نتایج جستجو برای: wiskott

تعداد نتایج: 1772  

Journal: :Indian Journal of Trauma and Emergency Pediatrics 2020

Journal: :LymphoSign journal 2021

Background: Wiskott-Aldrich syndrome (WAS) is an X-linked recessive disorder associated with combined immunodeficiency, microthrombocytopenia, eczema, and increased risk of autoimmunity cancer. Aim: To report the clinical presentation, immune features, genetic mutation in a patient novel gene, causing mild phenotype WAS. Methods: The patient’s chart was reviewed. We phenotypical laboratory char...

Journal: :Physical review. E, Statistical, nonlinear, and soft matter physics 2007
Shannon F Stewman Aaron R Dinner

We introduce a stochastic approach for self-assembly in systems far from equilibrium. The building blocks are represented by a lattice of discrete variables (Potts-like spins), and physically meaningful mechanisms are obtained by restricting transitions through spatially local rules based on experimental data. We use the method to study nucleation of filopodia-like bundles in a system consistin...

Journal: :Cell 2004
Hsin-Yi Henry Ho Rajat Rohatgi Andres M Lebensohn Le Ma Jiaxu Li Steven P Gygi Marc W Kirschner

An important signaling pathway to the actin cytoskeleton links the Rho family GTPase Cdc42 to the actin-nucleating Arp2/3 complex through N-WASP. Nevertheless, these previously identified components are not sufficient to mediate Cdc42-induced actin polymerization in a physiological context. In this paper, we describe the biochemical purification of Toca-1 (transducer of Cdc42-dependent actin as...

2006
Hsiu-Chuan Chou Inés M. Antón Mark R. Holt Claudia Curcio Stefania Lanzardo Austen Worth Siobhan Burns Adrian J. Thrasher Gareth E. Jones Yolanda Calle

The Wiskott-Aldrich Syndrome protein (WASP) is an adaptor protein that is essential for podosome formation in hematopoietic cells. Given that 80% of identified Wiskott-Aldrich Syndrome patients result from mutations in the binding site for WASP-interacting-protein (WIP), we examined the possible role of WIP in the regulation of podosome architecture and cell motility in dendritic cells (DCs). O...

Journal: :Science 2001
N Volkmann K J Amann S Stoilova-McPhie C Egile D C Winter L Hazelwood J E Heuser R Li T D Pollard D Hanein

The seven-subunit Arp2/3 complex choreographs the formation of branched actin networks at the leading edge of migrating cells. When activated by Wiskott-Aldrich Syndrome protein (WASp), the Arp2/3 complex initiates actin filament branches from the sides of existing filaments. Electron cryomicroscopy and three-dimensional reconstruction of Acanthamoeba castellanii and Saccharomyces cerevisiae Ar...

2013
Matthias Spiess Johan-Owen de Craene Alphée Michelot Bruno Rinaldi Aline Huber David G. Drubin Barbara Winsor Sylvie Friant

The spatial and temporal regulation of actin polymerization is crucial for various cellular processes. Members of the Wiskott-Aldrich syndrome protein (WASP) family activate the Arp2/3-complex leading to actin polymerization. The yeast Saccharomyces cerevisiae contains only one WASP homolog, Las17, that requires additional factors for its regulation. Lsb1 and Lsb2/Pin3 are two yeast homologous ...

Journal: :Molecular biology of the cell 2007
Anne Chabadel Inmaculada Bañon-Rodríguez David Cluet Brian B Rudkin Bernhard Wehrle-Haller Elisabeth Genot Pierre Jurdic Ines M Anton Frédéric Saltel

The actin cytoskeleton of mature osteoclasts (OCs) adhering to nonmineralized substrates is organized in a belt of podosomes reminiscent of the sealing zone (SZ) found in bone resorbing OCs. In this study, we demonstrate that the belt is composed of two functionally different actin-based domains: podosome cores linked with CD44, which are involved in cell adhesion, and a diffuse cloud associate...

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