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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Autors principals: Halene, Stephanie, Gaines, Peter, Sun, Hong, Zibello, Theresa, Lin, Sharon, Khanna-Gupta, Arati, Williams, Simon C., Perkins, Archibald, Krause, Diane, Berliner, Nancy
Format: Artigo
Idioma:Inglês
Publicat: 2009
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Article
Accés en línia: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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