BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 9662273)

  • 1. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in African Americans.
    Monaghan KG; Rybicki BA; Shurafa M; Feldman GL
    Am J Hematol; 1998 Jul; 58(3):213-7. PubMed ID: 9662273
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload.
    Barton EH; West PA; Rivers CA; Barton JC; Acton RT
    Blood Cells Mol Dis; 2001; 27(1):279-84. PubMed ID: 11358388
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls.
    Sánchez M; Bruguera M; Bosch J; Rodés J; Ballesta F; Oliva R
    J Hepatol; 1998 Nov; 29(5):725-8. PubMed ID: 9833909
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hemochromatosis gene HFE Cys282Tyr mutation analysis in a cohort of Northeast German hospitalized patients supports assumption of a North to South allele frequency gradient throughout Germany.
    Meier P; Schuff-Werner P; Steiner M
    Clin Lab; 2005; 51(9-10):539-43. PubMed ID: 16285477
    [TBL] [Abstract][Full Text] [Related]  

  • 5. HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology.
    Hanson EH; Imperatore G; Burke W
    Am J Epidemiol; 2001 Aug; 154(3):193-206. PubMed ID: 11479183
    [TBL] [Abstract][Full Text] [Related]  

  • 6. HFE gene mutation, C282Y causing hereditary hemochromatosis in Caucasian is extremely rare in Korean population.
    Lee JY; Yoo KH; Hahn SH
    J Korean Med Sci; 2000 Apr; 15(2):179-82. PubMed ID: 10803694
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inheritance of two HFE mutations in African Americans: cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency.
    Barton JC; Acton RT
    Genet Med; 2001; 3(4):294-300. PubMed ID: 11478530
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis.
    Barton JC; Shih WW; Sawada-Hirai R; Acton RT; Harmon L; Rivers C; Rothenberg BE
    Blood Cells Mol Dis; 1997; 23(1):135-45; discussion 145a-b. PubMed ID: 9215758
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.
    Gallego CJ; Burt A; Sundaresan AS; Ye Z; Shaw C; Crosslin DR; Crane PK; Fullerton SM; Hansen K; Carrell D; Kuivaniemi H; Derr K; de Andrade M; McCarty CA; Kitchner TE; Ragon BK; Stallings SC; Papa G; Bochenek J; Smith ME; Aufox SA; Pacheco JA; Patel V; Friesema EM; Erwin AL; Gottesman O; Gerhard GS; Ritchie M; Motulsky AG; Kullo IJ; Larson EB; Tromp G; Brilliant MH; Bottinger E; Denny JC; Roden DM; Williams MS; Jarvik GP
    Am J Hum Genet; 2015 Oct; 97(4):512-20. PubMed ID: 26365338
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.
    Jouanolle AM; Fergelot P; Gandon G; Yaouanq J; Le Gall JY; David V
    Hum Genet; 1997 Oct; 100(5-6):544-7. PubMed ID: 9341868
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence from a Ghanaian population of known African descent to support the proposition that hemochromatosis is a Caucasian disorder.
    Jeffery S; Crosby A; Plange-Rhule J; Amoah-Danquah J; Acheampong JW; Eastwood JB; Malik AK
    Genet Test; 1999; 3(4):375-7. PubMed ID: 10627947
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].
    Moreno L; Vallcorba P; Boixeda D; Cabello P; Bermejo F; San Román C
    Rev Clin Esp; 1999 Oct; 199(10):632-6. PubMed ID: 10589245
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of an unusual combination of mutations in the HFE gene for hemochromatosis.
    Thorstensen K; Asberg A; Kvitland M; Svaasand E; Hveem K; Bjerve KS
    Genet Test; 2000; 4(4):371-6. PubMed ID: 11216661
    [TBL] [Abstract][Full Text] [Related]  

  • 14. HFE gene mutations in coronary atherothrombotic disease.
    Calado RT; Franco RF; Pazin-Filho A; Simões MV; Marin-Neto JA; Zago MA
    Braz J Med Biol Res; 2000 Mar; 33(3):301-6. PubMed ID: 10719381
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Haplotype analysis of the HFE gene: implications for the origins of hemochromatosis related mutations.
    Aguilar-Martinez P; Thelcide C; Jeanjean P; Masmejean C; Giansily M; Schved JF
    Blood Cells Mol Dis; 1999; 25(3-4):166-9. PubMed ID: 10575542
    [No Abstract]   [Full Text] [Related]  

  • 16. Mutation analysis of the HFE gene in Brazilian populations.
    Agostinho MF; Arruda VR; Basseres DS; Bordin S; Soares MC; Menezes RC; Costa FF; Saad ST
    Blood Cells Mol Dis; 1999; 25(5-6):324-7. PubMed ID: 10660479
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An unusual case of hemochromatosis due to a new compound heterozygosity in HFE (p.[Gly43Asp;His63Asp]+[Cys282Tyr]): structural implications with respect to binding with transferrin receptor 1.
    Dupradeau FY; Pissard S; Coulhon MP; Cadet E; Foulon K; Fourcade C; Goossens M; Case DA; Rochette J
    Hum Mutat; 2008 Jan; 29(1):206. PubMed ID: 18157833
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
    Bittencourt PL; Palácios SA; Couto CA; Cançado EL; Carrilho FJ; Laudanna AA; Kalil J; Gayotto LC; Goldberg AC
    Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic expression of a novel C282Y/R226G compound heterozygous state in HFE hemochromatosis: molecular dynamics and biochemical studies.
    Cézard C; Rabbind Singh A; Le Gac G; Gourlaouen I; Ferec C; Rochette J
    Blood Cells Mol Dis; 2014 Jan; 52(1):27-34. PubMed ID: 23953397
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.
    Acton RT; Barton JC; Snively BM; McLaren CE; Adams PC; Harris EL; Speechley MR; McLaren GD; Dawkins FW; Leiendecker-Foster C; Holup JL; Balasubramanyam A;
    Ethn Dis; 2006; 16(4):815-21. PubMed ID: 17061732
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.