Direct interaction of the Wiskott-Aldrich syndrome protein with the GTPase Cdc42.
Wiskott-Aldrich syndrome (WAS) is an X-linked immunodeficiency disorder with the most severe pathology in the T lymphocytes and platelets. The disease arises from mutations in the gene encoding the WAS protein. T lymphocytes of affected males with WAS exhibit a severe disturbance of the actin cytosk...
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| Veröffentlicht in: | Proc Natl Acad Sci U S A |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
National Academy of Sciences
1996
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| Schlagworte: | |
| Online-Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC39296/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8643625/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.93.11.5615 |
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