ライフサイエンスコーパス: fungus

1 resistance function of WTK3 against the Bgt fungus.

2 e the potential to control the growth of the fungus.

3 e fission yeast clade, is one such dimorphic fungus.

4 ins predicted in the genome database of this fungus.

5 irulent bacteria and a virulent necrotrophic fungus.

6 oteins in response to the infection of blast fungus.

7 izontal gene transfer (HGT) from a rhizobial fungus.

8 l mosaic centromeres in this early-diverging fungus.

9 ion events and were less colonised by the AM fungus.

10 lpha in human macrophages infected with this fungus.

11 ed the PS synthase homolog (Cn Cho1) in this fungus.

12 transcriptional variability in the host and fungus.

13 pz1-Hal3 system in this important pathogenic fungus.

14 derophores, which induced iron stress on the fungus.

15 protein interactions (PPIs) between rice and fungus.

16 us and 8 that had never been observed in any fungus.

17 ysiology and pathogenicity of the rice blast fungus.

18 s sylvestris seedlings and each saprotrophic fungus.

19 m-mediated plant infection by the rice blast fungus.

20 duced decline in plant C allocated to the AM fungus.

21 he polarized growth and pathogenicity of the fungus.

22 ludes C. auris, a highly multidrug-resistant fungus.

23 nsferase (DBAT) have been identified in this fungus.

24 grass smut Ustilago maydis is the only smut fungus adapted to Brassicaceae hosts.

25 d and the kinetics of laccase from white rot fungus adsorption and its direct electro-catalytic activ

26 rmination and resistance to infection by the fungus Albugo laibachii, isolate Nc14.

27 e defenses against B. dendrobatidis, but the fungus also has a number of counterdefenses.

28 The fungus also produces carcinogenic mycotoxins, fumonisins

29 lated along with 11 known compounds from the fungus Alternaria alternata P1210.

30 no data on the major allergen Alt a 1 of the fungus Alternaria alternata.

31 Early blight, caused by the necrotrophic fungus Alternaria solani, is an increasing problem in po

32 llergens derived from the common saprophytic fungus, Alternaria alternata release ATP, which in turn

33 t had not previously been identified in this fungus and 8 that had never been observed in any fungus.

34 at the interface between an actively growing fungus and an iron-containing mineral, hematite.

35 cus neoformans is a ubiquitous environmental fungus and an opportunistic pathogen that causes fatal c

36 e apoptosis signaling pathway was induced by fungus and bacteria.

37 ng of phospholipid synthesis in a pathogenic fungus and indicate that PS synthase may be a useful tar

38 uense NJAU4742 and magnetite (Mt) as a model fungus and mineral system, we have shown for the first t

39 ome, potentially due to their effects on the fungus and other local immune cells.

40 rrence of infection of the amphibian chytrid fungus and ranaviruses during one season in two suscepti

41 ional pipeline to predict PPIs between blast fungus and rice.

42 xed carbon transferred from the plant to the fungus and several studies have begun to elucidate the m

43 The amphibian chytrid fungus and the viruses of the Ranavirus genus are alread

44 t by a globally devastating plant pathogenic fungus and to determine how impaired protein quality con

45 ved the structure of Dfg5 from a filamentous fungus and used in crystallo glycan fragment screening t

46 he dried extracellular matrix (ECM) from the fungus, and Ca oxalate crystals.

47 However, the allergens in this fungus are still unknown, limiting the development of di

48 ns between pathogenic and endophytic of this fungus are unknown.

49 bind to the Bateman domain of IMPDH from the fungus Ashbya gossypii with submicromolar affinities.

50 In the multinucleate filamentous fungus Ashbya gossypii, the RNA-binding protein Whi3 reg

51 e emissions of grape berries infected by the fungus Aspergillus carbonarius.

52 than 90% of the cell wall of the filamentous fungus Aspergillus fumigatus comprises polysaccharides.

53 ess response and virulence of the pathogenic fungus Aspergillus fumigatus, the leading etiology of in

54 t uncharacterized silent gene cluster of the fungus Aspergillus fumigatus, which is activated by the

55 ain proteins present in the human pathogenic fungus Aspergillus fumigatus.

56 Hyphal tip cells of the fungus Aspergillus nidulans are useful for studying long

57 performed on single spores (conidia) of the fungus Aspergillus nidulans in order to establish a base

58 In the filamentous fungus Aspergillus nidulans SPBs and septum-associated M

59 The model fungus Aspergillus nidulans synthesizes numerous seconda

60 In this study, the ability of the geoactive fungus Aspergillus niger to colonize and transform manga

61 In this work, the geoactive fungus Aspergillus niger was investigated for struvite t

62 by fermentation of sugars by the filamentous fungus Aspergillus terreus.

