Gardenghi, Sara

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice. [electronic resource] - The Journal of clinical investigation Dec 2010 - 4466-77 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

1558-8238

10.1172/JCI41717 doi


Animals
Antimicrobial Cationic Peptides--genetics
Base Sequence
DNA Primers--genetics
Disease Models, Animal
Erythropoiesis--drug effects
Gene Expression
Hepcidins
Humans
Iron--metabolism
Iron Overload--blood
Iron, Dietary--administration & dosage
Mice
Mice, Inbred C57BL
Mice, Mutant Strains
Mice, Transgenic
Recombinant Proteins--genetics
beta-Thalassemia--blood