ライフサイエンスコーパス: mildew

1 rasitica (P.p.) races Emoy2 and Emwa1 (downy mildew).

2 stresses (watermelon mosaic virus and downy mildew).

3 h levels of quantitative resistance to downy mildew.

4 s upon inoculation with a nonadapted powdery mildew.

5 interactions between Arabidopsis and powdery mildew.

6 R1, and fully enhanced resistance to powdery mildew.

7 asal and RPW8-mediated resistance to powdery mildew.

8 6S(l)#3, which confer resistance to powdery mildew.

9 a role that has been appropriated by powdery mildew.

10 confer broad-spectrum resistance to powdery mildew.

11 in penetration success by the barley powdery mildew.

12 to NHR in Arabidopsis against wheat powdery mildew.

13 rimary foliar diseases, Botrytis and powdery mildew.

14 ild type in response to infection by powdery mildew.

15 siphe cichoracearum, causal agent of powdery mildew.

16 that confers enhanced resistance to powdery mildew.

17 ated, EHM-focused resistance against powdery mildew.

18 entified as a susceptibility factor to downy mildew.

19 hesis and cell wall modification for powdery mildew.

20 NLS to it resulted in resistance to powdery mildew.

21 he corresponding avirulence genes in powdery mildew.

22 ng and extent of outbreaks of cucurbit downy mildew.

23 exhibit biological activity against powdery mildews.

24 s of uninucleate zoospores in multiple downy mildews.

25 re-invasive immune responses against powdery mildews.

26 putative chromatin regulator Enhanced Downy Mildew 2 (EDM2) as a cellular antisilencing factor and r

27 We identified EDM2 (enhanced downy mildew 2) in a genetic screen for RPP7 suppressors.

28 many angiosperms, the RESISTANCE TO POWDERY MILDEW 8 (RPW8)-CC domain containing NLR (RNL) subclass

29 ining a coiled-coil or RESISTANCE TO POWDERY MILDEW 8-like coiled-coil domain.

30 The Arabidopsis RESISTANCE TO POWDERY MILDEW 8.1 (RPW8.1) activates confined cell death and de

31 Arabidopsis RESISTANCE TO POWDERY MILDEW 8.2 (RPW8.2) is specifically induced by the powde

32 Arabidopsis thaliana RESISTANCE TO POWDERY MILDEW 8.2 (RPW8.2) is specifically targeted to the EHM

33 and molecular epidemiology of wheat powdery mildew, a disease caused by the biotrophic fungus Blumer

34 Powdery mildew, a fungal disease caused by Blumeria graminis f.

35 IVP-RNAi plants were more resistant to downy mildew and accumulated more salicylic acid (SA).

36 a forward genetic screen with barley powdery mildew and consequently characterized it by pathogen ass

37 uding enhanced disease resistance to powdery mildew and enhanced ethylene-induced senescence; thus, t

38 Extensive haplovariant mining in wheat mildew and related sublineages identified several ancien

39 silenced plants were more resistant to downy mildew and Soybean mosaic virus compared with vector con

40 Powdery mildews and other obligate biotrophic pathogens are high

41 eronospora parasitica (causal agent of downy mildew), and encodes an NBS-LRR type R protein with a pu

42 us Podosphaera pannosa, which causes powdery mildew, and the hemibiotrophic fungus Diplocarpon rosae,

43 es, those living in houses with pets, pests, mildew, and water damage, those whose parents had asthma

44 Powdery mildews are phytopathogens whose growth and reproduction

45 nergistically enhanced resistance to powdery mildew attack.

46 The perception of downy mildew avirulence (Arabidopsis thaliana Recognized [ATR]

47 By contrast, the nonhost barley powdery mildew Blumeria graminis f. sp. hordei (Bgh) typically f

48 penetration resistance to the barley powdery mildew Blumeria graminis f. sp. hordei.

49 nfection studies with the nonadapted powdery mildew Blumeria graminis f. sp. hordei.

50 fer durable and robust resistance to powdery mildew (Blumeria graminis), a biotrophic fungal leaf pat

51 mportant race-specific resistance to powdery mildew (Blumeria graminis).

52 Barley powdery mildew, Blumeria graminis f. sp. hordei (Bgh), is an obl

53 enetration resistance against barley powdery mildew, Blumeria graminis f. sp. hordei, and we isolated

54 resent the genome analysis of barley powdery mildew, Blumeria graminis f.sp. hordei (Blumeria), as we

55 ex, presence of water damage or visible mold/mildew, born in winter, breastfeeding, and being exposed

56 ight function in basal resistance to powdery mildew by influencing microtubule organization.

