BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

288 related articles for article (PubMed ID: 31452356)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. A novel stop codon mutation of TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.
    Zou G; Qi R; Ma M; Fu S; Liang Q; Bi X; Wang C; Hu X; Cai Y; Sheng X
    Ophthalmic Genet; 2022 Apr; 43(2):210-217. PubMed ID: 34738848
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-Exome Sequencing Analysis Identified Novel Mutations in the
    Yuan Y; Xu H; Zhang S; Zhang X; Zhang L; Yang Z
    Genet Test Mol Biomarkers; 2019 Oct; 23(10):722-727. PubMed ID: 31513438
    [No Abstract]   [Full Text] [Related]  

  • 6. Whole exome sequencing revealed 14 variants in NDP, FZD4, LRP5, and TSPAN12 genes for 20 families with familial exudative vitreoretinopathy.
    Dan H; Wang D; Huang Z; Shi Q; Zheng M; Xiao Y; Song Z
    BMC Med Genomics; 2022 Mar; 15(1):54. PubMed ID: 35277167
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Asymptomatic adults in a single family with familial exudative vitreoretinopathy and
    Carroll RM; Kim BJ
    Ophthalmic Genet; 2019 Oct; 40(5):474-479. PubMed ID: 31755339
    [No Abstract]   [Full Text] [Related]  

  • 8. Whole-Exome Sequencing Reveals Novel
    Chen C; Yang M; Huang L; Zhao R; Sundaresan P; Zhu X; Li S; Yang Z
    Genet Test Mol Biomarkers; 2021 Jun; 25(6):399-404. PubMed ID: 34077673
    [No Abstract]   [Full Text] [Related]  

  • 9. Novel Exon 7 Deletions in
    Jiang Z; Wang P
    Genes (Basel); 2023 Feb; 14(3):. PubMed ID: 36980859
    [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. 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]  

  • 12. 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]  

  • 13. Five novel dysfunctional variants in the TSPAN12 gene in familial exudative vitreoretinopathy.
    Wang Y; Lai Y; Jiang Z; Li S; Ding X
    Exp Eye Res; 2023 Sep; 234():109574. PubMed ID: 37451565
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12.
    Schatz P; Khan AO
    Acta Ophthalmol; 2017 Nov; 95(7):705-709. PubMed ID: 28211206
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Familial exudative vitreoretinopathy caused by a homozygous mutation in TSPAN12 in a cystic fibrosis infant.
    Savarese M; Spinelli E; Gandolfo F; Lemma V; Di Fruscio G; Padoan R; Morescalchi F; D'Agostino M; Savoldi G; Semeraro F; Nigro V; Bonatti S
    Ophthalmic Genet; 2014 Sep; 35(3):184-6. PubMed ID: 23834558
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy.
    Kashani AH; Learned D; Nudleman E; Drenser KA; Capone A; Trese MT
    Ophthalmology; 2014 Jan; 121(1):262-268. PubMed ID: 24084499
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.