Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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wetenschappelijk artikel

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наукова стаття, опублікована в жовтні 2018

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Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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P1476

Role of HAMP Genetic Variants on Pathophysiology of Iron Deficiency Anemia

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P2093

S K Pandey

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S Pandey

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V Shah

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P2860

Severe iron deficiency anemia in transgenic mice expressing liver hepcidin

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice

Hepcidin and iron homeostasis

The solution structure of human hepcidin, a peptide hormone with antimicrobial activity that is involved in iron uptake and hereditary hemochromatosis

A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload

Expression of hepcidin in hereditary hemochromatosis: evidence for a regulation in response to the serum transferrin saturation and to non-transferrin-bound iron

Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R)

Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis

Regulation of iron metabolism by hepcidin

P2888

s12291-017-0707-9

P304

479-482

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P31

scholarly article

P356

10.1007/S12291-017-0707-9

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2018-10-01T00:00:00Z

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P698

30319197

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P921

pathophysiology

P932

6170237

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