ライフサイエンスコーパス: Fusarium

1 l ulcers, particularly among those caused by Fusarium.

2 se(6), displayed enhanced resistance against Fusarium.

3 t has not always paralleled the evolution of Fusarium.

4 an important new tool for genetic studies of Fusarium.

5 Causative organisms included Fusarium (128 patients [40%]), Aspergillus (54 patients

6 = 14) was isolated in highest number whereas Fusarium (13.4%, N = 6) was the most common fungus speci

7 library alone (Aspergillus, 93% versus 69%; Fusarium, 84% versus 42%; and Scedosporium, 94% versus 1

8 Further results suggest that the anti-Fusarium activity of M6 may be transferable to maize and

9 the ATG gene with the most editing sites in Fusarium affected ascospore releasing.

10 lapse and black roots, symptoms similar to a Fusarium-Alternaria disease complex, recently characteri

11 Fusarium and Aspergillus species of mold are major cause

12 Fusarium and Aspergillus species were the two predominan

13 NAT enzymes in crop-compromising species of Fusarium and Aspergillus, identifying three groups of ho

14 t perspectives of what constitutes the genus Fusarium and how many species occur within the genus.

15 unctional divergence of two beta-tubulins in Fusarium and identified type II variations in FgTub2 res

16 Seed-coated M6 swarms towards root-invading Fusarium and is associated with the growth of root hairs

17 The genera Cladosporium, Fusarium and Penicillium were the fungi more frequently

18 olutionary antagonistic interactions between Fusarium and Streptomyces are driven by resource competi

19 found evidence for local adaptation between Fusarium and Streptomyces populations as indicated by si

20 cteria, decreasing the relative abundance of Fusarium, and increasing the fungal network complexity t

21 (coagulase-negative Staphylococcus, Candida, Fusarium, and Propionibacterium species).

22 sporium, Alternaria, Penicillium, Ulocadium, Fusarium, Arthrinium, Epicoccum, Aureobasidium, Curvular

23 mples the dominant genera were Cladosporium, Fusarium, Aspergillus, and Alternaria.

24 onale (46%), Fusarium cortaderiae (13%), and Fusarium austroamericanum (3%).

25 amacril also inhibits the ATPase activity of Fusarium avenaceum myosin-1 but has little or no inhibit

26 naturally occurring hemibiotrophic pathogen, Fusarium brachygibbosum Among all AGOs, only transcripts

27 ir influence on two native fungal pathogens, Fusarium brachygibbosum U4 and Alternaria sp. U10, and t

28 tracellular pH promotes infectious growth of Fusarium by stimulating phosphorylation of a conserved m

29 belief for natamycin treatment, whereas non-Fusarium cases had a 57.3% belief.

30 For Fusarium cases, the posterior demonstrated a 99.7% belie

31 fference attributable to improved results in Fusarium cases.

32 Fusarium circinatum is a harmful pathogenic fungus mostl

33 Zn(II) ions, using a mini-column packed with Fusarium-coated multi-walled carbon nanotubes and induct

34 has high levels of airborne Aspergillus and Fusarium conidia.

35 arum s.s. (37%), Fusarium meridionale (46%), Fusarium cortaderiae (13%), and Fusarium austroamericanu

36 Fusarium crown rot (FCR) of wheat and barley, predominan

37 found to mediate systemic resistance against Fusarium crown rot and to simultaneously improve tomato

38 ditions and following inoculation with fungi Fusarium culmorum.

39 Fusarium-damaged kernels and deoxynivalenol analyses sup

40 led to a significant decrease (p < 0.01) in Fusarium-damaged rachis rate, Fusarium-diseased kernel r

41 ling, diverse fungicides and resistance to a Fusarium-derived antibiotic.

42 xins in wheat three standardized approaches (Fusarium disease severity, PCR assays for Fusarium spp.

43 (p < 0.01) in Fusarium-damaged rachis rate, Fusarium-diseased kernel rate and DON content in harvest

44 ed Artemia survivorship and hyphal growth of Fusarium during the immature and mature stages.

