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Hax1 regulates neutrophil adhesion and motility through RhoA
Kostmann disease is an inherited severe congenital neutropenia syndrome associated with loss-of-function mutations in an adaptor protein HS1-associated protein X-1 (Hax1). How Hax1 regulates neutrophil function remains largely unknown. In this paper, we use ribonucleic acid interference to deplete H...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Rockefeller University Press
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3087009/ https://ncbi.nlm.nih.gov/pubmed/21518791 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1083/jcb.201010143 |
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