戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 turbances caused by seed transmission of two phytopathogenic agents, Alternaria brassicicola Abra43 (
2                                              Phytopathogenic and food spoilage microorganisms are maj
3 oth sampling areas the DNA of opportunistic, phytopathogenic and symbiotic fungi were detected, which
4 usarium species are among the most important phytopathogenic and toxigenic fungi.
5        Ocatin inhibits the growth of several phytopathogenic bacteria (Agrobacterium tumefaciens, Agr
6  induced in leaves after being challenged by phytopathogenic bacteria also has BEBT activity, whereas
7             Plasmids are common residents of phytopathogenic bacteria and contribute significantly to
8                Expansins are encoded by some phytopathogenic bacteria and evidence indicates that the
9 s of enhanced susceptibility to a variety of phytopathogenic bacteria and to the obligate biotrophic
10 romoting type III secretion system (T3SS) in phytopathogenic bacteria are induced at the start of inf
11               Most plasmids characterized in phytopathogenic bacteria are self-transmissible and poss
12 it is beginning to provide insights into how phytopathogenic bacteria cause disease on their hosts.
13                                              Phytopathogenic bacteria deliver effectors of disease in
14                   To overcome such immunity, phytopathogenic bacteria deliver virulence molecules cal
15                    To prevent this response, phytopathogenic bacteria deploy a repertoire of effector
16 water and nutrients for the proliferation of phytopathogenic bacteria during biotrophy.
17 y been considered as substrates exploited by phytopathogenic bacteria during plant infection.
18 toire of molecules putatively metabolized by phytopathogenic bacteria during their life cycle.
19 in studying the etiology and epidemiology of phytopathogenic bacteria from epidemics, as was done in
20                    This review describes how phytopathogenic bacteria have incorporated QS mechanisms
21  the most important groups of genes found in phytopathogenic bacteria in relationship to pathogenicit
22                              Avr-proteins of phytopathogenic bacteria include type III effector prote
23 pathway has revealed new mechanisms by which phytopathogenic bacteria infect plants.
24                                         Many phytopathogenic bacteria inject virulence effector prote
25                     However, its function in phytopathogenic bacteria is not yet understood.
26                                              Phytopathogenic bacteria possess a large number of genes
27 e applied this method to two isolates of the phytopathogenic bacteria Pseudomonas syringae.
28                         Xanthomonas spp. are phytopathogenic bacteria that can cause disease on a wid
29 retion system (T3SS) substrates found in all phytopathogenic bacteria that utilize a T3SS.
30             hrp genes control the ability of phytopathogenic bacteria to cause disease and to elicit
31  of mosaic and ever-changing plasmids allows phytopathogenic bacteria to maintain a dynamic, flexible
32                                Gram-negative phytopathogenic bacteria translocate effector proteins i
33                                         Many phytopathogenic bacteria use a type III secretion system
34  central role in the pathogenesis of diverse phytopathogenic bacteria(6).
35 alicylic acid (SA), methyl jasmonate (MeJA), phytopathogenic bacteria, and flagellin.
36   This reveals that, similar to effectors of phytopathogenic bacteria, recognition of filamentous pat
37                                Gram-negative phytopathogenic bacteria, such as Pseudomonas syringae,
38  their critical roles in the pathogenesis of phytopathogenic bacteria, the molecular functions and vi
39 d reveal a commonality between symbiotic and phytopathogenic bacteria.
40 ability to act as a biocontrol agent against phytopathogenic bacteria.
41 cess related to the PCD pathway activated by phytopathogenic bacteria.
42 onserved among many agriculturally important phytopathogenic bacteria.
43 eports linking actin with resistance against phytopathogenic bacteria.
44 eas homologs for the rest are found in other phytopathogenic bacteria.
45 namically and discriminately to infection by phytopathogenic bacteria.
46                             In addition, the phytopathogenic bacterial plasmid "mobilome" includes in
47 omonas syringae pv. syringae (Pss) and other phytopathogenic bacterial species.
