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396 related items for PubMed ID: 16597347

  • 1. The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.
    Chang B, Heckenlively JR, Bayley PR, Brecha NC, Davisson MT, Hawes NL, Hirano AA, Hurd RE, Ikeda A, Johnson BA, McCall MA, Morgans CW, Nusinowitz S, Peachey NS, Rice DS, Vessey KA, Gregg RG.
    Vis Neurosci; 2006; 23(1):11-24. PubMed ID: 16597347
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  • 2. Attenuation of oscillatory potentials in nob2 mice.
    Yu M, Peachey NS.
    Doc Ophthalmol; 2007 Nov; 115(3):173-86. PubMed ID: 17479213
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  • 3. Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.
    Lodha N, Bonfield S, Orton NC, Doering CJ, McRory JE, Mema SC, Rehak R, Sauvé Y, Tobias R, Stell WK, Bech-Hansen NT.
    Adv Exp Med Biol; 2010 Nov; 664():549-58. PubMed ID: 20238058
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  • 6. Photoreceptor degeneration in a new Cacna1f mutant mouse model.
    Dai X, Pang S, Wang J, FitzMaurice B, Pang J, Chang B.
    Exp Eye Res; 2019 Feb; 179():106-114. PubMed ID: 30445045
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  • 8. Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A).
    Waldner DM, Giraldo Sierra NC, Bonfield S, Nguyen L, Dimopoulos IS, Sauvé Y, Stell WK, Bech-Hansen NT.
    Channels (Austin); 2018 Jan 01; 12(1):17-33. PubMed ID: 29179637
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  • 9. Effects of presynaptic mutations on a postsynaptic Cacna1s calcium channel colocalized with mGluR6 at mouse photoreceptor ribbon synapses.
    Specht D, Wu SB, Turner P, Dearden P, Koentgen F, Wolfrum U, Maw M, Brandstätter JH, tom Dieck S.
    Invest Ophthalmol Vis Sci; 2009 Feb 01; 50(2):505-15. PubMed ID: 18952919
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  • 11. Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness.
    Gregg RG, Kamermans M, Klooster J, Lukasiewicz PD, Peachey NS, Vessey KA, McCall MA.
    J Neurophysiol; 2007 Nov 01; 98(5):3023-33. PubMed ID: 17881478
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  • 13. Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.
    Regus-Leidig H, Atorf J, Feigenspan A, Kremers J, Maw MA, Brandstätter JH.
    PLoS One; 2014 Nov 01; 9(1):e86769. PubMed ID: 24466230
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  • 16. Spontaneous activity promotes synapse formation in a cell-type-dependent manner in the developing retina.
    Soto F, Ma X, Cecil JL, Vo BQ, Culican SM, Kerschensteiner D.
    J Neurosci; 2012 Apr 18; 32(16):5426-39. PubMed ID: 22514306
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  • 19. Ablation of retinal horizontal cells from adult mice leads to rod degeneration and remodeling in the outer retina.
    Sonntag S, Dedek K, Dorgau B, Schultz K, Schmidt KF, Cimiotti K, Weiler R, Löwel S, Willecke K, Janssen-Bienhold U.
    J Neurosci; 2012 Aug 01; 32(31):10713-24. PubMed ID: 22855819
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  • 20. Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
    Dinet V, Ciccotosto GD, Delaunay K, Borras C, Ranchon-Cole I, Kostic C, Savoldelli M, El Sanharawi M, Jonet L, Pirou C, An N, Abitbol M, Arsenijevic Y, Behar-Cohen F, Cappai R, Mascarelli F.
    Mol Brain; 2016 Jun 08; 9(1):64. PubMed ID: 27267879
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