57 dozyma flocculosa for the control of powdery mildew by two Canadian research programs is presented.

58 escribe two barley (Hordeum vulgare) powdery mildew candidate secreted effector proteins, CSEP0105 an

59 Lettuce downy mildew caused by Bremia lactucae is the most important d

60 production is severely constrained by downy mildew caused by Sclerospora graminicola (Sacc.).

61 des Dm3 which determines resistance to downy mildew caused by the oomycete Bremia lactucae carrying t

62 Powdery mildew, caused by Blumeria graminis f. sp. tritici (Bgt)

63 Grapevine downy mildew, caused by the oomycete Plasmopara viticola (P. v

64 ly elusive 5' sequence of the barley powdery mildew chitin synthase gene, BgChs2, which includes a my

65 not associated with the collapse of powdery mildew colonies.

66 O2, MLO6 and MLO12 not only restrict powdery mildew colonization, but also affect interactions with a

67 ivation, and reduced susceptibility to downy mildew disease (Hyaloperonospora arabidopsidis).

68 associated with defense responses to powdery mildew disease but function in different signaling pathw

69 ar leafy vegetable, are susceptible to downy mildew disease caused by Bremia lactucae.

70 ment provided primed defence against powdery mildew disease caused by the biotrophic fungal pathogen,

71 of Arabidopsis confers resistance to powdery mildew disease caused by the fungus Erysiphe cichoracear

72 ide a novel strategy for controlling powdery mildew disease in crops.

73 lex inheritance of resistance to the powdery mildew disease in the model plant Arabidopsis thaliana,

74 e rwa2 and tbr mutants also suppress powdery mildew disease resistance in pmr6, a mutant defective in

75 study suggests that the Arabidopsis powdery mildew disease will be a suitable model system in which

76 p. hordei (Bgh), the causal agent of powdery mildew disease.

77 f. sp. hordei (Bgh), casual agent of powdery mildew disease.

78 sp hordei (Bgh), the causal agent of powdery mildew disease.

79 p. hordei (Bgh), the causal agent of powdery mildew disease.

80 f ABA signaling affects the outcome of downy mildew disease.

81 such as a recent outbreak of severe powdery mildew disease; furthermore, allergy to hazelnuts is an

82 Powdery mildew diseases are economically important diseases, cau

83 and accession Ms-0 was resistant, to powdery mildew diseases caused by Erysiphe cruciferarum UEA1 and

84 vinomyces spp., the causal agents of powdery mildew diseases on multiple plant species.

85 hogens Golovinomyces spp. that cause powdery mildew diseases on multiple plant species.

86 al species of the oomycetes that cause downy mildew diseases.

87 model system in which to investigate powdery mildew diseases.

88 otic and abiotic stresses, among which downy mildew (DM) is a severe biotic stress that is detrimenta

89 s sativus) is resistant to oomyceteous downy mildew (DM), bacterial angular leaf spot (ALS) and funga

90 gions associated with variation in aphid and mildew DNA load.

91 Previous screens for enhanced downy mildew (edm) mutants identified the co-chaperone SGT1b (

92 ntal changes in our understanding of powdery mildews (Erysiphales).

93 rabidopsis thaliana is a host to the powdery mildew Erysiphe cichoracearum and nonhost to Blumeria gr

94 Attack by the host powdery mildew Erysiphe cichoracearum usually results in success

95 o the nonadapted pea (Pisum sativum) powdery mildew Erysiphe pisi However, PLC2-silenced plants displ

96 phenotype, conferring resistance to powdery mildew (Erysiphe cichoracearum) and enhancing ethylene-i

97 enhanced sensitivity to the pathogen powdery mildew (Erysiphe cruciferarum) and fails to induce SA bi

98 itional inappropriate biotrophs, pea powdery mildew (Erysiphe pisi) and potato late blight (Phytophth

99 ose inoculated with a virulent, host powdery mildew, Erysiphe cichoracearum.

100 Barley powdery mildew, Erysiphe graminis f.sp. hordei, is an obligate b

101 I 1.14-2.04, and work environments with mold/mildew exposures [environments with possible exposures t

102 enic tomato variety resistant to the powdery mildew fungal pathogen using the CRISPR/Cas9 technology.

