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Yun Yuan

Showing results (141-150 of 544) with videos related to

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Mitochondrial DNA|April 9, 2014
The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosiaYinglin Leng, Yuhe Liu, Xiaojing Fang, et al.
Neuroscience Letters|February 25, 2014
Novel RYR1 missense mutations in six Chinese patients with central core diseaseMei Gu, Shu Zhang, Jing Hu, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 29, 2019
Homozygous splice-site mutation c.78 + 5G>A in PMP22 causes congenital hypomyelinating neuropathyRui Wu, Jun Fu, Lingchao Meng, et al.
Clinical Neuropathology|July 8, 2021
<i>PLEKHG5</i>-related autosomal recessive lower motor neuron disease with dysmyelination in peripheral nervesYuanfeng Miao, Meng Yu, Lingchao Meng, et al.
Acta Neuropathologica Communications|June 1, 2022
The polyG diseases: a new disease entityTongling Liufu, Yilei Zheng, Jiaxi Yu, et al.
Journal of Nanobiotechnology|December 17, 2023
Reprogramming mitochondrial metabolism of macrophages by miRNA-released microporous coatings to prevent peri-implantitisHongming Zhang, Yun Yuan, Hanxiao Xue, et al.
Journal of the Neurological Sciences|February 7, 2018
Survival analysis of a cohort of Chinese patients with mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) based on clinical featuresZhe Zhang, Danhua Zhao, Xiao Zhang, et al.
Chinese Medical Journal|September 21, 2016
Dysferlin Gene Mutation Spectrum in a Large Cohort of Chinese Patients with DysferlinopathySu-Qin Jin, Meng Yu, Wei Zhang, et al.
Zhonghua Yi Xue Za Zhi|December 5, 2009
[Expressions of PDCD5 and other apoptosis-related proteins in muscle of patients with mitochondrial cytopathy]Yong-fie Li, Zhao-xia Wang, Xu-guang Gao, et al.
Molecular Oral Microbiology|April 1, 2026
UCHL1 Exacerbates Periodontitis by Coordinating Mitochondrial Dysfunction and Endoplasmic Reticulum Stress in MacrophagesYun Yuan, Shengjia Ye, Hanxiao Xue, et al.
Pageof 55

Showing results (141-150 of 544) with videos related to

Sort By:
Pageof 55
Mitochondrial DNA|April 9, 2014
The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosiaYinglin Leng, Yuhe Liu, Xiaojing Fang, et al.
Neuroscience Letters|February 25, 2014
Novel RYR1 missense mutations in six Chinese patients with central core diseaseMei Gu, Shu Zhang, Jing Hu, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 29, 2019
Homozygous splice-site mutation c.78 + 5G>A in PMP22 causes congenital hypomyelinating neuropathyRui Wu, Jun Fu, Lingchao Meng, et al.
Clinical Neuropathology|July 8, 2021
<i>PLEKHG5</i>-related autosomal recessive lower motor neuron disease with dysmyelination in peripheral nervesYuanfeng Miao, Meng Yu, Lingchao Meng, et al.
Acta Neuropathologica Communications|June 1, 2022
The polyG diseases: a new disease entityTongling Liufu, Yilei Zheng, Jiaxi Yu, et al.
Journal of Nanobiotechnology|December 17, 2023
Reprogramming mitochondrial metabolism of macrophages by miRNA-released microporous coatings to prevent peri-implantitisHongming Zhang, Yun Yuan, Hanxiao Xue, et al.
Journal of the Neurological Sciences|February 7, 2018
Survival analysis of a cohort of Chinese patients with mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) based on clinical featuresZhe Zhang, Danhua Zhao, Xiao Zhang, et al.
Chinese Medical Journal|September 21, 2016
Dysferlin Gene Mutation Spectrum in a Large Cohort of Chinese Patients with DysferlinopathySu-Qin Jin, Meng Yu, Wei Zhang, et al.
Zhonghua Yi Xue Za Zhi|December 5, 2009
[Expressions of PDCD5 and other apoptosis-related proteins in muscle of patients with mitochondrial cytopathy]Yong-fie Li, Zhao-xia Wang, Xu-guang Gao, et al.
Molecular Oral Microbiology|April 1, 2026
UCHL1 Exacerbates Periodontitis by Coordinating Mitochondrial Dysfunction and Endoplasmic Reticulum Stress in MacrophagesYun Yuan, Shengjia Ye, Hanxiao Xue, et al.
Pageof 55