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1 m smegmatis , Mycobacterium tuberculosis and bacille Calmette-Guerin.
2 ce and C57BL/6 mice previously infected with bacille Calmette-Guerin.
3 ination of 10 of these 19 patients with live bacille Calmette-Guerin.
4 in or for those who cannot be immunized with bacille Calmette-Guerin.
5 h superficial bladder cancer who have failed bacille Calmette-Guerin.
6 autologous, DNP-modified vaccine mixed with bacille Calmette-Guerin.
7 acteria such as M. tuberculosis and M. bovis Bacille-Calmette-Guerin.
8 od to restrict growth of Mycobacterium bovis bacille Calmette Guerin and Mycobacterium tuberculosis w
9 n vitro activity against Mycobacterium bovis bacille Calmette-Guerin and virulent M. tuberculosis.
11 s to study the uptake of Mycobacterium bovis bacille Calmette Guerin (BCG) into murine macrophages.
13 from tuberculosis every year even though the bacille Calmette Guerin (BCG) vaccine has been available
14 ed as an intravesical agent in patients with bacille Calmette-Guerin (BCG) -refractory transitional c
15 led whole-promastigote vaccine cocktail plus bacille Calmette-Guerin (BCG) adjuvant significantly red
16 rget (ESAT)-6, that are absent from M. bovis bacille Calmette-Guerin (BCG) and most environmental myc
17 ow-growing mycobacteria, Mycobacterium bovis bacille Calmette-Guerin (BCG) and Mycobacterium avium, b
18 A human mycobacterial challenge model, using bacille Calmette-Guerin (BCG) as a surrogate for a Mycob
21 uated strain of Mycobacterium bovis known as bacille Calmette-Guerin (BCG) has been widely used as a
24 tify immune correlates of TB disease risk in Bacille Calmette-Guerin (BCG) immunized infants from the
25 CD8 T cells specific to Mycobacterium bovis bacille Calmette-Guerin (BCG) in the lungs, and the IFN-
28 obacterium smegmatis and Mycobacterium bovis bacille Calmette-Guerin (BCG) in which a very high propo
29 d major expansion during Mycobacterium bovis Bacille Calmette-Guerin (BCG) infection and a clear memo
30 th T cells responding to Mycobacterium bovis bacille Calmette-Guerin (BCG) infection and disrupt gran
35 urrently available vaccine for tuberculosis, bacille Calmette-Guerin (BCG) is the most widely used va
36 o, pleural mesothelial cells stimulated with bacille Calmette-Guerin (BCG) or interferon (IFN)-gamma
37 with IGRAs in individuals with a history of Bacille Calmette-Guerin (BCG) vaccination after infancy
38 sate to detect antibody responses induced by bacille Calmette-Guerin (BCG) vaccination and active tub
39 sessed using intradermal Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccination as a surrogate
40 ction with environmental mycobacteria and/or bacille Calmette-Guerin (BCG) vaccination compromise the
45 bacterial Ags in the context of experimental bacille Calmette-Guerin (BCG) vaccination, Ag-specific T
49 tection conferred by the Mycobacterium bovis bacille Calmette-Guerin (BCG) vaccine are multifaceted a
52 The existence of therapeutic agents and the bacille Calmette-Guerin (BCG) vaccine have not significa
53 er (250 days) than mice infected with either bacille Calmette-Guerin (BCG) vaccine or virulent M. tub
55 whole-cell melanoma vaccine, Canvaxin, plus Bacille Calmette-Guerin (BCG) versus placebo plus BCG.
56 )mac-infected macaques previously exposed to bacille Calmette-Guerin (BCG) were reinfected with BCG,
57 radiated autologous tumor cells admixed with bacille Calmette-Guerin (BCG) were used to vaccinate pat
62 is expressed in M. tuberculosis and M. bovis Bacille Calmette-Guerin (BCG), using reverse transcripti
63 obacterium smegmatis and Mycobacterium bovis bacille Calmette-Guerin (BCG), which respectively induce
64 rus of macaques (SIVmac)/Mycobacterium bovis bacille Calmette-Guerin (BCG)-coinfected macaque model.
65 an immunodeficiency virus (HIV)-infected and bacille Calmette-Guerin (BCG)-immunized adults with CD4
66 tuberculosis Ag 85A (M.85A), strongly boosts bacille Calmette-Guerin (BCG)-induced Ag 85A specific CD
67 ial protection in Mycobacterium bovis strain bacille Calmette-Guerin (BCG)-induced granulomas using a
69 N-gamma-secreting T cells when used alone in bacille Calmette-Guerin (BCG)-naive healthy volunteers.
70 cterium bovis bloodstream infection (BSI) in bacille Calmette-Guerin (BCG)-vaccinated children with h
79 ts were vaccinated with one of four doses of bacille Calmette-Guerin (BCG): The doses contained very
80 45 countries was 2.3 weeks (IQR 1.4-4.6) for bacille Calmette-Guerin (BCG); 2.4 weeks (1.2-3.3) for d
85 esus monkeys were immunized with recombinant bacille Calmette-Guerin expressing the full-length measl
86 toplasmically into macrophages infected with bacille Calmette-Guerin expressing the green fluorescent
90 infected with Mycobacterium tuberculosis or bacille Calmette-Guerin have been shown to facilitate pr
93 Mycobacterium tuberculosis vaccines to boost bacille Calmette-Guerin or for those who cannot be immun
94 nstrate that exposure of Mycobacterium bovis Bacille Calmette-Guerin or Mycobacterium marinum to thia
95 cells within hepatic granulomas triggered by Bacille Calmette-Guerin or Mycobacterium tuberculosis.
96 induced by infection with M. tuberculosis or bacille Calmette-Guerin, or treatment with LPS or TNF-al
97 vaccination involves the use of recombinant bacille Calmette-Guerin (rBCG) overexpressing protective
98 troduced and existing ones improved to treat bacille Calmette-Guerin-refractory superficial bladder c
99 cterium tuberculosis and Mycobacterium bovis bacille Calmette-Guerin, release MVs when growing in bot
101 tients who receive intravesical therapy with bacille Calmette-Guerin should be considered for ongoing
102 cterium tuberculosis and Mycobacterium bovis bacille Calmette-Guerin similarly home to established gr
103 acterial antigens shown previously to induce bacille Calmette-Guerin-specific gammadelta T cells.
104 chronic medical illness, isoniazid use, and bacille Calmette-Guerin strain did not substantially aff
106 candidate, M72/AS01, in a phase IIa trial of bacille Calmette-Guerin-vaccinated, HIV-uninfected, and
107 eactivity to nontuberculous mycobacteria and bacille Calmette-Guerin vaccination may account for a pr
111 fers poor specificity in those receiving the bacille Calmette-Guerin vaccine and poor sensitivity in
113 d, controlled trials of the effectiveness of bacille Calmette-Guerin vaccine in preventing active tub
117 inguish exposure to M. tuberculosis from the Bacille-Calmette-Guerin vaccine strain, they currently l
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