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Journal Abstract Search

198 related items for PubMed ID: 12196404

  • 1. Sequence variation and haplotype structure at the human HFE locus.
    Toomajian C, Kreitman M.
    Genetics; 2002 Aug; 161(4):1609-23. PubMed ID: 12196404
    [Abstract] [Full Text] [Related]

  • 2. Haplotype analysis of the H63D, IVS2+4t/c, and C282Y polymorphisms of the HFE gene reveals rare events of intragenic recombination.
    Curcio M, Fornaciari S, Mariotti ML, Chelazzi S, Scatena F, Presciuttini S.
    Eur J Haematol; 2008 Apr; 80(4):341-5. PubMed ID: 18182079
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  • 3. Co-selection of the H63D mutation and the HLA-A29 allele: a new paradigm of linkage disequilibrium?
    Cardoso CS, Alves H, Mascarenhas M, Gonçalves R, Oliveira P, Rodrigues P, Cruz E, de Sousa M, Porto G.
    Immunogenetics; 2002 Mar; 53(12):1002-8. PubMed ID: 11904676
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  • 4. Linkage disequilibrium between S65C HFE mutation and HLA A29-B44 haplotype in Terceira Island, Azores.
    Couto AR, Peixoto MJ, Garrett F, Laranjeira F, Cipriano T, Armas JB.
    Hum Immunol; 2003 Jun; 64(6):625-8. PubMed ID: 12770794
    [Abstract] [Full Text] [Related]

  • 5. Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis.
    Rubio JP, Bahlo M, Tubridy N, Stankovich J, Burfoot R, Butzkueven H, Chapman C, Johnson L, Marriott M, Mraz G, Tait B, Wilkinson C, Taylor B, Speed TP, Foote SJ, Kilpatrick TJ.
    Hum Genet; 2004 May; 114(6):573-80. PubMed ID: 15014978
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  • 6. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
    Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.
    Immunogenetics; 1998 Apr; 47(5):404-10. PubMed ID: 9510559
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  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central Sweden.
    Olsson KS, Ritter B, Hansson N, Chowdhury RR.
    Eur J Haematol; 2008 Jul; 81(1):36-46. PubMed ID: 18363869
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  • 9. 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 Jul; 34(1):38-47. PubMed ID: 15607698
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  • 11. The ethnospecific distribution of the HFE haplotypes for IVS2(+4)t/c, IVS4(-44)t/c, and IVS5(-47)g/a in populations of Russia and possible effects of these single-nucleotide polymorphisms in splicing.
    Mikhailova SV, Babenko VN, Voevoda MI, Romashchenko AG.
    Genet Test Mol Biomarkers; 2010 Aug; 14(4):461-9. PubMed ID: 20642366
    [Abstract] [Full Text] [Related]

  • 12. Natural selection on HFE in Asian populations contributes to enhanced non-heme iron absorption.
    Ye K, Cao C, Lin X, O'Brien KO, Gu Z.
    BMC Genet; 2015 Jun 10; 16():61. PubMed ID: 26054392
    [Abstract] [Full Text] [Related]

  • 13. Linkage disequilibrium analysis in Australian haemochromatosis patients indicates bipartite association with clinical expression.
    Pratiwi R, Fletcher LM, Pyper WR, Do KA, Crawford DH, Powell LW, Jazwinska EC.
    J Hepatol; 1999 Jul 10; 31(1):39-46. PubMed ID: 10424281
    [Abstract] [Full Text] [Related]

  • 14. H63D mutation in HFE gene is common in Indians and is associated with the European haplotype.
    Dhillon BK, Prakash S, Chandak GR, Chawla YK, Das R.
    J Genet; 2012 Aug 10; 91(2):229-32. PubMed ID: 22942096
    [No Abstract] [Full Text] [Related]

  • 15. Multicentric origin of hemochromatosis gene (HFE) mutations.
    Rochette J, Pointon JJ, Fisher CA, Perera G, Arambepola M, Arichchi DS, De Silva S, Vandwalle JL, Monti JP, Old JM, Merryweather-Clarke AT, Weatherall DJ, Robson KJ.
    Am J Hum Genet; 1999 Apr 10; 64(4):1056-62. PubMed ID: 10090890
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  • 18. The role of hemochromatosis susceptibility gene mutations in protecting against iron deficiency in celiac disease.
    Butterworth JR, Cooper BT, Rosenberg WM, Purkiss M, Jobson S, Hathaway M, Briggs D, Howell WM, Wood GM, Adams DH, Iqbal TH.
    Gastroenterology; 2002 Aug 10; 123(2):444-9. PubMed ID: 12145797
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  • 20. 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 Aug 10; 25(3-4):147-55. PubMed ID: 10575540
    [Abstract] [Full Text] [Related]

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