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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

Papers overview

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Highly Cited
2014
Highly Cited
2014
Wiskott-Aldrich syndrome gene therapy is feasible, but γ-retroviral vectors contribute a substantial risk of leukemogenesis… Expand
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Highly Cited
2011
Highly Cited
2011
Wiskott-Aldrich syndrome (WAS) is a primary immunodeficiency associated with an increased susceptibility to herpesvirus infection… Expand
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Highly Cited
2007
Highly Cited
2007
A large proportion of Wiskott-Aldrich syndrome (WAS) patients develop autoimmunity and allergy. CD4+CD25+FOXP3+ natural… Expand
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Highly Cited
2004
Highly Cited
2004
Short microvilli cover the surfaces of circulating mammalian lymphocytes. The surfaces of monocytes and neutrophils are very… Expand
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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… Expand
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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… Expand
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Review
2000
Review
2000
The biological mechanisms responsible for the pathophysiology of the Wiskott–Aldrich syndrome (WAS) have been shown to be linked… Expand
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Highly Cited
1998
Highly Cited
1998
Wiskott‐Aldrich syndrome (WAS) is a rare disease characterized by microthrombocytopenia, eczema and immune deficiency. In this… Expand
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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… Expand
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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… Expand
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