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Journal Abstract Search

239 related items for PubMed ID: 9804152

  • 1. A naturally occurring mouse model of X-linked congenital stationary night blindness.
    Pardue MT, McCall MA, LaVail MM, Gregg RG, Peachey NS.
    Invest Ophthalmol Vis Sci; 1998 Nov; 39(12):2443-9. PubMed ID: 9804152
    [Abstract] [Full Text] [Related]

  • 2. Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome.
    Candille SI, Pardue MT, McCall MA, Peachey NS, Gregg RG.
    Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2748-51. PubMed ID: 10509675
    [Abstract] [Full Text] [Related]

  • 3. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram.
    Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, Wycisk K, Mátyás G, Hoyng CB, Riemslag F, Meire F, Cremers FP, Berger W.
    Invest Ophthalmol Vis Sci; 2005 Nov; 46(11):4328-35. PubMed ID: 16249515
    [Abstract] [Full Text] [Related]

  • 4. Abnormalities of the photoreceptor-bipolar cell synapse in a substrain of C57BL/10 mice.
    Ruether K, Grosse J, Matthiessen E, Hoffmann K, Hartmann C.
    Invest Ophthalmol Vis Sci; 2000 Nov; 41(12):4039-47. PubMed ID: 11053310
    [Abstract] [Full Text] [Related]

  • 5. Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.
    Mansergh F, Orton NC, Vessey JP, Lalonde MR, Stell WK, Tremblay F, Barnes S, Rancourt DE, Bech-Hansen NT.
    Hum Mol Genet; 2005 Oct 15; 14(20):3035-46. PubMed ID: 16155113
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 98(5):3023-33. PubMed ID: 17881478
    [Abstract] [Full Text] [Related]

  • 7. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
    Bech-Hansen NT, Naylor MJ, Maybaum TA, Sparkes RL, Koop B, Birch DG, Bergen AA, Prinsen CF, Polomeno RC, Gal A, Drack AV, Musarella MA, Jacobson SG, Young RS, Weleber RG.
    Nat Genet; 2000 Nov 15; 26(3):319-23. PubMed ID: 11062471
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  • 9. Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.
    Scholl HP, Langrová H, Pusch CM, Wissinger B, Zrenner E, Apfelstedt-Sylla E.
    Invest Ophthalmol Vis Sci; 2001 Oct 15; 42(11):2728-36. PubMed ID: 11581222
    [Abstract] [Full Text] [Related]

  • 10. Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer.
    Ball SL, Powers PA, Shin HS, Morgans CW, Peachey NS, Gregg RG.
    Invest Ophthalmol Vis Sci; 2002 May 15; 43(5):1595-603. PubMed ID: 11980879
    [Abstract] [Full Text] [Related]

  • 11. Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.
    Hawes NL, Chang B, Hageman GS, Nusinowitz S, Nishina PM, Schneider BS, Smith RS, Roderick TH, Davisson MT, Heckenlively JR.
    Invest Ophthalmol Vis Sci; 2000 Sep 15; 41(10):3149-57. PubMed ID: 10967077
    [Abstract] [Full Text] [Related]

  • 12. Retinal degeneration in the nervous mutant mouse. III. Electrophysiological studies of the visual pathway.
    Ren JC, LaVail MM, Peachey NS.
    Exp Eye Res; 2000 Apr 15; 70(4):467-73. PubMed ID: 10865995
    [Abstract] [Full Text] [Related]

  • 13. Postreceptoral contributions to the light-adapted ERG of mice lacking b-waves.
    Shirato S, Maeda H, Miura G, Frishman LJ.
    Exp Eye Res; 2008 Jun 15; 86(6):914-28. PubMed ID: 18440505
    [Abstract] [Full Text] [Related]

  • 14. Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.
    Ruether K, Apfelstedt-Sylla E, Zrenner E.
    Ger J Ophthalmol; 1993 Nov 15; 2(6):429-35. PubMed ID: 8312830
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  • 16. Visual electrophysiological features of two naturally occurring mouse models with retinal dysfunction.
    Miyamoto M, Imai R, Sugimoto S, Aoki M, Nagai H, Ando T.
    Curr Eye Res; 2006 Apr 15; 31(4):329-35. PubMed ID: 16603466
    [Abstract] [Full Text] [Related]

  • 17. Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness).
    Chen J, Simon MI, Matthes MT, Yasumura D, LaVail MM.
    Invest Ophthalmol Vis Sci; 1999 Nov 15; 40(12):2978-82. PubMed ID: 10549660
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  • 19. Identification of the gene and the mutation responsible for the mouse nob phenotype.
    Gregg RG, Mukhopadhyay S, Candille SI, Ball SL, Pardue MT, McCall MA, Peachey NS.
    Invest Ophthalmol Vis Sci; 2003 Jan 15; 44(1):378-84. PubMed ID: 12506099
    [Abstract] [Full Text] [Related]

  • 20. RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis.
    Zeng Y, Takada Y, Kjellstrom S, Hiriyanna K, Tanikawa A, Wawrousek E, Smaoui N, Caruso R, Bush RA, Sieving PA.
    Invest Ophthalmol Vis Sci; 2004 Sep 15; 45(9):3279-85. PubMed ID: 15326152
    [Abstract] [Full Text] [Related]

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