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Journal Abstract Search

267 related items for PubMed ID: 19682985

  • 21. Effect of reduced retinal VLC-PUFA on rod and cone photoreceptors.
    Bennett LD, Brush RS, Chan M, Lydic TA, Reese K, Reid GE, Busik JV, Elliott MH, Anderson RE.
    Invest Ophthalmol Vis Sci; 2014 Apr 10; 55(5):3150-7. PubMed ID: 24722693
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  • 22. Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein.
    Ambasudhan R, Wang X, Jablonski MM, Thompson DA, Lagali PS, Wong PW, Sieving PA, Ayyagari R.
    Genomics; 2004 Apr 10; 83(4):615-25. PubMed ID: 15028284
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  • 23. Increased cone sensitivity to ABCA4 deficiency provides insight into macular vision loss in Stargardt's dystrophy.
    Conley SM, Cai X, Makkia R, Wu Y, Sparrow JR, Naash MI.
    Biochim Biophys Acta; 2012 Jul 10; 1822(7):1169-79. PubMed ID: 22033104
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  • 24. Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4.
    Grayson C, Molday RS.
    J Biol Chem; 2005 Sep 16; 280(37):32521-30. PubMed ID: 16036915
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  • 28. Long-term retinal cone survival and delayed alteration of the cone mosaic in a transgenic mouse model of stargardt-like dystrophy (STGD3).
    Kuny S, Filion MA, Suh M, Gaillard F, Sauvé Y.
    Invest Ophthalmol Vis Sci; 2014 Jan 21; 55(1):424-39. PubMed ID: 24334447
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  • 29. Mouse Models of Stargardt 3 Dominant Macular Degeneration.
    Barabas P, Gorusupudi A, Bernstein PS, Krizaj D.
    Adv Exp Med Biol; 2016 Jan 21; 854():137-43. PubMed ID: 26427404
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  • 30. Novel lipofuscin bisretinoids prominent in human retina and in a model of recessive Stargardt disease.
    Wu Y, Fishkin NE, Pande A, Pande J, Sparrow JR.
    J Biol Chem; 2009 Jul 24; 284(30):20155-66. PubMed ID: 19478335
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  • 32. Homozygous Expression of Mutant ELOVL4 Leads to Seizures and Death in a Novel Animal Model of Very Long-Chain Fatty Acid Deficiency.
    Hopiavuori BR, Deák F, Wilkerson JL, Brush RS, Rocha-Hopiavuori NA, Hopiavuori AR, Ozan KG, Sullivan MT, Wren JD, Georgescu C, Szweda L, Awasthi V, Towner R, Sherry DM, Anderson RE, Agbaga MP.
    Mol Neurobiol; 2018 Feb 24; 55(2):1795-1813. PubMed ID: 29168048
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  • 37. Loss of functional ELOVL4 depletes very long-chain fatty acids (> or =C28) and the unique omega-O-acylceramides in skin leading to neonatal death.
    Vasireddy V, Uchida Y, Salem N, Kim SY, Mandal MN, Reddy GB, Bodepudi R, Alderson NL, Brown JC, Hama H, Dlugosz A, Elias PM, Holleran WM, Ayyagari R.
    Hum Mol Genet; 2007 Mar 01; 16(5):471-82. PubMed ID: 17208947
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  • 39. The Elovl4 Spinocerebellar Ataxia-34 Mutation 736T>G (p.W246G) Impairs Retinal Function in the Absence of Photoreceptor Degeneration.
    Agbaga MP, Stiles MA, Brush RS, Sullivan MT, Machalinski A, Jones KL, Anderson RE, Sherry DM.
    Mol Neurobiol; 2020 Nov 01; 57(11):4735-4753. PubMed ID: 32780351
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  • 40. Delayed dark-adaptation and lipofuscin accumulation in abcr+/- mice: implications for involvement of ABCR in age-related macular degeneration.
    Mata NL, Tzekov RT, Liu X, Weng J, Birch DG, Travis GH.
    Invest Ophthalmol Vis Sci; 2001 Jul 01; 42(8):1685-90. PubMed ID: 11431429
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