63 isolated from a novel species of Australian fungus, Aspergillus nanangensis.

64 he capability of a ubiquitous geoactive soil fungus, Aspergillus niger, to affect the mobility of REE

65 y, we report the isolation of an onygenalean fungus associated with shell lesions in freshwater aquat

66 Yet, fungus-associated helper bacteria of the genus Mycetocol

67 will enable the detection of this ubiquitous fungus at the point-of-care, and could help to improve c

68 of AM fungal ecology, from the level of the fungus, at the plant community level, and to functional

69 Amphibian population declines caused by the fungus Batrachochytrium dendrobatidis (Bd) have prompted

70 predict infection prevalence of the chytrid fungus Batrachochytrium dendrobatidis (Bd) in a global a

71 lay a key role in spreading the frog-killing fungus Batrachochytrium dendrobatidis (Bd) in the natura

72 ce and intensity of infection of the chytrid fungus Batrachochytrium dendrobatidis (Bd), across a 3-y

73 ized driver of these declines is the chytrid fungus Batrachochytrium dendrobatidis, which causes the

74 diomycosis, a pandemic disease caused by the fungus Batrachochytrium dendrobatidis; however, some spe

75 The salamander chytrid fungus (Batrachochytrium salamandrivorans [Bsal]) is cau

76 Subsequent to the epidemic emergence of the fungus, Batrachochytrium salamandrivorans (Bsal), in mai

77 volution to occur, with the entomopathogenic fungus, Beauveria bassiana, and the red flour beetle, Tr

78 specific detergents in the insect pathogenic fungus, Beauveria bassiana.

79 bacterium from infecting the fungus, but the fungus became less tolerant to cell membrane stress.

80 mple of metabolic exaptation evolved in this fungus because the primary function of these ancient pro

81 tion, body size, and weaponry of male forked fungus beetles Bolitotherus cornutus as they influenced

82 a foliar disease caused by the necrotrophic fungus Bipolaris cookei (also known as Bipolaris sorghic

83 pot (TLS) disease caused by the necrotrophic fungus Bipolaris cookei in the SCP.

84 entral to zoospore phototaxis in the aquatic fungus Blastocladiella emersonii It has generated consid

85 ion of barley with the barley powdery mildew fungus Blumeria graminis f. sp. hordei (Bgh).

86 ng honeybees from pathogens (phytopathogenic fungus Botrytis cinerea and pathogenic bacteria, respect

87 ingae pv. tomato DC3000 and the necrotrophic fungus Botrytis cinerea As pldgamma1 mutant plants respo

88 ial pathogen Pseudomonas syringae and to the fungus Botrytis cinerea Furthermore, bsk5 mutant plants

89 g infection of Arabidopsis thaliana with the fungus Botrytis cinerea Indeed, in contrast to previous

90 wines are made with berries infected by the fungus Botrytis cinerea.

91 not prevent the bacterium from infecting the fungus, but the fungus became less tolerant to cell memb

92 se findings highlight the complex role a gut fungus can play in influencing the microbial communities

93 utrient-rich niches (i.e. tumors), where the fungus can proliferate and complete its life cycle.

94 This fungus can survive for years in soil as melanized micros

95 The fungus Candida albicans and the Gram-positive bacterium

96 ciated polymicrobial biofilms containing the fungus Candida albicans exist.

97 n of the oral mucosa caused by the commensal fungus Candida albicans IL-17R signaling is essential to

98 A recent study shows that the commensal fungus Candida albicans is an inducer of differentiation

99 tructure of Trl1 KIN-CPD from the pathogenic fungus Candida albicans, which adopts an extended confor

100 fection with a lethal dose of the pathogenic fungus Candida albicans.

101 w how dynamic resource movement may help the fungus capitalize on value differences across the trade

102 Ustilago maydis is a biotrophic fungus causing corn smut disease in maize.

103 Metarhizium majus and the stalked-cup lichen fungus Cladonia grayi.

104 pathogen Sporothrix schenckii, and the ergot fungus Claviceps purpurea.

