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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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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2014
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| Ämnen: | |
| Länkar: | 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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