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1 m, the causal agent of wheat and barley head blight.
2 ae (Xoo), the causal agent of bacterial leaf blight.
3 um graminearum, a causal agent of wheat head blight.
4 ffective against specific races of bacterial blight.
5 he cause of Stewart's vascular wilt and fire blight.
6 a, including the causal agent of potato late blight.
7 ria parasitica, the causal agent of chestnut blight.
8 e R1 resistance (R) gene against potato late blight.
9 s-like microbes and the cause of potato late blight.
10 re of the variation, up to 37.2% for foliage blight.
11  maturity, height, tuber blight, and foliage blight.
12 , a Gram-negative bacterium that causes rice blight.
13 hogen responsible for the plant disease fire blight.
14 ophthora infestans, the causal agent of late blight.
15 a4) at two field sites endemic for bacterial blight.
16 yphonectria parasitica, incitant of chestnut blight.
17 on in the phloem is characteristic of citrus blight.
18 ts that altered tissue structure accompanies blight.
19 ) offers a promising solution to manage late blight.
20 d signaling networks triggered by Alternaria blight.
21 nt lines that are most likely to resist rice blight.
22 fers persistent resistance to rice bacterial blight.
23 t wheat (T. aestivum) disease, Fusarium head blight.
24                                    In citrus blight, a decline disorder of unknown etiology, the tree
25 Malus domestica) cultivars resistant to fire blight, a devastating bacterial disease caused by Erwini
26  pathogen Erwinia amylovora that causes fire blight, a devastating disease of apple and pear, have be
27 or Jagger is the causal agent of Sclerotinia blight, a highly destructive disease of peanut (Arachis
28 g population for resistance to northern leaf blight, a maize disease of global economic importance.
29  oomycete Phytophthora infestans causes late blight, a ravaging disease of potato and tomato.
30 one, is now besieged by an aggressive foliar blight active over a broad temperature range when there
31 tein (ZBP) from phloem tissue of healthy and blight-affected citrus (Citrus sinensis [L.] Osbeck on C
32 e in response to wounding or other stress of blight-affected citrus.
33                                   The potato blight agent Phytophthora infestans secretes a range of
34                              Alternaria leaf blight (ALB), caused by a necrotrophic fungus Alternaria
35                          Apple scab and fire blight, along with Huanglongbing, canker, and tristeza v
36  phytopathogen Erwinia amylovora causes fire blight, an invasive disease that threatens a wide range
37  to enhance resistance to both southern leaf blight and anthracnose stalk rot caused by Cochliobolis
38 asis of resistance in rice to bacterial leaf blight and blast.
39 ne provides protection against a lethal leaf blight and ear mold disease caused by Cochliobolus carbo
40 aturity, short plants, and susceptibility to blight and explained 54.7, 26.5, 26.3, and 17.5% of the
41 uantitative resistance to both southern leaf blight and gray leaf spot.
42 tions for HsvA as a virulence factor in fire blight and may also provide a basis for strategies to co
43 enes that co-localize with QTL for bacterial blight and sheath blight disease resistance on rice chro
44                Gray leaf spot, northern leaf blight and southern leaf blight are three of the most de
45 the function of GhSWEETs in cotton bacterial blight and the promise of disrupting the TALE-binding si
46 of the variation for maturity, height, tuber blight, and foliage blight.
47 inct rice diseases, bacterial blight, sheath blight, and rice blast.
48 zae pv oryzae, the causal agent of bacterial blight, and the recessive allele is defeated by strains
49 resistance to anthracnose and Phomopsis stem blight; and, (iii) define regions of synteny between the
50 ual worldwide potato crop losses due to late blight are conservatively estimated at $6.7 billion.
51 spot, northern leaf blight and southern leaf blight are three of the most destructive foliar diseases
52 Golden Delicious were infected with the fire blight bacterium, highest MdB4H transcript levels were o
53                               Rice bacterial blight (BB) is a devastating rice disease.
54                                    Bacterial blight (BB), caused by Xanthomonas oryzae pathovar oryza
55 ovide a basis for strategies to control fire blight by inhibiting HsvA activity.
