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Journal Abstract Search

90 related items for PubMed ID: 16043865

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  • 2. Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration.
    Gamundi MJ, Hernan I, Maseras M, Baiget M, Ayuso C, Borrego S, Antiñolo G, Millán JM, Valverde D, Carballo M.
    Mol Vis; 2005 Nov 02; 11():922-8. PubMed ID: 16280978
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  • 4. Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes.
    Tubb BE, Bardien-Kruger S, Kashork CD, Shaffer LG, Ramagli LS, Xu J, Siciliano MJ, Bryan J.
    Genomics; 2000 Apr 15; 65(2):146-56. PubMed ID: 10783262
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  • 9. Ribozyme knockdown of the gamma-subunit of rod cGMP phosphodiesterase alters the ERG and retinal morphology in wild-type mice.
    Liu J, Timmers AM, Lewin AS, Hauswirth WW.
    Invest Ophthalmol Vis Sci; 2005 Oct 15; 46(10):3836-44. PubMed ID: 16186371
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  • 12. Caspase-1 ablation protects photoreceptors in a model of autosomal dominant retinitis pigmentosa.
    Samardzija M, Wenzel A, Thiersch M, Frigg R, Remé C, Grimm C.
    Invest Ophthalmol Vis Sci; 2006 Dec 15; 47(12):5181-90. PubMed ID: 17122101
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  • 15. Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP.
    Pawlyk BS, Smith AJ, Buch PK, Adamian M, Hong DH, Sandberg MA, Ali RR, Li T.
    Invest Ophthalmol Vis Sci; 2005 Sep 15; 46(9):3039-45. PubMed ID: 16123399
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  • 16. HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model.
    Kobayashi A, Higashide T, Hamasaki D, Kubota S, Sakuma H, An W, Fujimaki T, McLaren MJ, Weleber RG, Inana G.
    Invest Ophthalmol Vis Sci; 2000 Oct 15; 41(11):3268-77. PubMed ID: 11006213
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  • 17. Effect of p75NTR on the regulation of photoreceptor apoptosis in the rd mouse.
    Nakamura K, Harada C, Okumura A, Namekata K, Mitamura Y, Yoshida K, Ohno S, Yoshida H, Harada T.
    Mol Vis; 2005 Dec 29; 11():1229-35. PubMed ID: 16402023
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  • 18. Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
    Wycisk KA, Budde B, Feil S, Skosyrski S, Buzzi F, Neidhardt J, Glaus E, Nürnberg P, Ruether K, Berger W.
    Invest Ophthalmol Vis Sci; 2006 Aug 29; 47(8):3523-30. PubMed ID: 16877424
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  • 19. Altered expression of secreted frizzled-related protein-2 in retinitis pigmentosa retinas.
    Jones SE, Jomary C, Grist J, Stewart HJ, Neal MJ.
    Invest Ophthalmol Vis Sci; 2000 May 29; 41(6):1297-301. PubMed ID: 10798643
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