103 Powdery mildew fungal pathogens penetrate the plant cell wall an

104 naling in nonhost resistance against powdery mildew fungi and put PLDdelta forward as the main isofor

105 on phenotype upon challenge with the powdery mildew fungi Golovinomyces orontii and Erysiphe pisi, th

106 ial and quality, the three rusts and powdery mildew fungi have historically caused major crop losses

107 ich spores of adapted and nonadapted powdery mildew fungi showed reduced germination.

108 herwise virulent obligate biotrophic powdery mildew fungi such as Golovinomyces orontii.

109 s for viruses and for rust, smut and powdery mildew fungi that infect 473 plant species naturalized t

110 Penetration resistance to powdery mildew fungi, conferred by localized cell wall appositio

111 otype against adapted and nonadapted powdery mildew fungi.

112 ully resistant to otherwise virulent powdery mildew fungi.

113 membrane encasing the haustorium of powdery mildew fungi.

114 of defense components in response to powdery mildew fungi.

115 n of PEN3-GFP after inoculation with powdery mildew fungi.

116 vasive immunity against a nonadapted powdery mildew fungus (Blumeria graminis f.

117 ed resistance against the biotrophic powdery mildew fungus (Blumeria graminis f.sp. hordei), while MO

118 a wide spectrum of resistance to the powdery mildew fungus (PM), Erysiphe necator (Schw.) Burr., but

119 on formation due to infection by the powdery mildew fungus Blumeria f. sp. tritici.

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

121 NHR in Arabidopsis against the wheat powdery mildew fungus Blumeria graminis f. sp. tritici (Bgt).

122 Arabidopsis thaliana) and the barley powdery mildew fungus Blumeria graminis f.sp. hordei (Bgh) was i

123 nteraction of barley with the barley powdery mildew fungus Blumeria graminis f.sp. hordei.

124 o enhance resistance of wheat to the powdery mildew fungus Blumeria graminis f.sp. tritici, a novel e

125 conferring resistance to the oomycete downy mildew fungus Bremia lactucae map to the major resistanc

126 responses to a host-adapted virulent powdery mildew fungus but were impaired in preinvasive defenses

127 he mitochondrial genome of the grape powdery mildew fungus Erysiphe necator and a high-quality mitoch

128 Our findings imply that the mildew fungus has a repertoire of AVR genes, which may f

129 uring epiphytic growth, the cucurbit powdery mildew fungus Podosphaera xanthii expresses a family of

130 ntify AVR(a10) and AVR(k1) of barley powdery mildew fungus, Blumeria graminis f sp hordei (Bgh), and

131 bidopsis thaliana against the barley powdery mildew fungus, Blumeria graminis f. sp. hordei.

132 two MAP kinase genes from the barley powdery mildew fungus, Blumeria graminis.

133 tance against another nonadapted pea powdery mildew fungus, Erysiphe pisi.

134 also mediates defense to an adapted powdery mildew fungus, thus regulating a durable type of defense

135 ating Arabidopsis infection with the powdery mildew fungus, we find that the Arabidopsis atypical E2F

136 fector-induced HR in response to the powdery mildew fungus.

137 t cell inaccessible for the invading powdery mildew fungus.

138 all known isolates of the widespread powdery mildew fungus.

139 at are homologous with gEgh16 of the powdery mildew fungus.

140 fector-induced HR in response to the powdery mildew fungus.

141 ed 'step down' PCR to attain the full length mildew genomic clones.

142 netration resistance to the virulent powdery mildew Golovinomyces cichoracearum due to enhanced callo

143 h post inoculation with the virulent powdery mildew Golovinomyces cichoracearum.

144 Powdery mildew (Golovinomyces cichoracearum), one of the most pr

145 enhanced resistance to infection by powdery mildew (Golovinomyces cichoracearum).

146 We evaluated the effects of grape powdery mildew (GPM) as supplemental food, and habitat structura

147 The host-adapted powdery mildew had a reduced reproductive fitness on rop6(DN) pl

148 The resurgence of cucurbit downy mildew has dramatically influenced production of cucurbi

149 hronized with a higher expression of powdery mildew haustorial effectors, a sharp decline in the phot

150 PP2B confer recognition of Arabidopsis downy mildew (Hyaloperonospora arabidopsidis [Hpa]) isolate Ca

151 he 3221 mutant exhibited resistance to downy mildew (Hyaloperonospora arabidopsidis) and green peach

152 ts deficient in resistance to barley powdery mildew identified PENETRATION3 (PEN3).