56 Z-3-HAC protects wheat against Fusarium head blight by priming for enhanced JA-dependent defenses dur
57                                Fusarium head blight caused by Fusarium graminearum is one of the most
58                                         Head blight caused by Fusarium graminearum threatens world-wi
59               Biological control of chestnut blight caused by the filamentous ascomycete Cryphonectri
60                                    Bacterial blight caused by Xanthomonas arboricola pv. juglandis is
61 ly broad spectrum of resistance to bacterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo).
62 ly broad spectrum of resistance to bacterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo).
63                                      Boxwood blight, caused by Calonectria pseudonaviculata and Calon
64                                      Boxwood blight, caused by Calonectria pseudonaviculata, is a hig
65                                         Fire blight, caused by the bacterial phytopathogen Erwinia am
66                                         Fire blight, caused by the bacterium Erwinia amylovora, is a
67                                  Potato late blight, caused by the destructive Irish famine pathogen
68                                        Early blight, caused by the necrotrophic fungus Alternaria sol
69                                    Ascochyta blight, caused by the necrotrophic fungus Ascochyta rabi
70                                         Late blight, caused by the oomycete pathogen Phytophthora inf
71                                         Late blight, caused by the oomycete plant pathogen Phytophtho
72 re the most effective solution for bacterial blight, caused by Xanthomonas oryzae pv. oryzae (Xoo).
73             A protein associated with citrus blight (CB), a disease of unknown cause, was partially c
74 saic disease (CMD) and the cassava bacterial blight (CBB), and MECU72, resistant to cassava white fly
75 a Mosaic Disease (CMD) and Cassava Bacterial Blight (CBB), drought, and acid soils.
76                            Cassava bacterial blight (CBB), incited by Xanthomonas axonopodis pv. mani
77 (Xpm), the causal agent of cassava bacterial blight (CBB).
78 ant pathogen and causative agent of chestnut blight, contains three G alpha, one G beta, one G gamma
79 ution of redox-mediated pathways, Alternaria blight continues to infect crops in the Brassicaceae fam
80 ctions between host and pathogen during fire blight development and for the identification of resista
81 d it sheds new light on the mechanism of the blight disease caused by M. oryzae.
82                                  Rice sheath blight disease caused by Rhizoctonia solani Kuhn (telemo
83  the plant pathogen and causal agent of fire blight disease Erwinia amylovora has not been studied pr
84 nia amylovora, the cause of devastating fire blight disease in apple and pear, have shown that HsvA,
85  LMG 859, the causal agent of bacterial leaf blight disease in pomegranate.
86 winia amylovora, the causative agent of fire blight disease of apple and pear trees, causes disease o
87 ing plant pathogen causing necrotrophic fire blight disease of apple, pear, and other rosaceous plant
88  two fungal species causing a newly emergent blight disease of boxwood.
89 ophthora infestans, the causal agent of late blight disease of potato (Solanum tuberosum), depends on
90 hthora infestans, which is the cause of late blight disease of potato.
91  kinase XA21 confers resistance to bacterial blight disease of rice (Oryza sativa) caused by Xanthomo
92 es a high level of resistance against sheath blight disease of rice.
93 infestans, the agent of the devastating late blight disease of tomato (Lycopersicon esculentum) and p
94 sarium graminearum and F. culmorum cause ear blight disease on cereal crops worldwide.
95 ne race 6 (PR6) is unable to cause bacterial blight disease on rice lines containing the rice resista
96 ize with QTL for bacterial blight and sheath blight disease resistance on rice chromosome 2.
97 ction in Germany is highly resistant to fire blight disease, incited by different strains of the caus
98 ce (RNAi)-mediated resistance against sheath blight disease, we identified genes encoding proteins an
99 omato crops have fallen owing to potato late blight disease, which is caused by Phytophthora infestan
100 cific races of the causal agent of bacterial blight disease, Xanthomonas oryzae pv oryzae.
101  pv. oryzae (Xoo) races that cause bacterial blight disease.
102  specific function in facilitating bacterial blight disease.
103  Erwinia amylovora, the causal agent of fire blight disease.
104  the filamentous fungus that causes chestnut blight disease.
105 ta, the causal agent of boxwood (Buxus spp.) blight disease.
106 ing of AG1IA_04727 and suppression of sheath blight disease.
