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1 asthma (mice sensitized and challenged with aspergillus fumigatus).
2 unocompromised individuals that is caused by Aspergillus fumigatus.
3 ignated PerA, in the human pathogenic fungus Aspergillus fumigatus.
4 moderately active against a third pathogen, Aspergillus fumigatus.
5 irulence in the human opportunistic pathogen Aspergillus fumigatus.
6 of Ascomycota, including the human pathogen Aspergillus fumigatus.
7 oxygenase that is essential for virulence in Aspergillus fumigatus.
8 se (NRPS) gene cluster in the human pathogen Aspergillus fumigatus.
9 from this motif in a subtelomeric region of Aspergillus fumigatus.
10 rates within host cells and protects against Aspergillus fumigatus.
11 ion of SUN proteins in a filamentous fungus, Aspergillus fumigatus.
12 ampen the immune response against chitin and Aspergillus fumigatus.
13 l community to understand the human pathogen Aspergillus fumigatus.
14 nd an extended fungal panel; specific IgE to Aspergillus fumigatus.
15 gulators in the opportunistic human pathogen Aspergillus fumigatus.
16 terium Pseudomonas aeruginosa and the fungus Aspergillus fumigatus.
17 ure of the corneal scrapes were positive for aspergillus fumigatus.
18 infection with the invasive fungal pathogen Aspergillus fumigatus.
19 506, individually and in combination against Aspergillus fumigatus.
20 le species, the opportunistic human pathogen Aspergillus fumigatus.
21 irulence of the opportunistic human pathogen Aspergillus fumigatus.
22 ine monooxygenase from the pathogenic fungus Aspergillus fumigatus.
23 Netherlands might harbor triazole-resistant Aspergillus fumigatus.
24 Also, we have expanded prior ECV data for Aspergillus fumigatus.
25 es of Mucorales, but not Candida albicans or Aspergillus fumigatus.
26 pportunistic mold Aspergillus, most commonly Aspergillus fumigatus.
27 s (IA), a life-threatening disease caused by Aspergillus fumigatus.
28 ogenic fungi, including Candida albicans and Aspergillus fumigatus.
29 larly those caused by the opportunistic mold Aspergillus fumigatus.
30 disease progression between N. udagawae and Aspergillus fumigatus.
31 n by Df, Dermatophagoides pteronyssinus, and Aspergillus fumigatus.
32 es against the opportunistic fungal pathogen Aspergillus fumigatus.
33 infectious agents Listeria monocytogenes and Aspergillus fumigatus.
34 lycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus.
35 sults were available in 1 patient and showed Aspergillus fumigatus.
36 cluster in the opportunistic human pathogen Aspergillus fumigatus.
37 essential role in antifungal defense against Aspergillus fumigatus.
38 5 null (5) or Asp f 13 null (13) strains of Aspergillus fumigatus.
39 zed by an allergic immunological response to Aspergillus fumigatus.
41 hogens, including real-time visualization of Aspergillus fumigatus (5 d for culturing, 1-2 d for imag
43 sized that prenatal exposure of mice (F0) to Aspergillus fumigatus (A. fumigatus) would be associated
46 rate immune responses against fungi, such as Aspergillus fumigatus, a major fungal pathogen in humans
47 exposed to spores of the environmental mould Aspergillus fumigatus, a major opportunistic pathogen.
