ライフサイエンスコーパス: Aspergillus

1 entually pathology-proven AIFR (13:25, Mucor:Aspergillus).

2 ulmonary IMI after HCT, particularly for non-Aspergillus.

3 nly pneumonia due to nosocomial bacteria and Aspergillus.

4 mpounds against human-relevant fungi such as Aspergillus.

5 y did not relate to serum IgE positivity for Aspergillus.

6 tes of entry for opportunistic fungi such as Aspergillus.

7 into the initial epithelial host response to Aspergillus.

8 cies in the genera Candida, Saccharomyces or Aspergillus-accelerated oncogenesis.

9 f food-spoilage fungi under glycerol stress (Aspergillus aculeatinus and A. sclerotiicarbonarius); me

10 Reaction mechanism of apiosidase from Aspergillus aculeatus in commercial glycanase Viscozyme

11 Concordance with the Bio-Rad Aspergillus Ag assay (Bio Rad GM-EIA) and IMMY sona Aspe

12 Concordance with the Bio-Rad Aspergillus Ag assay (GM-EIA) was performed.

13 o identify selected toxigenic species of the Aspergillus and Fusarium genera isolated from grapes and

14 xin-producing fungal species from the genera Aspergillus and Fusarium using solid-state voltammetry i

15 has been approved for treatment of invasive Aspergillus and mucormycosis, we observed an increased r

16 The prevalences of Aspergillus and Scedosporium species were 40.8% and 5.2%

17 d therapy had significantly higher levels of Aspergillus and total fungus in their bronchoalveolar la

18 dominant genera were Cladosporium, Fusarium, Aspergillus, and Alternaria.

19 hromatographic technology (ICT) that detects Aspergillus antibodies (IgG and IgM) in less than 30 min

20 re as the only predictor and Group (Mucor vs Aspergillus) as the only outcome.

21 lly-relevant yeast (Cryptococcus) and molds (Aspergillus) at a concentration as low as 0.50 ug/mL.

22 essive therapeutic approach, has resulted in Aspergillus becoming the most commonly isolated pathogen

23 re outcomes for five major fungal pathogens: Aspergillus, Blastomyces, Coccidioides, Cryptococcus, an

24 The Aspergillus branching response is specific to a subset o

25 tional regulators that appear to mediate the Aspergillus branching response; one of the mutants is lo

26 vasive and granulomatous rhinosinusitis, and aspergillus bronchitis.

27 has the highest catalytic activity, whereas Aspergillus CAD is best adapted to a more acidic pH.

28 Similar to SpMae1(p), its homolog in Aspergillus carbonarius, AcDct(p), increased the malate

29 ions of grape berries infected by the fungus Aspergillus carbonarius.

30 The incidence rate of IPA and Aspergillus colonization was 30 of 1000 patient-y, and 6

31 Incidence of probable/proven IPA and Aspergillus colonization were assessed as per Internatio

32 s inhale several hundred to several thousand Aspergillus conidia (i.e., vegetative spores) daily and

33 In immunocompromised individuals, Aspergillus conidia can germinate into tissue-invasive h

34 Following inhalation, Aspergillus conidia deposit in the small airways, where

35 r rapid online concentration and analysis of Aspergillus conidia in bronchoalveolar lavage fluid usin

36 Among them, the median time to positive Aspergillus culture or GM positivity was 703 days (inter

37 Positive bronchoalveolar lavage for GM or Aspergillus cultures was reported for 15% (52/350) of LT

38 Patients with risk factors, positive Aspergillus cultures, or galactomannan (GM) received tar

39 s relatively low (<10%), despite unavoidable Aspergillus exposure in patients with a potentially simi

40 iety of fungi, including species of Candida, Aspergillus, Exserohilum, Cryptococcus, Histoplasma, and

41 e fermentation (SSF) with Aspergillus sojae, Aspergillus ficuum and their co-cultures on proximate co

42 dicated that SSF using Aspergillus sojae and Aspergillus ficuum can influence the physical, chemical

