226 related articles for article (PubMed ID: 19892936)
41. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
Barton JC; Wiener HW; Acton RT; Go RC
Blood Cells Mol Dis; 2005; 34(1):38-47. PubMed ID: 15607698
[TBL] [Abstract][Full Text] [Related]
42. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
Santos PC; Cançado RD; Pereira AC; Schettert IT; Soares RA; Pagliusi RA; Hirata RD; Hirata MH; Teixeira AC; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
Blood Cells Mol Dis; 2011 Apr; 46(4):302-7. PubMed ID: 21411349
[TBL] [Abstract][Full Text] [Related]
43. Gene expression profiling of Hfe-/- liver and duodenum in mouse strains with differing susceptibilities to iron loading: identification of transcriptional regulatory targets of Hfe and potential hemochromatosis modifiers.
Coppin H; Darnaud V; Kautz L; Meynard D; Aubry M; Mosser J; Martinez M; Roth MP
Genome Biol; 2007; 8(10):R221. PubMed ID: 17945001
[TBL] [Abstract][Full Text] [Related]
44. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S
Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764
[TBL] [Abstract][Full Text] [Related]
45. The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis.
Walsh A; Dixon JL; Ramm GA; Hewett DG; Lincoln DJ; Anderson GJ; Subramaniam VN; Dodemaide J; Cavanaugh JA; Bassett ML; Powell LW
Clin Gastroenterol Hepatol; 2006 Nov; 4(11):1403-10. PubMed ID: 16979952
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. Changes in the expression of intestinal iron transport and hepatic regulatory molecules explain the enhanced iron absorption associated with pregnancy in the rat.
Millard KN; Frazer DM; Wilkins SJ; Anderson GJ
Gut; 2004 May; 53(5):655-60. PubMed ID: 15082582
[TBL] [Abstract][Full Text] [Related]
48. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
[TBL] [Abstract][Full Text] [Related]
49. Immunohistochemistry of HFE in the duodenum of C282Y homozygotes with antisera for recombinant HFE protein.
Zuccon L; Corsi B; Levi S; Mattioli M; Fracanzani AL; Corti A; Albertini A; Sampietro M; Fargion S; Arosio P
Haematologica; 2000 Apr; 85(4):346-51. PubMed ID: 10756357
[TBL] [Abstract][Full Text] [Related]
50. Duodenal HFE expression and hepcidin levels determine body iron homeostasis: modulation by genetic diversity and dietary iron availability.
Ludwiczek S; Theurl I; Artner-Dworzak E; Chorney M; Weiss G
J Mol Med (Berl); 2004 Jun; 82(6):373-82. PubMed ID: 15173932
[TBL] [Abstract][Full Text] [Related]
51. Pathogenesis of hereditary hemochromatosis: genetics and beyond.
Britton RS; Fleming RE; Parkkila S; Waheed A; Sly WS; Bacon BR
Semin Gastrointest Dis; 2002 Apr; 13(2):68-79. PubMed ID: 12064862
[TBL] [Abstract][Full Text] [Related]
52. Apical distribution of HFE-beta2-microglobulin is associated with inhibition of apical iron uptake in intestinal epithelia cells.
Arredondo M; Tapia V; Rojas A; Aguirre P; Reyes F; Marzolo MP; Núñez MT
Biometals; 2006 Aug; 19(4):379-88. PubMed ID: 16841247
[TBL] [Abstract][Full Text] [Related]
53. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
Brissot P; Moirand R; Jouanolle AM; Guyader D; Le Gall JY; Deugnier Y; David V
J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799
[TBL] [Abstract][Full Text] [Related]
54. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
Cukjati M; Vaupotic T; Rupreht R; Curin-Serbec V
BMC Med Genet; 2007 Nov; 8():69. PubMed ID: 18036208
[TBL] [Abstract][Full Text] [Related]
55. Hereditary hemochromatosis.
Fix OK; Kowdley KV
Minerva Med; 2008 Dec; 99(6):605-17. PubMed ID: 19034258
[TBL] [Abstract][Full Text] [Related]
56. Pathways underlying iron accumulation in human nonalcoholic fatty liver disease.
Aigner E; Theurl I; Theurl M; Lederer D; Haufe H; Dietze O; Strasser M; Datz C; Weiss G
Am J Clin Nutr; 2008 May; 87(5):1374-83. PubMed ID: 18469261
[TBL] [Abstract][Full Text] [Related]
57. Protective role of calreticulin in HFE hemochromatosis.
Pinto JP; Ramos P; de Almeida SF; Oliveira S; Breda L; Michalak M; Porto G; Rivella S; de Sousa M
Free Radic Biol Med; 2008 Jan; 44(1):99-108. PubMed ID: 18045552
[TBL] [Abstract][Full Text] [Related]
58. Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four cases.
Barton JC; Lee PL; West C; Bottomley SS
Am J Hematol; 2006 Oct; 81(10):760-7. PubMed ID: 16838333
[TBL] [Abstract][Full Text] [Related]
59. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
Adams PC; Pankow JS; Barton JC; Acton RT; Leiendecker-Foster C; McLaren GD; Speechley M; Eckfeldt JH
Circ Cardiovasc Genet; 2009 Feb; 2(1):34-7. PubMed ID: 20031565
[TBL] [Abstract][Full Text] [Related]
60. 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]
[Previous] [Next] [New Search]
