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1 asthma (mice sensitized and challenged with aspergillus fumigatus).
2 sults were available in 1 patient and showed Aspergillus fumigatus.
3 cluster in the opportunistic human pathogen Aspergillus fumigatus.
4 essential role in antifungal defense against Aspergillus fumigatus.
5 5 null (5) or Asp f 13 null (13) strains of Aspergillus fumigatus.
6 zed by an allergic immunological response to Aspergillus fumigatus.
7 unocompromised individuals that is caused by Aspergillus fumigatus.
8 ignated PerA, in the human pathogenic fungus Aspergillus fumigatus.
9 moderately active against a third pathogen, Aspergillus fumigatus.
10 with an RGS4 antagonist after challenge with Aspergillus fumigatus.
11 irulence in the human opportunistic pathogen Aspergillus fumigatus.
12 of Ascomycota, including the human pathogen Aspergillus fumigatus.
13 oxygenase that is essential for virulence in Aspergillus fumigatus.
14 se (NRPS) gene cluster in the human pathogen Aspergillus fumigatus.
15 from this motif in a subtelomeric region of Aspergillus fumigatus.
16 rates within host cells and protects against Aspergillus fumigatus.
17 ion of SUN proteins in a filamentous fungus, Aspergillus fumigatus.
18 ampen the immune response against chitin and Aspergillus fumigatus.
19 l community to understand the human pathogen Aspergillus fumigatus.
20 nd an extended fungal panel; specific IgE to Aspergillus fumigatus.
21 gulators in the opportunistic human pathogen Aspergillus fumigatus.
22 terium Pseudomonas aeruginosa and the fungus Aspergillus fumigatus.
23 tant virulence factor of the fungal pathogen Aspergillus fumigatus.
24 ure of the corneal scrapes were positive for aspergillus fumigatus.
25 infection with the invasive fungal pathogen Aspergillus fumigatus.
26 506, individually and in combination against Aspergillus fumigatus.
27 irulence of the opportunistic human pathogen Aspergillus fumigatus.
28 est aspects of the innate immune response to Aspergillus fumigatus.
29 for a broad panel of pathogenic bacteria and Aspergillus fumigatus.
30 highlands of Panama and tested them against Aspergillus fumigatus.
31 ilm morphotypes of the human fungal pathogen Aspergillus fumigatus.
32 teins present in the human pathogenic fungus Aspergillus fumigatus.
33 le species, the opportunistic human pathogen Aspergillus fumigatus.
34 Netherlands might harbor triazole-resistant Aspergillus fumigatus.
35 infectious agents Listeria monocytogenes and Aspergillus fumigatus.
36 es during infection with the fungal pathogen Aspergillus fumigatus.
37 lycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus.
39 hogens, including real-time visualization of Aspergillus fumigatus (5 d for culturing, 1-2 d for imag
42 sized that prenatal exposure of mice (F0) to Aspergillus fumigatus (A. fumigatus) would be associated
43 rate immune responses against fungi, such as Aspergillus fumigatus, a major fungal pathogen in humans
44 exposed to spores of the environmental mould Aspergillus fumigatus, a major opportunistic pathogen.
49 irmed that the common fungal airway pathogen Aspergillus fumigatus activates heterologously-expressed
51 vely low challenge doses with the conidia of Aspergillus fumigatus administered to recombinase activa
52 HDM-exposed mothers, the magnitude of HDM or Aspergillus fumigatus (AF) extract-induced airway hyperr
53 rated synergistic antifungal effects against Aspergillus fumigatus (AF) in an in vitro human alveolus
54 of FasL expression in airway eosinophilia in Aspergillus fumigatus (Af)-induced sensitization and to
59 relevant fungi such as Candida albicans and Aspergillus fumigatus also form biofilms during infectio
60 and IgA reactivity to whole extract fungal (Aspergillus fumigatus, Alternaria alternata, Cryptococcu
61 gE or skin prick test response positivity to Aspergillus fumigatus, Alternaria alternata, or Cladospo
66 n, including lateral branching in pathogenic Aspergillus fumigatus and Aspergillus flavus, and appres
67 d a direct pH-dependent antifungal effect on Aspergillus fumigatus and Aspergillus nidulans; it incre
69 at infection with the human pathogenic fungi Aspergillus fumigatus and Candida albicans induces a dis
73 Azole resistance is an emerging problem in Aspergillus fumigatus and complicates the management of
74 scaffold, which showed high activity toward Aspergillus fumigatus and Cryptococcus neoformans at aci
75 en demonstrated against the fungal pathogens Aspergillus fumigatus and Cryptococcus neoformans, littl
76 s, caused most commonly by Candida albicans, Aspergillus fumigatus and Cryptococcus neoformans, resul
77 ad of agriculturally derived azole-resistant Aspergillus fumigatus and emerging threats such as multi
78 onse to alpha-(1,3)-glucan polysaccharide of Aspergillus fumigatus and ensuing CD4+ T-cell polarizati
79 lungs of mice sensitized and challenged with Aspergillus fumigatus and evaluated ex vivo in tissue cu
80 cy of pH- and calcium-mediated signalling in Aspergillus fumigatus and found that calcium chelation s
81 d juvenile Scnn1b-Tg and wild-type mice with Aspergillus fumigatus and house dust mite allergen and c
82 ue of 0.60 +/- 0.05 muM and to the NMOs from Aspergillus fumigatus and Mycobacterium smegmatis with K
85 ides produced by the opportunistic pathogens Aspergillus fumigatus and Pseudomonas aeruginosa, respec
87 ere highly susceptible to aeroallergens from Aspergillus fumigatus and the house dust mite, resulting
88 onditions may result from the interaction of Aspergillus fumigatus and the immune system of its human
94 bacterium tuberculosis, Salmonella enterica, Aspergillus fumigatus, and Epstein-Barr virus (EBV) and
95 hreatening lung disease caused by the fungus Aspergillus fumigatus, and is a leading cause of invasiv
96 cluding Pseudomonas aeruginosa, Haemophilus, Aspergillus fumigatus, and nontuberculous mycobacteria.
