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Journal Abstract Search

131 related items for PubMed ID: 17116709

  • 1. Accelerated transferrin degradation in HFE-deficient mice is associated with increased transferrin saturation.
    Chaudhury C, Kim J, Mehnaz S, Wani MA, Oberyszyn TM, Bronson CL, Mohanty S, Hayton WL, Robinson JM, Anderson CL.
    J Nutr; 2006 Dec; 136(12):2993-8. PubMed ID: 17116709
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  • 2. Iron uptake from plasma transferrin by the duodenum is impaired in the Hfe knockout mouse.
    Trinder D, Olynyk JK, Sly WS, Morgan EH.
    Proc Natl Acad Sci U S A; 2002 Apr 16; 99(8):5622-6. PubMed ID: 11943867
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  • 5. Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis.
    Waheed A, Grubb JH, Zhou XY, Tomatsu S, Fleming RE, Costaldi ME, Britton RS, Bacon BR, Sly WS.
    Proc Natl Acad Sci U S A; 2002 Mar 05; 99(5):3117-22. PubMed ID: 11867720
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  • 7. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb 05; 26(1):2-8. PubMed ID: 10772870
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  • 8. Disruption of hemochromatosis protein and transferrin receptor 2 causes iron-induced liver injury in mice.
    Delima RD, Chua AC, Tirnitz-Parker JE, Gan EK, Croft KD, Graham RM, Olynyk JK, Trinder D.
    Hepatology; 2012 Aug 05; 56(2):585-93. PubMed ID: 22383097
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  • 9. Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis.
    Ramos P, Guy E, Chen N, Proenca CC, Gardenghi S, Casu C, Follenzi A, Van Rooijen N, Grady RW, de Sousa M, Rivella S.
    Blood; 2011 Jan 27; 117(4):1379-89. PubMed ID: 21059897
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  • 11. Combined deletion of Hfe and transferrin receptor 2 in mice leads to marked dysregulation of hepcidin and iron overload.
    Wallace DF, Summerville L, Crampton EM, Frazer DM, Anderson GJ, Subramaniam VN.
    Hepatology; 2009 Dec 27; 50(6):1992-2000. PubMed ID: 19824072
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  • 12. Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: implications for cellular iron homeostasis.
    Salter-Cid L, Brunmark A, Li Y, Leturcq D, Peterson PA, Jackson MR, Yang Y.
    Proc Natl Acad Sci U S A; 1999 May 11; 96(10):5434-9. PubMed ID: 10318901
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  • 13. Blunted hepcidin response to inflammation in the absence of Hfe and transferrin receptor 2.
    Wallace DF, McDonald CJ, Ostini L, Subramaniam VN.
    Blood; 2011 Mar 10; 117(10):2960-6. PubMed ID: 21245482
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  • 16. Genetic study of variation in normal mouse iron homeostasis reveals ceruloplasmin as an HFE-hemochromatosis modifier gene.
    Gouya L, Muzeau F, Robreau AM, Letteron P, Couchi E, Lyoumi S, Deybach JC, Puy H, Fleming R, Demant P, Beaumont C, Grandchamp B.
    Gastroenterology; 2007 Feb 10; 132(2):679-86. PubMed ID: 17258727
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  • 18. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.
    Eur J Immunogenet; 2000 Jun 10; 27(3):129-34. PubMed ID: 10940080
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  • 19. Iron regulation of hepcidin despite attenuated Smad1,5,8 signaling in mice without transferrin receptor 2 or Hfe.
    Corradini E, Rozier M, Meynard D, Odhiambo A, Lin HY, Feng Q, Migas MC, Britton RS, Babitt JL, Fleming RE.
    Gastroenterology; 2011 Nov 10; 141(5):1907-14. PubMed ID: 21745449
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