Wiskott-Aldrich Syndrome Protein
"Wiskott-Aldrich Syndrome Protein" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
WASP protein is mutated in WISKOTT-ALDRICH SYNDROME and is expressed primarily in hematopoietic cells. It is the founding member of the WASP protein family and interacts with CDC42 PROTEIN to help regulate ACTIN polymerization.
| Descriptor ID |
D051316
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| MeSH Number(s) |
D05.750.078.730.912.500 D12.776.220.525.912.500
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Wiskott-Aldrich Syndrome Protein".
Below are MeSH descriptors whose meaning is more specific than "Wiskott-Aldrich Syndrome Protein".
This graph shows the total number of publications written about "Wiskott-Aldrich Syndrome Protein" by people in this website by year, and whether "Wiskott-Aldrich Syndrome Protein" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 2 | 0 | 2 |
| 2015 | 0 | 1 | 1 |
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Below are the most recent publications written about "Wiskott-Aldrich Syndrome Protein" by people in Profiles.
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Neonatal Thrombocytopenia: Etiology and Diagnosis. Pediatr Ann. 2015 Jul; 44(7):e175-80.
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Impaired cell adhesion, apoptosis, and signaling in WASP gene-disrupted Nalm-6 pre-B cells and recovery of cell adhesion using a transducible form of WASp. Int J Hematol. 2012 Mar; 95(3):299-310.
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Lymphocyte-dependent and Th2 cytokine-associated colitis in mice deficient in Wiskott-Aldrich syndrome protein. Gastroenterology. 2007 Oct; 133(4):1188-97.
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The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells. J Exp Med. 2007 Feb 19; 204(2):381-91.
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X inactivation in females with X-linked disease. N Engl J Med. 1998 Jan 29; 338(5):325-8.