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Journal Abstract Search

179 related items for PubMed ID: 24920245

  • 41. The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.
    Silva B, Pita L, Gomes S, Gonçalves J, Faustino P.
    Ann Hematol; 2014 Dec; 93(12):2063-6. PubMed ID: 25015054
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  • 44. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
    Lee PL, Gelbart T, West C, Halloran C, Beutler E.
    Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
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  • 45. Iron overload is rare in patients homozygous for the H63D mutation.
    Kelley M, Joshi N, Xie Y, Borgaonkar M.
    Can J Gastroenterol Hepatol; 2014 Apr; 28(4):198-202. PubMed ID: 24729993
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  • 49. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb; 26(1):2-8. PubMed ID: 10772870
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  • 52. Maternal hemochromatosis gene H63D single-nucleotide polymorphism and lead levels of placental tissue, maternal and umbilical cord blood.
    Kayaalti Z, Kaya-Akyüzlü D, Söylemez E, Söylemezoğlu T.
    Environ Res; 2015 Jul; 140():456-61. PubMed ID: 25981872
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  • 60. Pseudouridine-mediated stop codon readthrough in S. cerevisiae is sequence context-independent.
    Adachi H, Yu YT.
    RNA; 2020 Sep; 26(9):1247-1256. PubMed ID: 32434780
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