43 oteolytic activity of Aspergillus oryzae and Aspergillus flavipes enzymes, as well as to assess their

44 tivity against aflatoxin secreting strain of Aspergillus flavus (AF-LHP-S1) and 12 other food borne m

45 agricultural fields are occupied by complex Aspergillus flavus communities composed of isolates in m

46 a designer FADGDH was constructed by fusing Aspergillus flavus derived FADGDH (AfGDH) and a Phaneroc

47 s, a qualitative analytical method to detect Aspergillus flavus in food samples, based on the identif

48 Using Aspergillus flavus spores as a target organism, a compar

49 cies in all pulmonary syndromes, followed by Aspergillus flavus which is a common cause of allergic r

50 hing in pathogenic Aspergillus fumigatus and Aspergillus flavus, and appressorium formation in the ri

51 food fermentation and enzyme production, and Aspergillus flavus, food spoiler and mycotoxin producer.

52 A fusion enzyme composed of an Aspergillus flavus-derived flavin adenine dinucleotide g

53 NAi-5x) related to aflatoxin biosynthesis in Aspergillus flavus.

54 genic effects of thyme essential oil (EO) on Aspergillus flavus.

55 Opportunistic pathogens, including Aspergillus fumigatus (1.4%) and cytomegalovirus (6%), w

56 hogens, including real-time visualization of Aspergillus fumigatus (5 d for culturing, 1-2 d for imag

57 HDM-exposed mothers, the magnitude of HDM or Aspergillus fumigatus (AF) extract-induced airway hyperr

58 rated synergistic antifungal effects against Aspergillus fumigatus (AF) in an in vitro human alveolus

59 Candida auris, Cryptococcus neoformans, and Aspergillus fumigatus (SigmaFICI = 0.05-0.50).

60 Twelve bIFIs (Aspergillus fumigatus [5], Aspergillus species [2], Muco

61 irmed that the common fungal airway pathogen Aspergillus fumigatus activates heterologously-expressed

62 n, including lateral branching in pathogenic Aspergillus fumigatus and Aspergillus flavus, and appres

63 s, caused most commonly by Candida albicans, Aspergillus fumigatus and Cryptococcus neoformans, resul

64 onse to alpha-(1,3)-glucan polysaccharide of Aspergillus fumigatus and ensuing CD4+ T-cell polarizati

65 lungs of mice sensitized and challenged with Aspergillus fumigatus and evaluated ex vivo in tissue cu

66 n the organotypic bronchiole and cultures of Aspergillus fumigatus and Pseudomonas aeruginosa.

67 owever, Th17 cells that are crossreactive to Aspergillus fumigatus antigens can also drive exaggerate

68 Candida albicans and Aspergillus fumigatus are dangerous fungal pathogens wit

69 of lung inflammation in murine AA caused by Aspergillus fumigatus as well as its consequence on the

70 on induced increased mortality rates, higher Aspergillus fumigatus burden and reduced neutrophil recr

71 Recognition of Aspergillus fumigatus by the host immune system leads to

72 ential for host resistance against pulmonary Aspergillus fumigatus challenge through the regulation o

73 The most common fungus in asthmatics was Aspergillus fumigatus complex and this taxon accounted f

74 ere asthmatics and the most common fungus is Aspergillus fumigatus complex.

75 % of the cell wall of the filamentous fungus Aspergillus fumigatus comprises polysaccharides.

76 d cell death with apoptosis-like features in Aspergillus fumigatus conidia, the most prevalent human

77 Aspergillus fumigatus culture-positive patients were inv

78 In an Aspergillus fumigatus extract-induced inflammation model

79 Here we study the function of the Aspergillus fumigatus family of five Crh transglycosylas

80 The filamentous fungal pathogen Aspergillus fumigatus forms biofilms in vivo, and during

81 During infection, the fungal pathogen Aspergillus fumigatus forms biofilms that enhance its re

82 The laboratory also received 46 isolates of Aspergillus fumigatus from COVID-19 patients (including

83 Aspergillus fumigatus has widely evolved resistance to t

84 atients sensitized to airborne fungi such as Aspergillus fumigatus have more severe asthma.