48  of exopolysaccharide (EPS) synthesis in the phytopathogenic bacterium Pantoea stewartii ssp. stewart
49                                          The phytopathogenic bacterium Pantoea stewartii subsp. stewa
50                                          The phytopathogenic bacterium Pseudomonas syringae can suppr
51 or-gene disease resistance to strains of the phytopathogenic bacterium Pseudomonas syringae carrying
52 sis thaliana) following inoculation with the phytopathogenic bacterium Pseudomonas syringae pv tomato
53 dependent responses when challenged with the phytopathogenic bacterium Pseudomonas syringae.
54 vation of EFR and downstream immunity to the phytopathogenic bacterium Pseudomonas syringae.
55 the phytotoxin coronatine synthesized by the phytopathogenic bacterium Pseudomonas syringae.
56      Ralstonia (Pseudomonas) solanacearum, a phytopathogenic bacterium that appears to autoregulate i
57               Agrobacterium tumefaciens is a phytopathogenic bacterium that induces the 'crown gall'
58  hydathode infection by the adapted vascular phytopathogenic bacterium Xanthomonas campestris pv camp
59                  Biomultipliers, such as the phytopathogenic bacterium Xanthomonas hortorum pv. gardn
60         Xp10 is a lytic bacteriophage of the phytopathogenic bacterium Xanthomonas oryzae.
61 , in Ralstonia (Pseudomonas) solanacearum, a phytopathogenic bacterium, acyl-HSL production requires
62 virulence genes in Ralstonia solanacearum, a phytopathogenic bacterium, is controlled by a complex re
63 mplete and two draft genome sequences of the phytopathogenic bacterium, Xylella fastidiosa, which cau
64 s an important virulence determinant of this phytopathogenic bacterium.
65 ological systems: i) synthetic dsDNA and two phytopathogenic diseases, ii) the severe CB-form of Citr
66 sly shown that they promote infection by the phytopathogenic enterobacteria Dickeya dadantii and Erwi
67 A-binding protein referred to as CsrA or, in phytopathogenic Erwinia species, RsmA (repressor of stat
68 n-activated protein kinase (FsMAPK) from the phytopathogenic filamentous fungus F. solani f. sp. pisi
69 ve a putative or experimentally demonstrable phytopathogenic function.
70 idae are believed to occur commonly in their phytopathogenic fungal and plant hosts.
71 ssociated with a debilitating disease of its phytopathogenic fungal host.
72 iseases and/or reduce the virulence of their phytopathogenic fungal hosts.
73        It highlights what is known about the phytopathogenic fungal wall and what needs to be discove
74 ing new insights into pathogen initiation in phytopathogenic fungi and connect it to other autophagy-
75 owledge of the functions of MAPK cascades in phytopathogenic fungi and highlight the central role pla
76                   During interaction between phytopathogenic fungi and plants, fungal MAPKs help to p
77 ationship with other components and roles in phytopathogenic fungi are not well-characterized.
78 roles and regulatory mechanisms of m(6) A in phytopathogenic fungi are still largely unknown.
79                            Several potential phytopathogenic fungi associated with ARD, as well as en
80                                The idea that phytopathogenic fungi associated with tree-killing bark
81 exhibit antifungal activity against numerous phytopathogenic fungi at physiologically relevant concen
82 function analyses of two homologues from the phytopathogenic fungi Colletotrichum graminicola and C.
83                                              Phytopathogenic fungi encounter toxic environments durin
84 ruct and analyse a global atlas of potential phytopathogenic fungi from 20,312 samples across all con
85 he first lines of defense against fungi, but phytopathogenic fungi have developed different strategie
86                                              Phytopathogenic fungi have evolved an amazing diversity
87           We show a peak in the diversity of phytopathogenic fungi in mid-latitude regions, in contra
88 w this contributes to the infection cycle of phytopathogenic fungi is largely unknown.
89 ge of the complexes and their co-operator in phytopathogenic fungi is still fragmented.
90                  Germinating conidia of many phytopathogenic fungi must differentiate into an infecti
91              The germinating conidia of many phytopathogenic fungi on hosts must differentiate into a
92 are essential members across ecosystems, yet phytopathogenic fungi pose an increasing risk to crop yi
93                         Studies in different phytopathogenic fungi showed that appressorium formation
94 dins are iso-pimarane diterpenes produced by phytopathogenic fungi that display promising anticancer
95                                              Phytopathogenic fungi threaten global food security but
96                                         Many phytopathogenic fungi use infection structures (IFSs, i.
97 there is growing evidence that at least some phytopathogenic fungi use mannitol to suppress ROS-media
98 h their total antagonistic potential against phytopathogenic fungi was not reduced.
