Lin Zhang

发表

Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy

Peiquan Zhao, Xianjun Zhu, Qi Zhang, 2015, Scientific Reports.

Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft

Haixin Wang, Lulin Huang, Ziyan Wang, 2019, PLoS genetics.

A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy

S. Inoue, A. Laude, K. Nishida, 2016, Nature Genetics.

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.

Cholesterol homeostasis regulated by ABCA1 is critical for retinal ganglion cell survival

Xianjun Zhu, Yu Zhou, B. Gong, 2022, Science China Life Sciences.

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.

Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.

R. Kim, Xianjun Zhu, Lulin Huang, 2016, Genetic testing and molecular biomarkers.

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

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2021 .

Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population

R. Kim, Xianjun Zhu, Lulin Huang, 2016, Scientific Reports.

Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma.

Xianjun Zhu, Lin Zhang, Periasamy Sundaresan, 2017, Genetic testing and molecular biomarkers.

The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis

Huafu Chen, D. Yao, Xianjun Zhu, 2021, Science China Life Sciences.

ER complex proteins are required for rhodopsin biosynthesis and photoreceptor survival in Drosophila and mice

Xianjun Zhu, Tao Wang, Wenjia Lai, 2019, Cell Death & Differentiation.

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.

A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosa

Xianjun Zhu, K. Ramasamy, Lulin Huang, 2018, 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.

Hepatic Tmem30a Deficiency Causes Intrahepatic Cholestasis by Impairing Expression and Localization of Bile Salt Transporters.

Zhongjie Lu, Xianjun Zhu, Z. Ju, 2017, The American journal of pathology.

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.

Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa.

Xianjun Zhu, Zhenglin Yang, Lin Zhang, 2018, Genetic testing and molecular biomarkers.

Dysregulated m6A Modification Promotes Lipogenesis and Development of Non-alcoholic Fatty Liver Disease and Hepatocellular Carcinoma.

Xianjun Zhu, Zhenglin Yang, Lin Zhang, 2022, Molecular therapy : the journal of the American Society of Gene Therapy.

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.

Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy

Peiquan Zhao, Xianjun Zhu, Zhenglin Yang, 2022, Genes & diseases.

Deletion of phosphatidylserine flippase β-subunit Tmem30a in satellite cells leads to delayed skeletal muscle regeneration

Xianjun Zhu, Lin Zhang, Yeming Yang, 2021, Zoological research.

The endoplasmic reticulum membrane protein complex subunit Emc6 is essential for rhodopsin localization and photoreceptor cell survival

L. Wang, Xianjun Zhu, Lin Zhang, 2023, 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.

Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice

Xianjun Zhu, Zhilin Jiang, Lin Zhang, 2023, The FEBS journal.