107 vented the fungus from causing Fusarium head blight disease.
108 ing holoenzymes with Pi04314 to promote late blight disease.
109 nced resistant to most devastating bacterial blight diseases caused by Xanthomonas oryzae pv. oryzae
110 gens (causal agents of rice blast and sheath blight diseases) revealed that as more chr 8 OsGLP genes
111                                        Early blight (EB) caused by Alternaria linariae or Alternaria
112 Solanum lycopersicum L.) yield causing early blight (EB) disease in tropical environment.
113     Any factor reducing the rate of chestnut blight epidemics enhances hypovirus invasion.
114 ch play an important role in initiating fire blight epidemics.
115 aminearum is a causal agent of Fusarium head blight (FHB) and a deoxynivalenol (DON) producer.
116 stant genotype CI89831 against Fusarium head blight (FHB) based on metabolo-transcriptomics approach.
117 stant genotype CI89831 against Fusarium head blight (FHB) based on metabolo-transcriptomics approach.
118                                Fusarium head blight (FHB) caused by Fusarium graminearum (Fg) is a de
119      The devastating effect of Fusarium head blight (FHB) caused by Fusarium graminearum has led to s
120                                Fusarium head blight (FHB) caused by Fusarium graminearum is a devasta
121                                Fusarium Head Blight (FHB) caused by Fusarium graminearum pathogens co
122 ating defense response against Fusarium head blight (FHB) in barley.
123                                Fusarium head blight (FHB) is a cereal disease caused by Fusarium gram
124                                Fusarium head blight (FHB) is a devastating disease of wheat and barle
125                                Fusarium head blight (FHB) is a plant disease with serious economic an
126                                Fusarium head blight (FHB) is a severe disease of wheat (Triticum aest
127                                Fusarium head blight (FHB) management is a great challenge in barley a
128 minearum is a primary cause of Fusarium head blight (FHB) on wheat and barley.
129     Breeding for resistance to Fusarium head blight (FHB) relies strongly on a limited number of larg
130 ility of generating sources of Fusarium head blight (FHB) resistance.
131  DT696 is a source of moderate Fusarium head blight (FHB) resistance.
132                                Fusarium head blight (FHB), a fungal disease caused by Fusarium specie
133                                Fusarium head blight (FHB), caused by Fusarium graminearum, is a devas
134                                Fusarium head blight (FHB), which is mainly caused by Fusarium gramine
135 tivating disease resistance against the late blight fungal pathogen Phytophthora infestans.
136 ecimated by the introduction of the chestnut blight fungus (Cryphonectria parasitica) in the early 20
137 s isolated from strain NB631 of the chestnut blight fungus (Cryphonectria parasitica), a model filame
138 induced in a virulent strain of the chestnut blight fungus Cryphonectria parasitica (Murr.) Barr.
139          Hypovirus infection of the chestnut blight fungus Cryphonectria parasitica results in a spec
140 y (vic)] loci were disrupted in the chestnut blight fungus Cryphonectria parasitica using an adapted
141 e of two dicer genes, dcl-2, of the chestnut blight fungus Cryphonectria parasitica was recently show
142  attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica were used to cons
143                    Infection of the chestnut blight fungus Cryphonectria parasitica with Cryphonectri
144         Persistent infection of the chestnut blight fungus Cryphonectria parasitica with the prototyp
145  attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica, could serve as g
146 , and CHV-1/EP721, which infect the chestnut blight fungus Cryphonectria parasitica, differ in their
147  attenuation (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica, encodes two papa
148 g antiviral defense response in the chestnut blight fungus Cryphonectria parasitica, is inducible upo
149 orulation by the infected host, the chestnut blight fungus Cryphonectria parasitica, while being disp
150 e incompatibility (vic) loci of the chestnut blight fungus Cryphonectria parasitica.
151 tions on mycovirus infection of the chestnut blight fungus Cryphonectria parasitica.
152 ses, including pathogenesis, in the chestnut blight fungus Cryphonectria parasitica.
153 ed virulence (hypovirulence) of the chestnut blight fungus Cryphonectria parasitica.
154 ential for plant infection in the wheat head blight fungus Fusarium graminearum.
