BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 9410471)

  • 1. Impact of HLA-H mutations on iron stores in healthy elderly men and women.
    Garry PJ; Montoya GD; Baumgartner RN; Liang HC; Williams TM; Brodie SG
    Blood Cells Mol Dis; 1997 Aug; 23(2):277-87. PubMed ID: 9410471
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England.
    Willis G; Jennings BA; Goodman E; Fellows IW; Wimperis JZ
    Blood Cells Mol Dis; 1997 Aug; 23(2):288-91. PubMed ID: 9410472
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation analysis in hereditary hemochromatosis.
    Beutler E; Gelbart T; West C; Lee P; Adams M; Blackstone R; Pockros P; Kosty M; Venditti CP; Phatak PD; Seese NK; Chorney KA; Ten Elshof AE; Gerhard GS; Chorney M
    Blood Cells Mol Dis; 1996; 22(2):187-94; discussion 194a-194b. PubMed ID: 8931958
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HFE genotypes and haemochromatosis: quantifying the risks of disease.
    Lester S; Bardy P; McCluskey J
    Tissue Antigens; 1999 Sep; 54(3):282-4. PubMed ID: 10519366
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A population-based study of the clinical expression of the hemochromatosis gene.
    Olynyk JK; Cullen DJ; Aquilia S; Rossi E; Summerville L; Powell LW
    N Engl J Med; 1999 Sep; 341(10):718-24. PubMed ID: 10471457
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Relationship of body iron stores to levels of serum ferritin, serum iron, unsaturated iron binding capacity and transferrin saturation in patients with iron storage disease.
    Beutler E; Felitti V; Ho NJ; Gelbart T
    Acta Haematol; 2002; 107(3):145-9. PubMed ID: 11978935
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hemochromatosis in Ireland and HFE.
    Ryan E; O'keane C; Crowe J
    Blood Cells Mol Dis; 1998 Dec; 24(4):428-32. PubMed ID: 9851896
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetics of iron storage and hemochromatosis.
    Beutler E; Felitti V; Gelbart T; Ho N
    Drug Metab Dispos; 2001 Apr; 29(4 Pt 2):495-9. PubMed ID: 11259339
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence of HFE (hemochromatosis gene) mutations in unselected male patients with type 2 diabetes.
    Sampson MJ; Williams T; Heyburn PJ; Greenwood RH; Temple RC; Wimperis JZ; Jennings BA; Willis GA
    J Lab Clin Med; 2000 Feb; 135(2):170-3. PubMed ID: 10695662
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Carriers of the Complex Allele HFE c.[187C>G;340+4T>C] Have Increased Risk of Iron Overload in São Miguel Island Population (Azores, Portugal).
    Branco CC; Gomes CT; De Fez L; Bulhões S; Brilhante MJ; Pereirinha T; Cabral R; Rego AC; Fraga C; Miguel AG; Brasil G; Macedo P; Mota-Vieira L
    PLoS One; 2015; 10(10):e0140228. PubMed ID: 26501199
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hepatic iron overload in patients with chronic viral hepatitis: role of HFE gene mutations.
    Piperno A; Vergani A; Malosio I; Parma L; Fossati L; Ricci A; Bovo G; Boari G; Mancia G
    Hepatology; 1998 Oct; 28(4):1105-9. PubMed ID: 9755249
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New diallelic markers in the HLA region of chromosome 6.
    Beutler E; West C
    Blood Cells Mol Dis; 1997 Aug; 23(2):219-29. PubMed ID: 9268673
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The significance of the 187G (H63D) mutation in hemochromatosis.
    Beutler E
    Am J Hum Genet; 1997 Sep; 61(3):762-4. PubMed ID: 9326341
    [No Abstract]   [Full Text] [Related]  

  • 15. Body iron stores and iron restoration rate in Japanese patients with chronic hepatitis C as measured during therapeutic iron removal revealed neither increased body iron stores nor effects of C282Y and H63D mutations on iron indices.
    Shiono Y; Hayashi H; Wakusawa S; Sanae F; Takikawa T; Yano M; Yoshioka K; Saito H
    Nagoya J Med Sci; 2001 May; 64(1-2):51-7. PubMed ID: 11486601
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterozygosity for hereditary hemochromatosis is associated with more fibrosis in chronic hepatitis C.
    Smith BC; Gorve J; Guzail MA; Day CP; Daly AK; Burt AD; Bassendine MF
    Hepatology; 1998 Jun; 27(6):1695-9. PubMed ID: 9620344
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairs.
    Mura C; Le Gac G; Scotet V; Raguenes O; Mercier AY; Férec C
    J Med Genet; 2001 Sep; 38(9):632-6. PubMed ID: 11565552
    [No Abstract]   [Full Text] [Related]  

  • 18. Relationship between genotype, assessed by HLA typing, and phenotypic expression of iron status markers in families of 29 probands with hereditary haemochromatosis.
    Milman N; Fenger K; Graudal NA; Nielsen LS
    Dan Med Bull; 1994 Jun; 41(3):366-70. PubMed ID: 7924465
    [TBL] [Abstract][Full Text] [Related]  

  • 19. HLA-H and associated proteins in patients with hemochromatosis.
    Beutler E; West C; Gelbart T
    Mol Med; 1997 Jun; 3(6):397-402. PubMed ID: 9234244
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical characteristics of type 2 diabetes in patients with mutations of HFE.
    Dubois-Laforgue D; Caillat-Zucman S; Boitard C; Timsit J
    Diabetes Metab; 2000 Feb; 26(1):65-8. PubMed ID: 10705106
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.