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1 marker PR1, and fully enhanced resistance to powdery mildew.
2 omised basal and RPW8-mediated resistance to powdery mildew.
3 l)#2 and 6S(l)#3, which confer resistance to powdery mildew.
4 tif, and confer broad-spectrum resistance to powdery mildew.
5 ncrease in penetration success by the barley powdery mildew.
6 fungi, a role that has been appropriated by powdery mildew.
7 ributors to NHR in Arabidopsis against wheat powdery mildew.
8 ol the primary foliar diseases, Botrytis and powdery mildew.
9 A than wild type in response to infection by powdery mildew.
10 ngus Erysiphe cichoracearum, causal agent of powdery mildew.
11 leaf tissues and enhanced susceptibility to powdery mildew.
12 ed extrahaustorial membrane (EHM) induced by powdery mildew.
13 ase gene that confers enhanced resistance to powdery mildew.
14 in-affected mutants, and cells responding to powdery mildew.
15 t are an important susceptibility factor for powdery mildew.
16 erve as valuable resources for resistance to powdery mildew.
17 .2-activated, EHM-focused resistance against powdery mildew.
18 hotosynthesis and cell wall modification for powdery mildew.
19 dding an NLS to it resulted in resistance to powdery mildew.
20 about the corresponding avirulence genes in powdery mildew.
21 defenses upon inoculation with a nonadapted powdery mildew.
22 patible interactions between Arabidopsis and powdery mildew.
23 ective pre-invasive immune responses against powdery mildews.
24 orted to exhibit biological activity against powdery mildews.
26 ins belong to the coiled-coil, Resistance to Powdery Mildew 8, or Toll/interleukin-1 receptor subfami
31 genomics and molecular epidemiology of wheat powdery mildew, a disease caused by the biotrophic fungu
33 from host cells to biotrophic fungi such as powdery mildew across the plant-haustorium interface rem
34 k1-4 in a forward genetic screen with barley powdery mildew and consequently characterized it by path
35 es, including enhanced disease resistance to powdery mildew and enhanced ethylene-induced senescence;
36 es resistance to the adapted pathogen barley powdery mildew and non-adapted pathogen wheat stripe rus
38 the organization of mitochondrial genomes of powdery mildews and represent valuable resources for pop
39 hic fungus Podosphaera pannosa, which causes powdery mildew, and the hemibiotrophic fungus Diplocarpo
49 n to confer durable and robust resistance to powdery mildew (Blumeria graminis), a biotrophic fungal
53 n-host penetration resistance against barley powdery mildew, Blumeria graminis f. sp. hordei, and we
54 We present the genome analysis of barley powdery mildew, Blumeria graminis f.sp. hordei (Blumeria
55 HvRBK1 might function in basal resistance to powdery mildew by influencing microtubule organization.
56 and Pseudozyma flocculosa for the control of powdery mildew by two Canadian research programs is pres
57 re, we describe two barley (Hordeum vulgare) powdery mildew candidate secreted effector proteins, CSE
60 previously elusive 5' sequence of the barley powdery mildew chitin synthase gene, BgChs2, which inclu
62 genes MLO2, MLO6 and MLO12 not only restrict powdery mildew colonization, but also affect interaction
63 ese are associated with defense responses to powdery mildew disease but function in different signali
64 ed treatment provided primed defence against powdery mildew disease caused by the biotrophic fungal p
65 utation of Arabidopsis confers resistance to powdery mildew disease caused by the fungus Erysiphe cic
67 the complex inheritance of resistance to the powdery mildew disease in the model plant Arabidopsis th
69 This study suggests that the Arabidopsis powdery mildew disease will be a suitable model system i
76 tresses, such as a recent outbreak of severe powdery mildew disease; furthermore, allergy to hazelnut
78 ptible, and accession Ms-0 was resistant, to powdery mildew diseases caused by Erysiphe cruciferarum
85 -) and to the nonadapted pea (Pisum sativum) powdery mildew Erysiphe pisi However, PLC2-silenced plan
86 negative phenotype, conferring resistance to powdery mildew (Erysiphe cichoracearum) and enhancing et