155 tor present in the lipids of the potato late blight fungus Phytophthora infestans.
156                            The rice seedling blight fungus Rhizopus microsporus and its endosymbiont
157 uation) observed for strains of the chestnut blight fungus, Cryphonectria parasitica, harboring membe
158           Most hypovirulence in the chestnut blight fungus, Cryphonectria parasitica, is associated w
159 eport that DI RNA production in the chestnut blight fungus, Cryphonectria parasitica, persistently in
160 terized of a number of genes in the chestnut blight fungus, Cryphonectria parasitica, that are repres
161 al transcriptional responses of the chestnut blight fungus, Cryphonectria parasitica, to infection by
162 pMV1) from U.S. strain NB631 of the chestnut blight fungus, Cryphonectria parasitica, was the first v
163 ype, such as the hypoviruses of the chestnut-blight fungus, have been studied for their potential as
164 ne in Cryphonectria parasitica, the chestnut blight fungus, reduces the ability of the fungus to form
165  by the causal fungal agent of Fusarium head blight, Fusarium graminearum.
166 , causal agent of the tomato and potato late blight, generates important economic and environmental l
167 mportant foliar maize diseases-southern leaf blight, gray leaf spot and northern leaf blight-has been
168 ns causing necrotic symptoms such as blossom blights (group 1), and specialist flower pathogens which
169                                   Gummy stem blight (GSB) is a fungal disease affecting cucurbit crop
170  19th century from plants infected with late blight has shown that the potato famines of the 1840s we
171 eaf blight, gray leaf spot and northern leaf blight-has been identified on maize chromosome 9.
172 ns (Rpi) genes effective against potato late blight have been cloned, few have been cloned against ot
173  living fungal cells and cause rice seedling blight have been identified.
174 tive trait loci (QTL) for resistance to late blight, height, and maturity was performed on a tetraplo
175               Confidence in this approach is blighted however by lamentable inconsistency in publishe
176 olecular basis of resistance to Fusarium ear blight in cereal species is poorly understood.
177          It promotes the development of halo blight in common bean (Phaseolus vulgaris).
178  effective control strategy against chestnut blight in Europe.
179 an confer enhanced resistance to Sclerotinia blight in peanut.
180 dependent R gene for resistance to bacterial blight in rice (Oryza sativa).
181 d recessive forms of resistance to bacterial blight in rice.
182 erring race-specific resistance to bacterial blight in rice.
183 agnostic kit to enable analysis of bacterial blight in the field and identification of suitable resis
184                              Control of late blight in the United States and other developed countrie
185 rgely used in food industry against mold and blight in vegetables and fruits during transportation an
186 worldwide pathogen that causes Fusarium head blight in wheat, barley, maize and other grains.
187  that the average global risk of potato late blight increases initially, when compared with historic
188 oding MdBIS1 to MdBIS4 were cloned from fire-blight-infected shoots of apple 'Holsteiner Cox,' hetero
189 thora infestans (causal agent of potato late blight) inoculum and the subsequent risk of infection.
190                                         Fire blight is a devastating disease of apple and pear caused
191                                         Fire blight is a devastating disease of rosaceous plants caus
192 pression of the blossom-blight phase of fire blight is a key point in the management of this destruct
193  microbe and the causal agent of potato late blight, is based on a multilayered defense system.
194 ophthora infestans, the cause of potato late blight, is infamous for having triggered the Irish Great
195 oil fungus, Pythium irregulare, was found to blight jar1-1.
196 naria linariae or Alternaria solani and leaf blight (LB) caused by A. alternata are economically impo
197                                Fusarium head blight, leaf spotting diseases, and, more recently, whea
198 ive strategy from both an agronomic and late blight management perspective.
199 stics enables much greater precision in late blight management to produce recommendations that are si
200 mmercial potato varieties are susceptible to blight, many wild potato relatives show variation for re
201 hods with conventional management of blossom blight may be achievable by increasing the diversity of
202                           Northern corn leaf blight (NCLB) caused by the hemibiotrophic fungus Exsero
203 titative disease resistance to northern leaf blight (NLB) and secondarily for common rust resistance
204                                     Victoria blight of Avena sativa (oat) is caused by the fungus Coc
205  plant pathogen, is the causal agent of halo blight of bean.
