The controversial role of variants in HAMP , BMP 2 , FTL and SLC 40 A 1 genes

[1]  D. Lane,et al.  Mammalian iron homeostasis in health and disease: uptake, storage, transport, and molecular mechanisms of action. , 2013, Antioxidants & redox signaling.

[2]  M. P. Vaquero,et al.  Intronic SNP rs3811647 of the human transferrin gene modulates its expression in hepatoma cells. , 2012, Nutricion hospitalaria.

[3]  A. González-Quintela,et al.  Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant , 2010, BMC Genetics.

[4]  M. Podinovskaia,et al.  Monitoring the efficiency of iron chelation therapy: the potential of nontransferrin‐bound iron , 2010, Annals of the New York Academy of Sciences.

[5]  J. Eccleston,et al.  Mechanisms for the shuttling of plasma non-transferrin-bound iron (NTBI) onto deferoxamine by deferiprone. , 2010, Translational research : the journal of laboratory and clinical medicine.

[6]  C. Férec,et al.  Factors influencing disease phenotype and penetrance in HFE haemochromatosis , 2010, Human Genetics.

[7]  M. Ferrari,et al.  The -582A>G variant of the HAMP promoter is not associated with high serum ferritin levels in normal subjects , 2010, Haematologica.

[8]  J. Mosser,et al.  A common SNP near BMP2 is associated with severity of the iron burden in HFE p.C282Y homozygous patients: a follow-up study. , 2010, Blood cells, molecules & diseases.

[9]  M. Testi,et al.  Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major , 2009, Haematologica.

[10]  M. Baiget,et al.  Does the SLC40A1 gene modify HFE-related haemochromatosis phenotypes? , 2009, Annals of Hematology.

[11]  J. Mosser,et al.  Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance. , 2007, American journal of human genetics.

[12]  Y. Kohgo,et al.  Iron overload and cofactors with special reference to alcohol, hepatitis C virus infection and steatosis/insulin resistance. , 2007, World journal of gastroenterology.

[13]  M. Krawczak,et al.  Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients , 2005, Gut.

[14]  G. Ruggeri,et al.  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. , 2003, Clinical chemistry.

[15]  B. Baron,et al.  Regulation of the Tissue-Specific Expression of Transferrin Gene , 2002, Developmental Neuroscience.

[16]  Qian Wu,et al.  TMPRSS 6 , but not TF , TFR 2 or BMP 2 variants are associated with increased risk of iron-deficiency anemia , 2012 .