87 o shows enhanced sensitivity to the pathogen powdery mildew (Erysiphe cruciferarum) and fails to indu
88 ecent studies revealed partial resistance to powdery mildew (Erysiphe necator, PM) in V. sylvestris f
89 two additional inappropriate biotrophs, pea powdery mildew (Erysiphe pisi) and potato late blight (P
93 n-transgenic tomato variety resistant to the powdery mildew fungal pathogen using the CRISPR/Cas9 tec
95 ense signaling in nonhost resistance against powdery mildew fungi and put PLDdelta forward as the mai
96 infection phenotype upon challenge with the powdery mildew fungi Golovinomyces orontii and Erysiphe
97 d potential and quality, the three rusts and powdery mildew fungi have historically caused major crop
101 ypotheses for viruses and for rust, smut and powdery mildew fungi that infect 473 plant species natur
109 2-mediated resistance against the biotrophic powdery mildew fungus (Blumeria graminis f.sp. hordei),
110 exhibit a wide spectrum of resistance to the powdery mildew fungus (PM), Erysiphe necator (Schw.) Bur
112 in the interaction of barley with the barley powdery mildew fungus Blumeria graminis f. sp. hordei (B
113 asis of NHR in Arabidopsis against the wheat powdery mildew fungus Blumeria graminis f. sp. tritici (
114 dopsis (Arabidopsis thaliana) and the barley powdery mildew fungus Blumeria graminis f.sp. hordei (Bg
115 in the interaction of barley with the barley powdery mildew fungus Blumeria graminis f.sp. hordei.
116 proach to enhance resistance of wheat to the powdery mildew fungus Blumeria graminis f.sp. tritici, a
117 defense responses to a host-adapted virulent powdery mildew fungus but were impaired in preinvasive d
118 resent the mitochondrial genome of the grape powdery mildew fungus Erysiphe necator and a high-qualit
120 We identify AVR(a10) and AVR(k1) of barley powdery mildew fungus, Blumeria graminis f sp hordei (Bg
121 nous Arabidopsis thaliana against the barley powdery mildew fungus, Blumeria graminis f. sp. hordei.
124 VPS9a also mediates defense to an adapted powdery mildew fungus, thus regulating a durable type of
125 Investigating Arabidopsis infection with the powdery mildew fungus, we find that the Arabidopsis atyp
131 plete penetration resistance to the virulent powdery mildew Golovinomyces cichoracearum due to enhanc
135 anced resistance against the fungal pathogen powdery mildew, Golovinomyces cichoracearum and the viru
138 is synchronized with a higher expression of powdery mildew haustorial effectors, a sharp decline in
142 t3 mutants exhibited a dramatic reduction in powdery mildew-induced chloroplast TAGs, attributable to
143 -DNA insertion allele in DRP1E did not cause powdery mildew-induced lesions, suggesting that this phe
144 BTH protected wheat systemically against powdery mildew infection by affecting multiple steps in
145 ccharomyces cerevisiae and potential role in powdery mildew infection by gene ablation and overexpres
146 the hypersensitive response (HR) to restrict powdery mildew infection via the salicylic acid-dependen
147 istant transgenic lines during both types of powdery mildew infection, and neither the salicylic acid
148 E1 (EDR1) gene confer enhanced resistance to powdery mildew infection, enhanced senescence, and enhan
156 wn for its profound effect on the outcome of powdery mildew infections: when the appropriate MLO prot
157 tempted penetration by Bgh during the barley-powdery mildew interaction but is independent of gene-fo
161 We conclude that edr1-mediated resistance to powdery mildew is mediated, in part, by enhanced ABA sig
163 Erysiphe necator, the causal agent of grape powdery mildew, is a destructive pathogen of grapevines
167 gical aberrations and altered sensitivity to powdery mildews of rop6(DN) plants result from perturbat
169 edr1-mediated enhanced disease resistance to powdery mildew or spontaneous lesions, indicating that t
171 displayed enhanced disease resistance to the powdery mildew pathogen Erysiphe cichoracearum and ident
181 nhost to Blumeria graminis f. sp hordei, the powdery mildew pathogenic on barley (Hordeum vulgare).
182 ell as a comparison with the analysis of two powdery mildews pathogenic on dicotyledonous plants.