206  but its effects on controlling phytophthora blight of container-grown peppers have less been explore
207 alvacearum (Xcm) are essential for bacterial blight of cotton (BBC).
208 raskensis (Cn), which causes Goss's wilt and blight of maize.
209 an important plant pathogen that causes head blight of major cereal crops.
210 ungus Cochliobolus victoriae causes Victoria blight of oats (Avena sativa) and is pathogenic due to i
211 olus victoriae, the causal agent of victoria blight of oats, has been demonstrated to bind to the mit
212 olus victoriae, the causal agent of victoria blight of oats.
213 or Phytophthora infestans, which causes late blight of potato, and Phytophthora sojae, which affects
214 ve resistance to the rice blast fungus, late blight of potato, gray leaf spot of maize, bacterial wil
215 nthomonas oryzae pv. oryzae causes bacterial blight of rice (Oryza sativa L.), a major disease that c
216 istance gene xa5,for resistance to bacterial blight of rice (Oryza sativa), is dependent on the effec
217 Burkholderia glumae causes bacterial panicle blight of rice and produces major virulence factors, inc
218                                    Bacterial blight of rice is an important disease in Asia and Afric
219                                    Bacterial blight of rice is caused by the gamma-proteobacterium Xa
220 n increased host susceptibility to bacterial blight of rice.
221 e plant disease called scab or Fusarium head blight of wheat and barley has reached epidemic proporti
222  devastating and economically important head blight of wheat and related species.
223 13.6% of the variation for foliage and tuber blight on an additive model.
224 arum and related species cause Fusarium head blight on cultivated grasses, such as wheat and barley.
225 eafood-borne gastroenteritis worldwide and a blight on global aquaculture.
226 ls from the regressions of foliage and tuber blight on maturity were analyzed, there was no significa
227 m causes the important disease Fusarium head blight on various species of cereals, leading to contami
228 dverse events (iodine group: abortion, n=20; blighted ovum, and n=2; intrauterine death, n=2; placebo
229 e death, n=2; placebo group: abortion, n=22; blighted ovum, n=1; intrauterine death, n=2; early neona
230 issues, and tissues challenged with the late-blight pathogen (Phytophthora infestans).
231 f genetic diversity for both the potato late blight pathogen and for tuber-bearing Solanum spp.
232 ein is critical to the virulence of the fire blight pathogen Erwinia amylovora in host plants like ap
233 irulence regulator in the Gram-negative fire blight pathogen Erwinia amylovora.
234 center of origin not only of the potato late blight pathogen P. infestans, but also of several relate
235        RXLR effector Pi04089 from the potato blight pathogen Phytophthora infestans accumulates in th
236                   Effector AVR3a from potato blight pathogen Phytophthora infestans is translocated i
237                                   The potato blight pathogen Phytophthora infestans secretes effector
238 ants which, as shown for the infamous potato blight pathogen Phytophthora infestans, make up < 1% of
239 o-segregate with resistance towards the late blight pathogen Phytophthora infestans.
240 nfers resistance to strains of the bacterial blight pathogen Xanthomonas oryzae pv. oryzae (Xoo) that
241             The haploid, ascomycete chestnut blight pathogen, Cryphonectria parasitica, has previousl
242                                     The fire blight pathogen, Erwinia amylovora (EA), causes signific
243 script levels were also affected by the late blight pathogen, Phytophthora infestans.
244                                The bean halo blight pathogen, Pseudomonas syringae pv. phaseolicola (
245 ique to the incompatible interaction of late-blight pathogen, thereby providing a foundation for furt
246 QTLs that confer resistance to the bacterial blight pathogen, Xanthomonas campestris pv. malvacearum
247                  Adaptation of the bacterial blight pathogen, Xanthomonas oryzae pv. oryzae (Xoo), to
248  oryzae pv. oryzae (Xoo), the rice bacterial blight pathogen.
249                   Suppression of the blossom-blight phase of fire blight is a key point in the manage
250                     Famine took hold after a blight (Phytophthora infestans) destroyed virtually the
251 wdery mildew (Erysiphe pisi) and potato late blight (Phytophthora infestans).