51 and validated with 131 clinical isolates of Aspergillus fumigatus, A. flavus, A. niger, A. terreus,
52 mon medically important Aspergillus species (Aspergillus fumigatus, A. flavus, A. niger, and A. terre
53 n the basis of morphological features (e.g., Aspergillus fumigatus, A. lentulus, and Neosartorya udag
56 from the ergot biosynthetic gene cluster of Aspergillus fumigatus acts on chanoclavine-I aldehyde 1
58 vely low challenge doses with the conidia of Aspergillus fumigatus administered to recombinase activa
59 HDM-exposed mothers, the magnitude of HDM or Aspergillus fumigatus (AF) extract-induced airway hyperr
60 of FasL expression in airway eosinophilia in Aspergillus fumigatus (Af)-induced sensitization and to
63 ing module in the fumiquinazoline A producer Aspergillus fumigatus Af293 as well as a second anthrani
68 relevant fungi such as Candida albicans and Aspergillus fumigatus also form biofilms during infectio
69 and IgA reactivity to whole extract fungal (Aspergillus fumigatus, Alternaria alternata, Cryptococcu
70 gE or skin prick test response positivity to Aspergillus fumigatus, Alternaria alternata, or Cladospo
75 se against the opportunistic fungal pathogen Aspergillus fumigatus and are believed to be essential f
77 d a direct pH-dependent antifungal effect on Aspergillus fumigatus and Aspergillus nidulans; it incre
79 at infection with the human pathogenic fungi Aspergillus fumigatus and Candida albicans induces a dis
83 Azole resistance is an emerging problem in Aspergillus fumigatus and complicates the management of
84 scaffold, which showed high activity toward Aspergillus fumigatus and Cryptococcus neoformans at aci
85 en demonstrated against the fungal pathogens Aspergillus fumigatus and Cryptococcus neoformans, littl
86 s, caused most commonly by Candida albicans, Aspergillus fumigatus and Cryptococcus neoformans, resul
87 ad of agriculturally derived azole-resistant Aspergillus fumigatus and emerging threats such as multi
88 onse to alpha-(1,3)-glucan polysaccharide of Aspergillus fumigatus and ensuing CD4+ T-cell polarizati
89 lungs of mice sensitized and challenged with Aspergillus fumigatus and evaluated ex vivo in tissue cu
90 cy of pH- and calcium-mediated signalling in Aspergillus fumigatus and found that calcium chelation s
91 d juvenile Scnn1b-Tg and wild-type mice with Aspergillus fumigatus and house dust mite allergen and c
92 ue of 0.60 +/- 0.05 muM and to the NMOs from Aspergillus fumigatus and Mycobacterium smegmatis with K
95 ides produced by the opportunistic pathogens Aspergillus fumigatus and Pseudomonas aeruginosa, respec
97 identified in some fungal organisms, such as Aspergillus fumigatus and Schizosaccharomyces pombe, and
98 ere highly susceptible to aeroallergens from Aspergillus fumigatus and the house dust mite, resulting
99 onditions may result from the interaction of Aspergillus fumigatus and the immune system of its human
104 hreatening lung disease caused by the fungus Aspergillus fumigatus, and is a leading cause of invasiv
105 cluding Pseudomonas aeruginosa, Haemophilus, Aspergillus fumigatus, and nontuberculous mycobacteria.
106 ed literature about Aspergillus nidulans and Aspergillus fumigatus, and this annotation is provided w
107 cinetobacter baumannii, Candida albicans, or Aspergillus fumigatus; and treated intraperitoneally wit
110 entrations of Alternaria alternata allergen, Aspergillus fumigatus antigens, house dust mite and endo
111 Infections caused by triazole-resistant Aspergillus fumigatus are associated with a higher proba
112 breakthrough infections with fungal pathogen Aspergillus fumigatus are associated with caspofungin pr
114 llergens including Asp f 5 and Asp f 13 from Aspergillus fumigatus are thought to be important for in
116 acoccidioides brasiliensis, and occasionally Aspergillus fumigatus, are primary pulmonary pathogens o
117 and Candida krusei) or a mold 11-plex panel (Aspergillus fumigatus, Aspergillus flavus, Aspergillus n
118 us isolated from the human pathogenic fungus Aspergillus fumigatus, Aspergillus fumigatus tetramycovi
119 compared patterns of beta-glucan exposure in Aspergillus fumigatus, Aspergillus terreus, Rhizopus ory
120 molds (Paecilomyces variotii ATCC MYA-3630, Aspergillus fumigatus ATCC MYA-3626, A. flavus ATCC MYA-
121 rways of otherwise naive mice in response to Aspergillus fumigatus, but not ovalbumin sensitization a
122 the metabolic outcome of an interaction with Aspergillus fumigatus by influencing triacetylfusarinine
125 In susceptible individuals, exposure to Aspergillus fumigatus can lead to the development of ato
127 d 2008-2011, respectively; P=0.018), whereas Aspergillus fumigatus cases decreased (73.9/1000 vs. 49.
