556 related articles for article (PubMed ID: 10791995)
21. Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis.
Muckenthaler M; Roy CN; Custodio AO; Miñana B; deGraaf J; Montross LK; Andrews NC; Hentze MW
Nat Genet; 2003 May; 34(1):102-7. PubMed ID: 12704390
[TBL] [Abstract][Full Text] [Related]
22. Interaction of the hemochromatosis gene product HFE with transferrin receptor modulates cellular iron metabolism.
Eisenstein RS
Nutr Rev; 1998 Dec; 56(12):356-8. PubMed ID: 9884584
[TBL] [Abstract][Full Text] [Related]
23. Mechanisms and regulation of intestinal iron absorption.
Morgan EH; Oates PS
Blood Cells Mol Dis; 2002; 29(3):384-99. PubMed ID: 12547229
[TBL] [Abstract][Full Text] [Related]
24. Hepcidin: a putative iron-regulatory hormone relevant to hereditary hemochromatosis and the anemia of chronic disease.
Fleming RE; Sly WS
Proc Natl Acad Sci U S A; 2001 Jul; 98(15):8160-2. PubMed ID: 11459944
[No Abstract] [Full Text] [Related]
25. Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
Townsend A; Drakesmith H
Lancet; 2002 Mar; 359(9308):786-90. PubMed ID: 11888608
[TBL] [Abstract][Full Text] [Related]
26. Localization of iron transport and regulatory proteins in human cells.
Griffiths WJ; Kelly AL; Smith SJ; Cox TM
QJM; 2000 Sep; 93(9):575-87. PubMed ID: 10984552
[TBL] [Abstract][Full Text] [Related]
27. Function of the hemochromatosis protein HFE: Lessons from animal models.
Pantopoulos K
World J Gastroenterol; 2008 Dec; 14(45):6893-901. PubMed ID: 19058322
[TBL] [Abstract][Full Text] [Related]
28. Duodenal mRNA expression of iron related genes in response to iron loading and iron deficiency in four strains of mice.
Dupic F; Fruchon S; Bensaid M; Loreal O; Brissot P; Borot N; Roth MP; Coppin H
Gut; 2002 Nov; 51(5):648-53. PubMed ID: 12377801
[TBL] [Abstract][Full Text] [Related]
29. [Genetic hemochromatosis and the HFE gene].
Moirand R
Bull Acad Natl Med; 2000; 184(2):325-35; discussion 335-6. PubMed ID: 10989541
[TBL] [Abstract][Full Text] [Related]
30. Intestinal absorption of iron in HFE-1 hemochromatosis: local or systemic process?
Brissot P; Troadec MB; Loréal O
J Hepatol; 2004 Apr; 40(4):702-9. PubMed ID: 15030990
[No Abstract] [Full Text] [Related]
31. Pumping iron: the strange partnership of the hemochromatosis protein, a class I MHC homolog, with the transferrin receptor.
Enns CA
Traffic; 2001 Mar; 2(3):167-74. PubMed ID: 11260522
[TBL] [Abstract][Full Text] [Related]
32. Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene.
Montosi G; Donovan A; Totaro A; Garuti C; Pignatti E; Cassanelli S; Trenor CC; Gasparini P; Andrews NC; Pietrangelo A
J Clin Invest; 2001 Aug; 108(4):619-23. PubMed ID: 11518736
[TBL] [Abstract][Full Text] [Related]
33. Expression of stimulator of Fe transport is not enhanced in Hfe knockout mice.
Knutson MD; Levy JE; Andrews NC; Wessling-Resnick M
J Nutr; 2001 May; 131(5):1459-64. PubMed ID: 11340100
[TBL] [Abstract][Full Text] [Related]
34. The regulation of cellular iron metabolism.
Chua AC; Graham RM; Trinder D; Olynyk JK
Crit Rev Clin Lab Sci; 2007; 44(5-6):413-59. PubMed ID: 17943492
[TBL] [Abstract][Full Text] [Related]
35. Long-term sequelae of HFE deletion in C57BL/6 x 129/O1a mice, an animal model for hereditary haemochromatosis.
Lebeau A; Frank J; Biesalski HK; Weiss G; Srai SK; Simpson RJ; McKie AT; Bahram S; Gilfillan S; Schümann K
Eur J Clin Invest; 2002 Aug; 32(8):603-12. PubMed ID: 12190960
[TBL] [Abstract][Full Text] [Related]
36. [Hereditary hemochromatosis--new developments after discovery of the HFE gene].
Erhardt A; Niederau C; Osman Y; Häussinger D
Z Gastroenterol; 1999 Dec; 37(12):1179-85. PubMed ID: 10666843
[TBL] [Abstract][Full Text] [Related]
37. Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis.
Nicolas G; Viatte L; Lou DQ; Bennoun M; Beaumont C; Kahn A; Andrews NC; Vaulont S
Nat Genet; 2003 May; 34(1):97-101. PubMed ID: 12704388
[TBL] [Abstract][Full Text] [Related]
38. Haptoglobin modifies the hemochromatosis phenotype in mice.
Tolosano E; Fagoonee S; Garuti C; Valli L; Andrews NC; Altruda F; Pietrangelo A
Blood; 2005 Apr; 105(8):3353-5. PubMed ID: 15613548
[TBL] [Abstract][Full Text] [Related]
39. The functional significance of E277K and V295A HFE mutations.
Silva B; Martins R; Proença D; Fleming R; Faustino P
Br J Haematol; 2012 Aug; 158(3):399-408. PubMed ID: 22624560
[TBL] [Abstract][Full Text] [Related]
40. Hepcidin, a candidate modifier of the hemochromatosis phenotype in mice.
Nicolas G; Andrews NC; Kahn A; Vaulont S
Blood; 2004 Apr; 103(7):2841-3. PubMed ID: 14656876
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
