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217 related items for PubMed ID: 21349849

  • 1. Mutant HFE H63D protein is associated with prolonged endoplasmic reticulum stress and increased neuronal vulnerability.
    Liu Y, Lee SY, Neely E, Nandar W, Moyo M, Simmons Z, Connor JR.
    J Biol Chem; 2011 Apr 15; 286(15):13161-70. PubMed ID: 21349849
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  • 2. H63D HFE genotype accelerates disease progression in animal models of amyotrophic lateral sclerosis.
    Nandar W, Neely EB, Simmons Z, Connor JR.
    Biochim Biophys Acta; 2014 Dec 15; 1842(12 Pt A):2413-26. PubMed ID: 25283820
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  • 3. A mutation in the HFE gene is associated with altered brain iron profiles and increased oxidative stress in mice.
    Nandar W, Neely EB, Unger E, Connor JR.
    Biochim Biophys Acta; 2013 Jun 15; 1832(6):729-41. PubMed ID: 23429074
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  • 4. Prolyl-peptidyl isomerase, Pin1, phosphorylation is compromised in association with the expression of the HFE polymorphic allele, H63D.
    Hall EC, Lee SY, Simmons Z, Neely EB, Nandar W, Connor JR.
    Biochim Biophys Acta; 2010 Apr 15; 1802(4):389-95. PubMed ID: 20060900
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  • 10. HFE gene variants affect iron in the brain.
    Nandar W, Connor JR.
    J Nutr; 2011 Apr 01; 141(4):729S-739S. PubMed ID: 21346098
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  • 11. Consequences of expressing mutants of the hemochromatosis gene (HFE) into a human neuronal cell line lacking endogenous HFE.
    Lee SY, Patton SM, Henderson RJ, Connor JR.
    FASEB J; 2007 Feb 01; 21(2):564-76. PubMed ID: 17194693
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  • 15. Increased incidence of the Hfe mutation in amyotrophic lateral sclerosis and related cellular consequences.
    Wang XS, Lee S, Simmons Z, Boyer P, Scott K, Liu W, Connor J.
    J Neurol Sci; 2004 Dec 15; 227(1):27-33. PubMed ID: 15546588
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  • 17. Reduced white matter MRI transverse relaxation rate in cognitively normal H63D-HFE human carriers and H67D-HFE mice.
    Meadowcroft MD, Wang J, Purnell CJ, Peters DG, Eslinger PJ, Neely EB, Gill DJ, Vasavada M, Ali-Rahmani F, Yang QX, Connor JR.
    Brain Imaging Behav; 2016 Dec 15; 10(4):1231-1242. PubMed ID: 26660104
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  • 18. Contribution of different HFE genotypes to iron overload disease: a pooled analysis.
    Burke W, Imperatore G, McDonnell SM, Baron RC, Khoury MJ.
    Genet Med; 2000 Dec 15; 2(5):271-7. PubMed ID: 11399207
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  • 20. The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population.
    Sutedja NA, Sinke RJ, Van Vught PW, Van der Linden MW, Wokke JH, Van Duijn CM, Njajou OT, Van der Schouw YT, Veldink JH, Van den Berg LH.
    Arch Neurol; 2007 Jan 15; 64(1):63-7. PubMed ID: 17210810
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