Ön Alcatraz auktion Tanzania ferroportin železa muni biochemie Vara förvirrad helig jämnt
Ferroportin 1 - an overview | ScienceDirect Topics
IJMS | Free Full-Text | The Oral Ferroportin Inhibitor VIT-2763 Improves Erythropoiesis without Interfering with Iron Chelation Therapy in a Mouse Model of β-Thalassemia
Structural model of human ferroportin viewed along the membrane plane.... | Download Scientific Diagram
Structure of human ferroportin reveals molecular basis of iron homeostasis | bioRxiv
Structure of human ferroportin reveals molecular basis of iron homeostasis | bioRxiv
Ferroportin 1 - an overview | ScienceDirect Topics
Structure of human ferroportin bound to hepcidin reveals mechanisms of iron homeostasis | bioRxiv
Absorption of nonheme iron by intestinal epithelial cells (IECs).... | Download Scientific Diagram
Deciphering the molecular basis of ferroportin resistance to hepcidin: Structure/function analysis of rare SLC40A1 missense mutations found in suspected hemochromatosis type 4 patients - ScienceDirect
Systemic Iron Homeostasis and Erythropoiesis
Structural model of human ferroportin viewed along the membrane plane.... | Download Scientific Diagram
Hepcidin and iron regulatory proteins coordinately regulate ferroportin 1 expression in the brain of mice - Wang - 2019 - Journal of Cellular Physiology - Wiley Online Library
Interactions Between Ferroportin and Hephaestin in Rat Enterocytes Are Reduced After Iron Ingestion
Resistance of Ferroportin to Hepcidin Binding causes Exocrine Pancreatic Failure and Fatal Iron Overload - ScienceDirect
Ceruloplasmin-ferroportin system of iron traffic in vertebrates
Structural model of human ferroportin viewed along the membrane plane.... | Download Scientific Diagram
The hepcidin–ferroportin axis in the regulation of systemic iron (Fe)... | Download Scientific Diagram
IJMS | Free Full-Text | The Oral Ferroportin Inhibitor VIT-2763 Improves Erythropoiesis without Interfering with Iron Chelation Therapy in a Mouse Model of β-Thalassemia
JCI - Ferroportin mutation in autosomal dominant hemochromatosis: loss of function, gain in understanding