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Journal Abstract Search

195 related items for PubMed ID: 16357828

  • 1. Spatial and temporal expression patterns of the choroideremia gene in the mouse retina.
    Keiser NW, Tang W, Wei Z, Bennett J.
    Mol Vis; 2005 Dec 07; 11():1052-60. PubMed ID: 16357828
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  • 2. Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutations.
    Jacobson SG, Cideciyan AV, Sumaroka A, Aleman TS, Schwartz SB, Windsor EA, Roman AJ, Stone EM, MacDonald IM.
    Invest Ophthalmol Vis Sci; 2006 Sep 07; 47(9):4113-20. PubMed ID: 16936131
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  • 6. Clinical findings in a carrier of a new mutation in the choroideremia gene.
    Potter MJ, Wong E, Szabo SM, McTaggart KE.
    Ophthalmology; 2004 Oct 07; 111(10):1905-9. PubMed ID: 15465555
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  • 8. Sirt1 involvement in rd10 mouse retinal degeneration.
    Jaliffa C, Ameqrane I, Dansault A, Leemput J, Vieira V, Lacassagne E, Provost A, Bigot K, Masson C, Menasche M, Abitbol M.
    Invest Ophthalmol Vis Sci; 2009 Aug 07; 50(8):3562-72. PubMed ID: 19407027
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  • 9. Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with Rab geranylgeranyl transferase.
    Esposito G, De Falco F, Tinto N, Testa F, Vitagliano L, Tandurella IC, Iannone L, Rossi S, Rinaldi E, Simonelli F, Zagari A, Salvatore F.
    Hum Mutat; 2011 Dec 07; 32(12):1460-9. PubMed ID: 21905166
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  • 10. A practical diagnostic test for choroideremia.
    MacDonald IM, Mah DY, Ho YK, Lewis RA, Seabra MC.
    Ophthalmology; 1998 Sep 07; 105(9):1637-40. PubMed ID: 9754170
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  • 12. Single-base substitutions in the CHM promoter as a cause of choroideremia.
    Radziwon A, Arno G, K Wheaton D, McDonagh EM, Baple EL, Webb-Jones K, G Birch D, Webster AR, MacDonald IM.
    Hum Mutat; 2017 Jun 07; 38(6):704-715. PubMed ID: 28271586
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  • 15. Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical data.
    Preising MN, Wegscheider E, Friedburg C, Poloschek CM, Wabbels BK, Lorenz B.
    Ophthalmology; 2009 Jun 07; 116(6):1201-9.e1-2. PubMed ID: 19376587
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  • 17. Visual impairment and REP-1 gene mutations in Japanese choroideremia patients.
    Hayakawa M, Fujiki K, Hotta Y, Ito R, Ohki J, Ono J, Saito A, Nakayasu K, Kanai A, Ishidoh K, Kominami E, Yoshida K, Kim KC, Ohashi H.
    Ophthalmic Genet; 1999 Jun 07; 20(2):107-15. PubMed ID: 10420196
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  • 18. Expression of VLDLR in the retina and evolution of subretinal neovascularization in the knockout mouse model's retinal angiomatous proliferation.
    Hu W, Jiang A, Liang J, Meng H, Chang B, Gao H, Qiao X.
    Invest Ophthalmol Vis Sci; 2008 Jan 07; 49(1):407-15. PubMed ID: 18172119
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  • 19. Novel types of mutation in the choroideremia ( CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon.
    van den Hurk JA, van de Pol DJ, Wissinger B, van Driel MA, Hoefsloot LH, de Wijs IJ, van den Born LI, Heckenlively JR, Brunner HG, Zrenner E, Ropers HH, Cremers FP.
    Hum Genet; 2003 Aug 07; 113(3):268-75. PubMed ID: 12827496
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