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1 ps4 from Pseudomonas syringae and PopP2 from Ralstonia solanacearum.
2 effective in another P. syringae strain and Ralstonia solanacearum.
3 ound in phytopathogenic Xanthomonas spp. and Ralstonia solanacearum.
4 ella burnetii, as well as the plant pathogen Ralstonia solanacearum.
5 ltiple virulence genes in the plant pathogen Ralstonia solanacearum.
6 m Xanthomonas campestris pv. vesicatoria and Ralstonia solanacearum.
7 e similarity was with Ralstonia eutropha and Ralstonia solanacearum.
12 vorite pathogens, Phytophthora infestans and Ralstonia solanacearum, among others, are considered.
15 DNase activity in plant-pathogenic bacteria (Ralstonia solanacearum) and fungi (Cochliobolus heterost
16 binding module, a fucose-binding lectin from Ralstonia solanacearum, and human norovirus VA387 P part
20 ct invasion resistance to the plant pathogen Ralstonia solanacearum in microcosms and in tomato plant
21 YopJ effector produced by the plant pathogen Ralstonia solanacearum, in complex with inositol hexapho
29 ropeller formed by oligomerization as in the Ralstonia solanacearum lectin and not by sequential doma
30 iens, Pantoea stewartii, Erwinia carotovora, Ralstonia solanacearum, Pseudomonas syringae, Pseudomona
34 eudomonas syringae and the vascular pathogen Ralstonia solanacearum Thus, the GFP strand system can b
36 assessed the growth of a bacterial invader, Ralstonia solanacearum, when introduced into communities
38 winia amylovora, Pectobacterium carotovorum, Ralstonia solanacearum, Xanthomonas campestris, Xanthomo
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