ライフサイエンスコーパス: Aspergillus

1 lass in the management of diseases caused by Aspergillus.

2 affecting the quantity of asexual spores in Aspergillus.

3 ared with that for the Bruker library alone (Aspergillus, 93% versus 69%; Fusarium, 84% versus 42%; a

4 Utilizing Aspergillus, a fungal genus known for its rich secondary

5 digested with endo-polygalacturonase M2 from Aspergillus aculeatus and visualized by AFM.

6 ere misidentified by MALDI-TOF MS (including Aspergillus amoenus [n = 2] and Aspergillus calidoustus

7 found to expand during antifungal treatment (Aspergillus amstelodami, Epicoccum nigrum, and Wallemia

8 he most representative pathogenic molds (154 Aspergillus and 136 non-Aspergillus isolates) with the B

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

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

11 Aspergillus and Mucorales species cause severe infection

12 a natural carcinogenic mycotoxin produced by Aspergillus and Penicillium fungi and so it commonly app

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

14 Aspergillus and Serratia were somewhat more common in lo

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

16 with optimized commercial preparations from Aspergillus and Trichoderma.

17 ntifungal immunity (primarily to Candida and Aspergillus) and will also examine the emerging field of

18 f asthma symptoms suggests that Penicillium, Aspergillus, and Cladosporium species pose a respiratory

19 ed ceftriaxone administration and culturable Aspergillus, and demonstrated significantly increased in

20 The presence of Cladosporium, Alternaria, Aspergillus, and Penicillium species increased the exace

21 Cladosporium, Alternaria, Aspergillus, and Penicillium species were found to be pr

22 this study, we investigated whether certain Aspergillus antigens are more allergenic than others, as

23 spf2, Aspf3, and Aspf4, as well as two other Aspergillus antigens, Crf1 and Catalase1.

24 y which human neutrophils recognize and kill Aspergillus are poorly understood.

25 th a pro-inflammatory TH17-like phenotype in Aspergillus-associated immunopathology, and identifies k

26 vasive and granulomatous rhinosinusitis, and aspergillus bronchitis.

27 S (including Aspergillus amoenus [n = 2] and Aspergillus calidoustus [n = 1]) although 10 (3.1%) of t

28 ung or airways infection by endemic fungi or aspergillus can be diagnosed with respiratory sample cul

29 ciated with increased levels of Penicillium, Aspergillus, Cladosporium, and Alternaria species, altho

30 ndings reveal distinct killing mechanisms of Aspergillus conidia and hyphae by human neutrophils, lea

31 Human platelets were incubated with Aspergillus conidia and hyphae, isolated wall components

32 for effective host defense against Candida, Aspergillus, Cryptococcus, and others, with specific ele

33 d host immunity is fundamental to combatting Aspergillus diseases.

34 During disease, Aspergillus DNA burdens in blood are often at the limits

35 hain reaction (PCR)-based detection of serum Aspergillus DNA for the early diagnosis and therapy of i

36 ed monitoring strategy based on serum GM and Aspergillus DNA was associated with an earlier diagnosis

37 (bmGT) are secondary metabolites produced by Aspergillus during invasive, hyphal growth and may prove

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

39 two separate allergic stimuli (ovalbumin and Aspergillus extract), genetic removal of Muc5ac abolishe

40 (Ccl11) RNAs following pulmonary exposure to Aspergillus extract.

41 Penicillium roquefortii and Aspergillus flavipes presented optimum activity at tempe

42 aris essential oil (TEO) were evaluated upon Aspergillus flavus "in vitro".

43 Aspergillus flavus (8), however was the commonest amongs

44 over, treatment with voriconazole due to the Aspergillus flavus and meropenem due to the Pseudomonas

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

46 Aspergillus flavus is a filamentous fungus found in natu

47 Aflatoxin production by Aspergillus flavus is exacerbated by drought stress in t

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

49 ol, and perillyl alcohol were tested against Aspergillus flavus, Aspergillus ochraceus, Fusarium oxys

50 xin contamination, caused by fungal pathogen Aspergillus flavus, is a major quality and health proble

51 Aflatoxins are mycotoxins secreted by Aspergillus flavus, which can colonize the respiratory t

52 n of conidiation in Aspergillus fumigatus or Aspergillus flavus.

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

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

55 osure in mice sensitised and challenged with Aspergillus fumigatus (Af).

56 relevant fungi such as Candida albicans and Aspergillus fumigatus also form biofilms during infectio

57 and induction of innate immune responses to Aspergillus fumigatus and Candida albicans.