99 psular polysaccharides and the biocontrol of phytopathogenic fungi were enhanced at 28 degrees C.
100 portant driver of the global distribution of phytopathogenic fungi, and our models suggest that their
101 inants, to serve as bacterial antagonists to phytopathogenic fungi, and to secrete the highly useful
102  the variation (45%) in root lifespan, while phytopathogenic fungi, bacteria and herbivorous nematode
103          Finally, two of the most widespread phytopathogenic fungi, Fusarium oxysporum and Botrytis c
104 important role in the infection of plants by phytopathogenic fungi, given their involvement in signal
105 Oxalic acid is a virulence factor of several phytopathogenic fungi, including Sclerotinia sclerotioru
106 Sclerotinia sclerotiorum, one of devastating phytopathogenic fungi, inhibits chloroplast immunity and
107 TB) gene cluster is present in several other phytopathogenic fungi, prompting the search for biosynth
108                        Tentoxin, produced by phytopathogenic fungi, selectively affects the function
109 ates a molecular mechanism, used by multiple phytopathogenic fungi, that manipulates the highly conse
110 MS the first-reported overlapped proteome in phytopathogenic fungi, the "phosphomembranome" of B. cin
111 n structure (appressorium) formation in many phytopathogenic fungi.
112 FOX TF to ATG gene promoters is conserved in phytopathogenic fungi.
113 anscription and fruiting body development in phytopathogenic fungi.
114 get-specific genes remain largely unknown in phytopathogenic fungi.
115 lial growth inhibition against a spectrum of phytopathogenic fungi.
116 both virulence and vegetative growth in some phytopathogenic fungi.
117 C11, a compound with strong activity against phytopathogenic fungi.
118  and environmental stress in the devastating phytopathogenic fungi.
119  approaches to reduce potential threats from phytopathogenic fungi.
120 ined against five representative postharvest phytopathogenic fungi.
121 nctions in a variety of organisms, including phytopathogenic fungi.
122 ession of CWDE genes in both saprophytic and phytopathogenic fungi.
123 ding canola with resistance against multiple phytopathogenic fungi.
124  that is implicated in plant defense against phytopathogenic fungi.
125  of mannitol production and secretion in the phytopathogenic fungus Alternaria alternata in the prese
126 th three plant species, competition with the phytopathogenic fungus Bipolaris sorokiniana, and cooper
127 re, we show that the BcCrh1 protein from the phytopathogenic fungus Botrytis cinerea acts as a cytopl
128 nt and pollinating honeybees from pathogens (phytopathogenic fungus Botrytis cinerea and pathogenic b
129 ria innocua (L. innocua) bacteria as well as phytopathogenic fungus Botrytis cinerea.
130 re we show that RNAi can be expressed in the phytopathogenic fungus Colletotrichum acutatum (strain C
131 a RNA virus 1 (CfRV1), was identified in the phytopathogenic fungus Colletotrichum fructicola.
132                                       In the phytopathogenic fungus Cryphonectria parasitica, another
133 symbiotic fungi were detected, including the phytopathogenic fungus D. anthuriicola that was abundant
134                         Ustilago maydis is a phytopathogenic fungus exhibiting extreme resistance to
135 oxins, the endoplasmic reticulum (ER) of the phytopathogenic fungus Fusarium graminearum is reorganiz
136 ng the first report of a partitivirus from a phytopathogenic fungus infecting tea plants.
137           Macrophomate synthase (MPS) of the phytopathogenic fungus Macrophoma commelinae catalyzes t
138 he extracellular or secreted enzyme from the phytopathogenic fungus Magnaporthe grisea.
139 artitivirus 1 (ScPV1), was identified in the phytopathogenic fungus Sinodiscula camellicola, isolated
140 nstrated that tenuazonic acid (TeA) from the phytopathogenic fungus Stemphylium loti inhibits the pla
141 ycovirus responsible for hypervirulence on a phytopathogenic fungus through virion transfection, as w
142 verse propagules, such as teliospores of the phytopathogenic fungus Ustilago maydis and spores of the
143 r protein 4 (KP4) is a toxin secreted by the phytopathogenic fungus Ustilago maydis that inhibits the
144 s and resistance to Ceratocystis polonica, a phytopathogenic fungus vectored by the spruce bark beetl
145  (MOA) in Botrytis cinerea, a multiresistant phytopathogenic fungus.
