyu He, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 2, 2024
NF2 regulates IP3R-mediated Ca<sup>2+</sup> signal and apoptosis in meningiomasZhaoying Lei, Jie Niu, Huajian Cai, et al.
Gene|July 5, 2012
Mitochondrial ND5 12338T>C variant is associated with maternally inherited hypertrophic cardiomyopathy in a Chinese pedigreeZhong Liu, Yanrui Song, Shulian Gu, et al.
Journal of Medical Genetics|December 25, 2013
The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathyZhong Liu, Yanrui Song, Dan Li, et al.
Nanoscale|September 10, 2015
A high performance triboelectric nanogenerator for self-powered non-volatile ferroelectric transistor memoryHuajing Fang, Qiang Li, Wenhui He, et al.
Science China. Life Sciences|November 13, 2023
LncFASA promotes cancer ferroptosis via modulating PRDX1 phase separationXiao Fan, Fangzhou Liu, Xiang Wang, et al.
Optics Express|December 25, 2015
Infrared light gated MoS₂ field effect transistorHuajing Fang, Ziyuan Lin, Xinsheng Wang, et al.
Pageof 14

Showing results (101-110 of 140) with videos related to

Sort By:
Pageof 14
Nucleic Acids Research|February 22, 2005
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing lossHui Zhao, Wie-Yen Young, Qingfeng Yan, et al.
Cell & Bioscience|January 1, 2020
<i>Drosophila</i> Prominin-like, a homolog of CD133, interacts with ND20 to maintain mitochondrial functionXuexiang Wang, Huimei Zheng, Zexiao Jia, et al.
Frontiers in Genetics|November 8, 2019
A Novel Compound Heterozygous <i>CYP17A1</i> Variant Causes 17α-Hydroxylase/17, 20-Lyase DeficiencyHong Chen, Ke Yuan, Bingtao Zhang, et al.
Plos One|March 6, 2014
Mechanistic study on the nuclear modifier gene MSS1 mutation suppressing neomycin sensitivity of the mitochondrial 15S rRNA C1477G mutation in Saccharomyces cerevisiaeQiyin Zhou, Wei Wang, Xiangyu He, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 2, 2024
NF2 regulates IP3R-mediated Ca<sup>2+</sup> signal and apoptosis in meningiomasZhaoying Lei, Jie Niu, Huajian Cai, et al.
Gene|July 5, 2012
Mitochondrial ND5 12338T>C variant is associated with maternally inherited hypertrophic cardiomyopathy in a Chinese pedigreeZhong Liu, Yanrui Song, Shulian Gu, et al.
Journal of Medical Genetics|December 25, 2013
The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathyZhong Liu, Yanrui Song, Dan Li, et al.
Nanoscale|September 10, 2015
A high performance triboelectric nanogenerator for self-powered non-volatile ferroelectric transistor memoryHuajing Fang, Qiang Li, Wenhui He, et al.
Science China. Life Sciences|November 13, 2023
LncFASA promotes cancer ferroptosis via modulating PRDX1 phase separationXiao Fan, Fangzhou Liu, Xiang Wang, et al.
Optics Express|December 25, 2015
Infrared light gated MoS₂ field effect transistorHuajing Fang, Ziyuan Lin, Xinsheng Wang, et al.
Pageof 14