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Wiskott–Aldrich Syndrome protein deficiency perturbs the homeostasis of B-cell compartment in humans()
Wiskott–Aldrich Syndrome protein (WASp) regulates the cytoskeleton in hematopoietic cells and mutations in its gene cause the Wiskott–Aldrich Syndrome (WAS), a primary immunodeficiency with microthrombocytopenia, eczema and a higher susceptibility to develop tumors. Autoimmune manifestations, freque...
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| Asıl Yazarlar: | , , , , , , , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Academic Press
2014
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4012141/ https://ncbi.nlm.nih.gov/pubmed/24369837 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaut.2013.10.006 |
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