Ferroportin1: A new iron export molecule?

International Journal of Biochemistry and Cell Biology

Volumn 34, Issue 2, 2002, Pages 103-108

  Le, Nghia T V ^a   Richardson, Des R ^a  

^a HEART RESEARCH INSTITUTE   (Australia)

Author keywords

Absorption; Export; Ferroportin1; Hemochromatosis; IREG1; Iron; MTP1; Release

Indexed keywords

FERROPORTIN 1; MESSENGER RNA; OXIDOREDUCTASE; PROTEIN; UNCLASSIFIED DRUG;

5' UNTRANSLATED REGION; ARTICLE; CELLULAR DISTRIBUTION; DUODENUM; HEMOCHROMATOSIS; INTESTINE CELL; INTESTINE MUCOSA; IRON ABSORPTION; IRON DEFICIENCY; IRON KINETICS; IRON OVERLOAD; IRON RESPONSIVE ELEMENT; IRON TRANSPORT; LIVER; MACROPHAGE; NONHUMAN; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; SEQUENCE ANALYSIS; SIGNAL TRANSDUCTION; SPLEEN; SYNCYTIOTROPHOBLAST;

EID: 0036152949     PISSN: 13572725     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1357-2725(01)00104-2     Document Type: Short Survey

References (14)

1. Iron, free radicals, and oxidative injury
2. Iron homeostasis: New tales from the crypt
3. Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse
4. A novel mammalian iron-regulated protein involved in intracellular iron metabolism
5. Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
6. A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation
7. The molecular mechanisms of the metabolism and transport of iron in normal and neoplastic cells
8. The biochemical basis of the NADPH oxidase of phagocytes
9. A low-spin iron complex in human melanoma and rat hepatoma cells and a high-spin iron(II) complex in rat hepatoma cells
10. Effect of iron deficiency on placental transfer of iron and expression of iron transport proteins in vivo and in vitro
11. Cloning and characterization of a mammalian proton-coupled metal ion transporter
12. An iron-regulated ferric reductase associated with the absorption of dietary iron
13. Copper chaperones: Function, structure and copper-binding properties
14. A mutation on SLC11A3 is associated with autosomal dominant hemochromatosis