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 *

140 related articles for article (PubMed ID: 17879437)

  • 21. Establishment of a human induced pluripotent stem cell line (CSUASOi005-A), from peripheral blood mononuclear cells of a patient with X-linked juvenile retinoschisis carrying a novel mutation in RS1 gene.
    Mao S; Ding C; Zhou Y; Jing Y; Chen J; Guo Y; Liu J; Cui Z; Yan X; Gu J; Wang Y; Chen J; Tang S
    Stem Cell Res; 2020 Mar; 43():101718. PubMed ID: 32050117
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Intracellular retention of mutant retinoschisin is the pathological mechanism underlying X-linked retinoschisis.
    Wang T; Waters CT; Rothman AM; Jakins TJ; Römisch K; Trump D
    Hum Mol Genet; 2002 Nov; 11(24):3097-105. PubMed ID: 12417531
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. X-linked retinoschisis: a clinical and molecular genetic review.
    Tantri A; Vrabec TR; Cu-Unjieng A; Frost A; Annesley WH; Donoso LA
    Surv Ophthalmol; 2004; 49(2):214-30. PubMed ID: 14998693
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. X-linked retinoschisis--clinical manifestation, genetic and electrophysiological analysis of three generations with p.Arg197Cys mutation of RS1 gene.
    Ulinska M; Kmera-Muszynska M; Szulborski K; Broniek-Kowalik K; Franaszczyk M; Oldak M; Ploski R
    Klin Oczna; 2014; 116(3):187-92. PubMed ID: 25799783
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis.
    Gehrig A; White K; Lorenz B; Andrassi M; Clemens S; Weber BH
    Clin Genet; 1999 Jun; 55(6):461-5. PubMed ID: 10450864
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel truncating Rs1 mutation associated with X-linked juvenile retinoschisis.
    Jin ZB; Nao-I N
    Jpn J Ophthalmol; 2007; 51(1):71-3. PubMed ID: 17295148
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis.
    Gehrig A; Weber BH; Lorenz B; Andrassi M
    J Med Genet; 1999 Dec; 36(12):932-4. PubMed ID: 10636740
    [No Abstract]   [Full Text] [Related]  

  • 32. Focus on molecules: retinoschisin (RS1).
    Molday RS
    Exp Eye Res; 2007 Feb; 84(2):227-8. PubMed ID: 16600216
    [No Abstract]   [Full Text] [Related]  

  • 33. CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene.
    Langmann T; Lai CC; Weigelt K; Tam BM; Warneke-Wittstock R; Moritz OL; Weber BH
    Nucleic Acids Res; 2008 Nov; 36(20):6523-34. PubMed ID: 18927113
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic and clinical evaluation of juvenile retinoschisis.
    Kim JE; Ruttum MS; Koeberl MJ; Hassemer EL; Sidjanin DJ
    J AAPOS; 2009 Apr; 13(2):215-7. PubMed ID: 19393523
    [TBL] [Abstract][Full Text] [Related]  

  • 35. X-Linked Retinoschisis without Macular Retinoschisis: A New RS1 Mutation.
    Alfonso-Muñoz EA; Català-Mora J; Díaz-Cascajosa J
    Ophthalmol Retina; 2020 Jul; 4(7):719. PubMed ID: 32646553
    [No Abstract]   [Full Text] [Related]  

  • 36. Novel RS1 mutations associated with X-linked juvenile retinoschisis.
    Yi J; Li S; Jia X; Xiao X; Wang P; Guo X; Zhang Q
    Int J Mol Med; 2012 Apr; 29(4):644-8. PubMed ID: 22245991
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Two novel point mutations of the XLRS1 gene in patients with X-linked juvenile retinoschisis.
    Inoue Y; Yamamoto S; Inoue T; Fujikado T; Kusaka S; Ohguro N; Ohji M; Tano Y
    Am J Ophthalmol; 2002 Oct; 134(4):622-4. PubMed ID: 12383832
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Unusual phenotypic expression of an XLRS1 mutation in X-linked juvenile retinoschisis.
    Dodds JA; Srivastava AK; Holden KR
    J Child Neurol; 2006 Apr; 21(4):331-3. PubMed ID: 16900931
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. X-linked retinoschisis: clinical phenotype and RS1 genotype in 86 UK patients.
    Pimenides D; George ND; Yates JR; Bradshaw K; Roberts SA; Moore AT; Trump D
    J Med Genet; 2005 Jun; 42(6):e35. PubMed ID: 15937075
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.