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Journal Abstract Search

170 related items for PubMed ID: 12506099

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  • 2. Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retina.
    Pesch K, Zeitz C, Fries JE, Münscher S, Pusch CM, Kohler K, Berger W, Wissinger B.
    Invest Ophthalmol Vis Sci; 2003 May; 44(5):2260-6. PubMed ID: 12714669
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  • 6. Isolation and characterization of the leucine-rich proteoglycan nyctalopin gene (cNyx) from chick.
    Bech-Hansen NT, Cockfield J, Liu D, Logan CC.
    Mamm Genome; 2005 Oct; 16(10):815-24. PubMed ID: 16261423
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  • 7. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
    Pusch CM, Zeitz C, Brandau O, Pesch K, Achatz H, Feil S, Scharfe C, Maurer J, Jacobi FK, Pinckers A, Andreasson S, Hardcastle A, Wissinger B, Berger W, Meindl A.
    Nat Genet; 2000 Nov; 26(3):324-7. PubMed ID: 11062472
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  • 8. High susceptibility to experimental myopia in a mouse model with a retinal on pathway defect.
    Pardue MT, Faulkner AE, Fernandes A, Yin H, Schaeffel F, Williams RW, Pozdeyev N, Iuvone PM.
    Invest Ophthalmol Vis Sci; 2008 Feb; 49(2):706-12. PubMed ID: 18235018
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  • 10. 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
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  • 12. NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein.
    Zeitz C, Scherthan H, Freier S, Feil S, Suckow V, Schweiger S, Berger W.
    Invest Ophthalmol Vis Sci; 2003 Oct; 44(10):4184-91. PubMed ID: 14507859
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  • 15. NYX mutations in four families with high myopia with or without CSNB1.
    Zhou L, Li T, Song X, Li Y, Li H, Dan H.
    Mol Vis; 2015 Oct; 21():213-23. PubMed ID: 25802485
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  • 16. Presence of the Gpr179(nob5) allele in a C3H-derived transgenic mouse.
    Balmer J, Ji R, Ray TA, Selber F, Gassmann M, Peachey NS, Gregg RG, Enzmann V.
    Mol Vis; 2013 Oct; 19():2615-25. PubMed ID: 24415894
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  • 17. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
    Bijveld MM, Florijn RJ, Bergen AA, van den Born LI, Kamermans M, Prick L, Riemslag FC, van Schooneveld MJ, Kappers AM, van Genderen MM.
    Ophthalmology; 2013 Oct; 120(10):2072-81. PubMed ID: 23714322
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  • 18. Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB).
    Neuillé M, El Shamieh S, Orhan E, Michiels C, Antonio A, Lancelot ME, Condroyer C, Bujakowska K, Poch O, Sahel JA, Audo I, Zeitz C.
    PLoS One; 2014 Oct; 9(3):e90342. PubMed ID: 24598786
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  • 19. Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness.
    Qian H, Ji R, Gregg RG, Peachey NS.
    Vis Neurosci; 2015 Jan; 32():E004. PubMed ID: 26241901
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  • 20. Nystagmus in patients with congenital stationary night blindness (CSNB) originates from synchronously firing retinal ganglion cells.
    Winkelman BHJ, Howlett MHC, Hölzel MB, Joling C, Fransen KH, Pangeni G, Kamermans S, Sakuta H, Noda M, Simonsz HJ, McCall MA, De Zeeuw CI, Kamermans M.
    PLoS Biol; 2019 Sep; 17(9):e3000174. PubMed ID: 31513577
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