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Journal Abstract Search

134 related items for PubMed ID: 11940509

  • 21. Crystal structure of the hereditary haemochromatosis protein HFE complexed with transferrin receptor.
    Bennett MJ, Lebrón JA, Bjorkman PJ.
    Nature; 2000 Jan 06; 403(6765):46-53. PubMed ID: 10638746
    [Abstract] [Full Text] [Related]

  • 22. Comparison of the interactions of transferrin receptor and transferrin receptor 2 with transferrin and the hereditary hemochromatosis protein HFE.
    West AP, Bennett MJ, Sellers VM, Andrews NC, Enns CA, Bjorkman PJ.
    J Biol Chem; 2000 Dec 08; 275(49):38135-8. PubMed ID: 11027676
    [Abstract] [Full Text] [Related]

  • 23. Pumping iron: the strange partnership of the hemochromatosis protein, a class I MHC homolog, with the transferrin receptor.
    Enns CA.
    Traffic; 2001 Mar 08; 2(3):167-74. PubMed ID: 11260522
    [Abstract] [Full Text] [Related]

  • 24. Iron overload: molecular clues to its cause.
    Kühn LC.
    Trends Biochem Sci; 1999 May 08; 24(5):164-6. PubMed ID: 10322426
    [No Abstract] [Full Text] [Related]

  • 25. Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells.
    Waheed A, Parkkila S, Zhou XY, Tomatsu S, Tsuchihashi Z, Feder JN, Schatzman RC, Britton RS, Bacon BR, Sly WS.
    Proc Natl Acad Sci U S A; 1997 Nov 11; 94(23):12384-9. PubMed ID: 9356458
    [Abstract] [Full Text] [Related]

  • 26. The major histocompatibility complex-encoded HFE in iron homeostasis and immune function.
    Salter-Cid L, Peterson PA, Yang Y.
    Immunol Res; 2000 Nov 11; 22(1):43-59. PubMed ID: 10945226
    [Abstract] [Full Text] [Related]

  • 27. Patch-clamp capacitance measurements: new insights into the endocytic uptake of transferrin.
    Schwake L, Henkel AW, Riedel HD, Stremmel W.
    Blood Cells Mol Dis; 2002 Nov 11; 29(3):459-64. PubMed ID: 12547236
    [Abstract] [Full Text] [Related]

  • 28. 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 11; 26(1):2-8. PubMed ID: 10772870
    [Abstract] [Full Text] [Related]

  • 29. [Genetic hemochromatosis and the HFE gene].
    Moirand R.
    Bull Acad Natl Med; 2000 Feb 11; 184(2):325-35; discussion 335-6. PubMed ID: 10989541
    [Abstract] [Full Text] [Related]

  • 30. Expression of the hemochromatosis (HFE) gene modulates the cellular uptake of 67Ga.
    Chitambar CR, Wereley JP.
    J Nucl Med; 2003 Jun 11; 44(6):943-6. PubMed ID: 12791823
    [Abstract] [Full Text] [Related]

  • 31. Phenotypic expression of the HFE gene mutation (C282Y) among the hospitalised population.
    Moodie SJ, Maxwell JD.
    Gut; 2001 Jul 11; 49(1):156. PubMed ID: 11444237
    [No Abstract] [Full Text] [Related]

  • 32. Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives.
    Moirand R, Jouanolle AM, Brissot P, Le Gall JY, David V, Deugnier Y.
    Gastroenterology; 1999 Feb 11; 116(2):372-7. PubMed ID: 9922318
    [Abstract] [Full Text] [Related]

  • 33. [Relationship between HFE gene and hereditary hemochromatosis].
    Meng H, Hou Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Apr 11; 19(2):159-62. PubMed ID: 11941597
    [Abstract] [Full Text] [Related]

  • 34. Heterozygosity for the C282Y mutation in the hemochromatosis gene is associated with increased serum iron, transferrin saturation, and hemoglobin in young women: a protective role against iron deficiency?
    Datz C, Haas T, Rinner H, Sandhofer F, Patsch W, Paulweber B.
    Clin Chem; 1998 Dec 11; 44(12):2429-32. PubMed ID: 9836708
    [Abstract] [Full Text] [Related]

  • 35. The Q283P amino-acid change in HFE leads to structural and functional consequences similar to those described for the mutated 282Y HFE protein.
    Ka C, Le Gac G, Dupradeau FY, Rochette J, Férec C.
    Hum Genet; 2005 Sep 11; 117(5):467-75. PubMed ID: 15965644
    [Abstract] [Full Text] [Related]

  • 36. Overexpression of the hereditary hemochromatosis protein, HFE, in HeLa cells induces and iron-deficient phenotype.
    Corsi B, Levi S, Cozzi A, Corti A, Altimare D, Albertini A, Arosio P.
    FEBS Lett; 1999 Oct 22; 460(1):149-52. PubMed ID: 10571078
    [Abstract] [Full Text] [Related]

  • 37. Haemochromatosis: an inherited metal and toxicity syndrome.
    Cox TM, Kelly AL.
    Curr Opin Genet Dev; 1998 Jun 22; 8(3):274-81. PubMed ID: 9691000
    [Abstract] [Full Text] [Related]

  • 38. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
    Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.
    Immunogenetics; 1998 Apr 22; 47(5):404-10. PubMed ID: 9510559
    [Abstract] [Full Text] [Related]

  • 39. The hereditary hemochromatosis protein, HFE, specifically regulates transferrin-mediated iron uptake in HeLa cells.
    Roy CN, Penny DM, Feder JN, Enns CA.
    J Biol Chem; 1999 Mar 26; 274(13):9022-8. PubMed ID: 10085150
    [Abstract] [Full Text] [Related]

  • 40. Co-trafficking of HFE, a nonclassical major histocompatibility complex class I protein, with the transferrin receptor implies a role in intracellular iron regulation.
    Gross CN, Irrinki A, Feder JN, Enns CA.
    J Biol Chem; 1998 Aug 21; 273(34):22068-74. PubMed ID: 9705350
    [Abstract] [Full Text] [Related]

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