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SLC40A1 gene

Known as: solute carrier family 40 member 1, IREG1, FERROPORTIN 1 
National Institutes of Health

Related topics

Related topics

3 relations
HEMOCHROMATOSIS, TYPE 4SLC40A1 protein, humanmetal transporting protein 1

Papers overview

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2016
2016
Dietary iron concentration influences serum concentrations of manganese in rats consuming organic or inorganic sources of manganese.
To determine the effects of dietary Fe concentration on Mn bioavailability in rats fed inorganic or organic Mn sources, fifty… 
2012
2012
Hypoferraemia during the early inflammatory response is dependent on tumour necrosis factor activity in a murine model of protracted peritonitis.
On the grounds of clinical, in vitro and in vivo studies, tumour necrosis factor (TNF) is considered to be one of the… 
2011
2011
Chronic administration of 2-acetylaminofluorene alters the cellular iron metabolism in rat liver.
Dysregulated intracellular iron homeostasis has been found not only in rodent and human hepatocellular carcinomas but also in… 
2009
2009
Brain and retinal ferroportin 1 dysregulation in polycythaemia mice
2008
2008
Iron regulatory and bactericidal properties of human recombinant hepcidin expressed in Pichia pastoris.
2007
2007
The expression and regulation of the iron transport molecules hephaestin and IREG1
The amount of iron in the body is controlled at the point of absorption in the proximal small intestine. Dietary iron enters the… 
2006
2006
Effects of age and mineral intake on the regulation of iron absorption in infants
Review
2005
Review
2005
Trace element nutrition of infants--molecular approaches.
2004
2004
Iron overload in an African American woman with SS hemoglobinopathy and a promoter mutation in the X-linked erythroid-specific 5-aminolevulinate synthase (ALAS2) gene.
We report the case of an African American woman with sickle cell anemia and iron overload incompletely explained by erythrocyte… 
2004
2004
A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygote
A 62‐year‐old white man with a hemochromatosis phenotype was found to be heterozygous for the C282Y mutation of the HFE gene. The… 
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