153 in R-gene-mediated resistance against downy mildew in Arabidopsis and their regulatory control by th

154 s SA-dependent basal defense against powdery mildew in Arabidopsis.

155 A recent outbreak of sorghum downy mildew in Texas has led to the discovery of both metalax

156 confers resistance to Bremia lactucae (downy mildew) in 1033 accessions of Lactuca serriola (prickly

157 ts exhibited a dramatic reduction in powdery mildew-induced chloroplast TAGs, attributable to decreas

158 ertion allele in DRP1E did not cause powdery mildew-induced lesions, suggesting that this phenotype i

159 protected wheat systemically against powdery mildew infection by affecting multiple steps in the life

160 rsensitive response (HR) to restrict powdery mildew infection via the salicylic acid-dependent signal

161 ransgenic lines during both types of powdery mildew infection, and neither the salicylic acid-depende

162 ) gene confer enhanced resistance to powdery mildew infection, enhanced senescence, and enhanced prog

163 made Arabidopsis hypersusceptible to powdery mildew infection.

164 illa formation in the epidermis upon powdery mildew infection.

165 d in development and associated with powdery mildew infection.

166 which do not effectively block host powdery mildew infections.

167 ays played a role in blocking barley powdery mildew infections.

168 ts profound effect on the outcome of powdery mildew infections: when the appropriate MLO protein is a

169 penetration by Bgh during the barley-powdery mildew interaction but is independent of gene-for-gene r

170 bidopsis MLO genes implicated in the powdery mildew interaction.

171 ude that edr1-mediated resistance to powdery mildew is mediated, in part, by enhanced ABA signaling.

172 e necator, the causal agent of grape powdery mildew, is a destructive pathogen of grapevines worldwid

173 ergent alleles of ATR1NdWsB from eight downy mildew isolates and demonstrate that the ATR1NdWsB allel

174 aize, sugarcane, pearl millet and rose downy mildew isolates.

175 Powdery mildews may already be responding to climate change, sug

176 e logistic regression to investigate whether mildew/musty odour and increased concentrations of Alter

177 Reporting of a mildew/musty odour was associated with increased risk of

178 Exposure to a mildew/musty odour, as a proxy for exposure to fungus, w

179 Powdery mildews, obligate biotrophic fungal parasites on a wide

180 f Hyaloperonospora arabidopsidis (Hpa, downy mildew of Arabidopsis) contains at least 134 candidate R

181 Powdery mildew of barley, caused by Erysiphe graminis f. sp. hor

182 Downy mildew of spinach is caused by the obligate oomycete pat

183 errations and altered sensitivity to powdery mildews of rop6(DN) plants result from perturbations tha

184 been well demonstrated for rusts and powdery mildews of small grain crops.

185 l as from 5 related species that cause downy mildew on other hosts, the number of different bands det

186 92 in response to inoculation with the downy mildew oomycete pathogen Sclerospora graminicola.

187 iated enhanced disease resistance to powdery mildew or spontaneous lesions, indicating that these phe

188 te to pearl millet defense against the downy mildew pathogen by activating the expression of defense

189 d enhanced disease resistance to the powdery mildew pathogen Erysiphe cichoracearum and identified th

190 resistance (edr2) to the biotrophic powdery mildew pathogen Erysiphe cichoracearum.

191 not support the normal growth of the powdery mildew pathogen Erysiphe cichoracearum.

192 The biotrophic downy mildew pathogen Hyaloperonospora arabidopsidis encodes 1

193 ced immunity (iri) mutants against the downy mildew pathogen Hyaloperonospora arabidopsidis, yielding

194 ired for successful infection with the downy mildew pathogen Hyaloperonospora arabidopsidis.

195 We study the oomycete downy mildew pathogen of Arabidopsis, Hyaloperonospora arabido

196 Hyaloperonospora arabidopsidis, a downy mildew pathogen of the model plant Arabidopsis, has been

197 Interactions between barley and the powdery mildew pathogen, Blumeria graminis f. sp. hordei, (Bgh)

198 do not support normal growth of the powdery mildew pathogen, Erysiphe cichoracearum.

199 resistance to a wild isolate of the powdery mildew pathogen, Erysiphe cichoracearum.

200 a (gl1), which is susceptible to the powdery mildew pathogen, were performed.

201 pe plants inoculated with a virulent powdery mildew pathogen.

202 ce, resulting in reduced growth of a powdery mildew pathogen.

203 olumbia-0 (Col-0) virulent isolates of downy mildew pathogen.

