These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 20008721)

  • 1. Clinical presentation and genetic correlation of patients with mutations affecting the FZD4 gene.
    Drenser KA; Dailey W; Vinekar A; Dalal K; Capone A; Trese MT
    Arch Ophthalmol; 2009 Dec; 127(12):1649-54. PubMed ID: 20008721
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Frizzled-4 Variations Associated with Retinopathy and Intrauterine Growth Retardation: A Potential Marker for Prematurity and Retinopathy.
    Dailey WA; Gryc W; Garg PG; Drenser KA
    Ophthalmology; 2015 Sep; 122(9):1917-23. PubMed ID: 26119001
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with FZD4 mutations (H69Y and C181R).
    Omoto S; Hayashi T; Kitahara K; Takeuchi T; Ueoka Y
    Ophthalmic Genet; 2004 Jun; 25(2):81-90. PubMed ID: 15370539
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe retinopathy of prematurity associated with FZD4 mutations.
    Ells A; Guernsey DL; Wallace K; Zheng B; Vincer M; Allen A; Ingram A; DaSilva O; Siebert L; Sheidow T; Beis J; Robitaille JM
    Ophthalmic Genet; 2010 Mar; 31(1):37-43. PubMed ID: 20141357
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy.
    Toomes C; Bottomley HM; Scott S; Mackey DA; Craig JE; Appukuttan B; Stout JT; Flaxel CJ; Zhang K; Black GC; Fryer A; Downey LM; Inglehearn CF
    Invest Ophthalmol Vis Sci; 2004 Jul; 45(7):2083-90. PubMed ID: 15223780
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 44(3):313-317. PubMed ID: 36444989
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic overlap of familial exudative vitreoretinopathy (FEVR) with persistent fetal vasculature (PFV) caused by FZD4 mutations in two distinct pedigrees.
    Robitaille JM; Wallace K; Zheng B; Beis MJ; Samuels M; Hoskin-Mott A; Guernsey DL
    Ophthalmic Genet; 2009 Mar; 30(1):23-30. PubMed ID: 19172507
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy.
    Milhem RM; Ben-Salem S; Al-Gazali L; Ali BR
    Invest Ophthalmol Vis Sci; 2014 Apr; 55(6):3423-31. PubMed ID: 24744206
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.
    Qin M; Hayashi H; Oshima K; Tahira T; Hayashi K; Kondo H
    Hum Mutat; 2005 Aug; 26(2):104-12. PubMed ID: 15981244
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel frizzled-4 gene mutations in chinese patients with familial exudative vitreoretinopathy.
    Jia LY; Li XX; Yu WZ; Zeng WT; Liang C
    Arch Ophthalmol; 2010 Oct; 128(10):1341-9. PubMed ID: 20938005
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular Characterization of FZD4, LRP5, and TSPAN12 in Familial Exudative Vitreoretinopathy.
    Seo SH; Yu YS; Park SW; Kim JH; Kim HK; Cho SI; Park H; Lee SJ; Seong MW; Park SS; Kim JY
    Invest Ophthalmol Vis Sci; 2015 Aug; 56(9):5143-51. PubMed ID: 26244290
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity.
    Kondo H; Kusaka S; Yoshinaga A; Uchio E; Tawara A; Tahira T
    Mol Vis; 2013; 19():476-85. PubMed ID: 23441120
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease.
    Robitaille JM; Zheng B; Wallace K; Beis MJ; Tatlidil C; Yang J; Sheidow TG; Siebert L; Levin AV; Lam WC; Arthur BW; Lyons CJ; Jaakkola E; Tsilou E; Williams CA; Weaver RG; Shields CL; Guernsey DL
    Br J Ophthalmol; 2011 Apr; 95(4):574-9. PubMed ID: 21097938
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity.
    Dickinson JL; Sale MM; Passmore A; FitzGerald LM; Wheatley CM; Burdon KP; Craig JE; Tengtrisorn S; Carden SM; Maclean H; Mackey DA
    Clin Exp Ophthalmol; 2006; 34(7):682-8. PubMed ID: 16970763
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation spectrum of
    Rathi S; Jalali S; Musada GR; Patnaik S; Balakrishnan D; Hussain A; Kaur I
    Br J Ophthalmol; 2018 Feb; 102(2):276-281. PubMed ID: 28982955
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivity.
    Kondo H; Hayashi H; Oshima K; Tahira T; Hayashi K
    Br J Ophthalmol; 2003 Oct; 87(10):1291-5. PubMed ID: 14507768
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a fourth locus (EVR4) for familial exudative vitreoretinopathy (FEVR).
    Toomes C; Downey LM; Bottomley HM; Scott S; Woodruff G; Trembath RC; Inglehearn CF
    Mol Vis; 2004 Jan; 10():37-42. PubMed ID: 14737064
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy.
    Yang H; Li S; Xiao X; Wang P; Guo X; Zhang Q
    Mol Vis; 2012; 18():2438-46. PubMed ID: 23077402
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Retinal phenotype-genotype correlation of pediatric patients expressing mutations in the Norrie disease gene.
    Wu WC; Drenser K; Trese M; Capone A; Dailey W
    Arch Ophthalmol; 2007 Feb; 125(2):225-30. PubMed ID: 17296899
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel mutations in FZD4 and phenotype-genotype correlation in Chinese patients with familial exudative vitreoretinopathy.
    Tang M; Ding X; Li J; Hu A; Yuan M; Yang Y; Zhan Z; Li Z; Lu L
    Mol Vis; 2016; 22():917-32. PubMed ID: 27555740
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.