97 ed literature about Aspergillus nidulans and Aspergillus fumigatus, and this annotation is provided w
98 cinetobacter baumannii, Candida albicans, or Aspergillus fumigatus; and treated intraperitoneally wit
101 owever, Th17 cells that are crossreactive to Aspergillus fumigatus antigens can also drive exaggerate
102 entrations of Alternaria alternata allergen, Aspergillus fumigatus antigens, house dust mite and endo
103 Infections caused by triazole-resistant Aspergillus fumigatus are associated with a higher proba
104 breakthrough infections with fungal pathogen Aspergillus fumigatus are associated with caspofungin pr
106 llergens including Asp f 5 and Asp f 13 from Aspergillus fumigatus are thought to be important for in
108 acoccidioides brasiliensis, and occasionally Aspergillus fumigatus, are primary pulmonary pathogens o
109 of lung inflammation in murine AA caused by Aspergillus fumigatus as well as its consequence on the
110 and Candida krusei) or a mold 11-plex panel (Aspergillus fumigatus, Aspergillus flavus, Aspergillus n
111 us isolated from the human pathogenic fungus Aspergillus fumigatus, Aspergillus fumigatus tetramycovi
112 molds (Paecilomyces variotii ATCC MYA-3630, Aspergillus fumigatus ATCC MYA-3626, A. flavus ATCC MYA-
113 on induced increased mortality rates, higher Aspergillus fumigatus burden and reduced neutrophil recr
114 patients infected with a triazole-resistant Aspergillus fumigatus, but a direct comparison with tria
115 rways of otherwise naive mice in response to Aspergillus fumigatus, but not ovalbumin sensitization a
116 the metabolic outcome of an interaction with Aspergillus fumigatus by influencing triacetylfusarinine
120 In susceptible individuals, exposure to Aspergillus fumigatus can lead to the development of ato
123 rotein (FKBP12) from human fungal pathogens (Aspergillus fumigatus, Candida albicans, Cryptococcus ne
124 d 2008-2011, respectively; P=0.018), whereas Aspergillus fumigatus cases decreased (73.9/1000 vs. 49.
125 S (7-dimethylallyl tryptophan synthase) from Aspergillus fumigatus catalyze C(4)- and C(7)-prenylatio
128 ential for host resistance against pulmonary Aspergillus fumigatus challenge through the regulation o
129 traction, and lung inflammation in naive and Aspergillus fumigatus-challenged wild-type and Rgs5(-/-)
130 The most common fungus in asthmatics was Aspergillus fumigatus complex and this taxon accounted f
133 T) formation, are involved in the killing of Aspergillus fumigatus conidia and hyphae, using neutroph
134 blished a correlation between high levels of Aspergillus fumigatus conidia and the appearance of new
135 strated that repeated intranasal exposure to Aspergillus fumigatus conidia in C57BL/6 mice results in
136 operties of the human opportunistic pathogen Aspergillus fumigatus conidia is essential given the imp
137 e of healthy C57BL/6 mice to viable, resting Aspergillus fumigatus conidia leads to the development o
139 d cell death with apoptosis-like features in Aspergillus fumigatus conidia, the most prevalent human
143 derived metabolites differentially modulated Aspergillus fumigatus development, shifting from weak ve
145 Here we report a fluorogenic probe to image Aspergillus fumigatus directly in human pulmonary tissue
146 elevance of the SeptiFast assay in detecting Aspergillus fumigatus DNA in whole blood samples from 38
150 ack peripheral B cells) were sensitized with Aspergillus fumigatus extract and challenged with two in
151 ermatitis, we examined the effect of topical Aspergillus fumigatus extract exposure in wild-type and
155 with chronic granulomatous disease (CGD) is Aspergillus fumigatus followed by A. nidulans; other asp
156 ms to report a case of fungal keratitis with aspergillus fumigatus following ICRS implantation for co
160 The laboratory also received 46 isolates of Aspergillus fumigatus from COVID-19 patients (including
162 serum samples spiked with various amounts of Aspergillus fumigatus genomic DNA was distributed to 23
163 rdingly, beta-glucan surface exposure during Aspergillus fumigatus germination activates an Atg5-depe
165 innate responses to the major mold pathogen Aspergillus fumigatus has been restricted to specialized
171 ndida albicans, Cryptococcus neoformans, and Aspergillus fumigatus have transitioned from a rare curi
172 llosis, an infection caused predominantly by Aspergillus fumigatus, have increased due to the growing
