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A genetic variation associated with plasma erythropoietin and a non-coding transcript of PRKAR1A in sickle cell disease
Blood erythropoietin (EPO) increases primarily to hypoxia. In sickle cell anaemia (homozygous HBB(E6V); HbSS), plasma EPO is elevated due to hemolytic anaemia-related hypoxia. Hydroxyurea treatment reduces haemolysis and anaemia by increasing foetal haemoglobin, which leads to lower hypoxic transcri...
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| Udgivet i: | Hum Mol Genet |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6078595/ https://ncbi.nlm.nih.gov/pubmed/28173069 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw299 |
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