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Zixi Sun

Showing results (1-10 of 45) with videos related to

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American Journal of Medical Genetics. Part A|November 25, 2021
Leber congenital amaurosis as an initial manifestation in a Chinese patient with thiamine-responsive megaloblastic anemia syndromeShijing Wu, Zhisheng Yuan, Zixi Sun, et al.
Investigative Ophthalmology & Visual Science|February 7, 2024
Genotype-Phenotype Associations in an X-Linked Retinoschisis Patient Cohort: The Molecular Dynamic Insight and a Promising SD-OCT IndicatorXing Wei, Hui Li, Tian Zhu, et al.
Health Science Reports|November 30, 2023
Gender differences in the burden of multiple sclerosis in China from 1990 to 2019 and its 25-year projection: An analysis of the Global Burden of Diseases StudyHeng Wang, Xia Zhang, Heyan Li, et al.
Molecular Vision|February 2, 2018
Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalitiesZixi Sun, Qi Zhou, Huajin Li, et al.
Molecular Genetics & Genomic Medicine|January 31, 2020
Unilateral retinocytoma associated with a variant in the RB1 geneShijing Wu, Xuan Zou, Zixi Sun, et al.
Ocular Immunology and Inflammation|February 27, 2019
Ocular Features in Chinese Patients with Blau SyndromeShijing Wu, Linqing Zhong, Zixi Sun, et al.
Clinical Genetics|December 12, 2022
Novel homozygous variant in ARL2BP associated with retinitis pigmentosa, situs inversus, and male infertility in a Chinese patientTian Zhu, Hui Li, Xing Wei, et al.
Scientific Reports|February 7, 2018
A novel small deletion in the NHS gene associated with Nance-Horan syndromeHuajin Li, Lizhu Yang, Zixi Sun, et al.
Ophthalmic Genetics|July 7, 2020
Clinical and genetic study on two Chinese families with Wagner vitreoretinopathyHuajin Li, Hui Li, Lizhu Yang, et al.
Stem Cell Research|January 11, 2022
Generation of a human induced pluripotent stem cell line (PUMCHi018-A) from an early-onset severe retinal dystrophy patient with RDH12 mutationsXuan Zou, Shijing Wu, Tian Zhu, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|November 25, 2021
Leber congenital amaurosis as an initial manifestation in a Chinese patient with thiamine-responsive megaloblastic anemia syndromeShijing Wu, Zhisheng Yuan, Zixi Sun, et al.
Investigative Ophthalmology & Visual Science|February 7, 2024
Genotype-Phenotype Associations in an X-Linked Retinoschisis Patient Cohort: The Molecular Dynamic Insight and a Promising SD-OCT IndicatorXing Wei, Hui Li, Tian Zhu, et al.
Health Science Reports|November 30, 2023
Gender differences in the burden of multiple sclerosis in China from 1990 to 2019 and its 25-year projection: An analysis of the Global Burden of Diseases StudyHeng Wang, Xia Zhang, Heyan Li, et al.
Molecular Vision|February 2, 2018
Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalitiesZixi Sun, Qi Zhou, Huajin Li, et al.
Molecular Genetics & Genomic Medicine|January 31, 2020
Unilateral retinocytoma associated with a variant in the RB1 geneShijing Wu, Xuan Zou, Zixi Sun, et al.
Ocular Immunology and Inflammation|February 27, 2019
Ocular Features in Chinese Patients with Blau SyndromeShijing Wu, Linqing Zhong, Zixi Sun, et al.
Clinical Genetics|December 12, 2022
Novel homozygous variant in ARL2BP associated with retinitis pigmentosa, situs inversus, and male infertility in a Chinese patientTian Zhu, Hui Li, Xing Wei, et al.
Scientific Reports|February 7, 2018
A novel small deletion in the NHS gene associated with Nance-Horan syndromeHuajin Li, Lizhu Yang, Zixi Sun, et al.
Ophthalmic Genetics|July 7, 2020
Clinical and genetic study on two Chinese families with Wagner vitreoretinopathyHuajin Li, Hui Li, Lizhu Yang, et al.
Stem Cell Research|January 11, 2022
Generation of a human induced pluripotent stem cell line (PUMCHi018-A) from an early-onset severe retinal dystrophy patient with RDH12 mutationsXuan Zou, Shijing Wu, Tian Zhu, et al.
Pageof 5