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Hepcidin
Iron Regulation by Hepcidin
Hepcidin Is Not a Marker of Chronic Inflammation in Atherosclerosis Hepcidin Aterosklerozda Kronik Inflamasyonun Bir Göstergesi De¤Ildir
Hepcidin Therapeutics
Hepcidin the Key Regulator of Iron in the Blood St
The Correlation of the Hepcidin Ferritin Ratio and the Severity of Liver Cirrhosis
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The Potential for Transition Metal-Mediated Neurodegeneration in Amyotrophic Lateral Sclerosis
Inflammatory Markers and Hepcidin Are Elevated but Serum Iron Is
A Short Review of Iron Metabolism and Pathophysiology of Iron Disorders
Serum Hepcidin in Infants Born After 32 to 37 Wk of Gestational Age
Dysregulated Iron Metabolism in Polycythemia Vera: Etiology and Consequences
Iron Overload and Iron Chelation: the Inside Story
Iron Metabolism and Iron Disorders Revisited in the Hepcidin
HFE Gene Homeostatic Iron Regulator
Interpreting SERUM FERRITIN
Hepcidin-Ferroportin Interaction Controls Systemic Iron Homeostasis
Genetic Disorders Associated with Metal Metabolism
Hepcidin Protects Yellow Catfish (Pelteobagrus Fulvidraco)
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Regulation of Cell Surface Transferrin Receptor-2 by Iron-Dependent Cleavage and Release of a Soluble Form
Hepcidin and Sports Anemia Wei-Na Kong1,2, Guofen Gao1 and Yan-Zhong Chang1*
Hepcidin and Its Role in Iron Homeostasis
Iron—Too Much, Too Little, Too Late
Hepcidin and Ferritin Levels in Restless Legs Syndrome: a Case–Control Study
Hepcidin Therapeutics
Competitive Regulation of Hepcidin Mrna by Soluble and Cell-Associated Hemojuvelin
1 Expression of the Iron Exporter Ferroportin In
Multi-Copper Oxidases and Human Iron Metabolism
The Molecular Genetics of Haemochromatosis
Hepcidin, an Emerging and Important Player in Brain Iron Homeostasis Driton Vela*
Inherited Disorders of Transition Metal Metabolism: an Update
Transferrin Receptor 1 Mrna Is Downregulated in Placenta of Hepcidin Transgenic Embryos
Genetic Diseases Causing Iron Deficiency and Iron
Title Hepcidin Expression in Liver Cells
Disorders of Metal Metabolism Carlos Ferreira George Washington University
Genetic Testing for Hereditary Hemochromatosis AHS – M2012
First Phenotypic Description of Transferrin Receptor 2 Knockout