Related references
Note: Only part of the references are listed.WASP: a key immunological multitasker
Adrian J. Thrasher et al.
NATURE REVIEWS IMMUNOLOGY (2010)
Activating mutations of N-WASP alter Shigella pathogenesis
David A. Adamovich et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2009)
Recent advances in understanding the pathophysiology of Wiskott-Aldrich syndrome
Marita Bosticardo et al.
BLOOD (2009)
A large kindred with X-linked neutropenia with an I294T mutation of the Wiskott-Aldrich syndrome gene
Karolien Beel et al.
BRITISH JOURNAL OF HAEMATOLOGY (2009)
FOCUS ON RESEARCH The Many Causes of Severe Congenital Neutropenia
David C. Dale et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
A Syndrome with Congenital Neutropenia and Mutations in G6PC3
Kaan Boztug et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
The who, how and where of antigen presentation to B cells
Facundo D. Batista et al.
NATURE REVIEWS IMMUNOLOGY (2009)
WASP confers selective advantage for specific hematopoietic cell populations and serves a unique role in marginal zone B-cell homeostasis and function
Lisa S. Westerberg et al.
BLOOD (2008)
Wiskott-Aldrich syndrome
Luigi D. Notarangelo et al.
CURRENT OPINION IN HEMATOLOGY (2008)
The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency
Lawrence R. Shiow et al.
NATURE IMMUNOLOGY (2008)
Limiting the proliferation of polyploid cells
Neil J. Ganem et al.
CELL (2007)
Wiskott-Aldrich syndrome protein (WASP) and N-WASP are critical for T cell development
Vinicius Cotta-de-Almeida et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Unregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia
Dale A. Moulding et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2007)
Defective DNA repair and increased genomic instability in Cernunnos-XLF-deficient murine ES cells
Shan Zha et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
Christoph Klein et al.
NATURE GENETICS (2007)
Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia
Phil J. Ancliff et al.
BLOOD (2006)
Requirement for coronin 1 in T lymphocyte trafficking and cellular homeostasis
Niko Foeger et al.
SCIENCE (2006)
WASP deficiency leads to global defects of directed leukocyte migration in vitro and in vivo
SB Snapper et al.
JOURNAL OF LEUKOCYTE BIOLOGY (2005)
Wiskott-Aldrich syndrome protein deficiency leads to reduced B-cell adhesion, migration, and homing, and a delayed humoral immune response
L Westerberg et al.
BLOOD (2005)
A new method for rapidly generating gene-targeting vectors by engineering BACs through homologous recombination in bacteria
V Cotta-De-Almeida et al.
GENOME RESEARCH (2003)
Site-specific gene targeting in mouse embryonic stem cells with intact bacterial artificial chromosomes
Y Yang et al.
NATURE BIOTECHNOLOGY (2003)
Gene therapy for Wiskott-Aldrich syndrome: rescue of T-cell signaling and amelioration of colitis upon transplantation of retrovirally transduced hematopoietic stem cells in mice
C Klein et al.
BLOOD (2003)
Phosphorylation of tyrosine enhances the ability of WASp to stimulate actin polymerization and filopodium formation
GOC Cory et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
N-WASP deficiency reveals distinct pathways for cell surface projections and microbial actin-based motility
SB Snapper et al.
NATURE CELL BIOLOGY (2001)
Cdc42, Rac1, and the Wiskott-Aldrich syndrome protein are involved in the cytoskeletal regulation of B lymphocytes
L Westerberg et al.
BLOOD (2001)
A MAP kinase-dependent actin checkpoint ensures proper spindle orientation in fission yeast
Y Gachet et al.
NATURE (2001)
Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia
K Devriendt et al.
NATURE GENETICS (2001)
Autoinhibition and activation mechanisms of the Wiskott-Aldrich syndrome protein
AS Kim et al.
NATURE (2000)
Share Paper
