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 *

132 related articles for article (PubMed ID: 20373367)

  • 21. [Iron in the era of molecular biology].
    Deugnier Y; Moirand R; Brissot P; David V
    Pathol Biol (Paris); 1999 Nov; 47(9):938-44. PubMed ID: 10609274
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hemochromatosis gene mutations, body iron stores, dietary iron, and risk of colorectal adenoma in women.
    Chan AT; Ma J; Tranah GJ; Giovannucci EL; Rifai N; Hunter DJ; Fuchs CS
    J Natl Cancer Inst; 2005 Jun; 97(12):917-26. PubMed ID: 15956653
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Case report of a patient with non-alcoholic fatty liver disease, moderate iron overload who is homozygous for the S65C mutation in the HFE1 gene.
    Bernard PH; Ged C; Faivre E; Legac G; Bioulac-Sage P; Cassaigne A; de Verneuil H
    Eur J Med Genet; 2005; 48(2):195-8. PubMed ID: 16053912
    [No Abstract]   [Full Text] [Related]  

  • 24. Assessment of HFE mutations in patients with iron overload.
    Bittencourt PL
    Sao Paulo Med J; 2007 Jan; 125(1):65-7. PubMed ID: 17505690
    [No Abstract]   [Full Text] [Related]  

  • 25. Iron overload in cirrhosis-HFE genotypes and outcome after liver transplantation.
    Brandhagen DJ; Alvarez W; Therneau TM; Kruckeberg KE; Thibodeau SN; Ludwig J; Porayko MK
    Hepatology; 2000 Feb; 31(2):456-60. PubMed ID: 10655270
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The influence of hemochromatosis mutations on iron overload of thalassemia major.
    Longo F; Zecchina G; Sbaiz L; Fischer R; Piga A; Camaschella C
    Haematologica; 1999 Sep; 84(9):799-803. PubMed ID: 10477452
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients.
    Politou M; Kalotychou V; Pissia M; Rombos Y; Sakellaropoulos N; Papanikolaou G
    Haematologica; 2004 Apr; 89(4):490-2. PubMed ID: 15075083
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis.
    Nicolas G; Viatte L; Lou DQ; Bennoun M; Beaumont C; Kahn A; Andrews NC; Vaulont S
    Nat Genet; 2003 May; 34(1):97-101. PubMed ID: 12704388
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Non-HFE related hereditary iron overload].
    Brissot P; Jouanolle AM; Le Lan C; Loreal O; Deugnier Y; David V
    Gastroenterol Clin Biol; 2005 May; 29(5):565-8. PubMed ID: 15980752
    [No Abstract]   [Full Text] [Related]  

  • 30. Characteristics of HFE C282Y homozygotes younger than age 30 years.
    Barton JC; Felitti VJ; Lee P; Beutler E
    Acta Haematol; 2004; 112(4):219-21. PubMed ID: 15564736
    [No Abstract]   [Full Text] [Related]  

  • 31. HFE mutations in insulin resistance-associated hepatic iron overload.
    Guillygomarc'h A; Mendler MH; Moirand R; Jouanolle AM; David V; Deugnier Y
    J Hepatol; 2000 Sep; 33(3):515-6. PubMed ID: 11020014
    [No Abstract]   [Full Text] [Related]  

  • 32. Iron-independent specific protein expression pattern in the liver of HFE-deficient mice.
    Petrak J; Myslivcova D; Halada P; Cmejla R; Cmejlova J; Vyoral D; Vulpe CD
    Int J Biochem Cell Biol; 2007; 39(5):1006-15. PubMed ID: 17376729
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Absence of overt iron overload in two individuals compound heterozygotes for a 22 base pair deletion of exon 2 and the C282Y missense mutation of the HFE gene.
    Kinkely SM; Brown BD; Lyng AT; Harrison WK; Schep GN; Goddard-Hill AC; Aubrey ME; Lillicrap D; Taylor SA
    Clin Genet; 2003 Feb; 63(2):163-5. PubMed ID: 12630967
    [No Abstract]   [Full Text] [Related]  

  • 34. [HFE gene mutations in Tunisian major beta-Thalassemia and iron overload].
    Mellouli F; El Borgi W; Kaabi H; Ben Hassen E; Sassi R; Hmida H; Cherif G; Maamar M; Zouari B; Boukef K; Bejaoui M; Hmida S
    Transfus Clin Biol; 2006 Dec; 13(6):353-7. PubMed ID: 17303462
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Recent advances in the pathophysiology, diagnosis and treatment of hereditary hemochromatosis and other iron overload syndromes.
    Pirisi M; Avellini C; Scott CA; Toniutto P; Intersimone D; Aprile G; Branca B; Fumo E
    Adv Clin Path; 2001 Oct; 5(4):121-31. PubMed ID: 17582936
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hemochromatosis and iron-overload screening in a racially diverse population.
    Adams PC; Reboussin DM; Barton JC; McLaren CE; Eckfeldt JH; McLaren GD; Dawkins FW; Acton RT; Harris EL; Gordeuk VR; Leiendecker-Foster C; Speechley M; Snively BM; Holup JL; Thomson E; Sholinsky P;
    N Engl J Med; 2005 Apr; 352(17):1769-78. PubMed ID: 15858186
    [TBL] [Abstract][Full Text] [Related]  

  • 37. HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
    Barton JC; Acton RT; Leiendecker-Foster C; Lovato L; Adams PC; McLaren GD; Eckfeldt JH; McLaren CE; Reboussin DM; Gordeuk VR; Speechley MR; Reiss JA; Press RD; Dawkins FW;
    Genet Test; 2007; 11(3):269-75. PubMed ID: 17949288
    [TBL] [Abstract][Full Text] [Related]  

  • 38. EASL clinical practice guidelines for HFE hemochromatosis.
    European Association For The Study Of The Liver
    J Hepatol; 2010 Jul; 53(1):3-22. PubMed ID: 20471131
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Status of HFE mutation in thalassemia syndromes in north India.
    Agarwal S; Tewari D; Arya V; Moorchung N; Tripathi R; Chaudhuri G; Pradhan M
    Ann Hematol; 2007 Jul; 86(7):483-5. PubMed ID: 17401564
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis.
    Muckenthaler M; Roy CN; Custodio AO; Miñana B; deGraaf J; Montross LK; Andrews NC; Hentze MW
    Nat Genet; 2003 May; 34(1):102-7. PubMed ID: 12704390
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.