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Zhipeng Nie

Showing results (1-10 of 13) with videos related to

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Sensors (Basel, Switzerland)|September 23, 2016
Efficient Data Gathering Methods in Wireless Sensor Networks Using GBTR Matrix CompletionDonghao Wang, Jiangwen Wan, Zhipeng Nie, et al.
Human Mutation|June 8, 2026
A Novel <i>LMX1A</i> Frameshift Variant Underlies Familial Phenotypic Heterogeneity in DFNA7Chenyang Xu, Zhipeng Nie, Suyang Wang, et al.
Human Molecular Genetics|August 10, 2022
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathyZhipeng Nie, Chenghui Wang, Jiarong Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 11, 2017
[Progress in research on pathogenic genes and gene therapy for inherited retinal diseases]Ling Zhu, Cong Cao, Jiji Sun, et al.
Reviews on Environmental Health|May 10, 2023
Screen time and childhood attention deficit hyperactivity disorder: a meta-analysisHezuo Liu, Xiaorong Chen, Minhui Huang, et al.
Mitochondrion|June 6, 2017
Late onset nonsyndromic hearing loss in a Dongxiang Chinese family is associated with the 593T>C variant in the mitochondrial tRNA<sup>Phe</sup> geneXiaowan Chen, Zhipeng Nie, Fang Wang, et al.
Biomedical Reports|February 2, 2018
Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panelYu Dai, Chenghui Wang, Zhipeng Nie, et al.
The Journal of Biological Chemistry|February 21, 2021
An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal functionXiaofen Jin, Zengming Zhang, Zhipeng Nie, et al.
Oncotarget|November 16, 2017
Mitochondrial DNA depletion, mitochondrial mutations and high TFAM expression in hepatocellular carcinomaLihua Qiao, Guoqing Ru, Zhuochao Mao, et al.
Molecular Genetics & Genomic Medicine|December 2, 2024
A Novel Mutation Located in the N-Terminal Domain of MYO15A Caused Sensorineural Hearing LossYanli Wang, Zengping Liu, Yong Li, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Sensors (Basel, Switzerland)|September 23, 2016
Efficient Data Gathering Methods in Wireless Sensor Networks Using GBTR Matrix CompletionDonghao Wang, Jiangwen Wan, Zhipeng Nie, et al.
Human Mutation|June 8, 2026
A Novel <i>LMX1A</i> Frameshift Variant Underlies Familial Phenotypic Heterogeneity in DFNA7Chenyang Xu, Zhipeng Nie, Suyang Wang, et al.
Human Molecular Genetics|August 10, 2022
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathyZhipeng Nie, Chenghui Wang, Jiarong Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 11, 2017
[Progress in research on pathogenic genes and gene therapy for inherited retinal diseases]Ling Zhu, Cong Cao, Jiji Sun, et al.
Reviews on Environmental Health|May 10, 2023
Screen time and childhood attention deficit hyperactivity disorder: a meta-analysisHezuo Liu, Xiaorong Chen, Minhui Huang, et al.
Mitochondrion|June 6, 2017
Late onset nonsyndromic hearing loss in a Dongxiang Chinese family is associated with the 593T>C variant in the mitochondrial tRNA<sup>Phe</sup> geneXiaowan Chen, Zhipeng Nie, Fang Wang, et al.
Biomedical Reports|February 2, 2018
Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panelYu Dai, Chenghui Wang, Zhipeng Nie, et al.
The Journal of Biological Chemistry|February 21, 2021
An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal functionXiaofen Jin, Zengming Zhang, Zhipeng Nie, et al.
Oncotarget|November 16, 2017
Mitochondrial DNA depletion, mitochondrial mutations and high TFAM expression in hepatocellular carcinomaLihua Qiao, Guoqing Ru, Zhuochao Mao, et al.
Molecular Genetics & Genomic Medicine|December 2, 2024
A Novel Mutation Located in the N-Terminal Domain of MYO15A Caused Sensorineural Hearing LossYanli Wang, Zengping Liu, Yong Li, et al.
Pageof 2