45 Fungal mutants lacking a functional Fusarium (F)-RALF peptide failed to induce host alkalini

46 Three of the FSSC species (Fusarium falciforme, Fusarium keratoplasticum, and Fusar

47 een isolated from the rice pathogenic fungus Fusarium fujikuroi already more than 20 years ago.

48 Sequencing of the rice pathogen Fusarium fujikuroi revealed the presence of far more SM-

49 ndary metabolites produced by members of the Fusarium fujikuroi species complex (FFSC) and rare strai

50 several fusaria, including the rice pathogen Fusarium fujikuroi.

51 In Fusarium, fumonisin biosynthetic genes (FUM) are cluster

52 d by the presence of mycotoxins derived from Fusarium fungus, and, in particular, by deoxynivalenol (

53 ted toxigenic species of the Aspergillus and Fusarium genera isolated from grapes and cereals.

54 tion, redundancy analysis indicated that the Fusarium genera were significantly related to the diseas

55 Fusarium head blight (FHB) caused by Fusarium graminearum (Fg) is a devastating disease of cr

56 Fusarium graminearum (FG) is one of the major cereal inf

57 ina sp. LEB-18 phenolic extract (PE) against Fusarium graminearum (Fg) isolates.

58 ha-L-fucosidase from plant pathogenic fungus Fusarium graminearum (FgFCO1) actively releases fucose f

59 Expression of HopAI in Fusarium graminearum also mainly affected the activation

60 Trichoderma atroviride, the plant pathogens Fusarium graminearum and Colletotrichum graminicola, the

61 (1)CFU g(-1) and the species most found were Fusarium graminearum and Fusarium verticillioides with 2

62 the plasma membrane of the ascomycete fungi Fusarium graminearum and Neurospora crassa and induces a

63 could contribute to maize resistance against Fusarium graminearum and other fungal pathogens.

64 Mycotoxin-producing Fusarium graminearum and related species cause Fusarium

65 The ubiquitous filamentous fungus Fusarium graminearum causes the important disease Fusari

66 Infection of the Fusarium graminearum disruption mutant Deltafgl1, which

67 recovered via the heterologous expression of Fusarium graminearum GSK3 homolog gene FGK3, whose codin

68 ecific pollination and during infection with Fusarium graminearum In both Arabidopsis species, the la

69 Following Fusarium graminearum infection, we identified accumulati

70 Fusarium graminearum is a causal agent of Fusarium head

71 Fusarium head blight (FHB) caused by Fusarium graminearum is a devastating disease of cereal

72 Fusarium graminearum is a filamentous fungus and causes

73 Wheat scab caused by Fusarium graminearum is an important disease.

74 Fusarium graminearum is an important pathogen of wheat a

75 Fusarium graminearum is an important plant pathogen that

76 Fusarium head blight caused by Fusarium graminearum is one of the most destructive dise

77 nthesis of mycotoxin deoxynivalenol (DON) in Fusarium graminearum is regulated by two pathway-specifi

78 reticulum (ER) of the phytopathogenic fungus Fusarium graminearum is reorganized both in vitro and in

79 We also verified that the VdAtf1 ortholog in Fusarium graminearum mediates nitrogen metabolism, sugge

80 Fusarium Head Blight (FHB) caused by Fusarium graminearum pathogens constitutes a major threa

81 t and spiked into fungal culture filtrate of Fusarium graminearum respectively.

82 Four members of the Fusarium graminearum species complex were isolated: F. g

83 he primary inoculum in the wheat scab fungus Fusarium graminearum that was recently shown to have sex

84 Head blight caused by Fusarium graminearum threatens world-wide wheat producti

85 The role of the retromer complex in Fusarium graminearum was investigated using cell biologi

86 Ascospores are the primary inoculum in Fusarium graminearum, a causal agent of wheat head bligh

87 in the regulation of sterol biosynthesis in Fusarium graminearum, a fungal pathogen of cereal crops

88 d blight (FHB) is a cereal disease caused by Fusarium graminearum, a fungus able to produce type B tr

89 r events associated with host recognition in Fusarium graminearum, an economically important fungal p

90 c fungi B. cinerea, Alternaria brassicicola, Fusarium graminearum, and Sclerotinia sclerotiorum and y

91 the ascomycete fungi, Neurospora crassa and Fusarium graminearum, at micromolar concentrations.

