BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 25999676)

  • 1. Clinical presentations of X-linked retinoschisis in Taiwanese patients confirmed with genetic sequencing.
    Wang NK; Liu L; Chen HM; Tsai S; Chang TC; Tsai TH; Yang CM; Chao AN; Chen KJ; Kao LY; Yeung L; Yeh LK; Hwang YS; Wu WC; Lai CC
    Mol Vis; 2015; 21():487-501. PubMed ID: 25999676
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A phenotype-genotype correlation study of X-linked retinoschisis.
    Vincent A; Robson AG; Neveu MM; Wright GA; Moore AT; Webster AR; Holder GE
    Ophthalmology; 2013 Jul; 120(7):1454-64. PubMed ID: 23453514
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical findings and
    Chen C; Xie Y; Sun T; Tian L; Xu K; Zhang X; Li Y
    Mol Vis; 2020; 26():291-298. PubMed ID: 32300273
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis.
    Orès R; Mohand-Said S; Dhaenens CM; Antonio A; Zeitz C; Augstburger E; Andrieu C; Sahel JA; Audo I
    Ophthalmology; 2018 Oct; 125(10):1587-1596. PubMed ID: 29739629
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel gene mutation in a family with X-linked retinoschisis.
    Lai YH; Huang SP; Chen SP; Hu PS; Lin SF; Sheu MM; Wang HZ; Tsai RK
    J Formos Med Assoc; 2015 Sep; 114(9):872-80. PubMed ID: 24529551
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic findings in Hungarian patients with X-linked juvenile retinoschisis.
    Lesch B; Szabó V; Kánya M; Somfai GM; Vámos R; Varsányi B; Pámer Z; Knézy K; Salacz G; Janáky M; Ferencz M; Hargitai J; Papp A; Farkas A
    Mol Vis; 2008; 14():2321-32. PubMed ID: 19093009
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study.
    Vijayasarathy C; Ziccardi L; Zeng Y; Smaoui N; Caruso RC; Sieving PA
    Invest Ophthalmol Vis Sci; 2009 Nov; 50(11):5375-83. PubMed ID: 19474399
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Four novel RS1 gene mutations in Polish patients with X-linked juvenile retinoschisis.
    Skorczyk A; Krawczyński MR
    Mol Vis; 2012; 18():3004-12. PubMed ID: 23288992
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutations of the RS1 gene in a cohort of Chinese families with X-linked retinoschisis.
    Chen J; Xu K; Zhang X; Pan Z; Dong B; Li Y
    Mol Vis; 2014; 20():132-9. PubMed ID: 24505212
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene.
    Duncan JL; Ratnam K; Birch DG; Sundquist SM; Lucero AS; Zhang Y; Meltzer M; Smaoui N; Roorda A
    Invest Ophthalmol Vis Sci; 2011 Dec; 52(13):9614-23. PubMed ID: 22110067
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotypic expression of X-linked retinoschisis in Chinese families with mutations in the RS1 gene.
    Xu F; Xiang H; Jiang R; Dong F; Sui R
    Doc Ophthalmol; 2011 Aug; 123(1):21-7. PubMed ID: 21701876
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical features of X linked juvenile retinoschisis in Chinese families associated with novel mutations in the RS1 gene.
    Li X; Ma X; Tao Y
    Mol Vis; 2007 Jun; 13():804-12. PubMed ID: 17615541
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-Linked Retinoschisis: Deep Phenotyping and Genetic Characterization.
    Georgiou M; Finocchio L; Fujinami K; Fujinami-Yokokawa Y; Virgili G; Mahroo OA; Webster AR; Michaelides M
    Ophthalmology; 2022 May; 129(5):542-551. PubMed ID: 34822951
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia.
    Hewitt AW; FitzGerald LM; Scotter LW; Mulhall LE; McKay JD; Mackey DA
    Clin Exp Ophthalmol; 2005 Jun; 33(3):233-9. PubMed ID: 15932525
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic characterization of X-linked retinoschisis: Clinical, electroretinography, and optical coherence tomography variables.
    Neriyanuri S; Dhandayuthapani S; Arunachalam JP; Raman R
    Indian J Ophthalmol; 2016 Jul; 64(7):513-7. PubMed ID: 27609164
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comprehensive analysis of genetic and clinical characteristics of 30 patients with X-linked juvenile retinoschisis in China.
    Gao FJ; Dong JH; Wang DD; Chen F; Hu FY; Chang Q; Xu P; Liu W; Li JK; Huang Y; Wu JH; Xu GZ
    Acta Ophthalmol; 2021 Jun; 99(4):e470-e479. PubMed ID: 33124204
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT.
    Renner AB; Kellner U; Fiebig B; Cropp E; Foerster MH; Weber BH
    Doc Ophthalmol; 2008 Mar; 116(2):97-109. PubMed ID: 17987333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Truncation of retinoschisin protein associated with a novel splice site mutation in the RS1 gene.
    Lesch B; Szabó V; Kánya M; Varsányi B; Somfai GM; Hargitai J; Vámos R; Fiedler O; Farkas A
    Mol Vis; 2008 Aug; 14():1549-58. PubMed ID: 18728755
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in the XLRS1 gene in Thai families with X-linked juvenile retinoschisis.
    Atchaneeyasakul LO; Trinavarat A; Pituksung A; Jinda W; Thongnoppakhun W; Limwongse C
    Jpn J Ophthalmol; 2010 Jan; 54(1):89-93. PubMed ID: 20151283
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic variations in the hotspot region of RS1 gene in Indian patients with juvenile X-linked retinoschisis.
    Suganthalakshmi B; Shukla D; Rajendran A; Kim R; Nallathambi J; Sundaresan P
    Mol Vis; 2007 Apr; 13():611-7. PubMed ID: 17515881
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.