189 8.2 (RPW8.2) is specifically induced by the powdery mildew (PM) fungus (Golovinomyces cichoracearum)
190 the growth and reproduction of the virulent powdery mildew (PM) Golovinomyces orontii on Arabidopsis
191 factors exhibited altered expression at the powdery mildew (PM) infection site, with subsets of thes
195 evelopment of BSR to wheat yellow rust (YR), powdery mildew (PM), and leaf rust (LR) diseases elicite
198 esent as standing genetic variation in wheat powdery mildew prior to the Pm17 introgression, thereby
199 We identified and mapped three independent powdery mildew quantitative disease resistance loci, whi
200 RKY6, the MAP kinases AtMPK6 and AtMPK3, the powdery mildew R proteins RPW8.1 and RPW8.2, EDS1 and PR
201 essed by inoculations with non-host and host powdery mildews relative to non-inoculated control plant
203 are) cultivar C.I. 16151 (harboring the Mla6 powdery mildew resistance allele) and its fast neutron-d
204 olecular mechanisms underlying Pm13-mediated powdery mildew resistance and highlight the important ro
207 rts negative regulation on HR cell death and powdery mildew resistance by limiting the transcriptiona
208 ch on MLOs and novel breeding strategies for powdery mildew resistance by targeting MLO genes in vari
209 qualitative and quantitative traits against powdery mildew resistance by utilizing cluster and princ
210 (LRR) domain is responsible for the gain of powdery mildew resistance function of Pm5e, an allele en
212 g and functional characterization of Pm41, a powdery mildew resistance gene derived from WEW, which e
214 Here, we report the cloning of Pm57, a wheat powdery mildew resistance gene from Aegilops searsii.
215 Here, we report the map-based cloning of the powdery mildew resistance gene Pm13 from the wild wheat
216 Here, we report the map-based cloning of powdery mildew resistance gene Pm24 from Chinese wheat l
218 ne for N-mediated resistance to TMV and some powdery mildew resistance genes in barley provide the fi
219 and the plant defense response initiated by powdery mildew resistance genes in chromosomes 3S(l)#2 a
220 s similar to that conferred by "late-acting" powdery mildew resistance genes of wheat and barley.
221 Ae. comosa might harbor new stripe rust and powdery mildew resistance genes, respectively, therefore
223 we show that RPW8.2 from A. lyrata conferred powdery mildew resistance in A. thaliana, suggesting tha
224 nd outline a potential route for engineering powdery mildew resistance into susceptible crop species.
225 ced basal resistance and effector-triggered, powdery mildew resistance locus A12-mediated resistance
227 alleles of the Mla locus can dictate similar powdery mildew resistance phenotypes yet still require d
228 quivalent region from the orthologous barley powdery mildew resistance protein, MLA10, but is similar
229 gest that VpCDPK9 and VpCDPK13 contribute to powdery mildew resistance via positively regulating SA a
230 In accessions Wa-1, Kas-1, Stw-0 and Su-0, powdery mildew resistance was encoded by a semi-dominant
241 nalyses indicated that four loci, designated powdery mildew resistant 1-4 (pmr1-4), are defined by th
244 the infection phenotypes of two independent powdery mildew-resistant triple mutant lines with a rang
245 ed transgenic Arabidopsis lines that express POWDERY MILDEW RESISTANT4 (PMR4), which encodes a stress
249 5 gene rendered Arabidopsis resistant to the powdery mildew species Erysiphe cichoracearum and Erysip
253 ptible to E. orontii, a very closely related powdery mildew, suggesting that a very specific resistan
254 utagenized pmr5 seed selecting for increased powdery mildew susceptibility identified two previously
255 have revealed broader roles for MLOs beyond powdery mildew susceptibility, including regulating inte
257 ere more susceptible to the fungal pathogen, powdery mildew, than wild type as measured by conidiopho
258 ng of plant surfaces among distantly related powdery mildews that is based on KCS6-derived wax compon
260 ytopathogen but rather a biocontrol agent of powdery mildews; this relationship makes it unique for t
261 bidopsis inoculated with the non-host barley powdery mildew to those inoculated with a virulent, host
264 ell death and enhanced disease resistance to powdery mildew via the SA-dependent signaling pathway.
265 e-like cell death and enhanced resistance to powdery mildew via the salicylic acid-dependent signalin