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 *

335 related articles for article (PubMed ID: 28867931)

  • 1. Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathy.
    Huang XY; Zhuang H; Wu JH; Li JK; Hu FY; Zheng Y; Tellier LCAM; Zhang SH; Gao FJ; Zhang JG; Xu GZ
    Mol Vis; 2017; 23():605-613. PubMed ID: 28867931
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Mutation Spectrum of the LRP5, NDP, and TSPAN12 Genes in Chinese Patients With Familial Exudative Vitreoretinopathy.
    Tang M; Sun L; Hu A; Yuan M; Yang Y; Peng X; Ding X
    Invest Ophthalmol Vis Sci; 2017 Nov; 58(13):5949-5957. PubMed ID: 29181528
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Next-Generation Sequencing in the Familial Exudative Vitreoretinopathy-Associated Rhegmatogenous Retinal Detachment.
    Chen C; Wang Z; Sun L; Huang S; Li S; Zhang A; Luo X; Huang L; Ding X
    Invest Ophthalmol Vis Sci; 2019 Jun; 60(7):2659-2666. PubMed ID: 31237656
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The characteristics of digenic familial exudative vitreoretinopathy.
    Li Y; Peng J; Li J; Zhang Q; Li J; Zhang X; Fei P; She K; Zhao P
    Graefes Arch Clin Exp Ophthalmol; 2018 Nov; 256(11):2149-2156. PubMed ID: 30097784
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.
    Zhang L; Yang Y; Li S; Tai Z; Huang L; Liu Y; Zhu X; Di Y; Qu C; Jiang Z; Li Y; Zhang G; Kim R; Sundaresan P; Yang Z; Zhu X
    Genet Test Mol Biomarkers; 2016 Jul; 20(7):346-51. PubMed ID: 27228167
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. A start codon mutation of the TSPAN12 gene in Chinese families causes clinical heterogeneous familial exudative vitreoretinopathy.
    Li W; Wang Z; Sun Y; Wang Z; Bai J; Xing B; Sun X; Wang L; Li J; He W
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00948. PubMed ID: 31452356
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy.
    Mao J; Chen Y; Fang Y; Shao Y; Xiang Z; Li H; Zhao S; Chen Y; Shen L
    Ann Med; 2022 Dec; 54(1):3286-3298. PubMed ID: 36411543
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients.
    Salvo J; Lyubasyuk V; Xu M; Wang H; Wang F; Nguyen D; Wang K; Luo H; Wen C; Shi C; Lin D; Zhang K; Chen R
    Invest Ophthalmol Vis Sci; 2015 Feb; 56(3):1937-46. PubMed ID: 25711638
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic detection of two novel LRP5 pathogenic variants in patients with familial exudative vitreoretinopathy.
    Li J; Wang C; Zhang S; Cai B; Pan B; Sun C; Qi X; Ma C; Fang W; Jin K; Bi X; Jin Z; Zhuang W
    BMC Ophthalmol; 2023 Nov; 23(1):489. PubMed ID: 38030997
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Optical Coherence Tomography Angiography in Familial Exudative Vitreoretinopathy: Clinical Features and Phenotype-Genotype Correlation.
    Chen C; Liu C; Wang Z; Sun L; Zhao X; Li S; Luo X; Zhang A; Chong V; Lu L; Ding X
    Invest Ophthalmol Vis Sci; 2018 Dec; 59(15):5726-5734. PubMed ID: 30513533
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of LRP5 mutations in families with familial exudative vitreoretinopathy.
    Liu YQ; Zhu X; Li SJ; Yang YM; Yang M; Zhao PQ; Zhu XJ
    Yi Chuan; 2017 Mar; 39(3):241-249. PubMed ID: 28420620
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel mutation in
    Song Z; Li M; Wang C; Wang Y; Zhang L; Li N; Yang R; Sun P
    Ophthalmic Genet; 2022 Feb; 43(1):104-109. PubMed ID: 34445920
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.
    Xu Y; Huang L; Li J; Zhang Q; Fei P; Zhu X; Tai Z; Ma S; Gong B; Li Y; Zang W; Zhu X; Zhao P; Yang Z
    Mol Vis; 2014; 20():1296-306. PubMed ID: 25352738
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.