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 *

188 related articles for article (PubMed ID: 25168411)

  • 1. A novel deletion mutation in RS1 gene caused X-linked juvenile retinoschisis in a Chinese family.
    Huang Y; Mei L; Gui B; Su W; Liang D; Wu L; Pan Q
    Eye (Lond); 2014 Nov; 28(11):1364-9. PubMed ID: 25168411
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Thirty-two years follow-up of X-linked juvenile retinoschisis in a Chinese patient with RS1 mutation.
    Xu F; Sui R; Dong F
    Ophthalmic Genet; 2012 Jun; 33(2):77-82. PubMed ID: 22171610
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. X-Linked Retinoschisis: Phenotypic Variability in a Chinese Family.
    Xiao Y; Liu X; Tang L; Wang X; Coursey TG; Guo X; Li Z
    Sci Rep; 2016 Jan; 6():20118. PubMed ID: 26823236
    [TBL] [Abstract][Full Text] [Related]  

  • 13. R213W mutation in the retinoschisis 1 gene causes X-linked juvenile retinoschisis in a large Chinese family.
    Xu J; Gu H; Ma K; Liu X; Snellingen T; Sun E; Wang N; Liu N
    Mol Vis; 2010 Aug; 16():1593-600. PubMed ID: 20806044
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotypic and phenotypic diversity in X-linked retinoschisis: Findings from a South Indian patient cohort.
    Chowdhury S; Chermakani P; Baliga G; Anjanamurthy R; Sundaresan P
    Indian J Ophthalmol; 2024 Jun; 72(6):902-911. PubMed ID: 38317323
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Four Japanese male patients with juvenile retinoschisis: only three have mutations in the RS1 gene.
    Hayashi T; Omoto S; Takeuchi T; Kozaki K; Ueoka Y; Kitahara K
    Am J Ophthalmol; 2004 Nov; 138(5):788-98. PubMed ID: 15531314
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel XLRS1 gene mutations cause X-linked juvenile retinoschisis in Chinese families.
    Ma X; Li X; Wang L
    Jpn J Ophthalmol; 2008; 52(1):48-51. PubMed ID: 18369700
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Overlapping retinal phenotypes in a consanguineous family harboring mutations in CRB1 and RS1.
    Khan AO; El-Ghrably IA
    Ophthalmic Genet; 2019 Feb; 40(1):17-21. PubMed ID: 30608181
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two cases of X-linked juvenile retinoschisis with different optical coherence tomography findings and RS1 gene mutations.
    Chan WM; Choy KW; Wang J; Lam DS; Yip WW; Fu W; Pang CP
    Clin Exp Ophthalmol; 2004 Aug; 32(4):429-32. PubMed ID: 15281981
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.