204 Blumeria graminis f. sp hordei, the powdery mildew pathogenic on barley (Hordeum vulgare).

205 comparison with the analysis of two powdery mildews pathogenic on dicotyledonous plants.

206 solving among phylogenetically related downy mildew pathogens dramatically point out the need for sim

207 confers broad-spectrum resistance to powdery mildew pathogens.

208 ntrol resistance to a broad range of powdery mildew pathogens.

209 ing to incursions of new or reemerging downy mildew pathogens.

210 h avirulent Blumeria graminis (wheat powdery mildew) pathogens.

211 fers AtSgt1b-independent resistance to downy mildew (Peronospora parasitica) isolate Hiks1.

212 Powdery mildew (PM) caused by Podosphaera xanthii is a major pro

213 Powdery mildew (PM) caused by Podosphaera xanthii is one of the

214 W8.2) is specifically induced by the powdery mildew (PM) fungus (Golovinomyces cichoracearum) in the

215 wth and reproduction of the virulent powdery mildew (PM) Golovinomyces orontii on Arabidopsis (Arabid

216 exhibited altered expression at the powdery mildew (PM) infection site, with subsets of these playin

217 Tissue colonization by grape powdery mildew (PM) pathogen Erysiphe necator (Schw.) Burr trigg

218 Wheat powdery mildew (PM), caused by Blumeria graminis f.

219 Powdery mildew poses severe threats to wheat production.

220 standing genetic variation in wheat powdery mildew prior to the Pm17 introgression, thereby paving t

221 ntified and mapped three independent powdery mildew quantitative disease resistance loci, which act a

222 e MAP kinases AtMPK6 and AtMPK3, the powdery mildew R proteins RPW8.1 and RPW8.2, EDS1 and PR protein

223 inoculations with non-host and host powdery mildews relative to non-inoculated control plants accoun

224 report the map-based cloning of the powdery mildew resistance allele Pm5e from a Chinese wheat landr

225 tivar C.I. 16151 (harboring the Mla6 powdery mildew resistance allele) and its fast neutron-derived B

226 S5, NPR1 and SGT1b for activation of powdery mildew resistance and HR.

227 tive regulation on HR cell death and powdery mildew resistance by limiting the transcriptional amplif

228 omain is responsible for the gain of powdery mildew resistance function of Pm5e, an allele endemic to

229 barley (Hordeum vulgare), the Mla13 powdery mildew resistance gene confers Rar1-dependent, AvrMla13-

230 nctional characterization of Pm41, a powdery mildew resistance gene derived from WEW, which encodes a

231 Pm1a, the first powdery mildew resistance gene described in wheat, is part of a

232 , we report the map-based cloning of powdery mildew resistance gene Pm24 from Chinese wheat landrace

233 Here, the powdery mildew resistance gene Pm6Sl is cloned from the wild whe

234 -mediated resistance to TMV and some powdery mildew resistance genes in barley provide the first exam

235 plant defense response initiated by powdery mildew resistance genes in chromosomes 3S(l)#2 and 6S(l)

236 In cereals, several mildew resistance genes occur as large allelic series; f

237 r to that conferred by "late-acting" powdery mildew resistance genes of wheat and barley.

238 osa might harbor new stripe rust and powdery mildew resistance genes, respectively, therefore, they c

239 d and hexaploid wheats, harbors many powdery mildew resistance genes.

240 that RPW8.2 from A. lyrata conferred powdery mildew resistance in A. thaliana, suggesting that RPW8.2

241 ed organ morphogenesis and SA-mediated downy mildew resistance in cucumber.

242 ing that GB is a promising elicitor of downy mildew resistance in P. glaucum.

243 o assess candidate genes necessary for downy mildew resistance in spinach.

244 om Ethiopian landraces and nowadays controls mildew resistance in the majority of cultivated European

245 ne a potential route for engineering powdery mildew resistance into susceptible crop species.

246 * Barley (Hordeum vulgare L.) Mildew resistance locus a (Mla) confers allele-specific

247 Barley (Hordeum vulgare L.) Mildew resistance locus a (Mla) confers allele-specific

248 l resistance and effector-triggered, powdery mildew resistance locus A12-mediated resistance against

249 abidopsis thaliana), NORTIA, a member of the MILDEW RESISTANCE LOCUS O (MLO) family of proteins, play

250 Loss of barley Mildew Resistance Locus O (MLO) is known to confer durab

251 enes encoding protein homologs of the barley mildew resistance locus o (MLO) protein biochemically sh

252 The family of Mildew resistance Locus O (MLO) proteins is best known f

253 netically related Arabidopsis thaliana genes MILDEW RESISTANCE LOCUS O 4 (MLO4) and MLO11, encoding h

254 Among them, Arabidopsis MILDEW RESISTANCE LOCUS O3 (MLO3) was identified as a pr

255 of the Mla locus can dictate similar powdery mildew resistance phenotypes yet still require distinct

256 bidopsis thaliana) RLPs, including the downy mildew resistance protein RPP27.

