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1 rotein shows significant homology to RpfF in Xanthomonas campestris.
2 resistance to a virulent bacterial pathogen, Xanthomonas campestris.
3 omonas syringae, Pseudomonas aeruginosa, and Xanthomonas campestris.
4 a, Ralstonia (Pseudomonas) solanacearum, and Xanthomonas campestris.
5  of Ralstonia (Pseudomonas) solanacearum and Xanthomonas campestris.
6                        We have identified in Xanthomonas campestris a novel N-acetylornithine transca
7 acterial pathogens, Pseudomonas syringae and Xanthomonas campestris, and an oomycete, Peronospora par
8              Recently, it was shown that the Xanthomonas campestris AvrBs2 protein can be delivered d
9 to few pathovars of Pseudomonas syringae and Xanthomonas campestris, but also enhanced the growth of
10    While phenotypes of a DeltarpfF strain in Xanthomonas campestris could be complemented by its own
11                                The OleA from Xanthomonas campestris has been crystallized and its str
12  of Erwinia amylovora, Pseudomonas spp., and Xanthomonas campestris has impeded the control of severa
13        Tryptophan 2,3-dioxygenase (TDO) from Xanthomonas campestris is a highly specific heme-contain
14                                The bacterium Xanthomonas campestris is an economically important path
15 lus subtilis OhrR) and 2-Cys (represented by Xanthomonas campestris OhrR).
16 , mutagenesis of the active site cysteine in Xanthomonas campestris OleA (Cys(143)) enabled trapping
17  function of two B. subtilis homologs of the Xanthomonas campestris organic hydroperoxide resistance
18 tracellular enzymes and reduced virulence of Xanthomonas campestris pathovar campestris (Xcc).
19              XopN is a virulence factor from Xanthomonas campestris pathovar vesicatoria (Xcv) that i
20 onstrate that XopD, a type III effector from Xanthomonas campestris pathovar vesicatoria (Xcv), suppr
21 dependent hypersensitive response (HR) after Xanthomonas campestris pv campestris (Xcc) infection.
22                                              Xanthomonas campestris pv campestris (Xcc) is a plant pa
23 fense-eliciting activity of flagellins among Xanthomonas campestris pv campestris (Xcc) strains.
24 e adapted vascular phytopathogenic bacterium Xanthomonas campestris pv campestris (Xcc), the causal a
25 aliana accession Landsberg erecta (Ler) with Xanthomonas campestris pv campestris isolate 2D520 resul
26 om cold-treated, heat-treated, and pathogen (Xanthomonas campestris pv campestris)-infected plants, c
27  resistance gene are resistant to strains of Xanthomonas campestris pv vesicatoria (Xcv) expressing t
28 tion of tomato (Lycopersicon esculentum) and Xanthomonas campestris pv vesicatoria (Xcv), to examine
29 omato (Lycopersicon esculentum) and virulent Xanthomonas campestris pv vesicatoria (Xcv).
30 e 35S::Pto lines also were more resistant to Xanthomonas campestris pv vesicatoria and Cladosporium f
31 s of both genotypes with virulent bacterial (Xanthomonas campestris pv vesicatoria and Pseudomonas sy
32           AvrBsT is a type III effector from Xanthomonas campestris pv vesicatoria that is translocat
33 YopJ family effector from the plant pathogen Xanthomonas campestris pv vesicatoria, interacts with th
34 eviously identified 25.4-kbp pig region from Xanthomonas campestris pv. campestris (strain B-24).
35 p between the two signals in the Arabidopsis-Xanthomonas campestris pv. campestris (Xcc) compatible i
36 es and extracellular polysaccharide (EPS) in Xanthomonas campestris pv. campestris (Xcc) is regulated
37 ty acid signal DSF controls the virulence of Xanthomonas campestris pv. campestris (Xcc) to plants.