128 S (7-dimethylallyl tryptophan synthase) from Aspergillus fumigatus catalyze C(4)- and C(7)-prenylatio
133 traction, and lung inflammation in naive and Aspergillus fumigatus-challenged wild-type and Rgs5(-/-)
134 The most common fungus in asthmatics was Aspergillus fumigatus complex and this taxon accounted f
137 T) formation, are involved in the killing of Aspergillus fumigatus conidia and hyphae, using neutroph
138 mice were challenged with resting or swollen Aspergillus fumigatus conidia and monitored for survival
139 blished a correlation between high levels of Aspergillus fumigatus conidia and the appearance of new
140 strated that repeated intranasal exposure to Aspergillus fumigatus conidia in C57BL/6 mice results in
141 In this study, we demonstrate that uptake of Aspergillus fumigatus conidia induced drastic spatial re
142 operties of the human opportunistic pathogen Aspergillus fumigatus conidia is essential given the imp
143 e of healthy C57BL/6 mice to viable, resting Aspergillus fumigatus conidia leads to the development o
145 d cell death with apoptosis-like features in Aspergillus fumigatus conidia, the most prevalent human
148 derived metabolites differentially modulated Aspergillus fumigatus development, shifting from weak ve
151 Here we report a fluorogenic probe to image Aspergillus fumigatus directly in human pulmonary tissue
152 elevance of the SeptiFast assay in detecting Aspergillus fumigatus DNA in whole blood samples from 38
157 omologue of Old Yellow Enzyme encoded in the Aspergillus fumigatus ergot gene cluster catalyzes reduc
158 ack peripheral B cells) were sensitized with Aspergillus fumigatus extract and challenged with two in
159 ermatitis, we examined the effect of topical Aspergillus fumigatus extract exposure in wild-type and
160 In this study, we show that inhalation of Aspergillus fumigatus extract in mice induced a dramatic
164 with chronic granulomatous disease (CGD) is Aspergillus fumigatus followed by A. nidulans; other asp
165 ms to report a case of fungal keratitis with aspergillus fumigatus following ICRS implantation for co
167 ed and validated for rapid identification of Aspergillus fumigatus from the other species within the
169 serum samples spiked with various amounts of Aspergillus fumigatus genomic DNA was distributed to 23
170 rdingly, beta-glucan surface exposure during Aspergillus fumigatus germination activates an Atg5-depe
172 tandardized protocol for extracting DNA from Aspergillus fumigatus has been proposed by the European
173 innate responses to the major mold pathogen Aspergillus fumigatus has been restricted to specialized
177 ndida albicans, Cryptococcus neoformans, and Aspergillus fumigatus have transitioned from a rare curi
178 llosis, an infection caused predominantly by Aspergillus fumigatus, have increased due to the growing
179 VEGF reversed the antiangiogenic activity of Aspergillus fumigatus; however, VEGF induced the formati
180 /-) mice have an impaired ability to inhibit Aspergillus fumigatus hyphal growth in vitro and in infe
181 rologic tests (ImmunoCap total IgE, specific Aspergillus fumigatus IgE, and specific A fumigatus IgG)
182 st defense against Staphylococcus aureus and Aspergillus fumigatus in a murine X-linked gp91phox-defi
183 of persistent neutrophilic meningitis due to Aspergillus fumigatus in an immunocompetent man who had
187 al for survival of the fungal human pathogen Aspergillus fumigatus in the immunocompromised host lung
188 mmune defense against the opportunistic mold Aspergillus fumigatus In this study, we investigated the
189 CD11c(+) cells and controls Th2 responses to Aspergillus fumigatus in vitro in cystic fibrosis (CF) p
191 or pathways involved in innate resistance to Aspergillus fumigatus, including complement activation o
192 been shown to suppress house dust mite- and Aspergillus fumigatus-induced allergic inflammation in m
193 6 mediates this effect using mouse models of Aspergillus fumigatus-induced and house dust mite antige
202 pergillosis (IA) resulting from infection by Aspergillus fumigatus is a leading cause of death in imm
