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1 epidemiologic risk factor for acquisition of Blastomyces.
4 nary isolates of B. helicus identified among Blastomyces and Emmonsia isolates at the University of A
5 f the high level of cross-reactivity between Blastomyces and Histoplasma antigen EIAs, utilization of
8 were not resolved and the nearest outgroups (Blastomyces and Paracoccidioides) were too distant to un
9 e assessed performance of the Gotham BioTech Blastomyces antigen (GBA) enzyme immunoassay (EIA) (Port
11 lysis of 3,529 patients with Histoplasma and Blastomyces antigen testing performed on the same serum
13 or five major fungal pathogens: Aspergillus, Blastomyces, Coccidioides, Cryptococcus, and Histoplasma
14 United States-Histoplasma, Coccidioides, and Blastomyces-commonly known as endemic mycoses of North A
15 ew assay permitted retrospective analysis of Blastomyces cultures and primary clinical specimens from
17 ed by O-mannans decorating the C terminus of Blastomyces Dectin-2 ligand endoglucanase 2, can augment
18 fungal pulmonary infections with two agents, Blastomyces dermatitidis an extracellular pathogen, and
19 D4(+) T cells respond to a native epitope in Blastomyces dermatitidis and also in Histoplasma capsula
22 disease known in North America and caused by Blastomyces dermatitidis and Blastomyces gilchristii.
26 dhesin is indispensable for pathogenicity of Blastomyces dermatitidis and is thought to promote pulmo
27 g of the molecular bases of pathogenicity in Blastomyces dermatitidis and related systemic dimorphic
30 inically important discrepancy was observed (Blastomyces dermatitidis by culture and Cryptococcus neo
31 40/CD40L interactions in vaccine immunity to Blastomyces dermatitidis by immunizing CD40(-/-) and CD4
33 cally engineered, live, attenuated strain of Blastomyces dermatitidis carrying a targeted deletion at
34 e (3-week-old) mice killed nonphagocytizable Blastomyces dermatitidis cells less (25%) than did cells
36 ast cytosol extract (YCE) crude antigen from Blastomyces dermatitidis confers T-cell-mediated resista
37 in South Africa between 1967 and 2014, with Blastomyces dermatitidis considered to be the etiologica
38 ld was found to be positive by the AccuProbe Blastomyces dermatitidis Culture ID Test (Gen-Probe Inc.
40 Humans infected with the dimorphic fungus Blastomyces dermatitidis develop strong T-lymphocyte res
47 (Portland, ME) for quantitative detection of Blastomyces dermatitidis galactomannan (GM) in urine usi
48 genetically engineered attenuated strain of Blastomyces dermatitidis given s.c. as a vaccine, wherea
49 tools available for genetic manipulation of Blastomyces dermatitidis have enhanced our ability to st
50 vaccines to induce protection against lethal Blastomyces dermatitidis infection in mice and is far mo
55 ulmonary infection with the dimorphic fungus Blastomyces dermatitidis often progresses and requires t
57 R senses mannan on the surface of attenuated Blastomyces dermatitidis vaccine yeast and that MR(-/-)
58 found that serum inhibitory activity against Blastomyces dermatitidis was principally mediated by alb
60 emory after vaccination with transgenic (Tg) Blastomyces dermatitidis yeasts that display a model Ag,
61 oides posadasii, Histoplasma capsulatum, and Blastomyces dermatitidis), have soared recently, spurrin
63 f serum factors or MBL on the interaction of Blastomyces dermatitidis, a pulmonary fungal pathogen, w
64 gi Histoplasma capsulatum, Coccidioides spp, Blastomyces dermatitidis, and Paracoccidioides brasilien
65 role in phagocyte recognition and killing of Blastomyces dermatitidis, but little is known about how
66 igatus, Aspergillus terreus, Bipolaris spp., Blastomyces dermatitidis, Cladophialophora bantiana, Fus
67 to amplify DNA from Histoplasma capsulatum, Blastomyces dermatitidis, Coccidioides immitis, Paracocc
68 , a virulence factor in the dimorphic fungus Blastomyces dermatitidis, for expression in yeast and my
69 Blastomyces adhesin 1), a 120-kDa protein of Blastomyces dermatitidis, functions as an adhesin, immun
70 Pseudallescheria boydii, Rhizopus arrhizus, Blastomyces dermatitidis, Histoplasma capsulatum, and Sp
71 BAD1, an adhesin and immune modulator of Blastomyces dermatitidis, is an essential virulence fact
73 ved in specimens from patients infected with Blastomyces dermatitidis, Paracoccidioides brasiliensis,
76 nsia crescens, an agent of adiaspiromycosis, Blastomyces dermatitidis, the agent of blastomycosis, an
78 on caused by the soil-based dimorphic fungus Blastomyces dermatitidis, which is endemic throughout mu
88 asexualis isolates also resulted in positive Blastomyces DNA probe results, while Spiromastigoides sp
90 %), from 8 countries throughout all regions; Blastomyces emzantsi (n = 9, 26%), from South Africa; B.
92 All sequenced isolates were identified as Blastomyces gilchristii and clustered into a distinct ou
93 omycosis due to Blastomyces dermatitidis and Blastomyces gilchristii is a significant cause of respir
94 elated to but distinct from B. dermatitidis, Blastomyces gilchristii, and Blastomyces parvus The firs
102 . dermatitidis, Blastomyces gilchristii, and Blastomyces parvus The first group (n = 12) corresponded
103 yped case isolates that comprised 4 species: Blastomyces percursus (n = 22, 65%), from 8 countries th
104 rresponded to the recently described species Blastomyces percursus, and the other (n = 8) is describe
106 an enzyme immunoassay (EIA) compared to the Blastomyces quantitative EIA from MiraVista Diagnostics