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

59 ad of agriculturally derived azole-resistant Aspergillus fumigatus and emerging threats such as multi

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

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

62 cy of pH- and calcium-mediated signalling in Aspergillus fumigatus and found that calcium chelation s

63 d juvenile Scnn1b-Tg and wild-type mice with Aspergillus fumigatus and house dust mite allergen and c

64 ides produced by the opportunistic pathogens Aspergillus fumigatus and Pseudomonas aeruginosa, respec

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

66 ere highly susceptible to aeroallergens from Aspergillus fumigatus and the house dust mite, resulting

67 onditions may result from the interaction of Aspergillus fumigatus and the immune system of its human

68 Sensitisation to Aspergillus fumigatus and/or Penicillium chrysogenum was

69 Infections caused by triazole-resistant Aspergillus fumigatus are associated with a higher proba

70 breakthrough infections with fungal pathogen Aspergillus fumigatus are associated with caspofungin pr

71 in the growth and virulence of the pathogen Aspergillus fumigatus are unknown.

72 Aspergillus fumigatus can exploit the hypoxic microenvir

73 S (7-dimethylallyl tryptophan synthase) from Aspergillus fumigatus catalyze C(4)- and C(7)-prenylatio

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

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

76 % of the cell wall of the filamentous fungus Aspergillus fumigatus comprises polysaccharides.

77 T) formation, are involved in the killing of Aspergillus fumigatus conidia and hyphae, using neutroph

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

79 following subchronic inhalation exposure to Aspergillus fumigatus conidia.

80 Homology modeling of Aspergillus fumigatus DHODH has identified a predicted b

81 Here we report a fluorogenic probe to image Aspergillus fumigatus directly in human pulmonary tissue

82 elevance of the SeptiFast assay in detecting Aspergillus fumigatus DNA in whole blood samples from 38

83 (S) utilization by the human-pathogenic mold Aspergillus fumigatus during invasive growth.

84 ermatitis, we examined the effect of topical Aspergillus fumigatus extract exposure in wild-type and

85 In an Aspergillus fumigatus extract-induced inflammation model

86 rdingly, beta-glucan surface exposure during Aspergillus fumigatus germination activates an Atg5-depe

87 Azole resistance in Aspergillus fumigatus has emerged as a global health pro

88 The genome of Aspergillus fumigatus has four arsM genes encoding ArsMs

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

90 /-) mice have an impaired ability to inhibit Aspergillus fumigatus hyphal growth in vitro and in infe

91 Colonization by Aspergillus fumigatus in patients with cystic fibrosis (

92 mmune defense against the opportunistic mold Aspergillus fumigatus In this study, we investigated the

93 ere we show that the peroxiredoxin Asp f3 of Aspergillus fumigatus inactivates ROS.

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

95 nism different from that employed to control Aspergillus fumigatus infections.

96 Azole resistance in Aspergillus fumigatus is an increasing problem.

97 Aspergillus fumigatus is an opportunistic fungal pathoge

98 Aspergillus fumigatus is an opportunistic human pathogen

99 the protection against fungal infections by Aspergillus fumigatus is essential but not fully underst

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

101 Aspergillus fumigatus is the causative agent of allergic

102 Aspergillus fumigatus is the most virulent species withi

103 Aspergillus fumigatus is the opportunistic fungal pathog

104 Heterogeneity among Aspergillus fumigatus isolates results in unique virulen

105 illus species as well as azole resistance in Aspergillus fumigatus Its performance has been validated

106 cteria Pseudomonas aeruginosa and the fungus Aspergillus fumigatus M-CSF treatment during engraftment

107 -18 structures and a structural model of the Aspergillus fumigatus mtTyrRS showed that the overall to

108 and precocious activation of conidiation in Aspergillus fumigatus or Aspergillus flavus.

109 , CD8, and natural killer (NK) cells against Aspergillus fumigatus over 5 time points and compared th

110 The resistance assay was performed on Aspergillus fumigatus PCR-positive samples when a suffic

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

112 elicited by epicutaneous sensitization with Aspergillus fumigatus protein extract.

113 Aspergillus fumigatus remains the most common species in

114 racterized the fungal opportunistic pathogen Aspergillus fumigatus Sch9 homologue (SchA).

