BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 17899116)

  • 1. [Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy].
    Müller M; Kusserow C; Orth U; Klär-Dissars U; Laqua H; Gal A
    Ophthalmologe; 2008 Mar; 105(3):262-8. PubMed ID: 17899116
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement.
    Li P; Zhang HZ; Huff S; Nimmakayalu M; Qumsiyeh M; Yu J; Szekely A; Xu T; Pober BR
    Am J Med Genet A; 2006 Dec; 140(24):2721-9. PubMed ID: 17103440
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.
    Nallathambi J; Shukla D; Rajendran A; Namperumalsamy P; Muthulakshmi R; Sundaresan P
    Mol Vis; 2006 Sep; 12():1086-92. PubMed ID: 17093393
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A family harboring homozygous FZD4 deletion supports the existence of recessive FZD4-related familial exudative vitreoretinopathy.
    Khan AO; Lenzner S; Bolz HJ
    Ophthalmic Genet; 2017; 38(4):380-382. PubMed ID: 27668459
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Novel mutation in FZD4 gene in a Japanese pedigree with familial exudative vitreoretinopathy.
    Yoshida S; Arita R; Yoshida A; Tada H; Emori A; Noda Y; Nakao S; Fujisawa K; Ishibashi T
    Am J Ophthalmol; 2004 Oct; 138(4):670-1. PubMed ID: 15488808
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Severe form of familial exudative vitreoretinopathy caused by homozygous R417Q mutation in frizzled-4 gene.
    Kondo H; Qin M; Tahira T; Uchio E; Hayashi K
    Ophthalmic Genet; 2007 Dec; 28(4):220-3. PubMed ID: 18161623
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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; 51(5):2445-2455. PubMed ID: 30537745
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Variable reduction in Norrin signaling activity caused by novel mutations in
    Tian T; Zhang X; Zhang Q; Zhao P
    Mol Vis; 2019; 25():60-69. PubMed ID: 30820142
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Clinical and molecular evaluation of probands and family members with familial exudative vitreoretinopathy.
    Boonstra FN; van Nouhuys CE; Schuil J; de Wijs IJ; van der Donk KP; Nikopoulos K; Mukhopadhyay A; Scheffer H; Tilanus MA; Cremers FP; Hoefsloot LH
    Invest Ophthalmol Vis Sci; 2009 Sep; 50(9):4379-85. PubMed ID: 19324841
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.
    Toomes C; Bottomley HM; Jackson RM; Towns KV; Scott S; Mackey DA; Craig JE; Jiang L; Yang Z; Trembath R; Woodruff G; Gregory-Evans CY; Gregory-Evans K; Parker MJ; Black GC; Downey LM; Zhang K; Inglehearn CF
    Am J Hum Genet; 2004 Apr; 74(4):721-30. PubMed ID: 15024691
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 gene.
    Seemab S; Pervaiz N; Zehra R; Anwar S; Bao Y; Abbasi AA
    BMC Evol Biol; 2019 Mar; 19(1):72. PubMed ID: 30849938
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.