Pages that link to "Q24671532"
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The following pages link to Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene (Q24671532):
Displaying 50 items.
- A mouse model of juvenile hemochromatosis (Q24532268) (← links)
- Targeted mutagenesis of the murine transferrin receptor-2 gene produces hemochromatosis (Q24533580) (← links)
- Hereditary hemochromatosis in the post-HFE era (Q24646056) (← links)
- Ferroportin is a manganese-responsive protein that decreases manganese cytotoxicity and accumulation (Q24650332) (← links)
- Hepcidin revisited, disulfide connectivity, dynamics, and structure (Q24651444) (← links)
- Recent advances in understanding haemochromatosis: a transition state (Q24676226) (← links)
- The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease (Q24678328) (← links)
- SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent (Q24682642) (← links)
- Haemochromatosis (Q24685891) (← links)
- Impact of HFE genetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data (Q24814752) (← links)
- Hepcidin: regulation of the master iron regulator (Q26800198) (← links)
- Pharmacology of iron transport (Q27009387) (← links)
- Mechanisms of mammalian iron homeostasis (Q27010510) (← links)
- The SLC40 basolateral iron transporter family (IREG1/ferroportin/MTP1) (Q28183692) (← links)
- Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload (Q28279799) (← links)
- Impaired iron transport activity of ferroportin 1 in hereditary iron overload (Q28294061) (← links)
- Mechanisms of divalent metal toxicity in affective disorders (Q28384836) (← links)
- Acute Free-Iron Exposure Does Not Explain the Impaired Haemorheology Associated with Haemochromatosis (Q28552430) (← links)
- The European Hematology Association Roadmap for European Hematology Research: a consensus document (Q28830861) (← links)
- Zebrafish in hematology: sushi or science? (Q30481539) (← links)
- Investigation of the biophysical and cell biological properties of ferroportin, a multipass integral membrane protein iron exporter (Q30487384) (← links)
- Effects of iron loading on muscle: genome-wide mRNA expression profiling in the mouse (Q33303254) (← links)
- Null mutation in PGAP1 impairing Gpi-anchor maturation in patients with intellectual disability and encephalopathy (Q33553032) (← links)
- Hepcidin antagonists for potential treatments of disorders with hepcidin excess (Q33563777) (← links)
- Human macrophage ferroportin biology and the basis for the ferroportin disease (Q33628733) (← links)
- Stoichiometries of transferrin receptors 1 and 2 in human liver (Q33636603) (← links)
- Evolutionary mutant models for human disease (Q33686021) (← links)
- Targeting iron metabolism in drug discovery and delivery (Q33757232) (← links)
- Ferroportin1 is required for normal iron cycling in zebrafish (Q33774889) (← links)
- Hepatocyte-targeted HFE and TFR2 control hepcidin expression in mice (Q33806074) (← links)
- Pathophysiological consequences and benefits of HFE mutations: 20 years of research. (Q33815961) (← links)
- Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating plasma tumor necrosis factor-alpha and macrophage migration inhibitory factor concentrations in African children. (Q34065915) (← links)
- Intracellular iron transport and storage: from molecular mechanisms to health implications (Q34100135) (← links)
- Ferroportin disease: a systematic meta-analysis of clinical and molecular findings (Q34209183) (← links)
- Zebrafish as a model system for the study of hemostasis and thrombosis (Q34223444) (← links)
- The hemochromatosis protein HFE inhibits iron export from macrophages. (Q34388109) (← links)
- Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency (Q34410196) (← links)
- Normal iron metabolism and the pathophysiology of iron overload disorders (Q34427279) (← links)
- EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). (Q34483947) (← links)
- Gene therapy by allele selection in a mouse model of beta-thalassemia. (Q34519981) (← links)
- Interaction of the hereditary hemochromatosis protein HFE with transferrin receptor 2 is required for transferrin-induced hepcidin expression (Q34658174) (← links)
- Non-HFE haemochromatosis (Q34668872) (← links)
- Absorption of manganese and iron in a mouse model of hemochromatosis (Q34738248) (← links)
- Molecular pathogenesis of iron overload. (Q34739178) (← links)
- Ferristatin II promotes degradation of transferrin receptor-1 in vitro and in vivo (Q34875712) (← links)
- HFE and non-HFE hemochromatosis (Q34989227) (← links)
- Hypoxia-Inducible Factor-2α Mediates the Adaptive Increase of Intestinal Ferroportin During Iron Deficiency in Mice (Q35027929) (← links)
- Iron transport across the blood-brain barrier: development, neurovascular regulation and cerebral amyloid angiopathy (Q35032747) (← links)
- Zebrafish as a model for normal and malignant hematopoiesis (Q35070710) (← links)
- Heterozygous recipient and donor HFE mutations associated with a hereditary haemochromatosis phenotype after liver transplantation (Q35595454) (← links)