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Primary immunodeficiencies associated with eosinophiliaHuman Immunodeficiencies Related to Defective APC/T Cell InteractionCongenital defects in neutrophil dynamicsPlatelet actin nodules are podosome-like structures dependent on Wiskott-Aldrich syndrome protein and ARP2/3 complex.Differential gene expression analysis by RNA-seq reveals the importance of actin cytoskeletal proteins in erythroleukemia cells.Successful renal transplantation in a patient with a Wiskott-Aldrich syndrome protein (WASP) gene mutation.Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1CXCR4 signaling and function require the expression of the IgD-class B-cell antigen receptor.A human immunodeficiency syndrome caused by mutations in CARMIL2Nuclear role of WASp in gene transcription is uncoupled from its ARP2/3-dependent cytoplasmic role in actin polymerization.The actin binding proteins cortactin and HS1 are dispensable for platelet actin nodule and megakaryocyte podosome formation.Cytokine immunomodulation for the treatment of infectious diseases: lessons from primary immunodeficiencies.Insights into primary immune deficiency from quantitative microscopy.Current Status of Dedicator of Cytokinesis-Associated Immunodeficiency: DOCK8 and DOCK2.Cytoskeletal control of B cell responses to antigens.Activation of compensatory pathways via Rac2 in the absence of the Cdc42 effector Wiskott-Aldrich syndrome protein in Dendritic cells.Heme drives hemolysis-induced susceptibility to infection via disruption of phagocyte functions.An Amish founder mutation disrupts a PI(3)P-WHAMM-Arp2/3 complex-driven autophagosomal remodeling pathway.Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease.Nuclear Wiskott-Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells.Cytoskeletal function in the immune system.Disruption of Thrombocyte and T Lymphocyte Development by a Mutation in ARPC1B.Excitable Signal Transduction Networks in Directed Cell Migration.Wiskott-Aldrich syndrome protein: Emerging mechanisms in immunity.Nanoscale Dynamism of Actin Enables Secretory Function in Cytolytic Cells.Autonomous role of Wiskott-Aldrich Syndrome platelet deficiency in inducing autoimmunity and inflammation.Actin Filament Structures in Migrating Cells.Genome-wide transcriptome analysis identifies alternative splicing regulatory network and key splicing factors in mouse and human psoriasis.Neurological Manifestations of Primary Immunodeficiencies
P2860
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P2860
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Actin cytoskeletal defects in immunodeficiency
@ast
Actin cytoskeletal defects in immunodeficiency
@en
Actin cytoskeletal defects in immunodeficiency
@nl
type
label
Actin cytoskeletal defects in immunodeficiency
@ast
Actin cytoskeletal defects in immunodeficiency
@en
Actin cytoskeletal defects in immunodeficiency
@nl
prefLabel
Actin cytoskeletal defects in immunodeficiency
@ast
Actin cytoskeletal defects in immunodeficiency
@en
Actin cytoskeletal defects in immunodeficiency
@nl
P2093
P2860
P50
P921
P3181
P356
P1476
Actin cytoskeletal defects in immunodeficiency
@en
P2093
Adrian J. Thrasher
Dale A. Moulding
Dessislava Malinova
P2860
P304
P3181
P356
10.1111/IMR.12114
P407
P577
2013-11-01T00:00:00Z