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Article

The role of Wiskott-Aldrich Syndrome protein in activation and function of human T cells

2006-01-01

Abstract excerpt

Wiskott-Aldrich Syndrome (WAS) is a X-linked genetic disease caused by mutation in the gene encoding for the Wiskott-Aldrich Syndrome protein (WASP). WASP is specifically expressed in hematopoietic cells, where it regulates the reorganization of actin cytoskeleton in response to extracellular stimuli. WAS is characterized by micro-throm bocytopenia, eczema, immunodeficiency and high susceptibility to autoimmune di...

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Literature Corpus work
15032511-8d42-5a8f-ae45-2f0d5d512134
DOI
10.21954/ou.ro.0000fafc
Open publication

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