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 *

191 related articles for article (PubMed ID: 23568735)

  • 1. [Detection and prenatal diagnosis for RS1 gene mutations in two Chinese families with X-linked juvenile retinoschisis].
    Chu Y; Fang D; Hou QF; Wang LY; Guo XR; Wang YT; Liao SX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):199-202. PubMed ID: 23568735
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Gene symbol: RS1. Disease: Retinoschisis, X-Linked juvenile.
    Riveiro-Alvarez R; Cantalapiedra D; Vallespin E; Aguirre-Lamban J; Avila-Fernandez A; Gimenez-Pardo A; Trujillo-Tiebas MJ; Ayuso C
    Hum Genet; 2008 Jun; 123(5):551. PubMed ID: 20960647
    [No Abstract]   [Full Text] [Related]  

  • 11. X-linked juvenile retinoschisis (XLRS): a review of genotype-phenotype relationships.
    Kim DY; Mukai S
    Semin Ophthalmol; 2013; 28(5-6):392-6. PubMed ID: 24138048
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization of novel RS1 exonic deletions in juvenile X-linked retinoschisis.
    D'Souza L; Cukras C; Antolik C; Craig C; Lee JY; He H; Li S; Smaoui N; Hejtmancik JF; Sieving PA; Wang X
    Mol Vis; 2013; 19():2209-16. PubMed ID: 24227916
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel human pathological mutations. Gene symbol: RS1. Disease: X-linked juvenile retinoschisis.
    Riveiro-Alvarez R; Trujillo-Tiebas MJ; Gimenez A; Cantalapiedra D; Vallespin E; Aguirre-Lamban J; Villaverde C; Ayuso C
    Hum Genet; 2007 Jun; 121(5):647. PubMed ID: 17879437
    [No Abstract]   [Full Text] [Related]  

  • 14. Mutations in the RS1 gene in a Chinese family with X-linked juvenile retinoschisis.
    Hou Q; Chu Y; Guo Q; Wu D; Liao S
    Intractable Rare Dis Res; 2012 Feb; 1(1):30-4. PubMed ID: 25343070
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Design and Validation of a New MLPA-Based Assay for the Detection of RS1 Gene Deletions and Application in a Large Family with X-Linked Juvenile Retinoschisis.
    Nicoletti A; Ziccardi L; Maltese PE; Benedetti S; Palumbo O; Rendina M; D'Agruma L; Falsini B; Wang X; Bertelli M
    Genet Test Mol Biomarkers; 2017 Feb; 21(2):116-121. PubMed ID: 27997221
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Coexpression and interaction of wild-type and missense RS1 mutants associated with X-linked retinoschisis: its relevance to gene therapy.
    Dyka FM; Molday RS
    Invest Ophthalmol Vis Sci; 2007 Jun; 48(6):2491-7. PubMed ID: 17525175
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and molecular characterization of females affected by X-linked retinoschisis.
    Staffieri SE; Rose L; Chang A; De Roach JN; McLaren TL; Mackey DA; Hewitt AW; Lamey TM
    Clin Exp Ophthalmol; 2015; 43(7):643-7. PubMed ID: 25894957
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular genetic characteristics of X-linked retinoschisis in Koreans.
    Kim SY; Ko HS; Yu YS; Hwang JM; Lee JJ; Kim SY; Kim JY; Seong MW; Park KH; Park SS
    Mol Vis; 2009; 15():833-43. PubMed ID: 19390641
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.