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170 related items for PubMed ID: 12506099

  • 21. Receptive Field Sizes of Nyxnob Mouse Retinal Ganglion Cells.
    Hölzel MB, Howlett MHC, Kamermans M.
    Int J Mol Sci; 2022 Mar 16; 23(6):. PubMed ID: 35328623
    [Abstract] [Full Text] [Related]

  • 22. [Multimodal diagnostic of CSNB1 with NYX gene mutation].
    Rating P, Stöhr H, Neuhaus C, Schaperdoth-Gerlings B, Böhm MRR, Freimuth MA, Bechrakis NE.
    Ophthalmologe; 2019 Dec 16; 116(12):1207-1211. PubMed ID: 30980176
    [Abstract] [Full Text] [Related]

  • 23. Nyctalopin is essential for synaptic transmission in the cone dominated zebrafish retina.
    Bahadori R, Biehlmaier O, Zeitz C, Labhart T, Makhankov YV, Forster U, Gesemann M, Berger W, Neuhauss SC.
    Eur J Neurosci; 2006 Sep 16; 24(6):1664-74. PubMed ID: 17004930
    [Abstract] [Full Text] [Related]

  • 24. Species specific membrane anchoring of nyctalopin, a small leucine-rich repeat protein.
    O'Connor E, Eisenhaber B, Dalley J, Wang T, Missen C, Bulleid N, Bishop PN, Trump D.
    Hum Mol Genet; 2005 Jul 01; 14(13):1877-87. PubMed ID: 15905181
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency.
    Orhan E, Neuillé M, de Sousa Dias M, Pugliese T, Michiels C, Condroyer C, Antonio A, Sahel JA, Audo I, Zeitz C.
    Int J Mol Sci; 2021 Apr 23; 22(9):. PubMed ID: 33922602
    [Abstract] [Full Text] [Related]

  • 27. 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 23; 42(11):2728-36. PubMed ID: 11581222
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  • 31. Discrete visual defects in pearl mutant mice.
    Balkema GW, Mangini NJ, Pinto LH.
    Science; 1983 Mar 04; 219(4588):1085-7. PubMed ID: 6600521
    [Abstract] [Full Text] [Related]

  • 32. A Novel Approach for Integrating AF-SLO and SDOCT Imaging Data Demonstrates the Ability to Identify Early Retinal Abnormalities in Mutant Mice and Evaluate the Effects of Genetic and Pharmacological Manipulation.
    Bell BA, Bonilha VL, Samuels IS.
    Adv Exp Med Biol; 2018 Mar 04; 1074():167-173. PubMed ID: 29721941
    [Abstract] [Full Text] [Related]

  • 33. Differentiation of murine models of "negative ERG" by single and repetitive light stimuli.
    Tanimoto N, Akula JD, Fulton AB, Weber BH, Seeliger MW.
    Doc Ophthalmol; 2016 Apr 04; 132(2):101-9. PubMed ID: 26996188
    [Abstract] [Full Text] [Related]

  • 34. Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness.
    Orhan E, Prézeau L, El Shamieh S, Bujakowska KM, Michiels C, Zagar Y, Vol C, Bhattacharya SS, Sahel JA, Sennlaub F, Audo I, Zeitz C.
    Invest Ophthalmol Vis Sci; 2013 Dec 09; 54(13):8041-50. PubMed ID: 24222301
    [Abstract] [Full Text] [Related]

  • 35. The interphotoreceptor retinoid-binding protein (IRBP) of the chicken (Gallus gallus domesticus).
    Stenkamp DL, Calderwood JL, Van Niel EE, Daniels LM, Gonzalez-Fernandez F.
    Mol Vis; 2005 Sep 30; 11():833-45. PubMed ID: 16254552
    [Abstract] [Full Text] [Related]

  • 36. A common NYX mutation in Flemish patients with X linked CSNB.
    Leroy BP, Budde BS, Wittmer M, De Baere E, Berger W, Zeitz C.
    Br J Ophthalmol; 2009 May 30; 93(5):692-6. PubMed ID: 18617546
    [Abstract] [Full Text] [Related]

  • 37. The mouse X-linked juvenile retinoschisis cDNA: expression in photoreceptors.
    Reid SN, Akhmedov NB, Piriev NI, Kozak CA, Danciger M, Farber DB.
    Gene; 1999 Feb 18; 227(2):257-66. PubMed ID: 10023077
    [Abstract] [Full Text] [Related]

  • 38. Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect.
    Aguirre GD, Baldwin V, Pearce-Kelling S, Narfström K, Ray K, Acland GM.
    Mol Vis; 1998 Oct 30; 4():23. PubMed ID: 9808841
    [Abstract] [Full Text] [Related]

  • 39. Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
    Pang JJ, Chang B, Hawes NL, Hurd RE, Davisson MT, Li J, Noorwez SM, Malhotra R, McDowell JH, Kaushal S, Hauswirth WW, Nusinowitz S, Thompson DA, Heckenlively JR.
    Mol Vis; 2005 Feb 28; 11():152-62. PubMed ID: 15765048
    [Abstract] [Full Text] [Related]

  • 40. The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness.
    Feng L, Seymour AB, Jiang S, To A, Peden AA, Novak EK, Zhen L, Rusiniak ME, Eicher EM, Robinson MS, Gorin MB, Swank RT.
    Hum Mol Genet; 1999 Feb 28; 8(2):323-30. PubMed ID: 9931340
    [Abstract] [Full Text] [Related]


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