105 We identify the fungus comb, of Macrotermes subhyanus, as a potential bi

106 We found that the fungus: compensated for resource loss in the 'crash' tre

107 ynthetic algae to enter the hyphae of a soil fungus could tell us more about the evolution of these s

108 ted from strain NB631 of the chestnut blight fungus (Cryphonectria parasitica), a model filamentous f

109 rom U.S. strain NB631 of the chestnut blight fungus, Cryphonectria parasitica, was the first virus id

110 The pathogenic fungus Cryptococcus neoformans produces melanin within i

111 nin in the cell wall of the human pathogenic fungus Cryptococcus neoformans We observed that melanin

112 and CnHal3b (CNAG_07348) from the pathogenic fungus Cryptococcus neoformans.

113 Allocation of plant C to the AM fungus decreased dramatically following exposure to the

114 howed strong growth inhibition of the marine fungus Dendryphiella salina indicating an antifungal eco

115 Transporter1 To accumulate plant sugars, the fungus deploys its own set of sugar transporters, genera

116 auses powdery mildew, and the hemibiotrophic fungus Diplocarpon rosae, which causes black spot, we an

117 We assembled the genomes of the AM fungus Diversispora epigaea (formerly Glomus versiforme)

118 exocellular oxidase enzymes produced by this fungus during fruit contamination.

119 ered in the laboratory simply by growing the fungus either at room temperature (RT; which promotes hy

120 rocarpans produced in soybean seedlings upon fungus elicitation.

121 ustained once cell fusion occurred until the fungus enter the plant tissue.

122 eneralist predators of the nematode-trapping fungus family.

123 us (formerly Emmonsia helica) is a dimorphic fungus first isolated from a man with fungal encephaliti

124 LTTs) from a complex extract of the polypore fungus Fomitopsis pinicola.

125 yphonectria parasitica), a model filamentous fungus for studying virus-host interactions.

126 the ATG genes, except FgATG17, prevented the fungus from causing Fusarium head blight disease.

127 logical control of HB in the BI using a rust fungus from the Himalayan native range was implemented i

128 for plant infection in the wheat head blight fungus Fusarium graminearum.

129 G-LSR2 was horizontally transferred from the fungus Fusarium oxysporum f. sp. vasinfectum to V. dahli

130 uizhouense can overgrow another hypocrealean fungus Fusarium oxysporum, cause sporadic cell death and

131 nt work, for the first time, the filamentous fungus Fusarium sp. was utilized for devising a novel me

132 earlier reported Taxol-producing endophytic fungus, Fusarium solani from the standpoint of spores as

133 onomic composition support the microbiota of fungus-growing insects as convergent, despite difference

134 other hosts, the microbiota associated with fungus-growing insects presents a distinctive taxonomic

135 ndant features codified by the microbiota of fungus-growing insects suggest these communities occupyi

136 Here, by comparing fungus-growing insects to several hosts ranging diverse

137 tabolic pathways potentially relevant to the fungus-growing insects' ecosystems functioning.

138 Fungus-growing insects' symbiosis also hosts a bacterial

139 wth at 37 degrees C; in each ryp mutant, the fungus grows constitutively as hyphae regardless of temp

140 ss for around 10 days, during which time the fungus grows randomly across the leaf surface prior to e

141 y the bacterium culture inhibited to 100% of fungus growth and 100% of sclerotia production.

142 The CFS of X. szentirmaii inhibited > 98% of fungus growth from mycelium and sclerotia, whereas the v

143 se biogenic nanoparticles formed through the fungus-hematite interactions can behave as mimetic catal

144 rolytic mechanism in a GH45, Cel45A from the fungus Humicola insolens, via unbiased simulation approa

145 ) are being devastated by the invasive alien fungus Hymenoscyphus fraxineus, which causes ash dieback

146 The biosorption capacities of fungus immobilized iron oxide nanoparticles were found a

147 ng fungi above and beyond the assumed single fungus in lichen thalli [1-6].

148 ascus roseus, the most widespread decomposer fungus in maritime Antarctic fellfield soils, is reduced

149 antly higher levels of Aspergillus and total fungus in their bronchoalveolar lavage.

150 Aspergillus terreus is an allergenic fungus, in addition to causing infections in both humans

151 red for ciliogenesis, demonstrating that the fungus induced paralysis via the cilia of nematode senso

152 ntially expressed in comparisons both of the fungus infected with the wild-type bacterium vs. the mut

153 omotes the recruitment of neutrophils to the fungus-infected CNS, which mediates fungal clearance.

154 inflammasome activation, and of CXCL1 in the fungus-infected CNS.

