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C/EBP epsilon directs granulocytic versus monocytic lineage determination and confers chemotactic function via Hlx
OBJECTIVE: Mutations in the C/EBPε gene have been identified in the cells of patients with neutrophil specific granule deficiency (SGD), a rare congenital disorder marked by recurrent bacterial infections. Their neutrophils, in addition to lacking specific granules required for normal respiratory bu...
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| Main Authors: | , , , , , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2009
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2827304/ https://ncbi.nlm.nih.gov/pubmed/19925846 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exphem.2009.11.004 |
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