BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 18214793)

  • 1. Stargardt's disease and the ABCR gene.
    Westerfeld C; Mukai S
    Semin Ophthalmol; 2008; 23(1):59-65. PubMed ID: 18214793
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR.
    Cremers FP; van de Pol DJ; van Driel M; den Hollander AI; van Haren FJ; Knoers NV; Tijmes N; Bergen AA; Rohrschneider K; Blankenagel A; Pinckers AJ; Deutman AF; Hoyng CB
    Hum Mol Genet; 1998 Mar; 7(3):355-62. PubMed ID: 9466990
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease.
    Nasonkin I; Illing M; Koehler MR; Schmid M; Molday RS; Weber BH
    Hum Genet; 1998 Jan; 102(1):21-6. PubMed ID: 9490294
    [TBL] [Abstract][Full Text] [Related]  

  • 4. ABC transporters in ophthalmic disease.
    Westerfeld C
    Methods Mol Biol; 2010; 637():221-30. PubMed ID: 20419437
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa.
    Klevering BJ; Maugeri A; Wagner A; Go SL; Vink C; Cremers FP; Hoyng CB
    Ophthalmology; 2004 Mar; 111(3):546-53. PubMed ID: 15019334
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [From gene to disease: from the ABCA4 gene to Stargardt disease, cone-rod dystrophy and retinitis pigmentosa].
    Cremers FP; Maugeri A; Klevering BJ; Hoefsloot LH; Hoyng CB
    Ned Tijdschr Geneeskd; 2002 Aug; 146(34):1581-4. PubMed ID: 12224481
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Treatment with isotretinoin inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration.
    Radu RA; Mata NL; Nusinowitz S; Liu X; Sieving PA; Travis GH
    Proc Natl Acad Sci U S A; 2003 Apr; 100(8):4742-7. PubMed ID: 12671074
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis.
    Bini A; Sodi A; Passerini I; Menchini U; Torricelli F
    Clin Exp Ophthalmol; 2007 Nov; 35(8):777-9. PubMed ID: 17997789
    [TBL] [Abstract][Full Text] [Related]  

  • 9. ABCR unites what ophthalmologists divide(s).
    van Driel MA; Maugeri A; Klevering BJ; Hoyng CB; Cremers FP
    Ophthalmic Genet; 1998 Sep; 19(3):117-22. PubMed ID: 9810566
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stargardt's pigmentosa: A novel combination of two inherited retinal dystrophies.
    Bartol-Puyal FA; Méndez-Martínez S; Pardiñas Barón N; Ruiz-Moreno Ó; Pablo L
    Arch Soc Esp Oftalmol (Engl Ed); 2023 Nov; 98(11):665-669. PubMed ID: 37748682
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mutations in the ABCA4 gene in a family with Stargardt's disease and retinitis pigmentosa (STGD1/RP19)].
    Rudolph G; Kalpadakis P; Haritoglou C; Rivera A; Weber BH
    Klin Monbl Augenheilkd; 2002 Aug; 219(8):590-6. PubMed ID: 12353176
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The photoreceptor rim protein is an ABC transporter encoded by the gene for recessive Stargardt's disease (ABCR).
    Azarian SM; Travis GH
    FEBS Lett; 1997 Jun; 409(2):247-52. PubMed ID: 9202155
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.
    Weber BH; Sander S; Kopp C; Walker D; Eckstein A; Wissinger B; Zrenner E; Grimm T
    Br J Ophthalmol; 1996 Aug; 80(8):745-9. PubMed ID: 8949721
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's disease.
    Gerber S; Rozet JM; Bonneau D; Souied E; Weissenbach J; Frezal J; Munnich A; Kaplan J
    Hum Genet; 1995 Apr; 95(4):382-4. PubMed ID: 7705831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinoses.
    Gerber S; Odent S; Postel-Vinay A; Janin N; Dufier JL; Munnich A; Frezal J; Kaplan J
    J Med Genet; 1994 Mar; 31(3):222-3. PubMed ID: 8014971
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Light exposure stimulates formation of A2E oxiranes in a mouse model of Stargardt's macular degeneration.
    Radu RA; Mata NL; Bagla A; Travis GH
    Proc Natl Acad Sci U S A; 2004 Apr; 101(16):5928-33. PubMed ID: 15067110
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus.
    Rozet JM; Gerber S; Ghazi I; Perrault I; Ducroq D; Souied E; Cabot A; Dufier JL; Munnich A; Kaplan J
    J Med Genet; 1999 Jun; 36(6):447-51. PubMed ID: 10874631
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stargardt's disease and retinitis pigmentosa: different phenotypic presentations in the same family.
    Ozdek S; Onaran Z; Gürelik G; Bilgihan K; Acar C; Hasanreisoglu B
    Eye (Lond); 2005 Nov; 19(11):1222-5. PubMed ID: 15889047
    [No Abstract]   [Full Text] [Related]  

  • 19. [A special form of Stargardt's disease/fundus flavimaculatus].
    Suzuki R; Hirose T
    Nippon Ganka Gakkai Zasshi; 1996 Jul; 100(7):562-7. PubMed ID: 8741342
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial.
    Shroyer NF; Lewis RA; Allikmets R; Singh N; Dean M; Leppert M; Lupski JR
    Vision Res; 1999 Jul; 39(15):2537-44. PubMed ID: 10396622
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.