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Lulin Huang

Showing results (51-60 of 81) with videos related to

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Genetic Testing and Molecular Biomarkers|May 27, 2016
Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative VitreoretinopathyLin Zhang, Yeming Yang, Shujin Li, et al.
Plos One|November 19, 2013
A novel PRPF31 mutation in a large Chinese family with autosomal dominant retinitis pigmentosa and macular degenerationFang Lu, Lulin Huang, Chuntao Lei, et al.
Journal of Human Genetics|August 7, 2015
Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian populationYu Zhou, Bibhuti B Saikia, Zhilin Jiang, et al.
Molecular Vision|February 5, 2013
Evaluation of MMP2 as a candidate gene for high myopiaBo Gong, Xiaoqi Liu, Dingding Zhang, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|August 29, 2024
Genome-Wide Association Analysis Identifies LILRB2 Gene for Pathological MyopiaLingxi Jiang, Lulin Huang, Chao Dai, et al.
Scientific Reports|February 11, 2016
Associations of 6p21.3 Region with Age-related Macular Degeneration and Polypoidal Choroidal VasculopathyZimeng Ye, Ping Shuai, Yaru Zhai, et al.
Science China. Life Sciences|September 2, 2025
Exploring the role of VAV2 rare variants in primary open-angle glaucoma: genetic insights and pathophysiological mechanismsRunze Li, Yuhong Chen, Shanshan Zhang, et al.
Signal Transduction and Targeted Therapy|October 9, 2025
Single-cell RNA-seq reveals cell type-specific molecular and genetic associations with primary open-angle glaucomaHuaping Tian, Yuhong Chen, Tujing Zhao, et al.
Genes & Diseases|August 9, 2023
Dynamic human retinal pigment epithelium (RPE) and choroid architecture based on single-cell transcriptomic landscape analysisLulin Huang, Lin Ye, Runze Li, et al.
The Journal of Clinical Investigation|January 26, 2021
Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signalingXianjun Zhu, Mu Yang, Peiquan Zhao, et al.
Pageof 9

Showing results (51-60 of 81) with videos related to

Sort By:
Pageof 9
Genetic Testing and Molecular Biomarkers|May 27, 2016
Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative VitreoretinopathyLin Zhang, Yeming Yang, Shujin Li, et al.
Plos One|November 19, 2013
A novel PRPF31 mutation in a large Chinese family with autosomal dominant retinitis pigmentosa and macular degenerationFang Lu, Lulin Huang, Chuntao Lei, et al.
Journal of Human Genetics|August 7, 2015
Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian populationYu Zhou, Bibhuti B Saikia, Zhilin Jiang, et al.
Molecular Vision|February 5, 2013
Evaluation of MMP2 as a candidate gene for high myopiaBo Gong, Xiaoqi Liu, Dingding Zhang, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|August 29, 2024
Genome-Wide Association Analysis Identifies LILRB2 Gene for Pathological MyopiaLingxi Jiang, Lulin Huang, Chao Dai, et al.
Scientific Reports|February 11, 2016
Associations of 6p21.3 Region with Age-related Macular Degeneration and Polypoidal Choroidal VasculopathyZimeng Ye, Ping Shuai, Yaru Zhai, et al.
Science China. Life Sciences|September 2, 2025
Exploring the role of VAV2 rare variants in primary open-angle glaucoma: genetic insights and pathophysiological mechanismsRunze Li, Yuhong Chen, Shanshan Zhang, et al.
Signal Transduction and Targeted Therapy|October 9, 2025
Single-cell RNA-seq reveals cell type-specific molecular and genetic associations with primary open-angle glaucomaHuaping Tian, Yuhong Chen, Tujing Zhao, et al.
Genes & Diseases|August 9, 2023
Dynamic human retinal pigment epithelium (RPE) and choroid architecture based on single-cell transcriptomic landscape analysisLulin Huang, Lin Ye, Runze Li, et al.
The Journal of Clinical Investigation|January 26, 2021
Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signalingXianjun Zhu, Mu Yang, Peiquan Zhao, et al.
Pageof 9