85 ndida albicans, Cryptococcus neoformans, and Aspergillus fumigatus have transitioned from a rare curi

86 Our study demonstrates that Aspergillus fumigatus induces regulatory T-cells with a

87 lung function impairment was associated with Aspergillus fumigatus infection and prior lung surgery.

88 c enzyme A (SidA) ornithine hydroxylase from Aspergillus fumigatus is a fungal disease drug target in

89 osis caused by triazole-resistant strains of Aspergillus fumigatus is a growing public health concern

90 Aspergillus fumigatus is a human opportunistic fungal pa

91 Aspergillus fumigatus is a ubiquitous fungal pathogen ca

92 Aspergillus fumigatus is an environmental fungus that ca

93 Aspergillus fumigatus is an opportunistic fungal pathoge

94 s of azole resistance in the fungal pathogen Aspergillus fumigatus is limited.

95 is due to a TR46/Y121F/T289A azole-resistant Aspergillus fumigatus is reported.

96 The ubiquitous fungal pathogen Aspergillus fumigatus is the primary cause of opportunis

97 Aspergillus fumigatus isolate from the patient was more

98 Heterogeneity among Aspergillus fumigatus isolates results in unique virulen

99 However, the Aspergillus fumigatus PAMPs that are responsible for inf

100 images of an in vivo mouse disease model of aspergillus fumigatus pneumonia.

101 Aspergillus fumigatus remains the most common species in

102 Aspergillus fumigatus specifically caused production of

103 Attempts to correlate Aspergillus fumigatus strains from clinical infection or

104 -disease' in which mice rendered allergic to Aspergillus fumigatus were co-infected with influenza A

105 ed "shuttling." In Talaromyces marneffei and Aspergillus fumigatus zebrafish in vivo infections, live

106 Neosartorya fumigata (Aspergillus fumigatus) is the most common cause of invas

107 ScTOK, AfTOK1 (Aspergillus fumigatus), and H99TOK (Cryptococcus neoform

108 Aspergillus fumigatus, a ubiquitous human fungal pathoge

109 Aspergillus fumigatus, a ubiquitous mold, is a common ca

110 ophyton rubrum, Trichophyton mentagrophytes, Aspergillus fumigatus, and Candida albicans.

111 pathogenic fungi including Candida species, Aspergillus fumigatus, and Cryptococcus neoformans.

112 bacterium tuberculosis, Salmonella enterica, Aspergillus fumigatus, and Epstein-Barr virus (EBV) and

113 patients infected with a triazole-resistant Aspergillus fumigatus, but a direct comparison with tria

114 Aspergillus fumigatus, Candida albicans and Mycosphaerel

115 rotein (FKBP12) from human fungal pathogens (Aspergillus fumigatus, Candida albicans, Cryptococcus ne

116 llosis, an infection caused predominantly by Aspergillus fumigatus, have increased due to the growing

117 BS or mixed allergen ( Alternaria alternata, Aspergillus fumigatus, house dust mite, and ovalbumin) f

118 whether the presence of fungi, in particular Aspergillus fumigatus, in the airway correlated with ast

119 In the human pathogen Aspergillus fumigatus, the fungal-specific bZIP-type tra

120 ponse and virulence of the pathogenic fungus Aspergillus fumigatus, the leading etiology of invasive

121 racterized silent gene cluster of the fungus Aspergillus fumigatus, which is activated by the bacteri

122 ccharide galactosaminogalactan (GG) found in Aspergillus fumigatus, which is the most important airbo

123 been shown to suppress house dust mite- and Aspergillus fumigatus-induced allergic inflammation in m

124 est aspects of the innate immune response to Aspergillus fumigatus.

125 tant virulence factor of the fungal pathogen Aspergillus fumigatus.

126 for a broad panel of pathogenic bacteria and Aspergillus fumigatus.

127 highlands of Panama and tested them against Aspergillus fumigatus.