115 Aspergillus fumigatus siderophore (SidA), a member of cl

116 utcomes following repeated inhalation of dry Aspergillus fumigatus spores aerosolized at concentratio

117 Aspergillus fumigatus spores were delivered to the lungs

118 man pathogenic fungus Aspergillus fumigatus, Aspergillus fumigatus tetramycovirus-1 (AfuTmV-1), which

119 We used Aspergillus fumigatus to induce EoE in TRAIL-sufficient

120 Sensitization to animal dander, pollen, or Aspergillus fumigatus was associated with asthma.

121 Aspergillus fumigatus was the most commonly identified s

122 as aeruginosa, Streptococcus pneumoniae, and Aspergillus fumigatus when mice were heavily engrafted w

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

124 exposed to spores of the environmental mould Aspergillus fumigatus, a major opportunistic pathogen.

125 Using Aspergillus fumigatus, a respiratory pathogen, we charac

126 Aspergillus fumigatus, a ubiquitous human fungal pathoge

127 In contrast to Aspergillus fumigatus, A. terreus infections are associa

128 gE or skin prick test response positivity to Aspergillus fumigatus, Alternaria alternata, or Cladospo

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

130 hreatening lung disease caused by the fungus Aspergillus fumigatus, and is a leading cause of invasiv

131 cluding Pseudomonas aeruginosa, Haemophilus, Aspergillus fumigatus, and nontuberculous mycobacteria.

132 acoccidioides brasiliensis, and occasionally Aspergillus fumigatus, are primary pulmonary pathogens o

133 us isolated from the human pathogenic fungus Aspergillus fumigatus, Aspergillus fumigatus tetramycovi

134 ons with the opportunistic pathogenic fungus Aspergillus fumigatus, called aspergillosis.

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

136 C57BL/6 and BALB/c mice were exposed to Aspergillus fumigatus, O3, or both (3 ppm for 2 hours).

137 ffectors against the widely distributed mold Aspergillus fumigatus, which is a major threat for immun

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

139 lycerol (HOG) pathway in the fungal pathogen Aspergillus fumigatus.

140 sults were available in 1 patient and showed Aspergillus fumigatus.

141 cluster in the opportunistic human pathogen Aspergillus fumigatus.

142 essential role in antifungal defense against Aspergillus fumigatus.

143 5 null (5) or Asp f 13 null (13) strains of Aspergillus fumigatus.

144 zed by an allergic immunological response to Aspergillus fumigatus.

145 le species, the opportunistic human pathogen Aspergillus fumigatus.

146 Netherlands might harbor triazole-resistant Aspergillus fumigatus.

147 infectious agents Listeria monocytogenes and Aspergillus fumigatus.

148 They are activated by contact with Aspergillus fumigatus; putative consequences include ant

149 The utility of Aspergillus galactomannan (GM) and beta-D-glucan (BG) in

150 ma was spiked with various concentrations of Aspergillus genomic DNA before extraction following inte

151 s were spiked with various concentrations of Aspergillus genomic DNA for extraction, following intern

152 atus is the most virulent species within the Aspergillus genus and causes invasive infections with hi

153 Molecular tests for Aspergillus have been limited historically by lack of st

154 minate, the extracellular destruction of the Aspergillus hyphae needs opsonization by Abs and involve

155 lacking both AIM2 and NLRP3 fail to confine Aspergillus hyphae to inflammatory foci, leading to wide

156 es the complexities of molecular testing for Aspergillus in clinical mycology.

157 Aspergillus incidence was 55% in the lower superoxide-pr

158 Allergic manifestations of inhaled Aspergillus include allergic bronchopulmonary aspergillo

159 6944 or rs419598 was associated with reduced Aspergillus-induced interleukin 1beta and tumor necrosis

160 ld reverse the pro-inflammatory phenotype of Aspergillus-induced regulatory T-cells.

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

162 nd two occurred in the everolimus group (one aspergillus infection and one pneumonia aspiration).

163 Severe hypoxia was observed following Aspergillus infection in both models and correlated with

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

165 This is illustrated by the prevalence of Aspergillus infections in patients with neutropenia or p

166 The manifestations of Aspergillus infections include invasive aspergillosis, c

167 y a pivotal role in the host defense against Aspergillus infections.

168 to delineate antifungal drug efficacy in non-Aspergillus invasive mold infections (NAIMIs).

169 The fungal genus Aspergillus is of critical importance to humankind.

170 athogenic molds (154 Aspergillus and 136 non-Aspergillus isolates) with the BMD and Etest methods.

