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Zixi Sun

Showing results (11-20 of 45) with videos related to

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Scientific Reports|February 18, 2017
Molecular genetic and clinical evaluation of three Chinese families with X-linked ocular albinismXuan Zou, Hui Li, Lizhu Yang, et al.
Stem Cell Research|January 15, 2022
Generation of a human induced pluripotent stem cell line PUMCHi017-A from a Choroideremia patient with CHM mutationXiaoxu Han, Shijing Wu, Zixi Sun, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 8, 2022
Genetic polymorphisms of apolipoprotein E in nonarteritic anterior ischemic optic neuropathyYuyu Chou, Zixi Sun, Ye Wang, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 24, 2021
A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophyShijing Wu, Zhisheng Yuan, Zixi Sun, et al.
Investigative Ophthalmology & Visual Science|May 6, 2026
Independent Degeneration of Photoreceptors and Retinal Pigment Epithelium: Multimodal Imaging Evidence From Choroideremia CarriersXiaoxu Han, Yang Yu, Xing Wei, et al.
Eye and Vision (London, England)|February 24, 2026
Longitudinal and cross-sectional study of retinal phenotypes and visual function in choroideremia carriers: a new grading systemXiaoxu Han, Yang Yu, Jiaqi Ding, et al.
Ophthalmic Genetics|August 20, 2020
Variants at codon 838 in the <i>GUCY2D</i> gene result in different phenotypes of cone rod dystrophyZixi Sun, Shijing Wu, Tian Zhu, et al.
Stem Cell Research|August 22, 2021
Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variantsTian Zhu, Shijing Wu, Zixi Sun, et al.
American Journal of Ophthalmology|October 4, 2025
Ocular Manifestations of ROSAH Syndrome Caused by Different Mutations of the ALPK1 GeneZixi Sun, Xing Wei, Xiaoxu Han, et al.
Stem Cell Research|February 13, 2022
Generation of a human induced pluripotent stem cell line PUMCHi019-A from a dominant optic atrophy patient with an OPA1 mutationZixi Sun, Shijing Wu, Tian Zhu, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Scientific Reports|February 18, 2017
Molecular genetic and clinical evaluation of three Chinese families with X-linked ocular albinismXuan Zou, Hui Li, Lizhu Yang, et al.
Stem Cell Research|January 15, 2022
Generation of a human induced pluripotent stem cell line PUMCHi017-A from a Choroideremia patient with CHM mutationXiaoxu Han, Shijing Wu, Zixi Sun, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 8, 2022
Genetic polymorphisms of apolipoprotein E in nonarteritic anterior ischemic optic neuropathyYuyu Chou, Zixi Sun, Ye Wang, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 24, 2021
A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophyShijing Wu, Zhisheng Yuan, Zixi Sun, et al.
Investigative Ophthalmology & Visual Science|May 6, 2026
Independent Degeneration of Photoreceptors and Retinal Pigment Epithelium: Multimodal Imaging Evidence From Choroideremia CarriersXiaoxu Han, Yang Yu, Xing Wei, et al.
Eye and Vision (London, England)|February 24, 2026
Longitudinal and cross-sectional study of retinal phenotypes and visual function in choroideremia carriers: a new grading systemXiaoxu Han, Yang Yu, Jiaqi Ding, et al.
Ophthalmic Genetics|August 20, 2020
Variants at codon 838 in the <i>GUCY2D</i> gene result in different phenotypes of cone rod dystrophyZixi Sun, Shijing Wu, Tian Zhu, et al.
Stem Cell Research|August 22, 2021
Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variantsTian Zhu, Shijing Wu, Zixi Sun, et al.
American Journal of Ophthalmology|October 4, 2025
Ocular Manifestations of ROSAH Syndrome Caused by Different Mutations of the ALPK1 GeneZixi Sun, Xing Wei, Xiaoxu Han, et al.
Stem Cell Research|February 13, 2022
Generation of a human induced pluripotent stem cell line PUMCHi019-A from a dominant optic atrophy patient with an OPA1 mutationZixi Sun, Shijing Wu, Tian Zhu, et al.
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