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Items: 1 to 20 of 90

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.

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.

3.

HFE gene knockout produces mouse model of hereditary hemochromatosis.

Zhou XY, Tomatsu S, Fleming RE, Parkkila S, Waheed A, Jiang J, Fei Y, Brunt EM, Ruddy DA, Prass CE, Schatzman RC, O'Neill R, Britton RS, Bacon BR, Sly WS.

Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2492-7.

4.

Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis.

Fleming RE, Holden CC, Tomatsu S, Waheed A, Brunt EM, Britton RS, Bacon BR, Roopenian DC, Sly WS.

Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2707-11.

5.

The role of Hfe in transferrin-bound iron uptake by hepatocytes.

Chua AC, Herbison CE, Drake SF, Graham RM, Olynyk JK, Trinder D.

Hepatology. 2008 May;47(5):1737-44. doi: 10.1002/hep.22180.

PMID:
18393371
6.

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 5;99(5):3117-22.

7.

Iron-independent specific protein expression pattern in the liver of HFE-deficient mice.

Petrak J, Myslivcova D, Halada P, Cmejla R, Cmejlova J, Vyoral D, Vulpe CD.

Int J Biochem Cell Biol. 2007;39(5):1006-15.

PMID:
17376729
8.
9.
10.

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;132(2):679-86.

PMID:
17258727
11.

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;27(3):129-34.

PMID:
10940080
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.

13.

Increased susceptibility to Mycobacterium avium in hemochromatosis protein HFE-deficient mice.

Gomes-Pereira S, Rodrigues PN, Appelberg R, Gomes MS.

Infect Immun. 2008 Oct;76(10):4713-9. doi: 10.1128/IAI.00612-08.

14.

Duodenal mucosal reductase in wild-type and Hfe knockout mice on iron adequate, iron deficient, and iron rich feeding.

Simpson RJ, Debnam E, Beaumont N, Bahram S, Schümann K, Srai SK.

Gut. 2003 Apr;52(4):510-3.

15.

Regulation of iron absorption in Hfe mutant mice.

Ajioka RS, Levy JE, Andrews NC, Kushner JP.

Blood. 2002 Aug 15;100(4):1465-9.

16.

Physiologic systemic iron metabolism in mice deficient for duodenal Hfe.

Vujic Spasic M, Kiss J, Herrmann T, Kessler R, Stolte J, Galy B, Rathkolb B, Wolf E, Stremmel W, Hentze MW, Muckenthaler MU.

Blood. 2007 May 15;109(10):4511-7.

17.

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding.

Feder JN, Penny DM, Irrinki A, Lee VK, Lebrón JA, Watson N, Tsuchihashi Z, Sigal E, Bjorkman PJ, Schatzman RC.

Proc Natl Acad Sci U S A. 1998 Feb 17;95(4):1472-7.

19.

HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors.

Arya N, Chakrabrati S, Hegele RA, Adams PC.

Blood Cells Mol Dis. 1999 Oct-Dec;25(5-6):354-7.

PMID:
10660483
20.

Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: study of Italian cases.

Zanella A, Bianchi P, Iurlo A, Boschetti C, Taioli E, Vercellati C, Zappa M, Fermo E, Tavazzi D, Sampietro M.

Blood Cells Mol Dis. 2001 May-Jun;27(3):653-61.

PMID:
11482880
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