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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.
7 acterial pathogens, Pseudomonas syringae and Xanthomonas campestris, and an oomycete, Peronospora par
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
12 of Erwinia amylovora, Pseudomonas spp., and Xanthomonas campestris has impeded the control of severa
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
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.
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
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
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.
40 ) subgroup of the superfamily encoded by the Xanthomonas campestris pv. campestris str. ATCC 33913 ge
45 of the pepper Bs2 gene confers resistance to Xanthomonas campestris pv. vesicatoria (Xcv) pathogenic
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
57 rotein D), a type III secreted effector from Xanthomonas campestris pv. vesicatoria, is a desumoylati
63 ve structural and biochemical studies of the Xanthomonas campestris TDO and a related protein SO4414
66 enic bacteria, like Pseudomonas syringae and Xanthomonas campestris, use the type III secretion syste
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
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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