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 *

98 related articles for article (PubMed ID: 20642366)

  • 21. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry.
    Salvioni A; Mariani R; Oberkanins C; Moritz A; Mauri V; Pelucchi S; Riva A; Arosio C; Cerutti P; Piperno A
    Haematologica; 2003 Mar; 88(3):250-5. PubMed ID: 12651261
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
    Cimburova M; Putova I; Provaznikova H; Horak J
    Genet Epidemiol; 2002 Oct; 23(3):260-3. PubMed ID: 12384978
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic hemochromatosis, a Celtic disease: is it now time for population screening?
    Byrnes V; Ryan E; Barrett S; Kenny P; Mayne P; Crowe J
    Genet Test; 2001; 5(2):127-30. PubMed ID: 11551098
    [TBL] [Abstract][Full Text] [Related]  

  • 26. SNP and haplotype analysis reveals new HFE variants associated with iron overload trait.
    Yang Y; Férec C; Mura C
    Hum Mutat; 2011 Apr; 32(4):E2104-17. PubMed ID: 21412944
    [TBL] [Abstract][Full Text] [Related]  

  • 27. HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors.
    Arya N; Chakrabrati S; Hegele RA; Adams PC
    Blood Cells Mol Dis; 1999; 25(5-6):354-7. PubMed ID: 10660483
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Spectrum and haplotypes of the HFE hemochromatosis gene in Iran: H63D in beta-thalassemia major and the first E277K homozygous.
    Karimi M; Yavarian M; Delbini P; Harteveld CL; Farjadian S; Fiorelli G; Giordano PC
    Hematol J; 2004; 5(6):524-7. PubMed ID: 15570296
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina.
    Terzić R; Sehić A; Teran N; Terzić I; Peterlin B
    Coll Antropol; 2006 Sep; 30(3):555-7. PubMed ID: 17058523
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prevalence of H63D, S65C and C282Y mutations of the HFE gene in 1120 voluntary blood donors from Antioquia region of northwest Colombia.
    Avila-Gomez IC; Aristizabal-Bernal B; Jimenez-Del-Rio M; Velez-Pardo C
    Blood Cells Mol Dis; 2008; 40(3):449-51. PubMed ID: 18289891
    [No Abstract]   [Full Text] [Related]  

  • 31. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
    Vercesi E; Cerani P; Rolandi V; Rovati A; Bergamaschi G
    Haematologica; 2000 Aug; 85(8):787-91. PubMed ID: 10942923
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular analysis of A1AT (S and Z) and HFE (C282Y and H63D) gene mutations in Egyptian cases with HCV liver cirrhosis.
    Settin A; El-Bendary M; Abo-Al-Kassem R; El Baz R
    J Gastrointestin Liver Dis; 2006 Jun; 15(2):131-5. PubMed ID: 16802007
    [TBL] [Abstract][Full Text] [Related]  

  • 33. HFE gene polymorphisms and severity in Portuguese patients with multiple sclerosis.
    Bettencourt A; Silva AM; Santos E; Gomes S; Mendonça D; Costa PP; Faustino P; Silva BM
    Eur J Neurol; 2011 Apr; 18(4):663-6. PubMed ID: 20586792
    [TBL] [Abstract][Full Text] [Related]  

  • 34. HFE gene polymorphism defined by sequence-based typing of the Brazilian population and a standardized nomenclature for HFE allele sequences.
    Campos WN; Massaro JD; Martinelli ALC; Halliwell JA; Marsh SGE; Mendes-Junior CT; Donadi EA
    HLA; 2017 Oct; 90(4):238-242. PubMed ID: 28727322
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CAT53 and HFE alleles in Alzheimer's disease: a putative protective role of the C282Y HFE mutation.
    Correia AP; Pinto JP; Dias V; Mascarenhas C; Almeida S; Porto G
    Neurosci Lett; 2009 Jul; 457(3):129-32. PubMed ID: 19429178
    [TBL] [Abstract][Full Text] [Related]  

  • 36. An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy.
    Floreani A; Rosa Rizzotto E; Basso D; Navaglia F; Zaninotto M; Petridis I; DI Andrea O; Testa R; Marra M; Baldo V; Chiaramonte M
    Aliment Pharmacol Ther; 2007 Aug; 26(4):577-86. PubMed ID: 17661761
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Is the IVS2+4T>C variant of the HFE gene a splicing mutation or a polymorphism? A study in the Spanish population.
    de Lucas AP; Fulgencio MG; Robles JM; Sierra EM; del Rey Cerros MJ; Perez PM
    Genet Med; 2005 Mar; 7(3):212-3. PubMed ID: 15775762
    [No Abstract]   [Full Text] [Related]  

  • 38. 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; 34(1):38-47. PubMed ID: 15607698
    [TBL] [Abstract][Full Text] [Related]  

  • 39. An extensive analysis of the hereditary hemochromatosis gene HFE and neighboring histone genes: associations with childhood leukemia.
    Davis CF; Dorak MT
    Ann Hematol; 2010 Apr; 89(4):375-84. PubMed ID: 19806355
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
    Nie L; Ai XF; Zheng YZ; Li QH; Yang L; Xiao ZJ
    Zhonghua Xue Ye Xue Za Zhi; 2009 Apr; 30(4):223-8. PubMed ID: 19731820
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.