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Journal Abstract Search

215 related items for PubMed ID: 26165230

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  • 3. A novel F30S mutation in γS-crystallin causes autosomal dominant congenital nuclear cataract by increasing susceptibility to stresses.
    Wang KJ, Liao XY, Lin K, Xi YB, Wang S, Wan XH, Yan YB.
    Int J Biol Macromol; 2021 Mar 01; 172():475-482. PubMed ID: 33454329
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  • 5. Mutation causing self-aggregation in human gammaC-crystallin leading to congenital cataract.
    Talla V, Narayanan C, Srinivasan N, Balasubramanian D.
    Invest Ophthalmol Vis Sci; 2006 Dec 01; 47(12):5212-7. PubMed ID: 17122105
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  • 6. Congenital cataract-causing mutation βB1-L116P is prone to amyloid fibrils aggregation and protease degradation with low structural stability.
    Liu J, Xu W, Wang K, Chen F, Ren L, Xu J, Yao K, Chen X.
    Int J Biol Macromol; 2022 Jan 15; 195():475-482. PubMed ID: 34896472
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  • 7. Cataract-causing mutations L45P and Y46D promote γC-crystallin aggregation by disturbing hydrogen bonds network in the second Greek key motif.
    Fu C, Xu J, Jia Z, Yao K, Chen X.
    Int J Biol Macromol; 2021 Jan 15; 167():470-478. PubMed ID: 33278449
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  • 8. Cataract-causing defect of a mutant γ-crystallin proceeds through an aggregation pathway which bypasses recognition by the α-crystallin chaperone.
    Moreau KL, King JA.
    PLoS One; 2012 Jan 15; 7(5):e37256. PubMed ID: 22655036
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  • 11. Interactions and chaperone function of alphaA-crystallin with T5P gammaC-crystallin mutant.
    Liang JJ.
    Protein Sci; 2004 Sep 15; 13(9):2476-82. PubMed ID: 15322286
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  • 12. Overexpression of human γC-crystallin 5 bp duplication disrupts lens morphology in transgenic mice.
    Ma Z, Yao W, Theendakara V, Chan CC, Wawrousek E, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2011 Jul 23; 52(8):5369-75. PubMed ID: 21436266
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  • 13. Aggregation of Trp > Glu point mutants of human gamma-D crystallin provides a model for hereditary or UV-induced cataract.
    Serebryany E, Takata T, Erickson E, Schafheimer N, Wang Y, King JA.
    Protein Sci; 2016 Jun 23; 25(6):1115-28. PubMed ID: 26991007
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  • 14. Cataract-linked mutation R188H promotes βB2-crystallin aggregation and fibrillization during acid denaturation.
    Xi YB, Zhang K, Dai AB, Ji SR, Yao K, Yan YB.
    Biochem Biophys Res Commun; 2014 May 02; 447(2):244-9. PubMed ID: 24704203
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  • 15. Investigation of the early stages of human γD-crystallin aggregation process.
    Chang CK, Wang SS, Lo CH, Hsiao HC, Wu JW.
    J Biomol Struct Dyn; 2017 Apr 02; 35(5):1042-1054. PubMed ID: 27025196
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  • 16. Formation of amyloid fibrils in vitro from partially unfolded intermediates of human gammaC-crystallin.
    Wang Y, Petty S, Trojanowski A, Knee K, Goulet D, Mukerji I, King J.
    Invest Ophthalmol Vis Sci; 2010 Feb 02; 51(2):672-8. PubMed ID: 19684009
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  • 17. Effects of congenital cataract mutation R116H on alphaA-crystallin structure, function and stability.
    Pang M, Su JT, Feng S, Tang ZW, Gu F, Zhang M, Ma X, Yan YB.
    Biochim Biophys Acta; 2010 Apr 02; 1804(4):948-56. PubMed ID: 20079887
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  • 18. The importance of the last strand at the C-terminus in βB2-crystallin stability and assembly.
    Zhang K, Zhao WJ, Leng XY, Wang S, Yao K, Yan YB.
    Biochim Biophys Acta; 2014 Jan 02; 1842(1):44-55. PubMed ID: 24120835
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  • 19. Visualization of in situ intracellular aggregation of two cataract-associated human gamma-crystallin mutants: lose a tail, lose transparency.
    Talla V, Srinivasan N, Balasubramanian D.
    Invest Ophthalmol Vis Sci; 2008 Aug 02; 49(8):3483-90. PubMed ID: 18421082
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  • 20. Human αB-crystallin discriminates between aggregation-prone and function-preserving variants of a client protein.
    Sprague-Piercy MA, Wong E, Roskamp KW, Fakhoury JN, Freites JA, Tobias DJ, Martin RW.
    Biochim Biophys Acta Gen Subj; 2020 Mar 02; 1864(3):129502. PubMed ID: 31812542
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