38                                           In Xanthomonas campestris pv. campestris (Xcc), the protein
39                                              Xanthomonas campestris pv. campestris can express AvrXa2
40 ) subgroup of the superfamily encoded by the Xanthomonas campestris pv. campestris str. ATCC 33913 ge
41                                              Xanthomonas campestris pv. campestris, the causal agent
42 resistance to the bacterial blight pathogen, Xanthomonas campestris pv. malvacearum (Xcm).
43                    Whole-genome sequences of Xanthomonas campestris pv. raphani strain 756C and X. or
44                                   Strains of Xanthomonas campestris pv. vesicatoria (Xcv) carrying av
45 of the pepper Bs2 gene confers resistance to Xanthomonas campestris pv. vesicatoria (Xcv) pathogenic
46                       The bacterial pathogen Xanthomonas campestris pv. vesicatoria (Xcv) uses a type
47 with the disease-causing bacterial pathogen, Xanthomonas campestris pv. vesicatoria (Xcv).
48 igh titer inoculum of the non-host pathogen, Xanthomonas campestris pv. vesicatoria (Xcv).
49 he region was most similar to hrp genes from Xanthomonas campestris pv. vesicatoria and Ralstonia sol
50 ar characterization of the avrBs2 locus from Xanthomonas campestris pv. vesicatoria has revealed that
51 lene-insensitive tomato plants infected with Xanthomonas campestris pv. vesicatoria have greatly redu
52 esponse to virulent and avirulent strains of Xanthomonas campestris pv. vesicatoria in tomato (Lycope
53 , we show that infection of pepper plants by Xanthomonas campestris pv. vesicatoria strains expressin
54 ognizes and confers resistance to strains of Xanthomonas campestris pv. vesicatoria that contain the
55 rulence gene of the bacterial plant pathogen Xanthomonas campestris pv. vesicatoria triggers disease
56                                              Xanthomonas campestris pv. vesicatoria, causal agent of
57 rotein D), a type III secreted effector from Xanthomonas campestris pv. vesicatoria, is a desumoylati
58 inerea and the biotrophic bacterial pathogen Xanthomonas campestris pv. vesicatoria.
59 ity with a putative translocator, HrpF, from Xanthomonas campestris pv. vesicatoria.
60 shows homology to HrpF of the plant pathogen Xanthomonas campestris pv. vesicatoria.
61 uberculosis and AvrRxv of the plant pathogen Xanthomonas campestris pv. vesicatoria.
62                             Previous work on Xanthomonas campestris showed that the RpfC/RpfG two-com
63 ve structural and biochemical studies of the Xanthomonas campestris TDO and a related protein SO4414
64                                           In Xanthomonas campestris, the protein annotated as ornithi
65                                          The Xanthomonas campestris transcription regulator OhrR cont
66 enic bacteria, like Pseudomonas syringae and Xanthomonas campestris, use the type III secretion syste
67                     In this study, OleA from Xanthomonas campestris was expressed in Escherichia coli
68 -acetylglutamate synthase-kinase (NAGS-K) of Xanthomonas campestris, which is inhibited by arginine.
69    HfsA has sequence similarity to GumC from Xanthomonas campestris, which is involved in exopolysacc
70  such as Rhizobium meliloti (succinoglycan), Xanthomonas campestris (xanthan gum), and Salmonella ent
71 cterium carotovorum, Ralstonia solanacearum, Xanthomonas campestris, Xanthomonas oryzae, and Xylella
72 , several crystal structures of AOTCase from Xanthomonas campestris (xc) have been determined.
73       A genetic screen in the plant pathogen Xanthomonas campestris (Xcc) identified that XC_0250, wh
74 AGS-K) while it destabilized the NAGS-K from Xanthomonas campestris (XcNAGS-K).
75 idensis (sIDO) indoleamine 2,3-dioxygenases, Xanthomonas campestris (XcTDO) tryptophan 2,3-dioxygenas
76 , Erwinia chrysanthemi and carotovora (out), Xanthomonas campestris (xps), Pseudomonas aeruginosa (xc
77 nomeric tetratricopeptide repeat domain from Xanthomonas campestris YbgF, which is also able to trime

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