173 BS or mixed allergen ( Alternaria alternata, Aspergillus fumigatus, house dust mite, and ovalbumin) f
174 VEGF reversed the antiangiogenic activity of Aspergillus fumigatus; however, VEGF induced the formati
175 /-) mice have an impaired ability to inhibit Aspergillus fumigatus hyphal growth in vitro and in infe
176 rologic tests (ImmunoCap total IgE, specific Aspergillus fumigatus IgE, and specific A fumigatus IgG)
177 st defense against Staphylococcus aureus and Aspergillus fumigatus in a murine X-linked gp91phox-defi
178 of persistent neutrophilic meningitis due to Aspergillus fumigatus in an immunocompetent man who had
182 al for survival of the fungal human pathogen Aspergillus fumigatus in the immunocompromised host lung
183 mmune defense against the opportunistic mold Aspergillus fumigatus In this study, we investigated the
184 CD11c(+) cells and controls Th2 responses to Aspergillus fumigatus in vitro in cystic fibrosis (CF) p
185 whether the presence of fungi, in particular Aspergillus fumigatus, in the airway correlated with ast
187 or pathways involved in innate resistance to Aspergillus fumigatus, including complement activation o
188 been shown to suppress house dust mite- and Aspergillus fumigatus-induced allergic inflammation in m
189 6 mediates this effect using mouse models of Aspergillus fumigatus-induced and house dust mite antige
194 lung function impairment was associated with Aspergillus fumigatus infection and prior lung surgery.
199 c enzyme A (SidA) ornithine hydroxylase from Aspergillus fumigatus is a fungal disease drug target in
200 osis caused by triazole-resistant strains of Aspergillus fumigatus is a growing public health concern
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
220 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
234 illus species as well as azole resistance in Aspergillus fumigatus Its performance has been validated
235 ctin-1 displayed increased susceptibility to Aspergillus fumigatus lung infection in the presence of
236 cteria Pseudomonas aeruginosa and the fungus Aspergillus fumigatus M-CSF treatment during engraftment
237 ygen bubbles inactivate Escherichia coli and Aspergillus fumigatus, mainly by an oxygen gradient insi
241 -18 structures and a structural model of the Aspergillus fumigatus mtTyrRS showed that the overall to
243 on the genetic underpinnings of virulence in Aspergillus fumigatus, one of the most lethal fungal pat
245 , CD8, and natural killer (NK) cells against Aspergillus fumigatus over 5 time points and compared th
250 ere, we demonstrate that the fungal pathogen Aspergillus fumigatus possesses an active UAP (AfUAP1) t
253 Ultimately, by using overlapping peptides of Aspergillus fumigatus proteins, Aspergillus-specific T-c
256 tein 90 (Hsp90) is an essential chaperone in Aspergillus fumigatus representing an attractive antifun
263 utcomes following repeated inhalation of dry Aspergillus fumigatus spores aerosolized at concentratio
270 man pathogenic fungus Aspergillus fumigatus, Aspergillus fumigatus tetramycovirus-1 (AfuTmV-1), which
273 -ray scattering data for UGM from the fungus Aspergillus fumigatus, the causative agent of aspergillo
276 ponse and virulence of the pathogenic fungus Aspergillus fumigatus, the leading etiology of invasive
277 the in vitro volatile metabolite profile of Aspergillus fumigatus, the most common cause of IA, and
278 The Af12060 and Af12050 enzyme pair from Aspergillus fumigatus thereby converts FQF to FQA, while
280 model using the clinically relevant antigen Aspergillus fumigatus to determine the time kinetics of
282 hy was used to obtain structures of oxidized Aspergillus fumigatus UGM (AfUGM) complexed with NADPH a
283 tantially different from those described for Aspergillus fumigatus UGM, which is 45% identical to T.
284 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.
292 -disease' in which mice rendered allergic to Aspergillus fumigatus were co-infected with influenza A
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 racterized silent gene cluster of the fungus Aspergillus fumigatus, which is activated by the bacteri
299 ccharide galactosaminogalactan (GG) found in Aspergillus fumigatus, which is the most important airbo
300 ed "shuttling." In Talaromyces marneffei and Aspergillus fumigatus zebrafish in vivo infections, live