Inactivation of Bacillus anthracis spores in murine primary macrophages. - Wikidata - awgldk - TriplyDB

Inactivation of Bacillus anthracis spores in murine primary macrophages.

Inactivation of Bacillus anthracis spores in murine primary macrophages.

http://www.wikidata.org/entity/Q40230053

about

Bacillus anthracis factors for phagosomal escape Structural Insights into Inhibition of Bacillus anthracis Sporulation by a Novel Class of Non-heme Globin Sensor Domains Advax-adjuvanted recombinant protective antigen provides protection against inhalational anthrax that is further enhanced by addition of murabutide adjuvant Detection of anthrax toxin by an ultrasensitive immunoassay using europium nanoparticles Capillary morphogenesis protein-2 is the major receptor mediating lethality of anthrax toxin in vivo.Updating perspectives on the initiation of Bacillus anthracis growth and dissemination through its host.Nod1/Nod2-mediated recognition plays a critical role in induction of adaptive immunity to anthrax after aerosol exposure.Antimicrobial effects of interferon-inducible CXC chemokines against Bacillus anthracis spores and bacilli.Transcriptional and apoptotic responses of THP-1 cells to challenge with toxigenic, and non-toxigenic Bacillus anthracis.Tracking bacterial infection of macrophages using a novel red-emission pH sensor.Anthrax toxin uptake by primary immune cells as determined with a lethal factor-beta-lactamase fusion protein.In vitro intracellular trafficking of virulence antigen during infection by Yersinia pestis.Bacillus anthracis spore entry into epithelial cells is an actin-dependent process requiring c-Src and PI3K.Inflammasome sensor Nlrp1b-dependent resistance to anthrax is mediated by caspase-1, IL-1 signaling and neutrophil recruitment.Bacillus anthracis spore interactions with mammalian cells: relationship between germination state and the outcome of in vitro Key tissue targets responsible for anthrax-toxin-induced lethality.Cathelicidin administration protects mice from Bacillus anthracis spore challenge MyD88-dependent signaling protects against anthrax lethal toxin-induced impairment of intestinal barrier function.Anthrax toxin targeting of myeloid cells through the CMG2 receptor is essential for establishment of Bacillus anthracis infections in mice.Anthrolysin O and fermentation products mediate the toxicity of Bacillus anthracis to lung epithelial cells under microaerobic conditions.Characterization of Bacillus anthracis persistence in vivo.Lipoprotein biosynthesis by prolipoprotein diacylglyceryl transferase is required for efficient spore germination and full virulence of Bacillus anthracis.Mouse monoclonal antibodies to anthrax edema factor protect against infection.Impact of spores on the comparative efficacies of five antibiotics for treatment of Bacillus anthracis in an in vitro hollow fiber pharmacodynamic model.Bacillus anthracis TIR Domain-Containing Protein Localises to Cellular Microtubule Structures and Induces Autophagy.Effects of endogenous D-alanine synthesis and autoinhibition of Bacillus anthracis germination on in vitro and in vivo infections Delayed treatment with W1-mAb, a chimpanzee-derived monoclonal antibody against protective antigen, reduces mortality from challenges with anthrax edema or lethal toxin in rats and with anthrax spores in mice.Treatment of experimental anthrax with recombinant capsule depolymerase Contribution of toxins to the pathogenesis of inhalational anthrax.Saccharides cross-reactive with Bacillus anthracis spore glycoprotein as an anthrax vaccine component High-throughput, single-cell analysis of macrophage interactions with fluorescently labeled Bacillus anthracis spores.In vivo demonstration and quantification of intracellular Bacillus anthracis in lung epithelial cells Bacillus anthracis: interactions with the host and establishment of inhalational anthrax.Inhibition of Bacillus anthracis spore outgrowth by nisin Bacillus anthracis Spore Surface Protein BclA Mediates Complement Factor H Binding to Spores and Promotes Spore Persistence Resistance of human alveolar macrophages to Bacillus anthracis lethal toxin Oral vaccine delivery by recombinant spore probiotics.Activation of the classical complement pathway by Bacillus anthracis is the primary mechanism for spore phagocytosis and involves the spore surface protein BclA.Potential dissemination of Bacillus anthracis utilizing human lung epithelial cells.Mitochondrial proteins Bnip3 and Bnip3L are involved in anthrax lethal toxin-induced macrophage cell death.

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P2860

Inactivation of Bacillus anthracis spores in murine primary macrophages.

http://www.wikidata.org/entity/Q40230053

description

2006 nî lūn-bûn

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2006年の論文

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2006年论文

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2006年论文

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2006年论文

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name

Inactivation of Bacillus anthracis spores in murine primary macrophages.

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Inactivation of Bacillus anthracis spores in murine primary macrophages.

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Inactivation of Bacillus anthracis spores in murine primary macrophages.

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J.1462-5822.2006.00738.X

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Cellular Microbiology

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Inactivation of Bacillus anthracis spores in murine primary macrophages.

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Arthur I Aronson

http://www.w3.org/2001/XMLSchema#string

Daoguo Zhou

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Haijing Hu

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Qila Sa

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Theresa M Koehler

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P2860

Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production

Anthrax toxin edema factor: a bacterial adenylate cyclase that increases cyclic AMP concentrations of eukaryotic cells

Rab7: a key to lysosome biogenesis

Germination of Bacillus anthracis spores within alveolar macrophages.

Capsule synthesis by Bacillus anthracis is required for dissemination in murine inhalation anthrax

Signaling during the invasion of host cells by Toxoplasma gondii.

Roles of macrophages and neutrophils in the early host response to Bacillus anthracis spores in a mouse model of infection.

Efficient Salmonella entry requires activity cycles of host ADF and cofilin.

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