Dai E - Search Results

1

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

Zheng B, Dai Y, Liu Y, Shi W, Dai E, Han Y, Zheng D, Yu Y, Li M. Zheng B, et al. Among authors: dai y, dai e. Front Microbiol. 2017 Jun 13;8:1061. doi: 10.3389/fmicb.2017.01061. eCollection 2017. Front Microbiol. 2017. PMID: 28659886 Free PMC article.

2

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

Xiao H, Kou W, Yang Y, Dai E, Zhang X, Wen Y, Peng J, Fei P, Zhao P. Xiao H, et al. Among authors: dai e. Aesthetic Plast Surg. 2024 Feb;48(4):709-718. doi: 10.1007/s00266-022-03215-9. Epub 2022 Dec 27. Aesthetic Plast Surg. 2024. PMID: 36574028

3

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

Liu Y, Yang M, Fan L, He Y, Dai E, Liu M, Jiang L, Yang Z, Li S. Liu Y, et al. Among authors: dai e. Int J Biol Macromol. 2024 Feb;258(Pt 1):128570. doi: 10.1016/j.ijbiomac.2023.128570. Epub 2023 Dec 12. Int J Biol Macromol. 2024. PMID: 38096938

4

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

Dai E, Liu M, Li S, Zhang X, Wang S, Zhao R, He Y, Peng L, Lv L, Xiao H, Yang M, Yang Z, Zhao P. Dai E, et al. Invest Ophthalmol Vis Sci. 2024 Apr 1;65(4):1. doi: 10.1167/iovs.65.4.1. Invest Ophthalmol Vis Sci. 2024. PMID: 38558095 Free PMC article.

5

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

Peng L, Dai E, Xiao H, Zhao R, He Y, Li S, Yang M, Yang Z, Zhao P. Peng L, et al. Among authors: dai e. Mol Genet Genomic Med. 2022 Jun;10(6):e1949. doi: 10.1002/mgg3.1949. Epub 2022 Apr 13. Mol Genet Genomic Med. 2022. PMID: 35417085 Free PMC article.

6

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

Zhao R, Dai E, Wang S, Zhang X, He Y, Peng L, Zhao P, Yang Z, Yang M, Li S. Zhao R, et al. Among authors: dai e. Clin Genet. 2023 Mar;103(3):320-329. doi: 10.1111/cge.14273. Epub 2022 Dec 13. Clin Genet. 2023. PMID: 36453149

7

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

Li S, Yang M, Zhao R, Peng L, Liu W, Jiang X, He Y, Dai E, Zhang L, Yang Y, Shi Y, Zhao P, Yang Z, Zhu X. Li S, et al. Among authors: dai e. Genes Dis. 2022 Oct 11;10(6):2572-2585. doi: 10.1016/j.gendis.2022.10.003. eCollection 2023 Nov. Genes Dis. 2022. PMID: 37554197 Free PMC article.

8

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

Liu M, Dai E, Yang M, Li S, Fan L, Liu Y, Xiao H, Zhao P, Yang Z. Liu M, et al. Among authors: dai e. Invest Ophthalmol Vis Sci. 2024 Mar 5;65(3):31. doi: 10.1167/iovs.65.3.31. Invest Ophthalmol Vis Sci. 2024. PMID: 38517429 Free PMC article.

9

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

Peng Y, Zhao R, Dai E, Peng L, He Y, Li S, Yang M. Peng Y, et al. Among authors: dai e. Eur J Ophthalmol. 2022 Nov;32(6):3220-3226. doi: 10.1177/11206721221074209. Epub 2022 Jan 17. Eur J Ophthalmol. 2022. PMID: 35037517

10

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

Zhao R, Wang S, Zhao P, Dai E, Zhang X, Peng L, He Y, Yang M, Li S, Yang Z. Zhao R, et al. Among authors: dai e. Clin Exp Ophthalmol. 2022 May;50(4):441-448. doi: 10.1111/ceo.14037. Epub 2022 Feb 7. Clin Exp Ophthalmol. 2022. PMID: 35133048

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