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The Neutrophil Btk Signalosome Regulates Integrin Activation during Sterile Inflammation

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Immunodeficiency and severe susceptibility to bacterial infection associated with a loss-of-function homozygous mutation of MKL1

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The antimicrobial propeptide hCAP-18 plasma levels in neutropenia of various aetiologies: a prospective study

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Cell Surface Topography Is a Regulator of Molecular Interactions during Chemokine-Induced Neutrophil Spreading

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Actin cytoskeletal defects in immunodeficiency

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Homeostatic Regulation of Blood Neutrophil Counts

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Congenital Defects in Neutrophil Dynamics

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Animal Models of Human Granulocyte Diseases

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Leukocyte Adhesion Deficiencies

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De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome

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Fiji: an open-source platform for biological-image analysis

(2012) Johannes Schindelin et al.   NATURE METHODS

Critical Roles of the WASP N-Terminal Domain and Btk in LPS-Induced Inflammatory Response in Macrophages

(2012) Chisato Sakuma et al.   PLoS One

Genetic Defects in Severe Congenital Neutropenia: Emerging Insights into Life and Death of Human Neutrophil Granulocytes

(2011) Christoph Klein   Annual Review of Immunology

Activating WASP mutations associated with X-linked neutropenia result in enhanced actin polymerization, altered cytoskeletal responses, and genomic instability in lymphocytes

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Lifeact mice for studying F-actin dynamics

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Cdc42 Regulates Fcγ Receptor-mediated Phagocytosis through the Activation and Phosphorylation of Wiskott-Aldrich Syndrome Protein (WASP) and Neural-WASP

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The Many Causes of Severe Congenital Neutropenia

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Phosphorylation of WASp is a key regulator of activity and stability in vivo

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A large kindred with X-linked neutropenia with an I294T mutation of the Wiskott-Aldrich syndrome gene

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