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Journal Abstract Search

160 related items for PubMed ID: 31566834

  • 1. Frizzled 4 regulates ventral blood vessel remodeling in the zebrafish retina.
    Caceres L, Prykhozhij SV, Cairns E, Gjerde H, Duff NM, Collett K, Ngo M, Nasrallah GK, McMaster CR, Litvak M, Robitaille JM, Berman JN.
    Dev Dyn; 2019 Dec; 248(12):1243-1256. PubMed ID: 31566834
    [Abstract] [Full Text] [Related]

  • 2. The spectrum of genetic mutations in patients with asymptomatic mild familial exudative vitreoretinopathy.
    Chen C, Sun L, Li S, Huang L, Zhang T, Wang Z, Yu B, Ding X.
    Exp Eye Res; 2020 Mar; 192():107941. PubMed ID: 31987760
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  • 4. Whole-Gene Deletions of FZD4 Cause Familial Exudative Vitreoretinopathy.
    Huang L, Lu J, Zhang L, Zhang Z, Sun L, Li S, Zhang T, Chen L, Cao L, Ding X.
    Genes (Basel); 2021 Jun 27; 12(7):. PubMed ID: 34199009
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  • 5. Familial exudative vitreoretinopathy (FEVR) in a child with novel microarray-defined deletion of 11q14 previously diagnosed as retinopathy of prematurity (ROP).
    López-Cañizares A, Lazzarini TA, Mendoza C, Berrocal AM.
    Ophthalmic Genet; 2023 Jun 27; 44(3):313-317. PubMed ID: 36444989
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  • 6. A Novel Variant of the FZD4 Gene in a Chinese Family Causes Autosomal Dominant Familial Exudative Vitreoretinopathy.
    Yang L, Fu J, Cheng J, Wei C, Zhou Q, Ijaz I, Lv H, Fu J.
    Cell Physiol Biochem; 2018 Jun 27; 51(5):2445-2455. PubMed ID: 30537745
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  • 8. Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.
    Robitaille J, MacDonald ML, Kaykas A, Sheldahl LC, Zeisler J, Dubé MP, Zhang LH, Singaraja RR, Guernsey DL, Zheng B, Siebert LF, Hoskin-Mott A, Trese MT, Pimstone SN, Shastry BS, Moon RT, Hayden MR, Goldberg YP, Samuels ME.
    Nat Genet; 2002 Oct 27; 32(2):326-30. PubMed ID: 12172548
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  • 9. Role of NDP- and FZD4-Related Novel Mutations Identified in Patients with FEVR in Norrin/β-Catenin Signaling Pathway.
    Han S, Sun J, Yang L, Qi M.
    Biomed Res Int; 2020 Oct 27; 2020():7681926. PubMed ID: 32420371
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  • 11. Identification of Novel Mutations in the FZD4 and NDP Genes in Patients with Familial Exudative Vitreoretinopathy in South India.
    Zhu X, Sun K, Huang L, Ma S, Hao F, Yang Z, Sundaresan P, Zhu X.
    Genet Test Mol Biomarkers; 2020 Feb 27; 24(2):92-98. PubMed ID: 31999491
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  • 14. Symmetry of folds in FEVR: A genotype-phenotype correlation study.
    Wang Z, Chen C, Sun L, Zhang A, Liu C, Huang L, Ding X.
    Exp Eye Res; 2019 Sep 27; 186():107720. PubMed ID: 31299183
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  • 17. ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature.
    Collin RW, Nikopoulos K, Dona M, Gilissen C, Hoischen A, Boonstra FN, Poulter JA, Kondo H, Berger W, Toomes C, Tahira T, Mohn LR, Blokland EA, Hetterschijt L, Ali M, Groothuismink JM, Duijkers L, Inglehearn CF, Sollfrank L, Strom TM, Uchio E, van Nouhuys CE, Kremer H, Veltman JA, van Wijk E, Cremers FP.
    Proc Natl Acad Sci U S A; 2013 Jun 11; 110(24):9856-61. PubMed ID: 23716654
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  • 20. Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy.
    Fei P, Zhu X, Jiang Z, Ma S, Li J, Zhang Q, Zhou Y, Xu Y, Tai Z, Zhang L, Huang L, Yang Z, Zhao P, Zhu X.
    Sci Rep; 2015 Nov 04; 5():16120. PubMed ID: 26530129
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