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Journal Abstract Search

174 related items for PubMed ID: 32833997

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  • 2. Probing the changes in gene expression due to α-crystallin mutations in mouse models of hereditary human cataract.
    Andley UP, Tycksen E, McGlasson-Naumann BN, Hamilton PD.
    PLoS One; 2018; 13(1):e0190817. PubMed ID: 29338044
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  • 5. Analysis of amyloid-like secondary structure in the Cryab-R120G knock-in mouse model of hereditary cataracts by two-dimensional infrared spectroscopy.
    Alperstein AM, Molnar KS, Dicke SS, Farrell KM, Makley LN, Zanni MT, Andley UP.
    PLoS One; 2021; 16(9):e0257098. PubMed ID: 34520490
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  • 9. Oxysterol Compounds in Mouse Mutant αA- and αB-Crystallin Lenses Can Improve the Optical Properties of the Lens.
    Wang K, Hoshino M, Uesugi K, Yagi N, Pierscionek BK, Andley UP.
    Invest Ophthalmol Vis Sci; 2022 May 02; 63(5):15. PubMed ID: 35575904
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  • 11. AlphaA-crystallin R49Cneo mutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice.
    Andley UP.
    BMC Ophthalmol; 2009 Jul 20; 9():4. PubMed ID: 19619312
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  • 15. Loss of αBa-crystallin, but not αA-crystallin, increases age-related cataract in the zebrafish lens.
    Posner M, Garver T, Kaye T, Brdicka S, Suttle M, Patterson B, Farnsworth DR.
    Exp Eye Res; 2024 Jul 20; 244():109918. PubMed ID: 38705506
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  • 16. Alteration of protein-protein interactions of congenital cataract crystallin mutants.
    Fu L, Liang JJ.
    Invest Ophthalmol Vis Sci; 2003 Mar 20; 44(3):1155-9. PubMed ID: 12601044
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  • 17. The absence of SIRT3 and SIRT5 promotes the acetylation of lens proteins and improves the chaperone activity of α-crystallin in mouse lenses.
    Nandi SK, Nahomi RB, Harris PS, Michel CR, Fritz KS, Nagaraj RH.
    Exp Eye Res; 2019 May 20; 182():1-9. PubMed ID: 30849386
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  • 18. Genetics of crystallins: cataract and beyond.
    Graw J.
    Exp Eye Res; 2009 Feb 20; 88(2):173-89. PubMed ID: 19007775
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  • 19. Effects of alpha-crystallin on lens cell function and cataract pathology.
    Andley UP.
    Curr Mol Med; 2009 Sep 20; 9(7):887-92. PubMed ID: 19860667
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  • 20. A knock-in mouse model for the R120G mutation of αB-crystallin recapitulates human hereditary myopathy and cataracts.
    Andley UP, Hamilton PD, Ravi N, Weihl CC.
    PLoS One; 2011 Mar 18; 6(3):e17671. PubMed ID: 21445271
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