BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 9215758)

  • 1. 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]  

  • 2. 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]  

  • 3. Prevalence of the Cys282Tyr and His63Asp mutation in Flemish patients with hereditary hemochromatosis.
    Van Vlierberghe H; Messiaen L; Hautekeete M; De Paepe A; Elewaut A
    Acta Gastroenterol Belg; 2000; 63(3):250-3. PubMed ID: 11189980
    [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. Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.
    Carella M; D'Ambrosio L; Totaro A; Grifa A; Valentino MA; Piperno A; Girelli D; Roetto A; Franco B; Gasparini P; Camaschella C
    Am J Hum Genet; 1997 Apr; 60(4):828-32. PubMed ID: 9106528
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
    Barton JC; Sawada-Hirai R; Rothenberg BE; Acton RT
    Blood Cells Mol Dis; 1999; 25(3-4):147-55. PubMed ID: 10575540
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Genetics of hemochromatosis.
    Cullen LM; Anderson GJ; Ramm GA; Jazwinska EC; Powell LW
    Annu Rev Med; 1999; 50():87-98. PubMed ID: 10073265
    [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. Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis.
    Datz C; Lalloz MR; Vogel W; Graziadei I; Hackl F; Vautier G; Layton DM; Maier-Dobersberger T; Ferenci P; Penner E; Sandhofer F; Bomford A; Paulweber B
    J Hepatol; 1997 Nov; 27(5):773-9. PubMed ID: 9382962
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Hemochromatosis: association of severity of iron overload with genetic markers.
    Barton JC; Harmon L; Rivers C; Acton RT
    Blood Cells Mol Dis; 1996; 22(3):195-204. PubMed ID: 9075570
    [TBL] [Abstract][Full Text] [Related]  

  • 13. HFE codon 63/282 (H63D/C282Y) dimorphism in German patients with genetic hemochromatosis.
    Gottschalk R; Seidl C; Löffler T; Seifried E; Hoelzer D; Kaltwasser JP
    Tissue Antigens; 1998 Mar; 51(3):270-5. PubMed ID: 9550327
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda.
    Roberts AG; Whatley SD; Morgan RR; Worwood M; Elder GH
    Lancet; 1997 Feb; 349(9048):321-3. PubMed ID: 9024376
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Expression of hemochromatosis in homozygous subjects. Implications for early diagnosis and prevention.
    Powell LW; Summers KM; Board PG; Axelsen E; Webb S; Halliday JW
    Gastroenterology; 1990 Jun; 98(6):1625-32. PubMed ID: 2338199
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.