Rho GTPase Cdc42 is essential for B-lymphocyte development and activation.
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Rho GTPases in hematopoiesis and hemopathiesTargeting Cdc42 in cancerGenome-wide meta-analyses identify three loci associated with primary biliary cirrhosisThe immunosenescence-related gene Zizimin2 is associated with early bone marrow B cell development and marginal zone B cell formation.Cdc42 is a key regulator of B cell differentiation and is required for antiviral humoral immunity.FcγRIIB and autoimmunity.RhoA of the Rho family small GTPases is essential for B lymphocyte development.New insights into the DT40 B cell receptor cluster using a proteomic proximity labeling assayDistinct roles of Cdc42 in thymopoiesis and effector and memory T cell differentiationCoordination of IL-7 receptor and T-cell receptor signaling by cell-division cycle 42 in T-cell homeostasis.How B cells capture, process and present antigens: a crucial role for cell polarity.Exacerbated experimental arthritis in Wiskott-Aldrich syndrome protein deficiency: modulatory role of regulatory B cellsSignaling role of Cdc42 in regulating mammalian physiology.ARAP3 functions in hematopoietic stem cellsRhof promotes murine marginal zone B cell developmentThe Rho GTPase Cdc42 Is Essential for the Activation and Function of Mature B Cells.Cdc42-dependent actin dynamics controls maturation and secretory activity of dendritic cellsNiche WNT5A regulates the actin cytoskeleton during regeneration of hematopoietic stem cellsSignal transduction pathways in chronic inflammatory autoimmune disease: small GTPases.B Cells use Conserved Polarity Cues to Regulate Their Antigen Processing and Presentation Functions.The Small Rho GTPase TC10 Modulates B Cell Immune Responses.Dual inhibition of histone deacetylases and phosphoinositide 3-kinases: effects on Burkitt lymphoma cell growth and migration.A Chemoattractant-Guided Walk Through Lymphopoiesis: From Hematopoietic Stem Cells to Mature B Lymphocytes.Deletion of Dock10 in B Cells Results in Normal Development but a Mild Deficiency upon In Vivo and In Vitro Stimulations.The Small Rho GTPases Rac1 and Rac2 Are Important for T-Cell Independent Antigen Responses and for Suppressing Switching to IgG2b in Mice.Tuning of in vivo cognate B-T cell interactions by Intersectin 2 is required for effective anti-viral B cell immunity.Bone Marrow Myeloid Cells Regulate Myeloid-Biased Hematopoietic Stem Cells via a Histamine-Dependent Feedback Loop.A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome.Involvement of Zizimin2/3 in the age-related defect of peritoneal B-1a cells as a source of anti-bacterial IgM.
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Rho GTPase Cdc42 is essential for B-lymphocyte development and activation.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 11 August 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Rho GTPase Cdc42 is essential for B-lymphocyte development and activation.
@en
Rho GTPase Cdc42 is essential for B-lymphocyte development and activation.
@nl
type
label
Rho GTPase Cdc42 is essential for B-lymphocyte development and activation.
@en
Rho GTPase Cdc42 is essential for B-lymphocyte development and activation.
@nl
prefLabel
Rho GTPase Cdc42 is essential for B-lymphocyte development and activation.
@en
Rho GTPase Cdc42 is essential for B-lymphocyte development and activation.
@nl
P2093
P2860
P1433
P1476
Rho GTPase Cdc42 is essential for B-lymphocyte development and activation
@en
P2093
Chinavenmeni S Velu
P2860
P304
P356
10.1182/BLOOD-2009-04-214676
P407
P577
2009-08-11T00:00:00Z