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Journal Abstract Search

292 related items for PubMed ID: 10699176

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  • 7. Analysis of six candidate genes as potential modifiers of disease expression in canine XLPRA1, a model for human X-linked retinitis pigmentosa 3.
    Guyon R, Pearce-Kelling SE, Zeiss CJ, Acland GM, Aguirre GD.
    Mol Vis; 2007 Jul 11; 13():1094-105. PubMed ID: 17653054
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  • 8. RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa.
    Kirschner R, Rosenberg T, Schultz-Heienbrok R, Lenzner S, Feil S, Roepman R, Cremers FP, Ropers HH, Berger W.
    Hum Mol Genet; 1999 Aug 11; 8(8):1571-8. PubMed ID: 10401007
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  • 9. Retinal pathology of canine X-linked progressive retinal atrophy, the locus homologue of RP3.
    Zeiss CJ, Acland GM, Aguirre GD.
    Invest Ophthalmol Vis Sci; 1999 Dec 11; 40(13):3292-304. PubMed ID: 10586956
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  • 10. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
    Jacobson SG, Buraczynska M, Milam AH, Chen C, Järvaläinen M, Fujita R, Wu W, Huang Y, Cideciyan AV, Swaroop A.
    Invest Ophthalmol Vis Sci; 1997 Sep 11; 38(10):1983-97. PubMed ID: 9331262
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  • 11. XLPRA: a canine retinal degeneration inherited as an X-linked trait.
    Acland GM, Blanton SH, Hershfield B, Aguirre GD.
    Am J Med Genet; 1994 Aug 01; 52(1):27-33. PubMed ID: 7977457
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  • 12. Independent origin and restricted distribution of RPGR deletions causing XLPRA.
    Zangerl B, Johnson JL, Acland GM, Aguirre GD.
    J Hered; 2007 Aug 01; 98(5):526-30. PubMed ID: 17646274
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  • 13. X-linked retinitis pigmentosa associated with a 2-base pair insertion in codon 99 of the RP3 gene RPGR.
    Weleber RG, Butler NS, Murphey WH, Sheffield VC, Stone EM.
    Arch Ophthalmol; 1997 Nov 01; 115(11):1429-35. PubMed ID: 9366675
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  • 14. Mutations of RPGR in X-linked retinitis pigmentosa (RP3).
    Vervoort R, Wright AF.
    Hum Mutat; 2002 May 01; 19(5):486-500. PubMed ID: 11968081
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  • 15. Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa.
    Vervoort R, Lennon A, Bird AC, Tulloch B, Axton R, Miano MG, Meindl A, Meitinger T, Ciccodicola A, Wright AF.
    Nat Genet; 2000 Aug 01; 25(4):462-6. PubMed ID: 10932196
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  • 17. Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa.
    Zhao K, Wang L, Wang L, Wang L, Zhang Q, Wang Q.
    Ophthalmic Genet; 2001 Sep 01; 22(3):187-94. PubMed ID: 11559860
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  • 20. Identification of a 5' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3).
    Dry KL, Manson FD, Lennon A, Bergen AA, Van Dorp DB, Wright AF.
    Hum Mutat; 1999 Sep 01; 13(2):141-5. PubMed ID: 10094550
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