252 mylovora, the bacterium responsible for fire blight, relies on a type III secretion system and a sing
253 unctions of sRNAs in response to rice sheath blight remain unclear.
254 ly, pre-treatment with auxin enhanced sheath blight resistance by affecting endogenous auxin homeosta
255                                     All late blight resistance genes identified to date belong to the
256 e presence of the Solanum bulbocastanum late blight resistance genes Rpi-blb1 and Rpi-blb2, thereby e
257             American chestnuts with improved blight resistance have been developed through interspeci
258                             A major gene for blight resistance in Stirling was also mapped to LGXI.
259 'Idared', the locus (Mfu10) controlling fire blight resistance mapped on linkage group 10 (LG10) and
260 rtance, scientists have aggressively pursued blight resistance through various approaches.
261                                    Ascochyta blight resistance was evaluated at 3, 9, 11, 13, and 14
262 ess tolerance, photosynthetic activity, fire blight resistance, and other differences conferred by th
263 resistance, low alkaloids and Phomopsis stem blight resistance, highlighting different genetic contro
264 bean cultivars carrying the R1 gene for halo-blight resistance, such as Red Mexican.
265 ese four genes displayed broad spectrum late blight resistance.
266 -alkaloids and phenylpropanoids during early blight resistance.
267  programs intended to obtained Fusarium head blight resistance.
268 ckcrossing, and generated a nearly isogenic, blight-resistant 9311/Xa21 rice.
269  provides a new resource for developing late blight-resistant potato varieties.
270 n alternative strategy for developing sheath blight-resistant rice cultivars.
271                                              Blight-resistant rice lines are the most effective solut
272  DNA library from leaf tissue of the blister blight-resistant tea cultivar TRI2043 and functionally c
273                      Currently no gummy stem blight-resistant watermelon cultivars are available to g
274 ly used in China for controlling rice sheath blight, Rhizoctonia solani.
275  capsici Leonian, the causal agent of foliar blight, root rot, fruit rot and crown rot syndromes in s
276 ed knowledge about genetic diversity in fire blight S genes in diverse apple accessions and identifie
277                          South American leaf blight (SALB) of rubber has been the main constraint to
278                    The disease Fusarium head blight (scab) causes severe problems for farmers and for
279  primary etiological agents of Fusarium head blight (scab) of wheat and barley.
280                     The generation of sheath blight (ShB)-resistant transgenic rice plants through th
281 y to three distinct rice diseases, bacterial blight, sheath blight, and rice blast.
282 environments for resistance to southern leaf blight (SLB) disease caused by Cochliobolus heterostroph
283 as evaluated for resistance to southern leaf blight (SLB) disease.
284 M and DIPM gene families with a role in fire blight susceptibility (S genes) can help achieve sustain
285 rgeting the promoter region of the bacterial blight susceptibility genes, OsSWEET14 and OsSWEET11, we
286 ootstock is dwarfing and does not alter fire blight susceptibility of the scion.
287 ignificant associations (p < 0.05) with fire blight susceptibility traits, while two of these SNPs sh
288  develop apple cultivars with decreased fire blight susceptibility via marker-assisted breeding or bi
289 hisms) with significant associations to fire blight susceptibility.
290 essary to restrict pathogen growth and early blight symptom development in both potato foliage and tu
291  is a host susceptibility gene for bacterial blight targeted by the type III effector PthXo1.
292 obal effect of climate change on potato late blight, the disease that caused the Irish potato famine
293  oomycete Phytophthora infestans causes late blight, the potato disease that precipitated the Irish f
294 in wheat grains susceptible to fusarium head blight treated with fungicides, and to evaluate the rela
295                                      Boxwood blight was recorded in 61 of 86 weeks, with the highest
296        Hypovirulence has controlled chestnut blight well in some locations in Europe and in Michigan
297                                         Head blight, which is caused by mycotoxin-producing fungi of
298 sed methods to investigate cassava bacterial blight, which is caused by the pathogen Xanthomonas axon
299 urrent climatic conditions, the risk of late blight will increase in Scotland during the first half o
300 ice blast (Magnaporthe oryzae) and bacterial blight (Xanthomonas oryzae pv. oryzae).

 
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