These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 10707881)

  • 1. Rapid screening of the Cys282Tyr and His63Asp mutations in the HFE gene.
    Jardi R; Rodriguez-Frias F; Buti M; Costa X; Cotrina M; Olive G; Pascual C; Esteban R; Guardia J
    J Hepatol; 2000 Feb; 32(2):362-3. PubMed ID: 10707881
    [No 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. 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]  

  • 4. 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]  

  • 5. [Clinical usefulness of the detection of mutations of the HFE gene in hemochromatosis].
    Oliva R; Sánchez M; Bruguera M; Rodés J
    Gastroenterol Hepatol; 2000 Nov; 23(9):433-5. PubMed ID: 11126040
    [No Abstract]   [Full Text] [Related]  

  • 6. Diagnosis and management of haemochromatosis since the discovery of the HFE gene: a European experience.
    Br J Haematol; 2000 Jan; 108(1):31-9. PubMed ID: 10651721
    [No Abstract]   [Full Text] [Related]  

  • 7. Liver disorder and the HFE locus.
    Stewart SF; Day CP
    QJM; 2001 Sep; 94(9):453-6. PubMed ID: 11528007
    [No Abstract]   [Full Text] [Related]  

  • 8. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.
    Merryweather-Clarke AT; Pointon JJ; Shearman JD; Robson KJ; Jouanolle AM; Mosser A; David V; Le Gall JY; Halsall DJ; Elsey TS; Kelly A; Cox TM; Clare M; Bomford A; Vandwalle JL; Rochette J; Borot N; Coppin H; Roth MP; Ryan E; Crowe J; Totaro A; Gasparini P; Roetto A; Walker AP
    Nat Genet; 1999 Nov; 23(3):271. PubMed ID: 10545942
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Noll WW; Belloni DR; Stenzel TT; Grody WW
    Nat Genet; 1999 Nov; 23(3):271-2. PubMed ID: 10610176
    [No Abstract]   [Full Text] [Related]  

  • 11. Hemochromatosis with HFE gene mutation in a Japanese patient.
    Sohda T; Okubo R; Kamimura S; Ohkawara T
    Am J Gastroenterol; 2001 Aug; 96(8):2487-8. PubMed ID: 11513196
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Gomez PS; Parks S; Ries R; Tran TC; Gomez PF; Press RD
    Nat Genet; 1999 Nov; 23(3):272. PubMed ID: 10545944
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations.
    Merryweather-Clarke AT; Simonsen H; Shearman JD; Pointon JJ; Nørgaard-Pedersen B; Robson KJ
    Hum Mutat; 1999; 13(2):154-9. PubMed ID: 10094552
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 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. Haemochromatosis: diagnosis and management after the cloning of the HFE gene.
    Powell LW; Bassett ML
    Aust N Z J Med; 1998 Apr; 28(2):159-63. PubMed ID: 9612522
    [No Abstract]   [Full Text] [Related]  

  • 19. [Genetic hemochromatosis and the HFE gene].
    Moirand R
    Bull Acad Natl Med; 2000; 184(2):325-35; discussion 335-6. PubMed ID: 10989541
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Haemochromatosis: automated detection of the two point mutations in the HFE gene: Cys282Tyr and His63Asp.
    Klingler KR; Zech D; Wielckens K
    Clin Chem Lab Med; 2000 Dec; 38(12):1225-30. PubMed ID: 11205685
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.