215 the protection against fungal infections by Aspergillus fumigatus is essential but not fully underst
218 iods, and infection with the ubiquitous mold Aspergillus fumigatus is responsible for most cases of a
221 Fumitremorgin B endoperoxidase (FtmOx1) from Aspergillus fumigatus is the first reported alpha-ketogl
227 Here we show that purified afTMEM16, from Aspergillus fumigatus, is a dual-function protein: it is
228 Sensitization to fungi, such as the mold Aspergillus fumigatus, is increasingly becoming linked w
230 ulence factor of the human pathogenic fungus Aspergillus fumigatus, is the prototype of epipoly(thiod
233 illus species as well as azole resistance in Aspergillus fumigatus Its performance has been validated
234 ctin-1 displayed increased susceptibility to Aspergillus fumigatus lung infection in the presence of
235 cteria Pseudomonas aeruginosa and the fungus Aspergillus fumigatus M-CSF treatment during engraftment
236 ygen bubbles inactivate Escherichia coli and Aspergillus fumigatus, mainly by an oxygen gradient insi
240 -18 structures and a structural model of the Aspergillus fumigatus mtTyrRS showed that the overall to
242 on the genetic underpinnings of virulence in Aspergillus fumigatus, one of the most lethal fungal pat
244 , CD8, and natural killer (NK) cells against Aspergillus fumigatus over 5 time points and compared th
248 ere, we demonstrate that the fungal pathogen Aspergillus fumigatus possesses an active UAP (AfUAP1) t
251 Ultimately, by using overlapping peptides of Aspergillus fumigatus proteins, Aspergillus-specific T-c
254 tein 90 (Hsp90) is an essential chaperone in Aspergillus fumigatus representing an attractive antifun
259 utcomes following repeated inhalation of dry Aspergillus fumigatus spores aerosolized at concentratio
260 sed male Sprague-Dawley rats were exposed to Aspergillus fumigatus spores for an hour in an aerosol c
263 atophagoides pteronyssinus and from the mold Aspergillus fumigatus stimulated a rapid and robust prod
266 ly proposed single-locus typing strategy for Aspergillus fumigatus subtyping for interlaboratory repr
268 man pathogenic fungus Aspergillus fumigatus, Aspergillus fumigatus tetramycovirus-1 (AfuTmV-1), which
271 -ray scattering data for UGM from the fungus Aspergillus fumigatus, the causative agent of aspergillo
273 the in vitro volatile metabolite profile of Aspergillus fumigatus, the most common cause of IA, and
274 The Af12060 and Af12050 enzyme pair from Aspergillus fumigatus thereby converts FQF to FQA, while
276 model using the clinically relevant antigen Aspergillus fumigatus to determine the time kinetics of
278 photericin B, or caspofungin and exposure of Aspergillus fumigatus to voriconazole did not alter the
280 hy was used to obtain structures of oxidized Aspergillus fumigatus UGM (AfUGM) complexed with NADPH a
281 tantially different from those described for Aspergillus fumigatus UGM, which is 45% identical to T.
282 iderophore produced by the pathogenic fungus Aspergillus fumigatus under iron-limiting conditions.
283 misidentified from respiratory specimens as Aspergillus fumigatus using colonial and microscopic mor
285 -fold higher and the natamycin MIC90 against Aspergillus fumigatus was 4-fold higher in our study.
294 Fungal infections with Curvularia lunata and Aspergillus fumigatus were typically confined to the air
295 as aeruginosa, Streptococcus pneumoniae, and Aspergillus fumigatus when mice were heavily engrafted w
296 , including the opportunistic human pathogen Aspergillus fumigatus where SREBP is required for virule
297 ffectors against the widely distributed mold Aspergillus fumigatus, which is a major threat for immun
298 studies suggest the emergence of strains of Aspergillus fumigatus with acquired resistance to azoles
299 excellent activity against Candida spp. and Aspergillus fumigatus, with >or=98% of MIC results at <o
300 are nonpathogenic in D. melanogaster (e.g., Aspergillus fumigatus), Zygomycetes rapidly infect and k
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