Search Results - "Peacock, M. G."

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  1. 1

    Lethal effect of Rickettsia rickettsii on its tick vector (Dermacentor andersoni) by NIEBYLSKI, M. L, PEACOCK, M. G, SCHWAN, T. G

    Published in Applied and environmental microbiology (01-02-1999)
    “…Rickettsia rickettsii, the causative agent of Rocky Mountain spotted fever, was lethal for the majority of experimentally and transovarially infected Rocky…”
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  2. 2

    Directional actin polymerization associated with spotted fever group Rickettsia infection of Vero cells by HEINZEN, R. A, HAYES, S. F, PEACOCK, M. G, HACKSTADT, T

    Published in Infection and Immunity (01-05-1993)
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  3. 3

    Characterization of an endosymbiont infecting wood ticks, Dermacentor andersoni, as a member of the genus Francisella by Niebylski, M.L, Peacock, M.G, Fischer, E.R, Porcella, S.F, Schwan, T.G

    Published in Applied and Environmental Microbiology (01-10-1997)
    “…A microorganism (Dermacantor andersoni symbiont [DAS]) infecting Rocky Mountain wood ticks (D. andersoni) collected in the Bitterroot Mountains of western…”
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  4. 4

    Evidence for proteolytic cleavage of the 120-kilodalton outer membrane protein of rickettsiae: identification of an avirulent mutant deficient in processing by HACKSTADT, T, MESSER, R, CIEPLAK, W, PEACOCK, M. G

    Published in Infection and Immunity (01-01-1992)
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  5. 5

    Chlamydia psittaci IncA is phosphorylated by the host cell and is exposed on the cytoplasmic face of the developing inclusion by Rockey, D. D., Grosenbach, D., Hruby, D. E., Peacock, M. G., Heinzen, R. A., Hackstadt, T.

    Published in Molecular microbiology (01-04-1997)
    “…Chlamydiae are obligate intracellular bacteria that replicate within a non‐acidified vacuole called an inclusion. Chlamydia psittaci (strain GPIC) produces a…”
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  6. 6

    Comparison of enzyme-linked immunosorbent assay and complement fixation and indirect fluorescent-antibody tests for detection of Coxiella burnetii antibody by PETER, O, DUPUIS, G, PEACOCK, M. G, BURGDORFER, W

    Published in Journal of Clinical Microbiology (01-06-1987)
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  7. 7

    Serological evaluation of Q fever in humans: enhanced phase I titers of immunoglobulins G and A are diagnostic for Q fever endocarditis by PEACOCK, M. G, PHILIP, R. N, WILLIAMS, J. C, FAULKNER, R. S

    Published in Infection and immunity (1983)
    “…Serological parameters were compared in 15 cases of C. burnetii infection comprising 5 cases each of primary Q fever, chronic granulomatous hepatitis, and…”
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  8. 8

    ADP-Ribosyltransferase Activity of Pertussis Toxin and Immunomodulation by Bordetella pertussis by Black, W. J., Munoz, J. J., Peacock, M. G., Schad, P. A., Cowell, J. L., Burchall, J. J., Lim, M., Kent, A., Steinman, L., Falkow, S.

    “…Pertussis toxin is produced by the causative agent of whooping cough, Bordetella pertussis, and is an adenosine diphosphate (ADP)-ribosyltransferase capable of…”
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  9. 9

    Improved plaque assays for Rickettsia prowazekii in Vero76 cells by POLICASTRO, P. F, PEACOCK, M. G, HACKSTADT, T

    Published in Journal of clinical microbiology (1996)
    “…Typhus group rickettsiae, including Rickettsia prowazekii and R. typhi, produce visible plaques on primary chick embryo fibroblasts and low-passage mouse…”
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  10. 10

    Lipopolysaccharide variation in Coxiella burnetii: intrastrain heterogeneity in structure and antigenicity by Hackstadt, T, Peacock, M G, Hitchcock, P J, Cole, R L

    Published in Infection and immunity (1985)
    “…The authors isolated lipopolysaccharides (LPSs) from phase variants of Coxiella burnetii Nine Mile and compared the isolated LPS and C. burnetii cells by…”
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  11. 11

    Anaphylaxis or so-called encephalopathy in mice sensitized to an antigen with the aid of pertussigen (pertussis toxin) by MUNOZ, J. J, PEACOCK, M. G, HADLOW, W. J

    Published in Infection and Immunity (01-04-1987)
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  12. 12

    Microimmunofluorescence test for the serological study of rocky mountain spotted fever and typhus by Philip, R N, Casper, E A, Ormsbee, R A, Peacock, M G, Burgdorfer, W

    Published in Journal of Clinical Microbiology (01-01-1976)
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  13. 13

    Immunological and biological characterization of Coxiella burnetii, phases I and II, separated from host components by Williams, J C, Peacock, M G, McCaul, T F

    Published in Infection and Immunity (01-05-1981)
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  14. 14

    Humoral immune response to Q fever: enzyme-linked immunosorbent assay antibody response to Coxiella burnetii in experimentally infected guinea pigs by Williams, J C, Thomas, L A, Peacock, M G

    Published in Journal of Clinical Microbiology (01-12-1986)
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  15. 15

    Action of pertussigen (pertussis toxin) on serum IgE and on Fc epsilon receptors on lymphocytes by Munoz, J J, Peacock, M G

    Published in Cellular immunology (01-05-1990)
    “…Pertussigen (pertussis toxin (PT] is one of the most effective stimulators of IgE production in mice and rats. Employing flow microfluorimetric analysis (FMF),…”
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  16. 16

    Biochemical and immunological properties of Coxiella burnetii cell wall and peptidoglycan-protein complex fractions by Amano, K, Williams, J C, McCaul, T F, Peacock, M G

    Published in Journal of Bacteriology (01-12-1984)
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  17. 17

    Monoclonal antibodies distinguish phase variants of Coxiella burnetii by WILLIAMS, J. C, JOHNSTON, M. R, PEACOCK, M. G, THOMAS, L. A, STEWART, S, PORTIS, J. L

    Published in Infection and Immunity (01-01-1984)
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  18. 18

    Expression of Pertussis Toxin Correlates with Pathogenesis in Bordetella Species by Monack, D., Munoz, J. J., Peacock, M. G., Black, W. J., Falkow, S.

    Published in The Journal of infectious diseases (01-02-1989)
    “…Pertussis toxin is a principal determinant of virulence produced by Bordetella pertussis in the disease whooping cough and is the primary toxinogenic component…”
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  19. 19
  20. 20

    Identification of phase-specific antigenic fractions of Coxiella burnetii by enzyme-linked immunosorbent assay by Williams, J C, Thomas, LA, Peacock, M G

    Published in Journal of clinical microbiology (1986)
    “…Antigenic fractions of C. burnetii phase variants were identified with an enzyme-linked immunosorbent assay (ELISA). Immune sera from guinea pigs immunized…”
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