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3 were not resolved and the nearest outgroups (Blastomyces and Paracoccidioides) were too distant to un
4 fungal pulmonary infections with two agents, Blastomyces dermatitidis an extracellular pathogen, and
5 D4(+) T cells respond to a native epitope in Blastomyces dermatitidis and also in Histoplasma capsula
8 dhesin is indispensable for pathogenicity of Blastomyces dermatitidis and is thought to promote pulmo
9 g of the molecular bases of pathogenicity in Blastomyces dermatitidis and related systemic dimorphic
12 inically important discrepancy was observed (Blastomyces dermatitidis by culture and Cryptococcus neo
13 40/CD40L interactions in vaccine immunity to Blastomyces dermatitidis by immunizing CD40(-/-) and CD4
15 cally engineered, live, attenuated strain of Blastomyces dermatitidis carrying a targeted deletion at
16 e (3-week-old) mice killed nonphagocytizable Blastomyces dermatitidis cells less (25%) than did cells
18 ast cytosol extract (YCE) crude antigen from Blastomyces dermatitidis confers T-cell-mediated resista
19 ld was found to be positive by the AccuProbe Blastomyces dermatitidis Culture ID Test (Gen-Probe Inc.
21 Humans infected with the dimorphic fungus Blastomyces dermatitidis develop strong T-lymphocyte res
27 genetically engineered attenuated strain of Blastomyces dermatitidis given s.c. as a vaccine, wherea
28 tools available for genetic manipulation of Blastomyces dermatitidis have enhanced our ability to st
29 vaccines to induce protection against lethal Blastomyces dermatitidis infection in mice and is far mo
34 ulmonary infection with the dimorphic fungus Blastomyces dermatitidis often progresses and requires t
36 R senses mannan on the surface of attenuated Blastomyces dermatitidis vaccine yeast and that MR(-/-)
37 found that serum inhibitory activity against Blastomyces dermatitidis was principally mediated by alb
39 emory after vaccination with transgenic (Tg) Blastomyces dermatitidis yeasts that display a model Ag,
40 oides posadasii, Histoplasma capsulatum, and Blastomyces dermatitidis), have soared recently, spurrin
42 f serum factors or MBL on the interaction of Blastomyces dermatitidis, a pulmonary fungal pathogen, w
43 gi Histoplasma capsulatum, Coccidioides spp, Blastomyces dermatitidis, and Paracoccidioides brasilien
44 role in phagocyte recognition and killing of Blastomyces dermatitidis, but little is known about how
45 igatus, Aspergillus terreus, Bipolaris spp., Blastomyces dermatitidis, Cladophialophora bantiana, Fus
46 to amplify DNA from Histoplasma capsulatum, Blastomyces dermatitidis, Coccidioides immitis, Paracocc
47 , a virulence factor in the dimorphic fungus Blastomyces dermatitidis, for expression in yeast and my
48 Blastomyces adhesin 1), a 120-kDa protein of Blastomyces dermatitidis, functions as an adhesin, immun
49 Pseudallescheria boydii, Rhizopus arrhizus, Blastomyces dermatitidis, Histoplasma capsulatum, and Sp
50 BAD1, an adhesin and immune modulator of Blastomyces dermatitidis, is an essential virulence fact
52 ved in specimens from patients infected with Blastomyces dermatitidis, Paracoccidioides brasiliensis,
55 nsia crescens, an agent of adiaspiromycosis, Blastomyces dermatitidis, the agent of blastomycosis, an
57 on caused by the soil-based dimorphic fungus Blastomyces dermatitidis, which is endemic throughout mu
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