155 d smaller tumors compared to controls and to fungus-infected larvae.

156 CA01g05990 genes showed an early response to fungus infection in RF (24 h post-inoculation-HPI), bein

157 le provide insight into the process of blast fungus infection.

158 ole for the host in facilitating a bacterium-fungus infectious synergy, leading to disseminated staph

159 ed and 1,762 downregulated genes in RF under fungus inoculation.

160 eatment that helps to protect the seeds from fungus, insects, and nematodes after planting.

161 ns adhesin encoded by ALS3 While a bacterium-fungus interaction is required for systemic infection, t

162 rded decoy in this interaction, trapping the fungus into a recognition event.

163 ibute to the better understanding of how the fungus is able to facilitate wood decay and nutrient cyc

164 The same species of fungus is found in Europe but without associated mortali

165 and pathogen pressure from this cool-adapted fungus is high.

166 This fungus is listed as a quarantine pest in several parts o

167 The model rock-inhabiting microcolonial fungus Knufia petricola fractionates stable Mg isotopes

168 We showed that the ectomycorrhizal fungus Laccaria bicolor produces an array of lipochitool

169 tualistic symbiosis with the ectomycorrhizal fungus Laccaria bicolor, we sought to determine if host

170 icitors by human chitinases, thus making the fungus less susceptible to host immunosurveillance.

171 "global destroyer of crops", the soil-borne fungus Macrophomina phaseolina (Mp) infects more than 50

172 Rice blast disease caused by the fungus Magnaporthe grisea (M. grisea) is one of the most

173 grouped field populations of the rice blast fungus Magnaporthe oryzae (syn: Pyricularia oryzae) into

174 The fungus Magnaporthe oryzae causes blast, the most devasta

175 The fungus Magnaporthe oryzae causes devastating diseases of

176 The blast fungus Magnaporthe oryzae gains entry to its host plant

177 The pathogenic life cycle of the rice blast fungus Magnaporthe oryzae involves a series of morphogen

178 Wheat blast caused by the fungus Magnaporthe oryzae pathotype Triticum (MoT) is an

179 In the devastating blast fungus Magnaporthe oryzae(1), powerful glycoprotein-rich

180 ssorium-mediated infection in the rice blast fungus Magnaporthe oryzae, requires very-long-chain fatt

181 Here we show how, in the blast fungus Magnaporthe oryzae, terminating rice innate immun

182 8b-regulated rice immunity against the blast fungus Magnaporthe oryzae.

183 sed the function of MoHMT1 in the rice blast fungus, Magnaporthe oryzae.

184 One of these, the common skin resident fungus Malassezia restricta, is also linked to the prese

185 Here, we show how a symbiotic fungus mediates trade with a host root in response to di

186 For the poplar leaf rust fungus Melampsora larici-populina, the transcripts of it

187 hat were inoculated with the biotrophic rust fungus (Melampsora larici-populina) accumulated higher a

188 ust males infected with the entomopathogenic fungus Metarhizium acridum.

189 ified in the genome of the insect-pathogenic fungus Metarhizium rileyi.

190 become internalized within the hyphae of the fungus Mortierella elongata.

191 erium Mycoavidus sp. and the root-associated fungus Mortierella elongata.

192 Fusarium circinatum is a harmful pathogenic fungus mostly attacking Pinus species and also Pseudotsu

193 volatiles of X. szentirmaii cultures on the fungus mycelium and sclerotium inhibition; and evaluate

194 hispidin 3-hydroxylase, from the luminescent fungus Mycena chlorophos (McH3H), which catalyzes the co

195 d isolate as a model strain for the study of fungus-nematode interactions and demonstrates that trap

196 lation-mediated silencing in the filamentous fungus Neurospora crassa and identified a bromo-adjacent

197 The model filamentous fungus Neurospora crassa is capable of utilizing a varie

198 germinated asexual spores in the filamentous fungus Neurospora crassa rcd-1 alleles are highly polymo

199 ctive C4-oxidizing family AA9 LPMOs from the fungus Neurospora crassa, NcLPMO9A (NCU02240), NcLPMO9C

200 tic antifungal peptide PAF26 using the model fungus Neurospora crassa.

201 sion in a wild population of the filamentous fungus Neurospora crassa.

