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Journal Abstract Search

103 related items for PubMed ID: 16261423

  • 1. 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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  • 5. 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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  • 6. Localization of nyctalopin in the mammalian retina.
    Morgans CW, Ren G, Akileswaran L.
    Eur J Neurosci; 2006 Mar; 23(5):1163-71. PubMed ID: 16553780
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  • 7. Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.
    Scalabrino ML, Boye SL, Fransen KM, Noel JM, Dyka FM, Min SH, Ruan Q, De Leeuw CN, Simpson EM, Gregg RG, McCall MA, Peachey NS, Boye SE.
    Hum Mol Genet; 2015 Nov 01; 24(21):6229-39. PubMed ID: 26310623
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  • 8. 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 Nov 01; 21():213-23. PubMed ID: 25802485
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  • 9. Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness.
    Khan NW, Kondo M, Hiriyanna KT, Jamison JA, Bush RA, Sieving PA.
    J Neurophysiol; 2005 Jan 01; 93(1):481-92. PubMed ID: 15331616
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  • 11. 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 01; 44(10):4184-91. PubMed ID: 14507859
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  • 13. Mutations in NYX of individuals with high myopia, but without night blindness.
    Zhang Q, Xiao X, Li S, Jia X, Yang Z, Huang S, Caruso RC, Guan T, Sergeev Y, Guo X, Hejtmancik JF.
    Mol Vis; 2007 Mar 01; 13():330-6. PubMed ID: 17392683
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  • 14. [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 01; 116(12):1207-1211. PubMed ID: 30980176
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  • 15. 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
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  • 16. 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
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  • 17. 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 01; 24(6):1664-74. PubMed ID: 17004930
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  • 18. 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 01; 32():E004. PubMed ID: 26241901
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  • 19. A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness.
    Kondo M, Das G, Imai R, Santana E, Nakashita T, Imawaka M, Ueda K, Ohtsuka H, Sakai K, Aihara T, Kato K, Sugimoto M, Ueno S, Nishizawa Y, Aguirre GD, Miyadera K.
    PLoS One; 2015 Jan 01; 10(9):e0137072. PubMed ID: 26368928
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  • 20. 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 01; 120(10):2072-81. PubMed ID: 23714322
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