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Molecular Epidemiology and Risk Factors of Carbapenem-Resistant Klebsiella pneumoniae Infections in Eastern China

Frontiers in microbiology, 2017-06, Vol.8, p.1061-1061

2017

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

Genes & diseases, 2023-11, Vol.10 (6), p.2572-2585

2023

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CTNND1 variants cause familial exudative vitreoretinopathy through Wnt/Cadherin axis

JCI insight, 2022-07, Vol.7 (14)

2022

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A novel frameshift variant in the TSPAN12 gene causes autosomal dominant FEVR

Molecular genetics & genomic medicine, 2022-06, Vol.10 (6), p.e1949-n/a

2022

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Novel truncating variants in CTNNB1 cause familial exudative vitreoretinopathy

Journal of medical genetics, 2023-02, Vol.60 (2), p.174-182

2023

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Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients

Molecular genetics and genomics : MGG, 2024-12, Vol.299 (1), p.32-32, Article 32

2024

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Deciphering a crucial dimeric interface governing Norrin dimerization and the pathogenesis of familial exudative vitreoretinopathy

The FASEB journal, 2024-02, Vol.38 (4), p.e23493-n/a

2024

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Investigating the Impact of Dimer Interface Mutations on Norrin's Secretion and Norrin/β-Catenin Pathway Activation

Investigative ophthalmology & visual science, 2024-03, Vol.65 (3), p.31-31

2024

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Frameshift variants in the C-terminal of CTNNB1 cause familial exudative vitreoretinopathy by AXIN1-mediated ubiquitin-proteasome degradation condensation

International journal of biological macromolecules, 2024-02, Vol.258 (Pt 1), p.128570, Article 128570

2024

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Identification of Novel FZD4 Mutations in Familial Exudative Vitreoretinopathy and Investigating the Pathogenic Mechanisms of FZD4 Mutations

Investigative ophthalmology & visual science, 2024-04, Vol.65 (4), p.1-1

2024

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Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy

European journal of ophthalmology, 2022-11, Vol.32 (6), p.3220-3226

2022

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Administration Method and Potential Efficacy of Hyaluronidase for Hyaluronic Acid Filler-Related Vision Loss: A Systematic Review

Aesthetic plastic surgery, 2024-02, Vol.48 (4), p.709-718

2024

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A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy

Clinical genetics, 2023-03, Vol.103 (3), p.320-329

2023

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Identification of Two Novel Variants in the LRP5 Gene that Cause Familial Exudative Vitreoretinopathy

Genetic testing and molecular biomarkers, 2022-03, Vol.26 (3), p.146-151

2022

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Heterozygote loss‐of‐function variants in the LRP5 gene cause familial exudative vitreoretinopathy

Clinical & experimental ophthalmology, 2022-05, Vol.50 (4), p.441-448

2022

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Molecular Epidemiology and Risk Factors of Carbapenem-Resistant Klebsiella pneumoniae Infections in Eastern China

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

CTNND1 variants cause familial exudative vitreoretinopathy through Wnt/Cadherin axis

A novel frameshift variant in the TSPAN12 gene causes autosomal dominant FEVR

Novel truncating variants in CTNNB1 cause familial exudative vitreoretinopathy

Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients

Deciphering a crucial dimeric interface governing Norrin dimerization and the pathogenesis of familial exudative vitreoretinopathy

Investigating the Impact of Dimer Interface Mutations on Norrin's Secretion and Norrin/β-Catenin Pathway Activation

Frameshift variants in the C-terminal of CTNNB1 cause familial exudative vitreoretinopathy by AXIN1-mediated ubiquitin-proteasome degradation condensation

Identification of Novel FZD4 Mutations in Familial Exudative Vitreoretinopathy and Investigating the Pathogenic Mechanisms of FZD4 Mutations

Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy

Administration Method and Potential Efficacy of Hyaluronidase for Hyaluronic Acid Filler-Related Vision Loss: A Systematic Review

A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy

Identification of Two Novel Variants in the LRP5 Gene that Cause Familial Exudative Vitreoretinopathy

Heterozygote loss‐of‐function variants in the LRP5 gene cause familial exudative vitreoretinopathy

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