202 cellulolytic enzyme production by an aerobic fungus next to facultative anaerobic lactic acid bacteri

203 Candida albicans is a commensal fungus of human gastrointestinal and reproductive tracts

204 Candida albicans is a commensal fungus of the human gut, but also causes life-threatenin

205 s transmitted in nature via zoospores of the fungus Olpidium bornovanus While a number of plant virus

206 of the orientation of laccase from white rot fungus on multi-walled carbon nanotube surface modified

207 osis (snake fungal disease) is caused by the fungus Ophidiomyces ophiodiicola and threatens snake hea

208 se-responsive genes after infection with the fungus Ophiostoma novo-ulmi.

209 linked to carbon (C) transfer from plant to fungus or governed by sink-source dynamics.

210 ides the first evidence that the filamentous fungus P. graminis has evolved to produce fungal suppres

211 d is vanillyl-alcohol oxidase (VAO) from the fungus Penicillium simplicissimum For oxidation of pheno

212 tation and development in a plant endophytic fungus, Pestalotiopsis fici.

213 The MadC protein in the fungus Phycomyces blakesleeanus (Mucoromycotina) has bee

214 Citrus black spot (CBS) caused by the fungus Phyllosticta citricarpa occurs in tropical and su

215 s variation between four isolates of the ECM fungus Pisolithus microcarpus, in terms of gene regulati

216 al exocytosis and the roles of exocytosis in fungus-plant interactions.

217 ar1/KDM5 in Botrytis cinerea, the grey mould fungus, plays a crucial role in these processes.

218 re the mushroom holobiont, understood as the fungus plus associated microorganisms.

219 The inflammatory response to the fungus Pneumocystis jirovecii plays a central role in th

220 ages of infection by the obligate biotrophic fungus Podosphaera pannosa, which causes powdery mildew,

221 cuss the need for improved awareness of this fungus' potential link to cause disseminated and invasiv

222 The fungus produces several mycotoxins of which the fumonisi

223 d, we achieved 532 potential PPIs between 27 fungus proteins and 236 rice proteins.

224 ster regulators in rice interacting with the fungus proteins in response to the infection of blast fu

225 The psychrophilic (cold-loving) fungus Pseudogymnoascus destructans was discovered more

226 White-nose syndrome (WNS), caused by the fungus Pseudogymnoascus destructans, has caused widespre

227 White-nose syndrome (WNS) caused by the fungus, Pseudogymnoascus destructans (Pd) has killed mil

228 housands of dry-dispersed spores of the rust fungus Puccinia triticina being liberated from infected

229 The wheat leaf rust fungus, Puccinia triticina, is found in the major wheat

230 e they have been found to vector a symbiotic fungus, Raffaelea lauricola, the causal agent of the lau

231 nsects as convergent, despite differences in fungus-rearing by these insects.

232 M) fungus, Rhizophagus irregularis, when the fungus received an external supply of certain fatty acid

233 he timing of spore release would matter to a fungus remains an open question.

234 for their abilities to interact with the AM fungus Rhizophagus irregularis and the oomycete pathogen

235 runcatula plants were cocultured with the AM fungus Rhizophagus irregularis under high and low K(+) r

236 n colonization by the arbuscular mycorrhizal fungus Rhizophagus irregularis.

237 By supplying (33)P to an AM fungus (Rhizophagus irregularis) and (14)CO(2) to wheat,

238 production of an arbuscular mycorrhizal (AM) fungus, Rhizophagus irregularis, when the fungus receive

239 (formerly Burkholderia) rhizoxinica with the fungus Rhizopus microsporus, bacterial type III (T3) sec

240 omplete genome sequence of the basidiomycete fungus Rigidoporus microporus, a causative agent of the

241 ubstrate specificity of Cdc14 from the model fungus Saccharomyces cerevisiae (ScCdc14) are well-defin

242 The fungus, Sclerotinia sclerotiorum, causes white mold dise

243 PLC-MS analysis, and was able to identify 14 fungus secondary metabolites, namely aflatoxin B1, aflat

244 ta and CXCL1 was induced in microglia by the fungus-secreted toxin Candidalysin, in a manner dependen

245 e individualized and depend on the offending fungus, site and extent of IMD, comorbidities, hematolog

246 We show here that, in the fungus Sordaria macrospora, this critical transition is

247 For 25 of these, the effects were fungus specific, as opposed to general alterations in ph

248 ation procedure-, antifungal treatment-, and fungus-specific issues affect the risk of IFD relapse.

249 This fungus-specific system consists of a secreted zinc-bindi

250 deficiency in CARD9 causes susceptibility to fungus-specific, CNS-targeted infection.