92 we characterized the only RasGEF protein in Fusarium graminearum, FgCdc25, by combining genetic, cyt

93 In axenic cultures of Fusarium graminearum, in vitro feeding of CYP3RNA, a 791

94 head blight (FHB), which is mainly caused by Fusarium graminearum, is a destructive wheat disease tha

95 Fusarium head blight (FHB), caused by Fusarium graminearum, is a devastating disease of wheat

96 enotype CI9831, followed by inoculation with Fusarium graminearum, led to the down regulation of key

97 pathogen and phenamacril-susceptible species Fusarium graminearum, phenamacril-resistant Fusarium spe

98 ly characterized the FgMCM1 MADS-box gene in Fusarium graminearum, the causal agent of wheat and barl

99 se gene important for sexual reproduction in Fusarium graminearum, we found that two tandem stop codo

100 nase Cel5A, from the plant-pathogenic fungus Fusarium graminearum, whose production was increased by

101 estation with western corn rootworm (WCR) or Fusarium graminearum.

102 genes (ATGs) in the wheat pathogenic fungus Fusarium graminearum.

103 is phosphorylated at five conserved sites in Fusarium graminearum.

104 to pathogens including the toxigenic fungus Fusarium graminearum.

105 -2/Bub2/Cdc16) domain-containing proteins in Fusarium graminearum.

106 ent infection with the hemibiotrophic fungus Fusarium graminearum.

107 ortant for pathogenesis and morphogenesis in Fusarium graminearum.

108 causal fungal agent of Fusarium head blight, Fusarium graminearum.

109 iological and genetic functions of FgSch9 in Fusarium graminearum.

110 -vis the archetypal galactose 6-oxidase from Fusarium graminearum.

111 own mutants also showed higher resistance to Fusarium graminearum.

112 nt infection in the wheat head blight fungus Fusarium graminearum.

113 Ascospores are the primary inoculum in Fusarium graminearum.

114 but is important for splicing efficiency in Fusarium graminearum.

115 forms were determined using two isolates of Fusarium graminearum.

116 d the efficacy of clove oil nanoemulsions on Fusarium growth and mycotoxin during malting process.

117 ould be valuable efficient targets to reduce Fusarium growth and therefore to prevent food contaminat

118 reat diversity of fungal species (Cordyceps, Fusarium, Harpochytrium, Emericellopsis, Volutella, Clad

119 Fusarium graminearum is a causal agent of Fusarium head blight (FHB) and a deoxynivalenol (DON) pr

120 by barley resistant genotype CI89831 against Fusarium head blight (FHB) based on metabolo-transcripto

121 by barley resistant genotype CI89831 against Fusarium head blight (FHB) based on metabolo-transcripto

122 Fusarium head blight (FHB) caused by Fusarium graminearu

123 Fusarium head blight (FHB) caused by Fusarium graminearu

124 Fusarium Head Blight (FHB) caused by Fusarium graminearu

125 (TF) in modulating defense response against Fusarium head blight (FHB) in barley.

126 Fusarium head blight (FHB) is a cereal disease caused by

127 Fusarium head blight (FHB) is a severe disease of wheat

128 Fusarium head blight (FHB) management is a great challen

129 est the feasibility of generating sources of Fusarium head blight (FHB) resistance.

130 rum wheat line DT696 is a source of moderate Fusarium head blight (FHB) resistance.

