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 *

266 related articles for article (PubMed ID: 25352738)

  • 1. 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]  

  • 2. 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]  

  • 3. Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes.
    Yang H; Xiao X; Li S; Mai G; Zhang Q
    Mol Vis; 2011 Apr; 17():1128-35. PubMed ID: 21552475
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel frameshift variant in the TSPAN12 gene causes autosomal dominant FEVR.
    Peng L; Dai E; Xiao H; Zhao R; He Y; Li S; Yang M; Yang Z; Zhao P
    Mol Genet Genomic Med; 2022 Jun; 10(6):e1949. PubMed ID: 35417085
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy.
    Zhao R; Dai E; Wang S; Zhang X; He Y; Peng L; Zhao P; Yang Z; Yang M; Li S
    Clin Genet; 2023 Mar; 103(3):320-329. PubMed ID: 36453149
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR).
    Poulter JA; Davidson AE; Ali M; Gilmour DF; Parry DA; Mintz-Hittner HA; Carr IM; Bottomley HM; Long VW; Downey LM; Sergouniotis PI; Wright GA; MacLaren RE; Moore AT; Webster AR; Inglehearn CF; Toomes C
    Invest Ophthalmol Vis Sci; 2012 May; 53(6):2873-9. PubMed ID: 22427576
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy.
    Fei P; Zhu X; Jiang Z; Ma S; Li J; Zhang Q; Zhou Y; Xu Y; Tai Z; Zhang L; Huang L; Yang Z; Zhao P; Zhu X
    Sci Rep; 2015 Nov; 5():16120. PubMed ID: 26530129
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Large Deletions of TSPAN12 Cause Familial Exudative Vitreoretinopathy (FEVR).
    Seo SH; Kim MJ; Park SW; Kim JH; Yu YS; Song JY; Cho SI; Ahn JH; Oh YH; Lee JS; Lee S; Seong MW; Park SS; Kim JY
    Invest Ophthalmol Vis Sci; 2016 Dec; 57(15):6902-6908. PubMed ID: 28002565
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in the TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy.
    Kondo H; Kusaka S; Yoshinaga A; Uchio E; Tawara A; Hayashi K; Tahira T
    Am J Ophthalmol; 2011 Jun; 151(6):1095-1100.e1. PubMed ID: 21334594
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of Five Novel Variants in the TSPAN12 Gene in Chinese Families With Familial Exudative Vitreoretinopathy.
    Wang Y; Wang Q; Li S; Ding X
    Transl Vis Sci Technol; 2023 May; 12(5):29. PubMed ID: 37252707
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Symmetry of folds in FEVR: A genotype-phenotype correlation study.
    Wang Z; Chen C; Sun L; Zhang A; Liu C; Huang L; Ding X
    Exp Eye Res; 2019 Sep; 186():107720. PubMed ID: 31299183
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.