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WAS gene
Known as:
WASPA
, WASP
, Wiskott-Aldrich syndrome
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This gene is involved in signal transduction and plays a role in cell communication and organization.
National Institutes of Health
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Related topics
Related topics
7 relations
Cytoskeletal Modeling
Signal Transduction
WAS protein, human
WAS wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Critical requirement for the Wiskott-Aldrich syndrome protein in Th2 effector function.
V. Morales-Tirado
,
Dorothy K. Sojka
,
+4 authors
D. Fowell
Blood
2010
Corpus ID: 206883418
Patients with Wiskott-Aldrich syndrome (WAS) have numerous immune cell deficiencies, but it remains unclear how abnormalities in…
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Highly Cited
2008
Highly Cited
2008
Wiskott-Aldrich syndrome protein deficiency in B cells results in impaired peripheral homeostasis
A. Meyer-Bahlburg
,
S. Becker-Herman
,
+6 authors
D. Rawlings
Blood
2008
Corpus ID: 5734133
To more precisely identify the B-cell phenotype in Wiskott-Aldrich syndrome (WAS), we used 3 distinct murine in vivo models to…
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Highly Cited
2005
Highly Cited
2005
Defective nuclear translocation of nuclear factor of activated T cells and extracellular signal-regulated kinase underlies deficient IL-2 gene expression in Wiskott-Aldrich syndrome.
A. Cianferoni
,
M. Massaad
,
+4 authors
R. Geha
Journal of Allergy and Clinical Immunology
2005
Corpus ID: 37843806
Review
2005
Review
2005
WASP and the phenotypic range associated with deficiency.
L. Notarangelo
,
L. Notarangelo
,
H. Ochs
Current Opinion in Allergy and Clinical…
2005
Corpus ID: 34743652
PURPOSE OF REVIEW This review reports on the range of clinical phenotypes that are caused by mutations in the Wiskott-Aldrich…
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Highly Cited
2004
Highly Cited
2004
Differential contribution of Wiskott-Aldrich syndrome protein to selective advantage in T- and B-cell lineages.
A. Konno
,
T. Wada
,
+4 authors
F. Candotti
Blood
2004
Corpus ID: 12396995
Somatic mosaicism because of in vivo reversion has been recently reported in a small number of patients affected with Wiskott…
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Highly Cited
2003
Highly Cited
2003
Functional correction of T cells derived from patients with the Wiskott–Aldrich syndrome (WAS) by transduction with an oncoretroviral vector encoding the WAS protein
Ted S. Strom
,
W. Gabbard
,
+4 authors
A. Nienhuis
Gene Therapy
2003
Corpus ID: 23484979
T-cell dysfunction is thought to be central to the immunodeficiency state seen in patients with the Wiskott–Aldrich syndrome (WAS…
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Highly Cited
2002
Highly Cited
2002
Restoration of podosomes and chemotaxis in Wiskott-Aldrich syndrome macrophages following induced expression of WASp.
G. Jones
,
D. Zicha
,
G. Dunn
,
M. Blundell
,
A. Thrasher
International Journal of Biochemistry and Cell…
2002
Corpus ID: 6309389
Highly Cited
2002
Highly Cited
2002
Retrovirus-mediated WASP gene transfer corrects Wiskott-Aldrich syndrome T-cell dysfunction.
T. Wada
,
G. J. Jagadeesh
,
David L. Nelson
,
F. Candotti
Human Gene Therapy
2002
Corpus ID: 42606280
The Wiskott-Aldrich syndrome (WAS) is an X-linked disorder characterized by thrombocytopenia, eczema, and immunodeficiency. At…
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Highly Cited
2001
Highly Cited
2001
Cdc42, Rac1, and the Wiskott-Aldrich syndrome protein are involved in the cytoskeletal regulation of B lymphocytes.
L. Westerberg
,
Gediminas Greicius
,
S. Snapper
,
P. Aspenström
,
Eva Severinson
Blood
2001
Corpus ID: 25400672
Patients with the immunodeficiency disorder Wiskott-Aldrich syndrome (WAS) have lymphocytes with aberrant microvilli, and their T…
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1990
1990
Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome.
W. Greer
,
A. Somani
,
P. C. Kwong
,
M. Peacocke
,
L. Rubin
,
K. Siminovitch
Genomics
1990
Corpus ID: 23274257
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