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 *

168 related articles for article (PubMed ID: 1975556)

  • 1. HLA class I gene polymorphism in genetic hemochromatosis.
    Jouanolle AM; Yaouanq J; Blayau M; Périchon M; Fauchet R; Font MP; Le Gall JY; David V
    Hum Genet; 1990 Aug; 85(3):279-82. PubMed ID: 1975556
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ferritin H gene polymorphism in idiopathic hemochromatosis.
    David V; Papadopoulos P; Yaouanq J; Blayau M; Abel L; Zappone E; Perichon M; Drysdale J; Le Gall JY; Simon M
    Hum Genet; 1989 Jan; 81(2):123-6. PubMed ID: 2563249
    [TBL] [Abstract][Full Text] [Related]  

  • 3. DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family.
    David V; Paul P; Simon M; Le Gall JY; Fauchet R; Gicquel I; Dugast I; Le Mignon L; Yaouanq J; Cohen D
    Hum Genet; 1986 Oct; 74(2):113-20. PubMed ID: 2876944
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The HLA class I locus: analysis of RFLPs in hereditary hemochromatosis.
    Hansen JL; Kushner JP
    Cytogenet Cell Genet; 1989; 50(4):216-9. PubMed ID: 2572402
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutations occurring in hereditary hemochromatosis.
    Lynas C
    Blood; 1997 Nov; 90(10):4235-6. PubMed ID: 9354698
    [No Abstract]   [Full Text] [Related]  

  • 7. Hereditary hemochromatosis: a HpaI polymorphism within the HLA-H gene.
    Totaro A; Grifa A; Carella M; D'Ambrosio L; Valentino M; Roth MP; Borot N; Coppin H; Roetto A; Camaschella C; Gasparini P
    Mol Cell Probes; 1997 Jun; 11(3):229-30. PubMed ID: 9232622
    [No Abstract]   [Full Text] [Related]  

  • 8. A new highly polymorphic marker in the 5' untranslated region of HLA-F shows strong allelic association with haemochromatosis.
    Raha-Chowdhury R; Bowen DJ; Worwood M
    Hum Genet; 1996 Feb; 97(2):228-31. PubMed ID: 8566959
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of C282Y and H63D in the HFE gene.
    Pointon JJ; Merryweather-Clarke AT; Carella M; Robson KJ
    Genet Test; 2000; 4(2):115-20. PubMed ID: 10953949
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of HLA class I genes with restriction endonuclease fragments: implications for polymorphism of the human major histocompatibility complex.
    Cohen D; Paul P; Font MP; Cohen O; Sayagh B; Marcadet A; Busson M; Mahouy G; Cann HM; Dausset J
    Proc Natl Acad Sci U S A; 1983 Oct; 80(20):6289-92. PubMed ID: 6312451
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evaluation of a nucleic acid-based cross-linking assay to screen for hereditary hemochromatosis in healthy blood donors.
    Wylenzek C; Engelmann M; Holten D; Van Atta R; Wood M; Gathof B
    Clin Chem; 2000 Nov; 46(11):1853-5. PubMed ID: 11067829
    [No Abstract]   [Full Text] [Related]  

  • 12. [Detection of HFE polymorphism in German patients with hereditary hemochromatosis].
    Burggraf S; Olgemöller B
    Dtsch Med Wochenschr; 2000 Nov; 125(44):1346; author reply 1347. PubMed ID: 11109419
    [No Abstract]   [Full Text] [Related]  

  • 13. Iron beware: a common HFE gene polymorphism may prevent the accurate molecular diagnosis of homozygous hemochromatosis in low-risk, but not high-risk groups.
    Press RD
    Hepatology; 2000 Feb; 31(2):540-2. PubMed ID: 10655286
    [No Abstract]   [Full Text] [Related]  

  • 14. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.
    Gonzalez-Hevilla M; de Salamanca RE; Morales P; Martínez-Laso J; Fontanellas A; Castro MJ; Rojo R; Moscoso J; Zamora J; Serrano-Vela JI; Arnaiz-Villena A
    J Gastroenterol Hepatol; 2005 Mar; 20(3):456-62. PubMed ID: 15740492
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G
    Blood Cells Mol Dis; 2001; 27(2):549-56. PubMed ID: 11500066
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of a recombinant that locates the hereditary hemochromatosis gene telomeric to HLA-F.
    Calandro LM; Baer DM; Sensabaugh GF
    Hum Genet; 1995 Sep; 96(3):339-42. PubMed ID: 7649553
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Overestimation of HFE C282Y homozygous hemochromatosis prevalence as the result of a common primer-binding site polymorphism.
    Press RD
    Mol Diagn; 1999 Dec; 4(4):391-2. PubMed ID: 10671650
    [No Abstract]   [Full Text] [Related]  

  • 18. Where does the gene for hemochromatosis lie in relation to HLA-A?
    Jazwinska EC; Halliday JW; Powell LW
    Hepatology; 1994 Apr; 19(4):1050-1. PubMed ID: 8138245
    [No Abstract]   [Full Text] [Related]  

  • 19. Evidence for a polymorphism of HLA-G gene.
    Alizadeh M; Legras C; Semana G; Le Bouteiller P; Genetet B; Fauchet R
    Hum Immunol; 1993 Nov; 38(3):206-12. PubMed ID: 7906261
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial screening for genetic haemochromatosis by means of DNA markers.
    Yaouanq J; el Kahloun A; Chorney M; Jouanolle AM; Mauvieux V; Perichon M; Blayau M; Pontarotti P; Le Gall JY; David V
    J Med Genet; 1992 May; 29(5):320-2. PubMed ID: 1349923
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.