251 AS landscape during infection with the smut fungus (Sporisorium scitamineum) using a hybrid approach

252 osis is an infection caused by the dimorphic fungus Sporothrix schenckii and related species that oft

253 phosphorus was transferred to the host, the fungus successfully controlled resource value.

254 The fungus survives in the soil for up to 14 years by produc

255 nism at the protein level for the lignin/dye/fungus system.

256 rytis cinerea is a well-studied necrotrophic fungus taken as a model organism in fungal plant patholo

257 um, University of Texas Health San Antonio's Fungus Testing Laboratory, and Associated Regional and U

258 o telomere maintenance in Ustilago maydis, a fungus that bears strong resemblance to mammals with res

259 Aspergillus fumigatus is an environmental fungus that can cause invasive pulmonary aspergillosis w

260 Cryptococcus neoformans is an encapsulated fungus that causes cryptococcosis, an opportunistic infe

261 Verticillium dahliae is a soil-borne fungus that causes vascular wilt on numerous plants worl

262 Candida albicans, a ubiquitous commensal fungus that colonizes human mucosal tissues and skin, ca

263 Talaromyces marneffei is a dimorphic fungus that has emerged as an opportunistic pathogen par

264 Candida albicans-a yeast-like fungus that inhabits mucosal surfaces-is also a signific

265 entified two small molecules produced by the fungus that inhibit frog lymphocyte proliferation, methy

266 Cryptococcus neoformans is a basidiomycete fungus that is highly resistant to ionizing radiation an

267 is considered to be the main phytotoxin in a fungus that is responsible for cork oak decline.

268 Candida albicans is a pervasive commensal fungus that is the most common pathogen responsible for

269 rid-type centromere is found in a pathogenic fungus that lacks the key kinetochore component CENP-A.

270 ndida auris, an emerging multidrug-resistant fungus that presents a serious global health threat.

271 ushroom Pleurotus ostreatus is a carnivorous fungus that preys on nematodes to supplement its nitroge

272 ferred to as S. bescii, is a root-associated fungus that promotes plant growth in both its native swi

273 tated a radiation of social strategies, from fungus thieves to eusocial species to communities assemb

274 the top seven subnetworks affected by blast fungus through PPIs were investigated.

275 e the technical challenges that prevent this fungus to be a novel platform for industrial Taxol produ

276 nducing S. rapamycinicus, and thus helps the fungus to defend resources in the shared habitat against

277 metabolically describe the adaptation of the fungus to diminishing nutrients.

278 ssential gene, and heterokaryons allowed the fungus to maintain lethal CpRbp1-null mutant nuclei.

279 We found significant (15) N transfer from fungus to plant in all cultivars, and cultivar-specific

280 n of Ag NPs in the growth medium allowed the fungus to regain completely its ability of aflatoxin bio

281 le larva to ants within a colony exposed the fungus to the robust social immunity of ant societies.

282 Identification of the fungus Tremella as a consistent fourth component of wolf

283 Replicate populations of the filamentous fungus Trichoderma citrinoviride underwent 85 serial tra

284 When resources are limited, the hypocrealean fungus Trichoderma guizhouense can overgrow another hypo

285 The secretome of the cellulolytic model fungus Trichoderma reesei contains two GH7s, termed TrCe

286 tants of maize (Zea mays) and the beneficial fungus Trichoderma virens and identified 12-oxo-phytodie

287 The corn smut fungus uses two different mechanisms to control its cell

288 In the fungus Ustilago maydis, sexual pheromones elicit mating

289 , a virulence-promoting effector of the smut fungus Ustilago maydis.

290 The fungus Verticillium dahliae causes vascular wilt disease

291 The fungus Verticillium dahliae causes vascular wilt disease

292 The fungus Verticillium dahliae causes wilts of several hund

293 two of the six GH12 proteins produced by the fungus Verticillium dahliae Vd991, VdEG1 and VdEG3 acted

294 nce genome evolution in the plant pathogenic fungus Verticillium dahliae.

295 iderophores detection and later designed for fungus was adapted here for diffusive equilibrium in thi

296 The fungus was detected using real-time PCR in 26 (8.6%) spe

297 A biofilter with fungus was developed for efficient degradation of benzen

298 Meanwhile, the pathogenic genes of blast fungus were enriched in the predicted PPIs network when

299 sinks can limit plant C allocation to an AM fungus without hindering mycorrhizal-acquired nutrient u

300 emonstrated colonization of a widespread gut fungus (Zancudomyces culisetae) in a larval mosquito (Ae