131 Fusarium head blight (FHB), a fungal disease caused by F

132 Fusarium head blight (FHB), caused by Fusarium graminear

133 Fusarium head blight (FHB), which is mainly caused by Fu

134 leaf volatile Z-3-HAC protects wheat against Fusarium head blight by priming for enhanced JA-dependen

135 Fusarium head blight caused by Fusarium graminearum is o

136 t FgATG17, prevented the fungus from causing Fusarium head blight disease.

137 sarium graminearum and related species cause Fusarium head blight on cultivated grasses, such as whea

138 ium graminearum causes the important disease Fusarium head blight on various species of cereals, lead

139 s for breeding programs intended to obtained Fusarium head blight resistance.

140 cide residues in wheat grains susceptible to fusarium head blight treated with fungicides, and to eva

141 actor produced by the causal fungal agent of Fusarium head blight, Fusarium graminearum.

142 Fusarium head blight, leaf spotting diseases, and, more

143 bally important wheat (T. aestivum) disease, Fusarium head blight.

144 Baseline cultures grew Fusarium in 19 samples (27%), Aspergillus in 17 samples

145 Our sampling suggests that the Fusarium incarnatum-equiseti species complex (FIESC), wi

146 transferase (NAT) and has been identified in Fusarium infecting cereal plants as responsible for deto

147 0.01) in WFhb1-1 accumulation, 12 hours post Fusarium inoculation in non-Qfhb1-carrier wheat but not

148 Fusarium is a genus of filamentous fungi that contains m

149 The fungal genus Fusarium is one of the most important groups of plant-pa

150 tivity of a fungus from the ubiquitous genus Fusarium is related to the presence of nanometre-scale p

151 The fungus Fusarium is well known as a plant pathogen, but has rece

152 n elongation factor (TEF)-1alpha analysis of Fusarium isolates included FSSC 1-a, FOSC 33, and FDSC E

153 In this large susceptibility study, Fusarium isolates were least susceptible to voriconazole

154 Fusarium keratitis is common and often results in poor o

155 d not find a benefit for all corneal ulcers, Fusarium keratitis may benefit from the addition of oral

156 006 outbreak of contact lens (CL)-associated Fusarium keratitis, there may have been a rise in CL-ass

157 nt oral voriconazole on clinical outcomes in Fusarium keratitis.

158 ee of the FSSC species (Fusarium falciforme, Fusarium keratoplasticum, and Fusarium sp. FSSC 12) acco

159 ex were isolated: F. graminearum s.s. (37%), Fusarium meridionale (46%), Fusarium cortaderiae (13%),

160 escribe 2 patients with post-CAR-T-cell IMI (Fusarium, Mucorales) and review the published literature

161 cribe two patients with post-CAR-T-cell IMI (Fusarium, Mucorales) and review the published literature

162 Fusarium mycotoxin contamination in malting barley is of

163 This study investigated the Fusarium mycotoxin Nivalenol (NIV) on the metabolism of

164 espectively, but concentrations of the three Fusarium mycotoxins assessed were ~10 times lower than t

165 Emerging Fusarium mycotoxins were predominant in Italian samples

166 s study was concerned with the fate of these Fusarium mycotoxins within malting, brewing, milling and

167 urance systems are effective for maintaining Fusarium mycotoxins, but not OTA concentrations, below t

168 thy and its cause is hypothesised to involve Fusarium mycotoxins.

169 which were lower than TDI for all legislated Fusarium mycotoxins.

170 Fusarium (n = 126) and Aspergillus species (n = 52) were

171 sing the same biocatalyst in both processes, Fusarium oxysporum 152B.

172 f the most widespread phytopathogenic fungi, Fusarium oxysporum and Botrytis cinerea, were chosen to

173 ainst Rhizopus stolonifer, Botrytis cinerea, Fusarium oxysporum and Colletotrichum gloeosporioides.

