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 *

287 related articles for article (PubMed ID: 26472404)

  • 1. KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathy.
    Hu H; Xiao X; Li S; Jia X; Guo X; Zhang Q
    Br J Ophthalmol; 2016 Feb; 100(2):278-83. PubMed ID: 26472404
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.
    Robitaille JM; Gillett RM; LeBlanc MA; Gaston D; Nightingale M; Mackley MP; Parkash S; Hathaway J; Thomas A; Ells A; Traboulsi EI; Héon E; Roy M; Shalev S; Fernandez CV; MacGillivray C; Wallace K; Fahiminiya S; Majewski J; McMaster CR; Bedard K
    JAMA Ophthalmol; 2014 Dec; 132(12):1393-9. PubMed ID: 25124931
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel variants in familial exudative vitreoretinopathy patients with KIF11 mutations and the Genotype-Phenotype correlation.
    Chen C; Sun L; Li S; Huang L; Zhang T; Wang Z; Yu B; Luo X; Ding X
    Exp Eye Res; 2020 Oct; 199():108165. PubMed ID: 32730767
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole exome sequencing revealed novel pathogenic variants in Vietnamese patients with FEVR.
    Trang DT; Phu NM; Hung DM; Nhung VP; Ha NN; Thuong MTH; Ngoc TTB; Hiep NX; Ton ND; Hai NV; Ha NH
    Mol Vis; 2022; 28():480-491. PubMed ID: 37089697
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis.
    Li JK; Fei P; Li Y; Huang QJ; Zhang Q; Zhang X; Rao YQ; Li J; Zhao P
    Sci Rep; 2016 May; 6():26564. PubMed ID: 27212378
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation spectrum in a cohort with familial exudative vitreoretinopathy.
    Qu N; Li W; Han DM; Gao JY; Yang ZT; Jiang L; Liu TB; Chen YX; Jiang XS; Zhou L; Wu JH; Huang X
    Mol Genet Genomic Med; 2022 Sep; 10(9):e2021. PubMed ID: 35876299
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene.
    Kondo H; Matsushita I; Nagata T; Fujihara E; Hosono K; Uchio E; Hotta Y; Kusaka S
    Transl Vis Sci Technol; 2021 Jun; 10(7):18. PubMed ID: 34128965
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.
    Rao FQ; Cai XB; Cheng FF; Cheng W; Fang XL; Li N; Huang XF; Li LH; Jin ZB
    Invest Ophthalmol Vis Sci; 2017 May; 58(5):2623-2629. PubMed ID: 28494495
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Five novel copy number variations detected in patients with familial exudative vitreoretinopathy.
    Luo J; Li J; Zhang X; Li JK; Chen HJ; Zhao PQ; Fei P
    Mol Vis; 2021; 27():632-642. PubMed ID: 34924743
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Update on the Phenotypic and Genotypic Spectrum of
    Wang Y; Zhang Z; Huang L; Sun L; Li S; Zhang T; Ding X
    Genes (Basel); 2022 Apr; 13(4):. PubMed ID: 35456519
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection and quantification of a KIF11 mosaicism in a subject presenting familial exudative vitreoretinopathy with microcephaly.
    Karjosukarso DW; Cremers FPM; van Nouhuys CE; Collin RWJ
    Eur J Hum Genet; 2018 Dec; 26(12):1819-1823. PubMed ID: 30181612
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11.
    Yang J; Xiao X; Li S; Mai G; Jia X; Wang P; Sun W; Zhang Q
    Am J Ophthalmol; 2022 Mar; 235():178-187. PubMed ID: 34582765
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With Microcephaly.
    Hull S; Arno G; Ostergaard P; Pontikos N; Robson AG; Webster AR; Hogg CR; Wright GA; Henderson RHH; Martin CA; Jackson AP; Mansour S; Moore AT; Michaelides M
    Am J Ophthalmol; 2019 Nov; 207():87-98. PubMed ID: 31077665
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel mutation in
    Wang K; Zhang X; Tian T; Zhao P
    Mol Vis; 2021; 27():528-541. PubMed ID: 34526760
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and genetical features of probands and affected family members with familial exudative vitreoretinopathy in a large Chinese cohort.
    Wang S; Zhang X; Hu Y; Fei P; Xu Y; Peng J; Zhao P
    Br J Ophthalmol; 2021 Jan; 105(1):83-86. PubMed ID: 32238352
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy.
    Shurygina MF; Simonett JM; Parker MA; Mitchell A; Grigorian F; Lifton J; Nagiel A; Shpak AA; Dadali EL; Mishina IA; Weleber RG; Yang P; Pennesi ME
    Invest Ophthalmol Vis Sci; 2020 Nov; 61(13):2. PubMed ID: 33137195
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spectrum of Variants in 389 Chinese Probands With Familial Exudative Vitreoretinopathy.
    Li JK; Li Y; Zhang X; Chen CL; Rao YQ; Fei P; Zhang Q; Zhao P; Li J
    Invest Ophthalmol Vis Sci; 2018 Nov; 59(13):5368-5381. PubMed ID: 30452590
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Novel Insights Into the Phenotypical Spectrum of KIF11-Associated Retinopathy, Including a New Form of Retinal Ciliopathy.
    Birtel J; Gliem M; Mangold E; Tebbe L; Spier I; Müller PL; Holz FG; Neuhaus C; Wolfrum U; Bolz HJ; Charbel Issa P
    Invest Ophthalmol Vis Sci; 2017 Aug; 58(10):3950-3959. PubMed ID: 28785766
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.