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Journal Abstract Search

386 related items for PubMed ID: 3082264

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  • 2. Proteins of the cystic fibrosis respiratory tract. Fragmented immunoglobulin G opsonic antibody causing defective opsonophagocytosis.
    Fick RB, Naegel GP, Squier SU, Wood RE, Gee JB, Reynolds HY.
    J Clin Invest; 1984 Jul; 74(1):236-48. PubMed ID: 6429195
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  • 3. Association with phagocytic inhibition of anti-Pseudomonas aeruginosa immunoglobulin G antibody subclass levels in serum from patients with cystic fibrosis.
    Shryock TR, Mollé JS, Klinger JD, Thomassen MJ.
    J Clin Microbiol; 1986 Mar; 23(3):513-6. PubMed ID: 3082922
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  • 4. The immunoglobulin G subclass composition of immune complexes in cystic fibrosis. Implications for the pathogenesis of the Pseudomonas lung lesion.
    Hornick DB, Fick RB.
    J Clin Invest; 1990 Oct; 86(4):1285-92. PubMed ID: 2120286
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  • 5. Inhibition of the adherence of Pseudomonas aeruginosa to epithelial cells by IgG subclass antibodies.
    Morrin M, Reen DJ.
    J Med Microbiol; 1993 Dec; 39(6):459-66. PubMed ID: 8246266
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  • 11. IgG subclass antibodies to Pseudomonas aeruginosa in sera from patients with chronic Ps. aeruginosa infection investigated by ELISA.
    Pressler T, Pedersen SS, Espersen F, Høiby N, Koch C.
    Clin Exp Immunol; 1990 Sep; 81(3):428-34. PubMed ID: 2118845
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  • 13. Altered antibody isotype in cystic fibrosis: possible role in opsonic deficiency.
    Moss RB, Hsu YP, Sullivan MM, Lewiston NJ.
    Pediatr Res; 1986 May; 20(5):453-9. PubMed ID: 3714355
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  • 16. Pseudomonas respiratory infection in cystic fibrosis: a possible defect in opsonic IgG antibody?
    Fick RB, Reynolds HY.
    Bull Eur Physiopathol Respir; 1983 May; 19(2):151-61. PubMed ID: 6871494
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  • 17. IgG subclass responses to Pseudomonas aeruginosa a- and b-type flagellins in patients with cystic fibrosis: a prospective study.
    Lagacé J, Péloquin L, Kermani P, Montie TC.
    J Med Microbiol; 1995 Oct; 43(4):270-6. PubMed ID: 7562988
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  • 20. Specific IgG2 antibodies to Pseudomonas aeruginosa lipid A and lipopolysaccharide are early markers of chronic infection in patients with cystic fibrosis.
    Kronborg G, Pressler T, Fomsgaard A, Koch C, Høiby N.
    Infection; 1993 Oct; 21(5):297-302. PubMed ID: 8300245
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