A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton
Wiskott-Aldrich syndrome (WAS) is associated with mutations in the WAS protein (WASp), which plays a critical role in the initiation of T cell receptor–driven (TCR-driven) actin polymerization. The clinical phenotype of WAS includes susceptibility to infection, allergy, autoimmunity, and malignancy...
Main Authors: | , , , , , , , , , , , , , , , , , , |
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Other Authors: | |
Format: | Article |
Language: | en_US |
Published: |
American Society for Clinical Investigation
2017
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Online Access: | http://hdl.handle.net/1721.1/107953 https://orcid.org/0000-0003-2705-7245 |