128 ilm morphotypes of the human fungal pathogen Aspergillus fumigatus.

129 teins present in the human pathogenic fungus Aspergillus fumigatus.

130 es during infection with the fungal pathogen Aspergillus fumigatus.

131 with an RGS4 antagonist after challenge with Aspergillus fumigatus.

132 he performance of the recently released IMMY Aspergillus galactomannan enzyme immunoassay (IMMY GM-EI

133 The Aspergillus Galactomannan Lateral Flow Assay (LFA) is a

134 ity, and limited resources needed, the LDBio Aspergillus ICT is a suitable diagnostic tool for CPA in

135 The Aspergillus ICT lateral flow assay exhibits excellent se

136 Samples were applied to the LDBio Aspergillus ICT lateral flow assay, and results were rea

137 rgillus IgG titer was also compared with the Aspergillus ICT test line intensity or rate of developme

138 s, sensitivity and specificity for the LDBio Aspergillus ICT were 91.6% and 98.0%, respectively.

139 The ImmunoCAP Aspergillus IgG titer was also compared with the Aspergi

140 Results were compared with Aspergillus IgG titers in CPA patients, measured by Immu

141 Aspergillus IMI (n=51), Proven/Probable non-Aspergillus IMI (n=24), Possible IMI (n=20), and non-IMI

142 thin 14 days of diagnosis of Proven/Probable Aspergillus IMI (n=51), Proven/Probable non-Aspergillus

143 nsitivity, 79%; 95% CI, 56%-93%) compared to Aspergillus IMI (sensitivity, 31%; 95% CI, 19%-46%).

144 d higher sensitivity for Proven/Probable non-Aspergillus IMI (sensitivity, 79%; 95% CI, 56%-93%) comp

145 l 7 patients in the Aspergillus subgroup and Aspergillus in 1 patient with Possible IMI.

146 cultures grew Fusarium in 19 samples (27%), Aspergillus in 17 samples (24%), and other filamentous f

147 Allergic manifestations of inhaled Aspergillus include allergic bronchopulmonary aspergillo

148 ndings on craniofacial CT scans of Mucor and Aspergillus induced AIFR could be differentiated based o

149 Aspergillus-infected monocyte-derived DCs and neutrophil

150 Aspergillus-infected murine Mo-DCs and neutrophils recru

151 Enrichment of GT in Aspergillus-infected neutropenic lung correlated with fu

152 Patients with probable Aspergillus infection had a significantly longer median

153 : To estimate the prevalence and outcomes of Aspergillus infection in adults with suspected ventilato

154 Rationale: Aspergillus infection in patients with suspected ventila

155 sions: The estimated prevalence for probable Aspergillus infection in this geographically dispersed m

156 Patients were categorized as having probable Aspergillus infection using a definition comprising clin

157 evaluated, 24 met the definition of probable Aspergillus infection, giving an estimated prevalence of

158 ons (n = 26735, total cost $1.4 billion) and Aspergillus infections (n = 14820, total cost $1.2 billi

159 scuss novel concepts in host defense against Aspergillus infections and emphasize new insights in fun

160 o evaluate longitudinal associations between Aspergillus infections and lung disease in young childre

161 re used to determine the association between Aspergillus infections and the progression of structural

162 k (P = 0.008).Conclusions: Lower respiratory Aspergillus infections are associated with the progressi

163 sors activated in the context of Candida and Aspergillus infections are unknown.

164 Prevalence of Aspergillus infections did not significantly change (P =

165 riazoles are the mainstay of therapy against Aspergillus infections for treatment and prophylaxis.

166 The manifestations of Aspergillus infections include invasive aspergillosis, c

167 lococcus aureus, Pseudomonas aeruginosa, and Aspergillus infections were all associated with worse CT

168 Aspergillus infections were also associated with markers

169 s to develop pulmonary infections, including Aspergillus infections.

170 The genus Aspergillus is ubiquitous in the environment and contain

171 llus Ag assay (Bio Rad GM-EIA) and IMMY sona Aspergillus lateral flow assay was assessed.