174 Formae speciales (ff.spp.) of the fungus Fusarium oxysporum are often polyphyletic within the spe

175 Fusarium oxysporum f. lycopersici (Fol), the causal agen

176 genotypes with respect to resistance against Fusarium oxysporum f. sp. ciceri Race1 (Foc1), we demons

177 n the FSA biosynthetic gene (FUB) cluster in Fusarium oxysporum f. sp. cubense tropical race 4 (Foc T

178 omologue of the yeast SNARE protein Vam7p in Fusarium oxysporum f. sp. lycopersici (Fol), a fungal pa

179 mosomes within strains pathogenic to tomato (Fusarium oxysporum f. sp. lycopersici) and pea (Fusarium

180 of a set of strains of the melon wilt fungus Fusarium oxysporum f. sp. melonis (Fom), bioinformatics-

181 Identity of the effector genes of Fusarium oxysporum f. sp. niveum (Fon) races that affect

182 st crown rot caused by a soilborne pathogen, Fusarium oxysporum f. sp. radicis lycopersici.

183 was horizontally transferred from the fungus Fusarium oxysporum f. sp. vasinfectum to V. dahliae and

184 yses suggested that G-LSR2 was acquired from Fusarium oxysporum f. vasinfectum through horizontal gen

185 Panama disease caused by Fusarium oxysporum f.sp. cubense infection on banana is

186 Resistance to wilt fungus Fusarium oxysporum f.sp. matthioli (FOM) is a polygenic

187 of a set of strains of the melon wilt fungus Fusarium oxysporum f.sp. melonis (Fom), bioinformatics-b

188 in BM was studied by applying a lipase from Fusarium oxysporum in the process.

189 Genome sequencing of Fusarium oxysporum revealed that pathogenic forms of thi

190 eromone from the plant pathogenic ascomycete Fusarium oxysporum revealed the presence of a central be

191 When infecting a host plant, the fungus Fusarium oxysporum secretes several effector proteins in

192 The Fusarium oxysporum species complex (FOSC) comprises a mu

193 e Fusarium solani species complex (FSSC) and Fusarium oxysporum species complex (FOSC), the most comm

194 and one each within the FIESC (1-a) and the Fusarium oxysporum species complex (ST-33) were widespre

195 Here, we show that the root-infecting fungus Fusarium oxysporum uses a functional homologue of the pl

196 (Botrytis cinerea, Pseudomonas syringae, and Fusarium oxysporum) were used to demonstrate potential t

197 capsulatum, Coccidioides immitis/posadasii, Fusarium oxysporum, Aspergillus spp., and Bipolaris spp.

198 nse can overgrow another hypocrealean fungus Fusarium oxysporum, cause sporadic cell death and arrest

199 t Aspergillus flavus, Aspergillus ochraceus, Fusarium oxysporum, Saccharomyces cerevisiae and Candida

200 tants, as shown for Pseudomonas syringae and Fusarium oxysporum.

201 i species complex (FFSC) and rare strains of Fusarium oxysporum.

202 y 20% to 30% and increased susceptibility to Fusarium pathogens.

203 and further elucidating the role of Six6 in Fusarium-plant interactions.

204 larity to the closely related partitiviruses Fusarium poae virus 1 and Penicillium stoloniferum virus

205 reciprocal inhibition among Streptomyces and Fusarium populations from prairie soil, and explore anti

206 Fusarium proliferatum causes diverse diseases of many ec

207 predominantly caused by the fungal pathogen Fusarium pseudograminearum, is a disease of economic sig

208 hout yield penalty, providing a solution for Fusarium resistance breeding.

209 ization of an orphan gene (Triticum aestivum Fusarium Resistance Orphan Gene [TaFROG]) as a component

210 portant clade of veterinary relevance within Fusarium Six of the multilocus STs within the FSSC (3+4-

211 -containing poly(butylene adipate) films and Fusarium solani cutinase (FsC).

212 polytic activity of three microbial lipases: Fusarium solani cutinase, Rv0183, and LipY from Mycobact

213 -adipate ratio by Rhizopus oryzae lipase and Fusarium solani cutinase.

214 reported Taxol-producing endophytic fungus, Fusarium solani from the standpoint of spores as seed in

215 crobial peptide (CRAMP) in a murine model of Fusarium solani keratitis.