171 PCR assay based on amplification of the pan-Aspergillus ITS1/5.8S ribosomal operon.

172 at had PK or EK for failed TPK conducted for Aspergillus keratitis showed better outcomes in terms of

173 perienced repeated pulmonary infections with Aspergillus, leading to multiple hospitalizations and lo

174 Mechanistically, Aspergillus melanin inhibits NADPH oxidase-dependent act

175 gnostic setting, but failure to identify non-Aspergillus molds limits its usefulness.

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

177 The Aspergillus nidulans 7-TMD receptor PalH senses alkaline

178 crystal structures of C-terminally truncated Aspergillus nidulans and Coccidioides posadasii mtTyrRSs

179 terised all Fur proteins of the model fungus Aspergillus nidulans and discovered novel functions and

180 educe the secondary metabolite background in Aspergillus nidulans and minimize the rediscovery of com

181 However, Aspergillus nidulans and vertebrate Nup2 also locate to

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

183 In the filamentous fungus Aspergillus nidulans BrlA triggers the central developme

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

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

186 The Aspergillus nidulans genome encodes 16 putative GPCRs, b

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

188 the model fungi Saccharomyces cerevisiae and Aspergillus nidulans However, the roles of myosins in th

189 ges during mitosis, which in vertebrates and Aspergillus nidulans involves movement of Nup2 from NPCs

190 ment (conidiation) in the filamentous fungus Aspergillus nidulans is governed by orchestrated gene ex

191 During Aspergillus nidulans mitosis peripheral nuclear pore com

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

193 is work, we investigated the contribution of Aspergillus nidulans sphingolipid Delta8-desaturase (Sde

194 We show that the nearly essential Aspergillus nidulans syntaxin PepA(Pep12) , present in a

195 The model fungus Aspergillus nidulans synthesizes numerous secondary meta

196 Tolerance of Aspergillus nidulans to alkalinity and elevated cation c

197 riptional response of the filamentous fungus Aspergillus nidulans to the presence of high and low glu

198 Using the filamentous fungus Aspergillus nidulans we found that hitchhiking is mediat

199 xternal intron (experimentally confirmed for Aspergillus nidulans).

200 discovery of VezA, a vezatin-like protein in Aspergillus nidulans, as a factor critical for early end

201 of mitochondrial morphology and function in Aspergillus nidulans, systematic characterization was ca

202 cent protein fusions of four SAC proteins in Aspergillus nidulans, the homologs of Mad2, Mps1, Bub1/B

203 tracking MT +end-binding proteins (+TIPS) in Aspergillus nidulans, we find that MTs are regulated to

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

205 This investigation focuses on clathrin in Aspergillus nidulans, with the aim of understanding its

206 cence microscopy that KlpA-a kinesin-14 from Aspergillus nidulans-is a context-dependent bidirectiona

207 rine transporter from the filamentous fungus Aspergillus nidulans.

208 the last few decades--Neurospora crassa and Aspergillus nidulans.

209 zae but was dissimilar to the non-oleaginous Aspergillus nidulans.

210 F-kB like fungal regulators VosA and VelB in Aspergillus nidulans.

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

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

213 Aspergillus niger also precipitated lead oxalate during

214 Aspergillus niger and Paecilomyces javanicus grew in 5 m

215 industry) and brandy distillery wastes with Aspergillus niger and Rhizopus oligosporus were investig

216 In the present work Aspergillus niger beta-glucosidase is immobilized within

217 Trichoderma and Aspergillus niger cellulases activities were determined

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

219 nd purified alpha-casein (alphas-CN) with an Aspergillus niger derived prolyl endoproteinase (An-PEP)

220 sing Escherichia coli expressing recombinant Aspergillus niger epoxide hydrolase as the model enzyme

221 Using Aspergillus niger Fdc1 as a model system, we reveal that

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

223 as a dough and bread improver, similarly to Aspergillus niger glucose oxidase (GOX).

224 gh resolution x-ray structures of a PME from Aspergillus niger in deglycosylated and Asn-linked N-ace

225 d and identified as Penicillium oxalicum and Aspergillus niger respectively in this study.

226 tnC from the kotanin biosynthetic pathway of Aspergillus niger was expressed in Saccharomyces cerevis

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

228 ausing parasite Plasmodium vivax, the fungus Aspergillus niger, and the TEM-family of beta-lactamase

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

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

231 The direct detection of Aspergillus nucleic acid in clinical specimens has the p

232 al resolution was used to collect spectra of Aspergillus ochraceus, a mold producer of ochratoxin A (

233 ohol were tested against Aspergillus flavus, Aspergillus ochraceus, Fusarium oxysporum, Saccharomyces

234 of life were not detected for patients with Aspergillus or other non-Fusarium species as the causati

235 ucoid P. aeruginosa (OR, 0.77; P = .013) and Aspergillus (OR, 0.47; P = .039), but not Staphylococcus

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

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

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

239 euromutilin cluster was reconstructed within Aspergillus oryzae giving production of pleuromutilin in

240 Aspergillus oryzae showed stability at all pH values stu

241 y flour fermented with Monascus purpureus or Aspergillus oryzae.