172 lyses revealed that these isolates belong to Aspergillus latus, an allodiploid hybrid species.

173 rformance of the recently released IMMY sona Aspergillus LFA when testing serum samples.

174 The IMMY sona Aspergillus LFA, when used with a cube reader, provides

175 s suggested that airway fungi, in particular Aspergillus may impinge on clinical phenotype in asthma.

176 hermolysin and a non-specific peptidase from Aspergillus melleus), contained a varying peptide profil

177 McfDNA-Seq also identified non-Aspergillus molds in an additional 7 patients in the Asp

178 nbreakthrough IMIs shows a shift towards non-Aspergillus molds with a significantly increased proport

179 and 23 (10 mg/kg) protected in an ovalbumin/Aspergillus mouse asthma model, and PEG conjugate 12 red

180 In mice, a GAG-deficient Aspergillus mutant (Deltagt4c) did not elicit protective

181 d from a novel species of Australian fungus, Aspergillus nanangensis.

182 ), and the ascomycetes Neurospora crassa and Aspergillus nidulans (Fungi), and bring to light develop

183 leaching of calcium hydroxide from concrete, Aspergillus nidulans (MAD1445), a pH regulatory mutant,

184 with aspergillosis originally identified as Aspergillus nidulans (section Nidulantes) that are actua

185 Hyphal tip cells of the fungus Aspergillus nidulans are useful for studying long-range

186 s and demonstrate that the Raman signal from Aspergillus nidulans conidia originates in pigment molec

187 on of a 237 residue deacetylase (AnCDA) from Aspergillus nidulans FGSC A4.

188 We have developed a genetic screen in Aspergillus nidulans for negative regulators of fungal S

189 the melanin pathway, we utilized an advanced Aspergillus nidulans heterologous system for the express

190 is by heterologous pathway reconstruction in Aspergillus nidulans identified the multicopper oxidase

191 med on single spores (conidia) of the fungus Aspergillus nidulans in order to establish a baseline me

192 In the filamentous fungus Aspergillus nidulans SPBs and septum-associated MTOCs we

193 ated dynein activation in the model organism Aspergillus nidulans Specifically, we found that overexp

194 The model fungus Aspergillus nidulans synthesizes numerous secondary meta

195 functional expression of a mammalian NAT in Aspergillus nidulans Thus, our results provide a potenti

196 entation using heterologous RanBP genes from Aspergillus nidulans was successful, suggesting that the

197 In Aspergillus nidulans, a donor-disrupted stwintron (intro

198 In Aspergillus nidulans, the WCC and the phytochrome intera

199 ons affecting early-endosome distribution in Aspergillus nidulans, we identified the prp40A(L438*) mu

200 Using Aspergillus nidulans, we show that AP-2 has a clathrin-i

201 We have identified a similar system in Aspergillus nidulans, where Upf1 is required for the reg

202 ns the cellular and metabolic development in Aspergillus nidulans.

203 ate the usage of a prolyl endopeptidase from Aspergillus niger (An-PEP) for HDX-MS.

204 ependent glucose dehydrogenase, derived from Aspergillus niger (AnGDH), was characterized.

205 ns Zygosaccharomyces bailii (ATCC 42476) and Aspergillus niger (ATCC 6275 (M68)).

206 tolerance of two typical filamentous fungi, Aspergillus niger and Penicillium oxalicum.

207 ifungal efficacy against Penicillium sp. and Aspergillus niger but low effective against Rhizopus sp.

208 The orthologous transcript of Aspergillus niger can be alternatively spliced; the exon

209 Trichoderma and Aspergillus niger cellulases activities were determined

210 (Cu2 (CO3 )(OH)2 ) and bioaccumulated within Aspergillus niger colonies when grown on different inorg

211 the emulsions assays were conducted against Aspergillus niger given its strong resistance and its re

212 with Botrytis cinerea, Penicillium expansum, Aspergillus niger or A. carbonarius.

