WAS gene

Known as: WASPA, WASP, Wiskott-Aldrich syndrome 
This gene is involved in signal transduction and plays a role in cell communication and organization.
National Institutes of Health

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Highly Cited
2014
Highly Cited
2014
Wiskott-Aldrich syndrome (WAS) is characterized by microthrombocytopenia, immunodeficiency, autoimmunity, and susceptibility to… (More)
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2007
2007
The Wiskott-Aldrich syndrome (WAS) is characterized by defective cytoskeletal dynamics affecting multiple immune cell lineages… (More)
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2006
2006
Wiskott-Aldrich syndrome (WAS) is a life-threatening X-linked primary immunodeficiency characterized by infections, hemorrhages… (More)
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Highly Cited
2004
Highly Cited
2004
Wiskott-Aldrich syndrome (WAS) is an X-linked primary immunodeficiency with a median survival below the age of 20 due to… (More)
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2003
2003
Revertant mosaicism due to true back mutations or second-site mutations has been identified in several inherited disorders. The… (More)
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Highly Cited
2002
Highly Cited
2002
The Wiskott-Aldrich syndrome (WAS) is a primary immunodeficiency disorder caused by a mutation in WAS protein (WASp) that results… (More)
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Highly Cited
2000
Highly Cited
2000
Wiskott-Aldrich syndrome (WAS) is an X-linked recessive disorder originally characterized by the clinical triad eczema… (More)
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Review
1998
Review
1998
In 1937, Wiskott described three brothers with congenital thrombocytopenia, bloody diarrhea, eczema, and recurrent ear infections… (More)
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Highly Cited
1997
Highly Cited
1997
Wiskott-Aldrich syndrome (WAS) and X-linked thrombocytopenia (XLT), caused by mutations of the WAS protein (WASP) gene, represent… (More)
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Highly Cited
1997
Highly Cited
1997
Wiskott-Aldrich syndrome (WAS) is an X-linked immunodeficiency caused by mutations that affect the WAS protein (WASP) and… (More)
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