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Biomedicines
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September 28, 2024
Preservation of Mitochondrial Function by SkQ1 in Skin Fibroblasts Derived from Patients with Leber's Hereditary Optic Neuropathy Is Associated with the PINK1/PRKN-Mediated Mitophagy
Jin Xu, Yan Li, Shun Yao, et al.
Frontiers in Molecular Neuroscience
|
August 1, 2022
Multi-mtDNA Variants May Be a Factor Contributing to Mitochondrial Function Variety in the Skin-Derived Fibroblasts of Leber's Hereditary Optic Neuropathy Patients
Shun Yao, Qingru Zhou, Mingzhu Yang, et al.
Cell Death Discovery
|
August 15, 2022
A novel mutation located in the intermembrane space domain of AFG3L2 causes dominant optic atrophy through decreasing the stability of the encoded protein
Lin Yang, Xiuxiu Jin, Ya Li, et al.
FASEB Bioadvances
|
November 8, 2024
Mitochondrial functional impairment in <i>ARL3</i>-mutation related rod-cone dystrophy
Xiaoli Zhang, Shun Yao, Lujia Zhang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 8, 2024
Mechanisms underlying morphological and functional changes of cilia in fibroblasts derived from patients bearing ARL3<sup>T31A</sup> and ARL3<sup>T31A/C118F</sup> mutations
Xiaoli Zhang, Shun Yao, Lujia Zhang, et al.
Neuroscience
|
February 19, 2026
The retinal nerve fiber layer mean thickness in patients with early Parkinson's disease reflects striatal dopamine function
Xiaoxue Shi, Keke Liang, Jianjun Ma, et al.
Neurobiology of Disease
|
December 17, 2023
Structural changes in the retina and serum HMGB1 levels are associated with decreased cognitive function in patients with Parkinson's disease
Keke Liang, Xiaohuan Li, Qingge Guo, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
Biomedicines
|
September 28, 2024
Preservation of Mitochondrial Function by SkQ1 in Skin Fibroblasts Derived from Patients with Leber's Hereditary Optic Neuropathy Is Associated with the PINK1/PRKN-Mediated Mitophagy
Jin Xu, Yan Li, Shun Yao, et al.
Frontiers in Molecular Neuroscience
|
August 1, 2022
Multi-mtDNA Variants May Be a Factor Contributing to Mitochondrial Function Variety in the Skin-Derived Fibroblasts of Leber's Hereditary Optic Neuropathy Patients
Shun Yao, Qingru Zhou, Mingzhu Yang, et al.
Cell Death Discovery
|
August 15, 2022
A novel mutation located in the intermembrane space domain of AFG3L2 causes dominant optic atrophy through decreasing the stability of the encoded protein
Lin Yang, Xiuxiu Jin, Ya Li, et al.
FASEB Bioadvances
|
November 8, 2024
Mitochondrial functional impairment in <i>ARL3</i>-mutation related rod-cone dystrophy
Xiaoli Zhang, Shun Yao, Lujia Zhang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 8, 2024
Mechanisms underlying morphological and functional changes of cilia in fibroblasts derived from patients bearing ARL3<sup>T31A</sup> and ARL3<sup>T31A/C118F</sup> mutations
Xiaoli Zhang, Shun Yao, Lujia Zhang, et al.
Neuroscience
|
February 19, 2026
The retinal nerve fiber layer mean thickness in patients with early Parkinson's disease reflects striatal dopamine function
Xiaoxue Shi, Keke Liang, Jianjun Ma, et al.
Neurobiology of Disease
|
December 17, 2023
Structural changes in the retina and serum HMGB1 levels are associated with decreased cognitive function in patients with Parkinson's disease
Keke Liang, Xiaohuan Li, Qingge Guo, et al.
Page
of 3