213 gether with recombinant proteins: the fungal Aspergillus niger PhyA or the bacterial Escherichia coli

214 Aspergillus tubingensis, a member of the Aspergillus niger species complex, was most prevalent fr

215 s study, the ability of the geoactive fungus Aspergillus niger to colonize and transform manganese no

216 Aspergillus niger was able to colonize and penetrate man

217 Aspergillus niger was capable of solubilizing natural (f

218 In this work, the geoactive fungus Aspergillus niger was investigated for struvite transfor

219 alyze the process, and beta-glucosidase from Aspergillus niger was selected.

220 Saprobic fungi, such as Aspergillus niger, grow as colonies consisting of a netw

221 demonstrated a superior performance against Aspergillus niger, isolated from spoiled pomegranate, co

222 successful history of citrate production in Aspergillus niger, the molecular mechanism of citrate ac

223 ility of a ubiquitous geoactive soil fungus, Aspergillus niger, to affect the mobility of REE in mona

224 , Paecilomyces formosus, Rhizopus oryzae and Aspergillus niger.

225 enzymes (CAZymes) of the filamentous fungus Aspergillus niger.

226 The reductive aminase from Aspergillus oryzae (AspRedAm) was combined with a single

227 an NADP(H)-dependent reductive aminase from Aspergillus oryzae (AspRedAm, Uniprot code Q2TW47) that

228 ilk subjected to the proteolytic activity of Aspergillus oryzae and Aspergillus flavipes enzymes, as

229 nd polyaniline chitosan nanocomposites bound Aspergillus oryzae beta-galactosidase.

230 through rational heterologous expression in Aspergillus oryzae coupled with isolation and detailed s

231 ther alternative extraction methods based on Aspergillus oryzae fermentation and alpha-amylase hydrol

232 in which the reductive aminase (RedAm) from Aspergillus oryzae is combined with either (i) a 1 degre

233 soybean flour (DSF) by Monascus purpureus or Aspergillus oryzae on the bioactive compounds.

234 For the fermentation by Aspergillus oryzae, all the function responses were infl

235 and beneficial Aspergillus species, such as Aspergillus oryzae, used in food fermentation and enzyme

236 nt increase in pyrazines was observed in the Aspergillus oryzae-fermented samples, while higher level

237 Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae.

238 ER) on aflatoxins accumulation by a selected Aspergillus parasiticus strain in maize at 0.95 a(w) wer

239 ond, the review focuses on novel concepts of Aspergillus pathogenesis and highlights emerging knowled

240 , fungal culture, galactomannan antigen, and aspergillus PCR are useful tests.

241 plantation, respiratory virus infection, and Aspergillus PCR positivity were all significant risk fac

242 time PCR and, with clinical risk factors and Aspergillus PCR results, subjected to multilogistic regr

243 for stress, using a number of model systems (Aspergillus penicillioides; Bacillus subtilis; Escherich

244 been inserted following the sentence ending "Aspergillus phytase" in the third paragraph of the artic

245 rella, Rhodotorula, Penicillium, Thelebolus, Aspergillus, Poaceicola, Glarea and Lecanora were the do

246 Aspergillus positive BAL correlated with increased plasm

247 Aspergillus quadrilineatus endo-beta-mannanase effective

248 Aspergillus quadrilineatus RSNK-1 produced a multi-enzym

249 nulosporus with an unknown close relative of Aspergillus quadrilineatus, both in section Nidulantes.

250 Promoting epithelial transmigration with Aspergillus required prolonged exposure with live restin

251 clinically important fungi (CIF), defined as Aspergillus, Scedosporium, and Trichosporon species and

252 entity of a set of 34 clinical isolates from Aspergillus section Circumdati from the United States an

253 to determine whether traditional markers of Aspergillus sensitization related to the presence of Asp

254 claudin-18 null and wild-type mice following aspergillus sensitization.

255 Thus, the study indicated that SSF using Aspergillus sojae and Aspergillus ficuum can influence t

256 fects of solid-state fermentation (SSF) with Aspergillus sojae, Aspergillus ficuum and their co-cultu

257 6), or both (n = 4); three patients cultured Aspergillus sp. in BAL fluid.

