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N-WASP is required for B-cell–mediated autoimmunity in Wiskott-Aldrich syndrome
Mutations of the Wiskott-Aldrich syndrome gene (WAS) are responsible for Wiskott-Aldrich syndrome (WAS), a disease characterized by thrombocytopenia, eczema, immunodeficiency, and autoimmunity. Mice with conditional deficiency of Was in B lymphocytes (B/WcKO) have revealed a critical role for WAS pr...
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| Udgivet i: | Blood |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society of Hematology
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4713162/ https://ncbi.nlm.nih.gov/pubmed/26468226 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2015-05-643817 |
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