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1 Andean Puna, including strains of the genus Micrococcus.
2 (6), Corynebacterium (8), Lactobacillus (2), Micrococcus (2), Neisseria mucosa (1), Escherichia coli
3 of a common ancestor for linear plasmids in Micrococcus and suggests that horizontal gene transfer l
4 nase (IKK) mutant forms completely inhibited micrococcus- and PGN-induced activation of NF-kappaB and
8 nging from 45% identity for the homolog from Micrococcus luteus (FtsZ[Ml]) to 91% identity for the ho
9 lf thymus, salmon testes, and the bacterium, micrococcus luteus (lysodeikticus) containing different
14 opin A gene was induced by the G(+) bacteria Micrococcus luteus and Staphylococcus aureus, but not by
16 ssessed by qualitative agar plate test using Micrococcus luteus as substrate showing that both the un
17 exhibit biphasic kinetics in the clearing of Micrococcus luteus cell suspensions, suggesting preferen
19 the D52A and D52A/N46A ChEWL complexes with Micrococcus luteus cells are 3- and 4-fold higher, respe
20 were challenged with Gram-positive bacteria Micrococcus luteus In this setting, osa knockdown had a
23 e synthesis of a tetrasaccharide fragment of Micrococcus luteus teichuronic acid containing N-acetyl-
26 uence similarity to the Escherichia coli and Micrococcus luteus UvrA proteins involved in excision re
27 y against Bacillus subtilis (but not against Micrococcus luteus), as well as against the parental and
29 Four genomic DNAs of differing GC content (Micrococcus luteus, 72% GC; Escherichia coli, 50% GC; ca
30 Transcription termination factor Rho from Micrococcus luteus, a high G + C Gram-positive bacterium
32 , Escherichia coli, Lactobacillus plantarum, Micrococcus luteus, and Staphylococcus aureus support th
33 as purified from the Gram-positive bacterium Micrococcus luteus, and the complete gene sequence was d
34 te inhibited the growth of Escherichia coli, Micrococcus luteus, Bacillus subtilis, and Klebsiella pn
37 ricidal activity against both Gram-positive (Micrococcus luteus, Staphylococcus aureus, Bacillus subt
39 of resuscitation-promoting factor (Rpf) from Micrococcus luteus, which is an extremely potent anti-do
54 conferring protection to fluorescein-labeled Micrococcus lysodeikticus from lysozyme-mediated hydroly
55 e activity of immune pupal hemolymph against Micrococcus lysodeikticus was 11 times greater when comp
56 lysozyme sensing concept based on the use of Micrococcus lysodeikticus whole cells adsorbed on graphe
57 I of ascorbate peroxidase and catalase from Micrococcus lysodeikticus, in which the radical has been
60 ceeding 30 kb in total) in all three studied Micrococcus megaplasmids indicates a clear evolutionary
61 C4 promoter accessibility as demonstrated by micrococcus nuclease digestion (P<0.05) and chromatin im
62 ium, Cutibacterium acnes, Lactobacillus, and Micrococcus), PPA and NPA ranged from 84.5% to 100% and
63 teria Actinomyces, Anaerococcus, Finegoldia, Micrococcus, Prevotella and Propionibacterium at all tim
66 thalate-grown Arthrobacter keyseri (formerly Micrococcus sp.) 12B to the corresponding 2-substituted
69 lococci, aerobic and anaerobic diphtheroids, Micrococcus spp., Bacillus spp., and viridans group stre
70 ulase-negative Staphylococcus strains, and 8 Micrococcus strains) in freshly reconstituted master mix