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Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors
Diamond-Blackfan anemia (DBA) is a congenital disorder characterized by the failure of erythroid progenitor differentiation, severely curtailing red blood cell production. Because many DBA patients fail to respond to corticosteroid therapy, there is considerable need for therapeutics for this disord...
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| Publicado en: | Sci Transl Med |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5501179/ https://ncbi.nlm.nih.gov/pubmed/28179501 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scitranslmed.aah5645 |
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