163 related articles for article (PubMed ID: 19228389)
41. HFE based re-evaluation of heterozygous hemochromatosis.
Moirand R; Guyader D; Mendler MH; Jouanolle AM; Le Gall JY; David V; Brissot P; Deugnier Y
Am J Med Genet; 2002 Sep; 111(4):356-61. PubMed ID: 12210292
[TBL] [Abstract][Full Text] [Related]
42. 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. PubMed ID: 17376729
[TBL] [Abstract][Full Text] [Related]
43. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
Nie L; Ai XF; Zheng YZ; Li QH; Yang L; Xiao ZJ
Zhonghua Xue Ye Xue Za Zhi; 2009 Apr; 30(4):223-8. PubMed ID: 19731820
[TBL] [Abstract][Full Text] [Related]
44. Serum hepcidin and macrophage iron correlate with MCP-1 release and vascular damage in patients with metabolic syndrome alterations.
Valenti L; Dongiovanni P; Motta BM; Swinkels DW; Bonara P; Rametta R; Burdick L; Frugoni C; Fracanzani AL; Fargion S
Arterioscler Thromb Vasc Biol; 2011 Mar; 31(3):683-90. PubMed ID: 21183736
[TBL] [Abstract][Full Text] [Related]
45. 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; 227(1):27-33. PubMed ID: 15546588
[TBL] [Abstract][Full Text] [Related]
46. Frequency of the hemochromatosis gene (HFE) variants in a Jordanian Arab population and in diabetics from the same region.
Alkhateeb A; Uzrail A; Bodoor K
Dis Markers; 2009; 27(1):17-22. PubMed ID: 19822954
[TBL] [Abstract][Full Text] [Related]
47. HFE polymorphisms affect survival of brain tumor patients.
Lee SY; Slagle-Webb B; Sheehan JM; Zhu J; Muscat JE; Glantz M; Connor JR
J Neurooncol; 2015 Mar; 122(1):97-104. PubMed ID: 25491948
[TBL] [Abstract][Full Text] [Related]
48. Iron genes, iron load and risk of Alzheimer's disease.
Lehmann DJ; Worwood M; Ellis R; Wimhurst VL; Merryweather-Clarke AT; Warden DR; Smith AD; Robson KJ
J Med Genet; 2006 Oct; 43(10):e52. PubMed ID: 17047092
[TBL] [Abstract][Full Text] [Related]
49. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.
de Tayrac M; Roth MP; Jouanolle AM; Coppin H; le Gac G; Piperno A; Férec C; Pelucchi S; Scotet V; Bardou-Jacquet E; Ropert M; Bouvet R; Génin E; Mosser J; Deugnier Y
J Hepatol; 2015 Mar; 62(3):664-72. PubMed ID: 25457201
[TBL] [Abstract][Full Text] [Related]
50. Primary osteoarthritis in the ankle joint is associated with finger metacarpophalangeal osteoarthritis and the H63D mutation in the HFE gene: evidence for a hemochromatosis-like polyarticular osteoarthritis phenotype.
Carroll GJ
J Clin Rheumatol; 2006 Jun; 12(3):109-13. PubMed ID: 16755236
[TBL] [Abstract][Full Text] [Related]
51. Hepatic iron metabolism gene expression profiles in HFE associated hereditary hemochromatosis.
Gleeson F; Ryan E; Barrett S; Russell J; Crowe J
Blood Cells Mol Dis; 2007; 38(1):37-44. PubMed ID: 17098454
[TBL] [Abstract][Full Text] [Related]
52. Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City.
Baptista-González HA; Rosenfeld-Mann F; Trueba-Gómez R; Bermejo-Martínez L; Méndez-Sánchez N
Ann Hepatol; 2007; 6(1):55-60. PubMed ID: 17297430
[TBL] [Abstract][Full Text] [Related]
53. Modifying factors of the HFE hemochromatosis phenotype.
Deugnier Y; Mosser J
Expert Rev Gastroenterol Hepatol; 2008 Aug; 2(4):531-40. PubMed ID: 19072401
[TBL] [Abstract][Full Text] [Related]
54. Maternal iron metabolism gene variants modify umbilical cord blood lead levels by gene-environment interaction: a birth cohort study.
Karwowski MP; Just AC; Bellinger DC; Jim R; Hatley EL; Ettinger AS; Hu H; Wright RO
Environ Health; 2014 Oct; 13():77. PubMed ID: 25287020
[TBL] [Abstract][Full Text] [Related]
55. The effect of HFE polymorphisms on cardiac iron overload in patients with beta-thalassemia major.
Turedi A; Oymak Y; Meşe T; Yaman Y; Bayraktaroglu S; Alpman A; Ozkinay F; Aydınok Y; Vergin C
Pediatr Hematol Oncol; 2013 Nov; 30(8):755-60. PubMed ID: 24087894
[TBL] [Abstract][Full Text] [Related]
56. HFE gene mutations in Polish patients with disturbances of iron metabolism: an initial assessment.
Sikorska K; Bielawski KP; Stalke P; Lakomy EA; Michalska Z; Witczak-Malinowska K; Romanowski T
Int J Mol Med; 2005 Dec; 16(6):1151-6. PubMed ID: 16273299
[TBL] [Abstract][Full Text] [Related]
57. Possible roles of the hereditary hemochromatosis protein, HFE, in regulating cellular iron homeostasis.
Enns CA
Biol Res; 2006; 39(1):105-11. PubMed ID: 16629171
[TBL] [Abstract][Full Text] [Related]
58. Associations of iron metabolism genes with blood manganese levels: a population-based study with validation data from animal models.
Claus Henn B; Kim J; Wessling-Resnick M; Téllez-Rojo MM; Jayawardene I; Ettinger AS; Hernández-Avila M; Schwartz J; Christiani DC; Hu H; Wright RO
Environ Health; 2011 Nov; 10():97. PubMed ID: 22074419
[TBL] [Abstract][Full Text] [Related]
59. The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.
Silva B; Pita L; Gomes S; Gonçalves J; Faustino P
Ann Hematol; 2014 Dec; 93(12):2063-6. PubMed ID: 25015054
[TBL] [Abstract][Full Text] [Related]
60. HFE genetic variability, body iron stores, and the risk of type 2 diabetes in U.S. women.
Qi L; Meigs J; Manson JE; Ma J; Hunter D; Rifai N; Hu FB
Diabetes; 2005 Dec; 54(12):3567-72. PubMed ID: 16306377
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