216 o inhibitory effect on the motor activity of Fusarium solani myosin-1, human myosin-1c, and D. discoi

217 st (named as SDFsC) by expressing the enzyme Fusarium solani pisi cutinase (FsC) on the cell surface

218 e sources of human pathogenic strains in the Fusarium solani species complex (FSSC) and Fusarium oxys

219 lates (47/67 = 70.1%) were nested within the Fusarium solani species complex (FSSC), and these includ

220 Three isolates (Fusarium solani, Aspergillus fumigatus, Candida albicans

221 arium oxysporum f. sp. lycopersici) and pea (Fusarium 'solani' f. sp. pisi).

222 ota showed a predominance of Alternaria sp., Fusarium sp. and Epicoccum sp. Microdochium nivale (23%)

223 e inhibitor of class I myosin in susceptible Fusarium sp. Chemerin is a leukocyte attractant, adipoki

224 ; however, strains of F. keratoplasticum and Fusarium sp. FSSC 12 were mostly (25/27) isolated from m

225 um falciforme, Fusarium keratoplasticum, and Fusarium sp. FSSC 12) accounted for four-fifths of the v

226 , for the first time, the filamentous fungus Fusarium sp. was utilized for devising a novel method fo

227 ipants, 72 (30.4%) were culture positive for Fusarium species (41 [56.9%] male and 31 [43.1%] female;

228 tification of Aspergillus, Scedosporium, and Fusarium species (n = 28) by matrix-assisted laser desor

229 [5], Aspergillus species [2], Mucorales [2], Fusarium species [2], and Candida glabrata [1]) occurred

230 ubgroup analyses looking at ulcers caused by Fusarium species and adjusting for baseline best spectac

231 mptomatic native grasses for the presence of Fusarium species and confirmed infected grasses as hosts

232 sses for the presence of mycotoxin-producing Fusarium species and evaluated the ability of these fung

233 id (FSA) is a phytotoxin produced by several Fusarium species and has been associated with plant dise

234 Aspergillus and Fusarium species are important causes of fungal infectio

235 d for patients with Aspergillus or other non-Fusarium species as the causative organism (1.5 points [

236 conazole, and especially among patients with Fusarium species as the causative organism.

237 ferase (GST) and confers broad resistance to Fusarium species by detoxifying trichothecenes through d

238 exerts its antifungal effect on susceptible Fusarium species by inhibiting the ATPase activity of th

239 FB1) is a carcinogenic mycotoxin produced by Fusarium species contaminating maize.

240 pathogens and is active with malonyl-CoA in Fusarium species infecting cereals.

241 Compared to other organisms, Fusarium species isolates had the highest MICs to vorico

242 However, these Fusarium species may have had a longer evolutionary hist

243 sm subgroups, there was some suggestion that Fusarium species might have a decreased rate of perforat

244 Fumonisins are mycotoxins produced by Fusarium species that commonly live in maize.

245 ead blight (FHB), a fungal disease caused by Fusarium species that produce food toxins, currently dev

246 Mycotoxin-producing Fusarium species were shown to be prevalent in phylogene

247 Fusarium graminearum, phenamacril-resistant Fusarium species, and the mycetozoan model organism Dict

248 h American grasses are commonly inhabited by Fusarium species, but appear to accommodate these toxige

249 hows highly inhibitory activity towards some Fusarium species, but not to other fungi, indicating tha

250 itative disease resistance to plants against Fusarium species.

251 t UBL1 has a broader role in virulence among Fusarium species.

252 ntative strains of F. circinatum and related Fusarium species.

253 Here, a newly developed Fusarium-specific monoclonal antibody (mAb ED7) was used

254 ere able to quantify mycotoxins and identify Fusarium spp.

255 hogens, including Botrytis cinerea and three Fusarium spp.

256 p., Cryptococcus spp., Aspergillus spp., and Fusarium spp.

