Shanshan Zhang

发表

A new hand-held holder optimizes the parameters of the laser-induced choroidal neovascularization model in mice.

B. Xue, Shanshan Zhang, Li Gan, 2020, Experimental eye research.

Identification of novel variants in the FZD4 gene associated with familial exudative vitreoretinopathy in Chinese families

Peiquan Zhao, Lulin Huang, Zhenglin Yang, 2019, Clinical & experimental ophthalmology.

Whole-Exome Sequencing Analysis Identified Novel Mutations in the TSPAN12 Gene in Chinese Families with Familial Exudative Vitreoretinopathy.

Zhenglin Yang, Lin Zhang, Huijuan Xu, 2019, Genetic testing and molecular biomarkers.

Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2019, Genetics in Medicine.

Deep Sc-RNA sequencing decoding the molecular dynamic architecture of the human retina

Lulin Huang, Ling Zhong, Yi Shi, 2022, Science China Life Sciences.

Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2021 .

Whole-Exome Sequencing Identified DLG1 as a Candidate Gene for Familial Exudative Vitreoretinopathy.

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2021, Genetic testing and molecular biomarkers.

Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis

Dean Y. Li, Xianjun Zhu, C. Mardin, 2019, Genetics in Medicine.

TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis

Xianjun Zhu, Lin Zhang, Shujin Li, 2019, Journal of Cell Science.

Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice.

Xianjun Zhu, Zhilin Jiang, Lin Zhang, 2020, Human molecular genetics.

Targeted next-generation sequencing reveals that a compound heterozygous mutation in phosphodiesterase 6a gene leads to retinitis pigmentosa in a Chinese family

Xianjun Zhu, Zhenglin Yang, Lin Zhang, 2018, Ophthalmic genetics.

Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells

Xianjun Zhu, Zhilin Jiang, Lin Zhang, 2018, Cell Death & Disease.

Loss of Tmem30a leads to photoreceptor degeneration

Xianjun Zhu, Xiong Zhu, Zhilin Jiang, 2017, Scientific Reports.

Untargeted metabolomics for uncovering plasma biological markers of wet age-related macular degeneration

Haixin Wang, Yanhui Deng, Lulin Huang, 2021, Aging.

Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2019, Genetics in Medicine.

Overexpression of Twist1 in vascular endothelial cells promotes pathological retinal angiogenesis in mice

Lin Zhang, Huijuan Xu, Kuanxiang Sun, 2022, Zoological research.

Loss of Tmem30a leads to photoreceptor degeneration

Xianjun Zhu, Xiong Zhu, Zhilin Jiang, 2017, Scientific Reports.

Whole‐exome sequencing revealed HKDC1 as a candidate gene associated with autosomal‐recessive retinitis pigmentosa

Peiquan Zhao, Xianjun Zhu, Rui Chen, 2018, Human molecular genetics.

Dynamic human retinal pigment epithelium (RPE) and choroid architecture based on single-cell transcriptomic landscape analysis

Lulin Huang, B. Gong, Zhenglin Yang, 2022, Genes & diseases.

Catenin alpha 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/beta-catenin signaling.

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2021, The Journal of clinical investigation.

Big data reveals deep associations in physical examination indicators and can help predict overall underlying health status

Haixin Wang, Yanhui Deng, Lulin Huang, 2019, bioRxiv.