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Pseudomonas aeruginosa infection in cystic fibrosis. Diagnostic and prognostic significance of Pseudomonas aeruginosa precipitins determined by means of crossed immunoelectrophoresis.
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Adherence of streptococcus pyogenes, Escherichia coli, and Pseudomonas aeruginosa to fibronectin-coated and uncoated epithelial cells.
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Modulation of surface CD11/CD18 glycoproteins (Mo1, LFA-1, p150,95) by human mononuclear phagocytes.
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In vitro inhibition of lymphocyte proliferation by Pseudomonas aeruginosa phenazine pigments.
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Inhibition of human natural killer cell activity by Pseudomonas aeruginosa alkaline protease and elastase.
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Leukotriene B4 production by the human alveolar macrophage: a potential mechanism for amplifying inflammation in the lung.
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Selective modulation of the CD4 molecular complex by Pseudomonas aeruginosa alkaline protease and elastase.
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Inhibitory effect of cystic fibrosis serum on pseudomonas phagocytosis by rabbit and human alveolar macrophages.
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Biochemical and pathologic evidence for proteolytic destruction of lung connective tissue in cystic fibrosis.
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Immunologic investigations of mucoid strains of Pseudomonas aeruginosa: comparison of susceptibility to opsonic antibody in mucoid and nonmucoid strains.
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Microbial elastases. A comparative study.
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Immune complexes and complement abnormalities in patients with cystic fibrosis. Increased mortality associated with circulating immune complexes and decreased function of the alternative complement pathway.
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Evidence for the presence of components of the alternative (properdin) pathway of complement activation in respiratory secretions.
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Cleavage of IgG by elastase-like protease (ELP) of human polymorphonuclear leukocytes (PMN): isolation and characterization of Fab and Fc fragments and low-molecular-weight peptides. Stimulation of granulocyte function by ELP-derived Fab and Fc fragments.
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Complement receptor expression on neutrophils at an inflammatory site, the Pseudomonas-infected lung in cystic fibrosis.
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Granulocyte neutral proteases and Pseudomonas elastase as possible causes of airway damage in patients with cystic fibrosis.
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Cystic fibrosis pseudomonas opsonins. Inhibitory nature in an in vitro phagocytic assay.
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N Engl J Med. 1988 Aug 11;319(6):338-43
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Inhibition of human lymphocyte proliferation and cleavage of interleukin-2 by Pseudomonas aeruginosa proteases.
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Opsonic defect in patients with cystic fibrosis of the pancreas.
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Analysis of proteins and respiratory cells obtained from human lungs by bronchial lavage.
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