257 t frequent microbe (10/17; 59%), followed by Fusarium spp. (4/17; 24%), Pseudomonas aeruginosa (2/17;

258 Common causes include Candida spp., Fusarium spp. and Aspergillus spp..

259 s (Fusarium disease severity, PCR assays for Fusarium spp. identification and mycotoxin quantificatio

260 nd subsequent analysis was realized using 15 Fusarium spp. isolates.

261 ypes: order Mucorales, Aspergillus spp., and Fusarium spp.) significantly prolonged the time to wound

262 or non-Aspergillus molds (Mucoromycotina and Fusarium spp.).

263 neoformans and C. gattii, 98.6% and 100% for Fusarium spp., and 96.2% and 99.9% for Rhodotorula spp.,

264 versity and evolutionary relationships of 67 Fusarium strains from veterinary sources, most of which

265 n-19-ol against Fusarium verticillioides and Fusarium subglutinans may indicate pathogen defensive fu

266 so identified in the distantly related genus Fusarium, suggesting convergent evolution.

267 An approach to defining and identifying Fusarium that places the needs of the community of users

268 evidence that horizontal gene transfer from Fusarium to Vd991 contributed significantly to its adapt

269 and classify three agriculturally important Fusarium toxins in wheat.

270 ed calibration curves were used to determine Fusarium toxins in wheat.

271 otoxin method was developed for 12 different Fusarium toxins including modified mycotoxins in beer (d

272 None of the other monitored Fusarium toxins like 15-acetyldeoxynivalenol, HT2- and T

273 Cut off levels for all three Fusarium toxins were validated using blank wheat and whe

274 assay was developed and validated for three Fusarium toxins, deoxynivalenol (DON), zearalenone (ZEA)

275 The predominant species were Stachybotrys, Fusarium, Trichoderma and Cochlonema.

276 Fusarium ulcers randomized to oral voriconazole had a 0.

277 though there may have been some effect among Fusarium ulcers.

278 ngal species from the genera Aspergillus and Fusarium using solid-state voltammetry is described.

279 The mycelial growth of Fusarium verticillioides (Sacc.) Nirenberg was reduced s

280 ber officinale Roscoe) was evaluated against Fusarium verticillioides (Saccardo) Nirenberg.

281 develop a rapid method for identification of Fusarium verticillioides and F. graminearum.

282 19-ol and syn-pimara-7,15-dien-19-ol against Fusarium verticillioides and Fusarium subglutinans may i

283 d SHs was explored during biotic stress with Fusarium verticillioides infection.

284 Fusarium verticillioides is a fungal pathogen that is re

285 Fusarium verticillioides produces fumonisin mycotoxins d

286 ies most found were Fusarium graminearum and Fusarium verticillioides with 26% and 12% of incidence,

287 Pokkah boeng, caused by Fusarium verticillioides, is a serious disease in sugarc

288 d in the Fvmcm1 mutants of the heterothallic Fusarium verticillioides.

289 Corn plants contaminated with Fusarium verticilloides were harvested at two dates and

290 Fusarium virguliforme is a soil borne pathogen that caus

291 ophthora sojae and the fungal plant pathogen Fusarium virguliforme that are pathogenic to soybean (Gl

292 dying growth, germination and sporulation in Fusarium virguliforme that causes sudden death syndrome

293 We exploited the broad host range of Fusarium virguliforme to identify differential fungal re

294 Sudden death syndrome (SDS), caused by Fusarium virguliforme, is one of the top yield-limiting

295 For fungi, the relative abundance of Fusarium was decreased with wheat straw addition.

296 t induces resistance response in chickpea to Fusarium wilt disease by modulating the transcription of

297 to enhance the defense of watermelon against Fusarium wilt disease.

298 Though watermelon Fusarium wilt is a severe soil-borne disease, the effect

299 ful to select melon cultivars to avoid melon Fusarium wilt, but also to monitor how quickly a Fom pop

300 ed distributions, notably tropical race 4 of Fusarium wilt, rival its impact.