242 Bacillus circulans, Kluyveromyces lactis and Aspergillus oryzae.

243 tarch aerogel and led to slower lethality of Aspergillus parasiticus cells inoculated on pistachio nu

244 tous fungus and an important plant pathogen, Aspergillus parasiticus, without inhibiting fungal growt

245 anding mycelium of a popular plant pathogen, Aspergillus parasiticus.

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

247 With the proposal to include Aspergillus PCR in the revised European Organization for

248 s (IA) have been established by the European Aspergillus PCR Initiative for the testing of whole bloo

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

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

251 This study confirms that Aspergillus PCR testing of plasma provides robust perfor

252 Aspergillus PCR testing of serum provides technical simp

253 Standardized Aspergillus PCR was performed on 423 whole-blood pellets

254 Standardized Aspergillus PCR was performed on plasma and serum sample

255 The sensitivity and specificity for Aspergillus PCR when testing serum were 68.4% and 76.2%,

256 While some comparison of the performance of Aspergillus PCR when testing these different sample type

257 The current study focused on germination of Aspergillus penicillioides, a xerophile which is also ab

258 Spores from a variety of species, including Aspergillus penicillioides, Eurotium halophilicum, Xeroc

259 ustralian database for the identification of Aspergillus, Scedosporium, and Fusarium species (n = 28)

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

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

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

263 d airway responsiveness following intranasal aspergillus sensitization.

264 able to accurately identify 133/144 (93.6%) Aspergillus sp. isolates to the species level.

265 The dominant fungal genera were Aspergillus sp., Rhizopus sp., Penicillium sp. and Saroc

266 nome sequences for ten novel, highly diverse Aspergillus species and compared these in detail to sist

267 st that has the ability to detect a range of Aspergillus species as well as azole resistance in Asper

268 Doxycycline-exposed, Aspergillus species extract-challenged CC10-IL-15 bitran

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

270 The ability of neutrophils to interfere with Aspergillus species hyphal growth was impaired after HSC

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

272 Fusarium and Aspergillus species were the two predominant molds accou

273 ween invasive fungi (eg, Candida species and Aspergillus species) and pathogenic bacteria can be part

274 ve pathogens of these outbreaks were usually Aspergillus species, but Zygomycetes and other fungi wer

275 rol and bioremediation technologies based on Aspergillus species.

276 s the second transesterification reaction in Aspergillus species.

277 dole alkaloids isolated from Penicillium and Aspergillus species.

278 ndida species and fungistatic action against Aspergillus species.

279 An Aspergillus-specific lateral-flow device (LFD), quantita

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

281 posttransplantation airway colonization with Aspergillus spp.

282 Aspergillus spp. (17%) and Staphylococcus aureus (10.7%)

283 Etest MIC values were consistently lower for Aspergillus spp. (EAs of <90%).

284 When wounds with Mucorales and Aspergillus spp. growth were compared, there was no sign

285 an 100 strains from the four main pathogenic Aspergillus spp. revealed minimal inhibitory concentrati

286 oides immitis/posadasii, Fusarium oxysporum, Aspergillus spp., and Bipolaris spp.) was also identifie

287 e molds (predominant types: order Mucorales, Aspergillus spp., and Fusarium spp.) significantly prolo

288 uses include Candida spp., Fusarium spp. and Aspergillus spp..

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

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

291 study was to improve the thermostability of Aspergillus sulphureus acidic xylanase.

292 hunamides A-G, were isolated from the fungus Aspergillus taichungensis (IBT 19404).

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

294 Aspergillus terreus is an airborne human fungal pathogen

295 A fungus called Aspergillus terreus produces a secondary metabolite in r

296 errein production were studied in the fungus Aspergillus terreus to elucidate the contribution of ter

297 entation of sugars by the filamentous fungus Aspergillus terreus.

298 roliferative cyclic tripeptide isolated from Aspergillus versicolor ZLN-60, is reported herein.

299 sentation of Candida spp. was reduced, while Aspergillus, Wallemia, and Epicoccum spp. were increased

300 in response to environmental Alternaria and Aspergillus, was elevated in children with a maternal hi