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 *

163 related articles for article (PubMed ID: 30820268)

  • 1. Comprehensive analysis of
    de Campos WN; Massaro JD; Cançado ELR; Wiezel CEV; Simões AL; Teixeira AC; de Souza FF; Mendes-Junior CT; Martinelli ALC; Donadi EA
    World J Hepatol; 2019 Feb; 11(2):186-198. PubMed ID: 30820268
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R; Seidl C; Schilling S; Braner A; Seifried E; Hoelzer D; Kaltwasser JP
    Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC; Cançado RD; Pereira AC; Schettert IT; Soares RA; Pagliusi RA; Hirata RD; Hirata MH; Teixeira AC; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
    Blood Cells Mol Dis; 2011 Apr; 46(4):302-7. PubMed ID: 21411349
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Carriers of the Complex Allele HFE c.[187C>G;340+4T>C] Have Increased Risk of Iron Overload in São Miguel Island Population (Azores, Portugal).
    Branco CC; Gomes CT; De Fez L; Bulhões S; Brilhante MJ; Pereirinha T; Cabral R; Rego AC; Fraga C; Miguel AG; Brasil G; Macedo P; Mota-Vieira L
    PLoS One; 2015; 10(10):e0140228. PubMed ID: 26501199
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Genetic variants associated with the progression of hepatocellular carcinoma in hepatitis C Egyptian patients.
    Motawi TK; Shaker OG; Ismail MF; Sayed NH
    Gene; 2013 Sep; 527(2):516-20. PubMed ID: 23845776
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P; Esculié-Coste C; Bismuth M; Giansily-Blaizot M; Larrey D; Schved JF
    Blood Cells Mol Dis; 2001; 27(1):290-3. PubMed ID: 11358390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 25(3-4):147-55. PubMed ID: 10575540
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
    Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L
    Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
    Hellerbrand C; Bosserhoff AK; Seegers S; Lingner G; Wrede C; Lock G; Schölmerich J; Büttner R
    Scand J Gastroenterol; 2001 Nov; 36(11):1211-6. PubMed ID: 11686223
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 123(2):444-9. PubMed ID: 12145797
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ancestral association between HLA and HFE H63D and C282Y gene mutations from northwest Colombia.
    Rodriguez LM; Giraldo MC; Velasquez LI; Alvarez CM; Garcia LF; Jimenez-Del-Rio M; Velez-Pardo C
    Genet Mol Biol; 2015 Mar; 38(1):8-13. PubMed ID: 25983618
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL; Filho R; Cruz S; Franco R; Tavella M; Secaf M; Ramalho L; Zucoloto S; Rodrigues S; Zago M
    Genet Mol Res; 2005 Mar; 4(1):31-8. PubMed ID: 15841433
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?
    Aguilar-Martinez P; Bismuth M; Picot MC; Thelcide C; Pageaux GP; Blanc F; Blanc P; Schved JF; Larrey D
    Gut; 2001 Jun; 48(6):836-42. PubMed ID: 11358905
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnostic utility of HFE variants in Spanish patients: association with HLA alleles and role in susceptibility to acute lymphoblastic leukemia.
    Rodríguez-López R; Donoso M; Fernández-Cavada M; González LM; Margallo A; Corral C; Gallego M; García de Cáceres MT; Herrera T; González C; Vagace JM; Gervasini G
    Gene; 2013 Feb; 514(1):31-5. PubMed ID: 23178241
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association between heterozygosity for HFE gene mutations and hepatitis viruses in hepatocellular carcinoma.
    Fracanzani AL; Fargion S; Stazi MA; Valenti L; Amoroso P; Cariani E; Sangiovanni A; Tommasini M; Rossini A; Bertelli C; Fatta E; Patriarca V; Brescianini S; Stroffolini T
    Blood Cells Mol Dis; 2005; 35(1):27-32. PubMed ID: 15894495
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.