258 o aeroallergen alkaline protease 1 (Alp1) of Aspergillus sp., because proteases are critical componen

259 Twelve bIFIs (Aspergillus fumigatus [5], Aspergillus species [2], Mucorales [2], Fusarium species

260 ignificantly change (P = 0.669).Conclusions: Aspergillus species and P. aeruginosa are commonly prese

261 Rationale: Recent data show that Aspergillus species are prevalent respiratory infections

262 Aspergillus species are regarded as relatively infrequen

263 cillium arenicola and echinocandin-producing Aspergillus species belong to the family Aspergillaceae

264 rhinosinusitis (AIFR) caused by Mucor versus Aspergillus species by evaluating computed tomography ra

265 c comparison taking advantage of 20 resolved Aspergillus species genomes revealed that DNA recognitio

266 Resistance mechanisms for Candida and Aspergillus species have been extensively described and

267 ighlights the need to further evaluate early Aspergillus species infections and the feasibility, risk

268 Azole resistance among Candida and Aspergillus species is one of the greatest challenges to

269 1%, 2.5 years; P. aeruginosa, 8%, 2.4 years; Aspergillus species, 11%, 3.2 years; and H. influenzae,

270 lavi encompasses both harmful and beneficial Aspergillus species, such as Aspergillus oryzae, used in

271 repressor of fungal secondary metabolism in Aspergillus species.

272 dole alkaloids isolated from Penicillium and Aspergillus species.

273 Detecting Aspergillus-specific IgG is critical to diagnosing chron

274 tted and subjected to galactomannan testing, Aspergillus-specific PCR, and microscopy and culture.

275 allodiploid hybrids formed by the fusion of Aspergillus spinulosporus with an unknown close relative

276 , drug interactions, and azole resistance in Aspergillus spp limit therapy.

277 Results showed the inhibition of Aspergillus spp. and B. bruxellensis inhibited in low co

278 Solid-state fermentation (SSF) by Aspergillus spp. and Mucor spp. on green canephora coffe

279 ncluding cytomegalovirus), fungal (including Aspergillus spp. and non-Aspergillus spp. molds), and No

280 ombined concentrations antimicrobials, while Aspergillus spp. and T. macrosporus were inhibited at 45

281 , fungal (including Aspergillus spp. and non-Aspergillus spp. molds), and Nocardia infections.

282 s including Candida spp., Cryptococcus spp., Aspergillus spp., and Fusarium spp.

283 With use of an Aspergillus strain expressing CndF and CndE, feeding var

284 This is the first study introducing an Aspergillus strain for benzene removal and these results

285 MIC) values against non-albicans Candida and Aspergillus strains.

286 lus molds in an additional 7 patients in the Aspergillus subgroup and Aspergillus in 1 patient with P

287 ation of mammalian transporters in the model Aspergillus system.

288 ctooligosaccharides (FOS) was obtained using Aspergillus tamarii NKRC 1229 mycelial fructosyltransfer

289 lator laeA, and deletion of mcrA homologs in Aspergillus terreus and Penicillum canescens alters the

290 Aspergillus terreus is an allergenic fungus, in addition

291 technological production of itaconic acid by Aspergillus terreus We have elucidated the crystal struc

292 Attenuating the Taxol yield of Aspergillus terreus with the subculturing and storage we

293 entation of sugars by the filamentous fungus Aspergillus terreus.

294 ble to species of Candida, Cryptococcus, and Aspergillus Treating fungal infections is challenging, i

295 Aspergillus tubingensis, a member of the Aspergillus nig

296 eling revealed conservation in zebrafish and Aspergillus We identified 8 active-site residues critica

297 Only P. aeruginosa and Aspergillus were associated with progression in CT score

298 confidence interval, 0.3-1.6; P = 0.003) and Aspergillus with trapped air (difference, 3.2; 95% confi

299 The presence of Aspergillus within the airway did not relate to serum Ig

300 lus sensitization related to the presence of Aspergillus within the airway.