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Wenmin Sun

Showing results (21-30 of 95) with videos related to

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Eye (London, England)|November 27, 2021
Clinical features and genetic spectrum of NMNAT1-associated retinal degenerationZhen Yi, Shiqiang Li, Siyu Wang, et al.
Frontiers in Cell and Developmental Biology|March 8, 2021
Dominant RP in the Middle While Recessive in Both the N- and C-Terminals Due to <i>RP1</i> Truncations: Confirmation, Refinement, and QuestionsJunwen Wang, Xueshan Xiao, Shiqiang Li, et al.
Acta Ophthalmologica|July 6, 2019
RPE65 mutation frequency and phenotypic variation according to exome sequencing in a tertiary centre for genetic eye diseases in ChinaShiqiang Li, Xueshan Xiao, Zhen Yi, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 28, 2021
Pathogenic variants and associated phenotypic spectrum of TSPAN12 based on data from a large cohortWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|February 26, 2021
Confirming and expanding the phenotypes of <i>FZD5</i> variants: Coloboma, inferior chorioretinal hypoplasia, and high myopiaYi Jiang, Jiamin Ouyang, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|August 16, 2012
PAX6 mutations identified in 4 of 35 families with microcorneaPanfeng Wang, Wenmin Sun, Shiqiang Li, et al.
Ebiomedicine|May 27, 2020
Comparative exome sequencing reveals novel candidate genes for retinitis pigmentosaZhen Yi, Jiamin Ouyang, Wenmin Sun, et al.
Investigative Ophthalmology & Visual Science|January 14, 2026
Genetic Landscape and Clinical Characterization of FRMD7-Related Infantile Nystagmus Based on Large In-House Datasets and Literature ReviewShu Liu, Shiqiang Li, Yingwei Wang, et al.
Molecular Vision|April 18, 2013
Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataractThomas M Bennett, Giovanni Maraini, Chongfei Jin, et al.
Experimental Eye Research|December 21, 2020
Spectrum-frequency and genotype-phenotype analysis of rhodopsin variantsHualei Luo, Xueshan Xiao, Shiqiang Li, et al.
Pageof 10

Showing results (21-30 of 95) with videos related to

Sort By:
Pageof 10
Eye (London, England)|November 27, 2021
Clinical features and genetic spectrum of NMNAT1-associated retinal degenerationZhen Yi, Shiqiang Li, Siyu Wang, et al.
Frontiers in Cell and Developmental Biology|March 8, 2021
Dominant RP in the Middle While Recessive in Both the N- and C-Terminals Due to <i>RP1</i> Truncations: Confirmation, Refinement, and QuestionsJunwen Wang, Xueshan Xiao, Shiqiang Li, et al.
Acta Ophthalmologica|July 6, 2019
RPE65 mutation frequency and phenotypic variation according to exome sequencing in a tertiary centre for genetic eye diseases in ChinaShiqiang Li, Xueshan Xiao, Zhen Yi, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 28, 2021
Pathogenic variants and associated phenotypic spectrum of TSPAN12 based on data from a large cohortWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|February 26, 2021
Confirming and expanding the phenotypes of <i>FZD5</i> variants: Coloboma, inferior chorioretinal hypoplasia, and high myopiaYi Jiang, Jiamin Ouyang, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|August 16, 2012
PAX6 mutations identified in 4 of 35 families with microcorneaPanfeng Wang, Wenmin Sun, Shiqiang Li, et al.
Ebiomedicine|May 27, 2020
Comparative exome sequencing reveals novel candidate genes for retinitis pigmentosaZhen Yi, Jiamin Ouyang, Wenmin Sun, et al.
Investigative Ophthalmology & Visual Science|January 14, 2026
Genetic Landscape and Clinical Characterization of FRMD7-Related Infantile Nystagmus Based on Large In-House Datasets and Literature ReviewShu Liu, Shiqiang Li, Yingwei Wang, et al.
Molecular Vision|April 18, 2013
Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataractThomas M Bennett, Giovanni Maraini, Chongfei Jin, et al.
Experimental Eye Research|December 21, 2020
Spectrum-frequency and genotype-phenotype analysis of rhodopsin variantsHualei Luo, Xueshan Xiao, Shiqiang Li, et al.
Pageof 10