146 ulence while reducing vegetative growth in a phytopathogenic fungus.
147 e required for plant infection in this model phytopathogenic fungus.
148          The circular single-stranded DNA of phytopathogenic geminiviruses is propagated by three mod
149 e genomes of plant pathogens compared to non-phytopathogenic genomes (saprotrophs, endo- and ectomyco
150         We sought to establish whether these phytopathogenic genomic patterns hold across diverse tax
151    Pectobacterium atrosepticum SCRI1043 is a phytopathogenic Gram-negative enterobacterium.
152 ixed populations, cells of N. crassa and the phytopathogenic gray mold Botrytis cinerea coordinate th
153  6 predicted LAGs are indeed involved in the phytopathogenic lifestyle of Burkholderia plantarii and
154 e of genomic signatures in predicting fungal phytopathogenic lifestyles and traits during biosurveill
155 on this first functional reconstruction of a phytopathogenic microbe, we spotlight an unusual respira
156 roducts that attract insects, defend against phytopathogenic microbes and combat human diseases.
157 ike proteins (NLPs) are produced by numerous phytopathogenic microbes that cause important crop disea
158 idopsis plants can respond to VCs emitted by phytopathogenic microorganisms by triggering pPGI-indepe
159                          Plant resistance to phytopathogenic microorganisms mainly relies on the acti
160 opalus rusticus is a suspected vector of the phytopathogenic nematode, Bursaphelenchus xylophilus, th
161 teorin, and inhibition of Pythium ultimum, a phytopathogenic oomycete sensitive to pyoluteorin.
162                                              Phytopathogenic oomycetes cause some of the most devasta
163 aphrinomycotina and Saccharomycotina, and in phytopathogenic Oomycetes, but neither other eukaryotes
164 es revealed they all have orthologs in other phytopathogenic or symbiotic bacteria, and are involved
165        Plant resistance to disease caused by phytopathogenic organisms is often triggered by the abil
166 solates and amplified a subset of putatively phytopathogenic P. syringae in a manner causally consist
167 onB-dependent receptor, which is utilized by phytopathogenic Pectobacterium spp. to obtain iron from
168 thogenicity, we were unable to demonstrate a phytopathogenic phenotype for B. thailandensis in three
169                         While the organism's phytopathogenic potential has been well documented, it h
170 ce of A. thaliana to infection with virulent phytopathogenic Pseudomonas syringae strains.
171 ytotoxin synthesized by several pathovars of phytopathogenic Pseudomonas syringae.
172  TTSS pathway targeting signals suggest that phytopathogenic Pseudomonas, Xanthomonas, and Ralstonia
173  of microbiota that suppress the soil-borne, phytopathogenic Ralstonia solanacearum bacterium.
174              Dimorphic pathogens such as the phytopathogenic smut fungi, Ustilago maydis and Microbot
175     In addition, many economically important phytopathogenic species are nested within this complex.
176           The genus Verticillium encompasses phytopathogenic species that cause vascular wilts of pla
177 in the overall levels of gene duplication in phytopathogenic species versus non-pathogenic relatives
178  cluster is widespread within biocontrol and phytopathogenic strains of the enterobacteria, Serratia
179 24 and its NLR targets analysed in different phytopathogenic stresses revealed differential and mutua
180  (HGT) has played a role in the evolution of phytopathogenic traits in fungi and oomycetes.
181  they suck phloem sap and act as vectors for phytopathogenic viruses, aphids pose a threat to crop yi
182 uction of plant defense-related responses by phytopathogenic xanthomonads in leaves of pepper (Capsic
183                   TAL effectors delivered by phytopathogenic Xanthomonas species are DNA-sequence-spe
184 re bacterial Type-III effector proteins from phytopathogenic Xanthomonas species that act as transcri
185 a spp. and is very similar to T3SSs found in phytopathogenic Xanthomonas spp. and Ralstonia solanacea
186                                          The phytopathogenic y-proteobacteria, Pectobacterium carotov

 
Page Top