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 *

116 related articles for article (PubMed ID: 25850353)

  • 1. Compound heterozygous C282Y/Q283P and Q283P/H63D mutations in haemochromatosis.
    van Gammeren A; de Baar E; Schrauwen L; van Wijngaarden P
    Br J Haematol; 2015 Nov; 171(4):650-1. PubMed ID: 25850353
    [No Abstract]   [Full Text] [Related]  

  • 2. The Q283P amino-acid change in HFE leads to structural and functional consequences similar to those described for the mutated 282Y HFE protein.
    Ka C; Le Gac G; Dupradeau FY; Rochette J; Férec C
    Hum Genet; 2005 Sep; 117(5):467-75. PubMed ID: 15965644
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect.
    Le Gac G; Dupradeau FY; Mura C; Jacolot S; Scotet V; Esnault G; Mercier AY; Rochette J; Férec C
    Blood Cells Mol Dis; 2003; 30(3):231-7. PubMed ID: 12737937
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Compound heterozygote (C282Y/H63D) of hereditary hemochromatosis in a 16-year-old girl with hypoplastic kidney.
    Kaczorowska-Hac B; Sikorska K; Bielawski KP; Schramm K; Balcerska A
    Int J Hematol; 2007 May; 85(4):300-3. PubMed ID: 17483072
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.
    Simsek H; Balaban YH; Yilmaz E; Sumer H; Buyukasik Y; Cengiz C; Ozcebe O; Hascelik G; Tatar G
    Ann Hematol; 2005 Oct; 84(10):646-9. PubMed ID: 15871018
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
    Himmelmann A; Bortoluzzi L; Jansen S; Fehr J
    Schweiz Med Wochenschr; 2000 Aug; 130(31-32):1112-9. PubMed ID: 11008304
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect.
    Oberkanins C
    Blood Cells Mol Dis; 2003; 31(2):173; author reply 174. PubMed ID: 12972020
    [No Abstract]   [Full Text] [Related]  

  • 9. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.
    de Diego C; Murga MJ; Martínez-Castro P
    Genet Test; 2004; 8(3):263-7. PubMed ID: 15727249
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Prevalence of hemochromatosis-associated mutations in the hemochromatosis gene in the Danish population].
    Larsen LE; Ellervik C; Appleyard M; Nordestgaard BG; Birgens H; Tybjaerg-Hansen A
    Ugeskr Laeger; 2002 Sep; 164(39):4545-7. PubMed ID: 12380399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in a Venezuelan sample.
    Vizzi E; Loureiro CL; Gerder M; de las Nieves Garcia-Casal M; Rodríguez-Larralde A; Gerace L; Ludert JE; Liprandi F; Pujol FH
    Ann Hematol; 2005 Nov; 84(12):802-6. PubMed ID: 15995871
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.
    De Marco F; Liguori R; Giardina MG; D'Armiento M; Angelucci E; Lucariello A; Morante R; Cimino L; Galeota-Lanza A; Tarantino G; Ascione A; Budillon G; Vecchione R; Martinelli R; Matarazzo M; De Simone V
    Clin Chem Lab Med; 2004 Jan; 42(1):17-24. PubMed ID: 15061375
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population.
    Lin A; Yan WH; Xu HH; Zhu M; Zhou MY
    Tissue Antigens; 2007 Sep; 70(3):252-5. PubMed ID: 17661915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frequency and spectrum of hemochromatosis mutations in Tunisia.
    Zorai A; Harteveld CL; Rachdi R; Dellagi K; Abbes S; Delbini P; Giordano PC
    Hematol J; 2003; 4(6):433-5. PubMed ID: 14671616
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Hereditary hemochromatosis: the clinical significance of the S65C mutation.
    Asberg A; Thorstensen K; Hveem K; Bjerve KS
    Genet Test; 2002; 6(1):59-62. PubMed ID: 12180078
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP; Popp RA; Militaru MS; Farcaş MF; Crişan TO; Gana I; Cucuianu A; Pop IV
    J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [From gene to disease; HFE-mutations in primary haemochromatosis].
    Swinkels DW; Jacobs EM
    Ned Tijdschr Geneeskd; 2003 Apr; 147(14):652-6. PubMed ID: 12712648
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.