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Zixi Sun

Showing results (31-40 of 45) with videos related to

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American Journal of Ophthalmology|December 25, 2025
Natural history of CNGA1-associated retinitis pigmentosa in a large Chinese cohort revealing an optimal intervention windowYue Liu, Dingding Zhang, Yunyu Zhou, et al.
Ophthalmology. Retina|April 4, 2026
Expanding the Clinical and Genetic Spectrum of TTLL5-Associated Retinal Dystrophy: A Single-Center Cohort StudyYunyu Zhou, Yue Liu, Huan Chen, et al.
American Journal of Medical Genetics. Part A|August 2, 2023
Ocular manifestations of mitochondrial neurogastrointestinal encephalomyopathy: A case report and literature reviewHeng Wang, Gechong Ruan, Shan Yang, et al.
Investigative Ophthalmology & Visual Science|September 19, 2025
Exon Skipping Therapy Restores Ciliary Function in USH2A-Related Retinal DegenerationWuyi Li, Yamei Li, Yunyu Zhou, et al.
Retina (Philadelphia, Pa.)|August 23, 2018
PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHYXuan Zou, Qing Fu, Sha Fang, et al.
Gene Therapy|June 3, 2020
Treating Bietti crystalline dystrophy in a high-fat diet-exacerbated murine model using gene therapyBin Qu, Shijing Wu, Guanyi Jiao, et al.
American Journal of Ophthalmology|December 9, 2022
Clinical and Molecular Features of a Chinese Cohort With Syndromic and Nonsyndromic Retinal Dystrophies Related to the CEP290 GeneTian Zhu, Yue Shen, Zixi Sun, et al.
BMJ Open|February 24, 2019
Prevalence and risk factors for pterygium: a cross-sectional study in Han and Manchu ethnic populations in Hebei, ChinaZhouxian Pan, Jiantao Cui, Guangliang Shan, et al.
Journal of Medical Genetics|September 16, 2016
<i>CEP78</i> is mutated in a distinct type of Usher syndromeQing Fu, Mingchu Xu, Xue Chen, et al.
Human Molecular Genetics|February 25, 2016
Mutations in POMGNT1 cause non-syndromic retinitis pigmentosaMingchu Xu, Takeyuki Yamada, Zixi Sun, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Ophthalmology|December 25, 2025
Natural history of CNGA1-associated retinitis pigmentosa in a large Chinese cohort revealing an optimal intervention windowYue Liu, Dingding Zhang, Yunyu Zhou, et al.
Ophthalmology. Retina|April 4, 2026
Expanding the Clinical and Genetic Spectrum of TTLL5-Associated Retinal Dystrophy: A Single-Center Cohort StudyYunyu Zhou, Yue Liu, Huan Chen, et al.
American Journal of Medical Genetics. Part A|August 2, 2023
Ocular manifestations of mitochondrial neurogastrointestinal encephalomyopathy: A case report and literature reviewHeng Wang, Gechong Ruan, Shan Yang, et al.
Investigative Ophthalmology & Visual Science|September 19, 2025
Exon Skipping Therapy Restores Ciliary Function in USH2A-Related Retinal DegenerationWuyi Li, Yamei Li, Yunyu Zhou, et al.
Retina (Philadelphia, Pa.)|August 23, 2018
PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHYXuan Zou, Qing Fu, Sha Fang, et al.
Gene Therapy|June 3, 2020
Treating Bietti crystalline dystrophy in a high-fat diet-exacerbated murine model using gene therapyBin Qu, Shijing Wu, Guanyi Jiao, et al.
American Journal of Ophthalmology|December 9, 2022
Clinical and Molecular Features of a Chinese Cohort With Syndromic and Nonsyndromic Retinal Dystrophies Related to the CEP290 GeneTian Zhu, Yue Shen, Zixi Sun, et al.
BMJ Open|February 24, 2019
Prevalence and risk factors for pterygium: a cross-sectional study in Han and Manchu ethnic populations in Hebei, ChinaZhouxian Pan, Jiantao Cui, Guangliang Shan, et al.
Journal of Medical Genetics|September 16, 2016
<i>CEP78</i> is mutated in a distinct type of Usher syndromeQing Fu, Mingchu Xu, Xue Chen, et al.
Human Molecular Genetics|February 25, 2016
Mutations in POMGNT1 cause non-syndromic retinitis pigmentosaMingchu Xu, Takeyuki Yamada, Zixi Sun, et al.
Pageof 5