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Fuxin Zhao

Showing results (31-40 of 50) with videos related to

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Nature Communications|December 16, 2025
Decreased scleral Wnt5a<sup>hi</sup> fibroblasts exacerbate myopia progression by disrupting extracellular matrix homeostasis in miceHe Zhu, Wei Chen, Xuemei Ling, et al.
Frontiers in Genetics|February 4, 2022
<i>PDE4B</i> Proposed as a High Myopia Susceptibility Gene in Chinese PopulationFuxin Zhao, Wei Chen, Hui Zhou, et al.
Biochemical and Biophysical Research Communications|September 8, 2009
Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutationFuxin Zhao, Minqiang Guan, Xiangtian Zhou, et al.
Journal of Medical Genetics|December 15, 2020
Dysfunction of VIPR2 leads to myopia in humans and miceFuxin Zhao, Qihang Li, Wei Chen, et al.
Molecular Genetics and Metabolism|August 24, 2010
Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutationMinglian Zhang, Xiangtian Zhou, Chengwu Li, et al.
Biochemical and Biophysical Research Communications|August 10, 2010
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese familiesJuanjuan Zhang, Xiangtian Zhou, Jian Zhou, et al.
Journal of Human Genetics|January 17, 2014
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese familiesYanchun Ji, Min Liang, Juanjuan Zhang, et al.
Experimental Eye Research|September 10, 2021
Declines in PDE4B activity promote myopia progression through downregulation of scleral collagen expressionFuxin Zhao, Hui Zhou, Wei Chen, et al.
Investigative Ophthalmology & Visual Science|July 29, 2015
Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic NeuropathyPingping Jiang, Min Liang, Juanjuan Zhang, et al.
Ophthalmology|December 7, 2010
Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese familiesXiao-Ling Liu, Xiangtian Zhou, Jian Zhou, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Nature Communications|December 16, 2025
Decreased scleral Wnt5a<sup>hi</sup> fibroblasts exacerbate myopia progression by disrupting extracellular matrix homeostasis in miceHe Zhu, Wei Chen, Xuemei Ling, et al.
Frontiers in Genetics|February 4, 2022
<i>PDE4B</i> Proposed as a High Myopia Susceptibility Gene in Chinese PopulationFuxin Zhao, Wei Chen, Hui Zhou, et al.
Biochemical and Biophysical Research Communications|September 8, 2009
Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutationFuxin Zhao, Minqiang Guan, Xiangtian Zhou, et al.
Journal of Medical Genetics|December 15, 2020
Dysfunction of VIPR2 leads to myopia in humans and miceFuxin Zhao, Qihang Li, Wei Chen, et al.
Molecular Genetics and Metabolism|August 24, 2010
Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutationMinglian Zhang, Xiangtian Zhou, Chengwu Li, et al.
Biochemical and Biophysical Research Communications|August 10, 2010
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese familiesJuanjuan Zhang, Xiangtian Zhou, Jian Zhou, et al.
Journal of Human Genetics|January 17, 2014
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese familiesYanchun Ji, Min Liang, Juanjuan Zhang, et al.
Experimental Eye Research|September 10, 2021
Declines in PDE4B activity promote myopia progression through downregulation of scleral collagen expressionFuxin Zhao, Hui Zhou, Wei Chen, et al.
Investigative Ophthalmology & Visual Science|July 29, 2015
Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic NeuropathyPingping Jiang, Min Liang, Juanjuan Zhang, et al.
Ophthalmology|December 7, 2010
Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese familiesXiao-Ling Liu, Xiangtian Zhou, Jian Zhou, et al.
Pageof 5