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Journal Abstract Search

267 related items for PubMed ID: 29203866

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  • 4. The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking.
    Bachmann-Gagescu R, Phelps IG, Stearns G, Link BA, Brockerhoff SE, Moens CB, Doherty D.
    Hum Mol Genet; 2011 Oct 15; 20(20):4041-55. PubMed ID: 21816947
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  • 5. Knocking out lca5 in zebrafish causes cone-rod dystrophy due to impaired outer segment protein trafficking.
    Qu Z, Yimer TA, Xie S, Wong F, Yu S, Liu X, Han S, Ma J, Lu Z, Hu X, Qin Y, Huang Y, Lv Y, Li J, Tang Z, Liu F, Liu M.
    Biochim Biophys Acta Mol Basis Dis; 2019 Oct 01; 1865(10):2694-2705. PubMed ID: 31348989
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  • 7. Ciliary genes arl13b, ahi1 and cc2d2a differentially modify expression of visual acuity phenotypes but do not enhance retinal degeneration due to mutation of cep290 in zebrafish.
    Lessieur EM, Song P, Nivar GC, Piccillo EM, Fogerty J, Rozic R, Perkins BD.
    PLoS One; 2019 Oct 01; 14(4):e0213960. PubMed ID: 30970040
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  • 8. Rhodopsin Trafficking and Mistrafficking: Signals, Molecular Components, and Mechanisms.
    Nemet I, Ropelewski P, Imanishi Y.
    Prog Mol Biol Transl Sci; 2015 Oct 01; 132():39-71. PubMed ID: 26055054
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  • 11. Gypenosides attenuate retinal degeneration in a zebrafish retinitis pigmentosa model.
    Alhasani RH, Zhou X, Biswas L, Li X, Reilly J, Zeng Z, Shu X.
    Exp Eye Res; 2020 Dec 01; 201():108291. PubMed ID: 33049273
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  • 12. RPGRIP1 is mutated in Leber congenital amaurosis: a mini-review.
    Koenekoop RK.
    Ophthalmic Genet; 2005 Dec 01; 26(4):175-9. PubMed ID: 16352478
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  • 13. Variabilities in retinal function and structure in a canine model of cone-rod dystrophy associated with RPGRIP1 support multigenic etiology.
    Das RG, Marinho FP, Iwabe S, Santana E, McDaid KS, Aguirre GD, Miyadera K.
    Sci Rep; 2017 Oct 09; 7(1):12823. PubMed ID: 28993665
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  • 15. Loss of ift122, a Retrograde Intraflagellar Transport (IFT) Complex Component, Leads to Slow, Progressive Photoreceptor Degeneration Due to Inefficient Opsin Transport.
    Boubakri M, Chaya T, Hirata H, Kajimura N, Kuwahara R, Ueno A, Malicki J, Furukawa T, Omori Y.
    J Biol Chem; 2016 Nov 18; 291(47):24465-24474. PubMed ID: 27681595
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  • 17. Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis.
    Pawlyk BS, Bulgakov OV, Liu X, Xu X, Adamian M, Sun X, Khani SC, Berson EL, Sandberg MA, Li T.
    Hum Gene Ther; 2010 Aug 18; 21(8):993-1004. PubMed ID: 20384479
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  • 19. Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy.
    Lu Z, Hu X, Liu F, Soares DC, Liu X, Yu S, Gao M, Han S, Qin Y, Li C, Jiang T, Luo D, Guo AY, Tang Z, Liu M.
    Sci Rep; 2017 Apr 05; 7():46098. PubMed ID: 28378834
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