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Lulin Huang

Showing results (41-50 of 81) with videos related to

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Cellular and Molecular Life Sciences : CMLS|March 4, 2026
SDF2L1 modulates oxLDL-induced endoplasmic reticulum stress, protein aggregation, and O-mannosylation in myocardial infarction and lung cancerHuaping Tian, Tujing Zhao, Xiaoyi Huang, et al.
Journal of Ophthalmology|July 1, 2015
Exome Sequencing Identified a Recessive RDH12 Mutation in a Family with Severe Early-Onset Retinitis PigmentosaBo Gong, Bo Wei, Lulin Huang, et al.
Cell Death & Disease|February 18, 2026
Unveiling ZNF124 as a novel determinant in neurodegeneration: orchestration of photoreceptor homeostasis through MSX2 transcriptional regulationYeming Yang, Xiaoyan Jiang, Shujin Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 6, 2019
Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathyLin Zhang, Xiang Zhang, Huijuan Xu, et al.
Ophthalmic Genetics|June 15, 2018
A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridiaXiaoqi Liu, Yaqi Wu, Zequn Miao, et al.
Scientific Reports|September 28, 2016
Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosaYin Yang, Yeming Yang, Lulin Huang, et al.
Scientific Reports|November 5, 2015
Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathyPing Fei, Xiong Zhu, Zhilin Jiang, et al.
Science China. Life Sciences|October 12, 2025
Unveiling the choroidal immune landscape revealed interferon-gamma and TNF-alpha as novel therapeutic targets in dry AMDLin Ye, Tujing Zhao, Huaping Tian, et al.
Molecular Vision|October 30, 2014
Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathyYu Xu, Lulin Huang, Jing Li, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|December 13, 2021
Variants in the Wnt co-receptor LRP6 are associated with familial exudative vitreoretinopathyShujin Li, Mu Yang, Yunqi He, et al.
Pageof 9

Showing results (41-50 of 81) with videos related to

Sort By:
Pageof 9
Cellular and Molecular Life Sciences : CMLS|March 4, 2026
SDF2L1 modulates oxLDL-induced endoplasmic reticulum stress, protein aggregation, and O-mannosylation in myocardial infarction and lung cancerHuaping Tian, Tujing Zhao, Xiaoyi Huang, et al.
Journal of Ophthalmology|July 1, 2015
Exome Sequencing Identified a Recessive RDH12 Mutation in a Family with Severe Early-Onset Retinitis PigmentosaBo Gong, Bo Wei, Lulin Huang, et al.
Cell Death & Disease|February 18, 2026
Unveiling ZNF124 as a novel determinant in neurodegeneration: orchestration of photoreceptor homeostasis through MSX2 transcriptional regulationYeming Yang, Xiaoyan Jiang, Shujin Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 6, 2019
Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathyLin Zhang, Xiang Zhang, Huijuan Xu, et al.
Ophthalmic Genetics|June 15, 2018
A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridiaXiaoqi Liu, Yaqi Wu, Zequn Miao, et al.
Scientific Reports|September 28, 2016
Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosaYin Yang, Yeming Yang, Lulin Huang, et al.
Scientific Reports|November 5, 2015
Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathyPing Fei, Xiong Zhu, Zhilin Jiang, et al.
Science China. Life Sciences|October 12, 2025
Unveiling the choroidal immune landscape revealed interferon-gamma and TNF-alpha as novel therapeutic targets in dry AMDLin Ye, Tujing Zhao, Huaping Tian, et al.
Molecular Vision|October 30, 2014
Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathyYu Xu, Lulin Huang, Jing Li, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|December 13, 2021
Variants in the Wnt co-receptor LRP6 are associated with familial exudative vitreoretinopathyShujin Li, Mu Yang, Yunqi He, et al.
Pageof 9