257 Here, we report that the broad-spectrum mildew resistance protein RPW8.2 from Arabidopsis thalia

258 t region from the orthologous barley powdery mildew resistance protein, MLA10, but is similar to the

259 essions Wa-1, Kas-1, Stw-0 and Su-0, powdery mildew resistance was encoded by a semi-dominant allele.

260 The key SNV associated with powdery mildew resistance will be useful for marker-assisted sel

261 n direct contrast to their increased powdery mildew resistance, both pmr5 and pmr6 plants are highly

262 oria is key for RPW8-mediated broad-spectrum mildew resistance.

263 landraces represent a rich source of powdery mildew resistance.

264 screened for spontaneous mutations in downy mildew resistance.

265 eral R genes that confer bacterial and downy mildew resistance.

266 , pre-mature senescence and enhanced powdery mildew resistance.

267 -35-1, appear to positively regulate powdery mildew resistance.

268 barley cv Morex that spans the Mla (powdery mildew) resistance locus.

269 nations of host resistance genes, designated Mildew-resistance locus (Ml), and cognate pathogen aviru

270 eage, and are homologs of the barley powdery mildew-resistance protein MLA10.

271 Mapping studies revealed that powdery mildew resistances in Kas-1, Wa-1, Te-0, Su-0 and Stw-0

272 indicated that four loci, designated powdery mildew resistant 1-4 (pmr1-4), are defined by this colle

273 Surprisingly, here we found that powdery mildew resistant 4 (pmr4), a mutant lacking pathogen-ind

274 The Arabidopsis mutant powdery mildew resistant 5 (pmr5) carries a mutation in a putati

275 ection phenotypes of two independent powdery mildew-resistant triple mutant lines with a range of mic

276 genic Arabidopsis lines that express POWDERY MILDEW RESISTANT4 (PMR4), which encodes a stress-induced

277 We also show here that DOWNY MILDEW RESISTANT6 (AtDMR6), the Arabidopsis homologous e

278 p. hordei, which cause leaf rust and powdery mildew, respectively.

279 root rot (Rps1, Rps2, and Rps3), and powdery mildew (rmd).

280 Resistance to powdery mildew (Rmd-c), Phytophthora stem and root rot (Rps2), a

281 endered Arabidopsis resistant to the powdery mildew species Erysiphe cichoracearum and Erysiphe oront

282 Powdery mildew species Oidium neolycopersici (On) can cause seri

283 Erysiphe vaccinii is an emerging powdery mildew species that is impacting the blueberry industry.

284 rica, where it hybridized with unknown grass mildew species.

285 um TAG biosynthesis does not support powdery mildew spore production.

286 o E. orontii, a very closely related powdery mildew, suggesting that a very specific resistance mecha

287 10) define a core set conserved in all three mildews, suggesting that most effectors represent specie

288 ed pmr5 seed selecting for increased powdery mildew susceptibility identified two previously characte

289 susceptible to the fungal pathogen, powdery mildew, than wild type as measured by conidiophore produ

290 pairs studied in detail using DNA from downy mildews that attack maize (P. maydis & P. philippinensis

291 ant surfaces among distantly related powdery mildews that is based on KCS6-derived wax components.

292 For plant pathogenic fungi, such as powdery mildews, that survive only on a limited number of host p

293 gen but rather a biocontrol agent of powdery mildews; this relationship makes it unique for the study

294 inoculated with the non-host barley powdery mildew to those inoculated with a virulent, host powdery

295 ommon parasite Peronospora parasitica (downy mildew) to study the evolution of resistance specificity

296 xplaining 21-31% of the variation in powdery mildew tolerance.

297 h and enhanced disease resistance to powdery mildew via the SA-dependent signaling pathway.

298 ell death and enhanced resistance to powdery mildew via the salicylic acid-dependent signaling pathwa

299 rolling for age, ethnicity, medication, mold/mildew, water leaks, and season of sampling.

300 of three Phytophthora species and one downy mildew were identified and could serve as useful phyloge