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Modulation of hepcidin as therapy for primary and secondary iron overload disorders: pre-clinical models and approaches

CORRECTING INEFFECTIVE ERYTHROPOIESIS AND IRON DYSREGULATION BY REGULATING HEPCIDIN EXPRESSION: Unbalanced hemoglobin α- and β-chain expression in the thalassemias, results in anemia, extramedullary hematopoiesis and ineffective erythropoiesis leading to secondary iron overload even in the absence o...

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Hlavní autoři: Schmidt, Paul J., Fleming, Mark D.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2014
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3942790/
https://ncbi.nlm.nih.gov/pubmed/24589273
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hoc.2013.11.004
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