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 *

276 related articles for article (PubMed ID: 19759876)

  • 1. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis.
    Bittencourt PL; Marin ML; Couto CA; Cançado EL; Carrilho FJ; Goldberg AC
    Clinics (Sao Paulo); 2009; 64(9):837-41. PubMed ID: 19759876
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Analysis of HFE and TFR2 gene mutations in patients with acute leukemia.
    Veneri D; Franchini M; Krampera M; de Matteis G; Solero P; Pizzolo G
    Leuk Res; 2005 Jun; 29(6):661-4. PubMed ID: 15863206
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. HFE gene mutations an Apulian population: allele frequencies.
    Pietrapertosa A; Vitucci A; Campanale D; Palma A; Renni R; Delios G; Tannoia N
    Eur J Epidemiol; 2003; 18(7):685-9. PubMed ID: 12952143
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
    Bittencourt PL; Palácios SA; Couto CA; Cançado EL; Carrilho FJ; Laudanna AA; Kalil J; Gayotto LC; Goldberg AC
    Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M; Vaupotic T; Rupreht R; Curin-Serbec V
    BMC Med Genet; 2007 Nov; 8():69. PubMed ID: 18036208
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.
    Del-Castillo-Rueda A; Moreno-Carralero MI; Cuadrado-Grande N; Alvarez-Sala-Walther LA; Enríquez-de-Salamanca R; Méndez M; Morán-Jiménez MJ
    Gene; 2012 Oct; 508(1):15-20. PubMed ID: 22890139
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload.
    Barton EH; West PA; Rivers CA; Barton JC; Acton RT
    Blood Cells Mol Dis; 2001; 27(1):279-84. PubMed ID: 11358388
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
    Milić S; Ristić S; Starčević-Čizmarević N; Brajenović-Milić B; Crnić-Martinović M; Kapović M; Peterlin B; Štimac D
    Med Sci Monit; 2011 Oct; 17(10):CR552-6. PubMed ID: 21959608
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload.
    De Gobbi M; Daraio F; Oberkanins C; Moritz A; Kury F; Fiorelli G; Camaschella C
    Haematologica; 2003 Apr; 88(4):396-401. PubMed ID: 12681966
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload.
    Biasiotto G; Belloli S; Ruggeri G; Zanella I; Gerardi G; Corrado M; Gobbi E; Albertini A; Arosio P
    Clin Chem; 2003 Dec; 49(12):1981-8. PubMed ID: 14633868
    [TBL] [Abstract][Full Text] [Related]  

  • 16. S65C and other mutations in the haemochromatosis gene in the Czech population.
    Cimburová M; Půtová I; Provazníková H; Pintérová D; Horák J
    Folia Biol (Praha); 2005; 51(6):172-6. PubMed ID: 16419611
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload.
    Cançado RD; Guglielmi AC; Vergueiro CS; Rolim EG; Figueiredo MS; Chiattone CS
    Sao Paulo Med J; 2006 Mar; 124(2):55-60. PubMed ID: 16878186
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.
    Leão GD; Freire JM; Cunha Fernandes AL; Moura de Oliveira TM; Leão ND; Gil EA; de Vasconcelos RC; Azevedo JP; de Farias Sales VS; de Araújo Moura Lemos TM; Leão MD; do Nascimento FF; Maciel JF; de Freitas RV; de Souza Paiva A; Cavalcanti GB
    J Clin Lab Anal; 2014 May; 28(3):178-85. PubMed ID: 24395214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20.
    Zarifian Yeganeh R; Akbari Kelishomi M; Ahmadpour Jenaghard A; Salmani B; Vahidi Z; Makvand M; Azad M; Kooshki M; Bouraqi Y; Azarkeivan A; Najmabadi H; Neishabury M
    Genet Test Mol Biomarkers; 2024 Jul; 28(7):289-296. PubMed ID: 38980801
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.