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1 ight mass spectrometry (MALDI-TOF MS) (e.g., Streptococcus oralis).
2 udopneumoniae, Streptococcus pneumoniae, and Streptococcus oralis.
3 iae, 12 were Streptococcus mitis, and 1 were Streptococcus oralis.
4 ayers of Streptococcus gordonii Blackburn or Streptococcus oralis 10557 on enamel chips were placed o
5 burn, 10558, Streptococcus mitis 10712, 903, Streptococcus oralis 10557, 9811, and Streptococcus sang
6 e tooth surface (Streptococcus gordonii DL1, Streptococcus oralis 34, and Actinomyces naeslundii T14V
7 al bacteria, Actinomyces naeslundii T14V and Streptococcus oralis 34, is dependent upon production of
10 streptococci examined, except one strain of Streptococcus oralis (35037), rapidly induced up-regulat
11 cluding Streptococcus sanguinis (3 strains), Streptococcus oralis (4 strains), and Streptococcus muta
12 ical blood cultures with Streptococcus mitis/Streptococcus oralis and 1/3 blood cultures spiked with
13 coccus gordonii, Streptococcus sanguinis, or Streptococcus oralis and a quadculture containing all 4
14 mutans grown with sucrose in the presence of Streptococcus oralis and Actinomyces naeslundii steadily
15 ggregation receptor polysaccharides (RPS) of Streptococcus oralis and related species are recognized
16 stant to cleavage by the IgA1 proteases from Streptococcus oralis and Streptococcus mitis biovar 1 st
17 , Tannerella forsythia, Treponema denticola, Streptococcus oralis, and Actinomyces naeslundii levels.
18 treptococcus sobrinus, Streptococcus mutans, Streptococcus oralis, and Candida albicans in the saliva
20 s yielded a mutant defective in adherence to Streptococcus oralis, and revealed the essential role of
21 A within typical and atypical S. pneumoniae, Streptococcus oralis, and Streptococcus mitis strains.
22 unts and proportions of Streptococcus mitis, Streptococcus oralis, and Streptococcus mutans, whereas
25 ell as Actinomyces naeslundii ATCC 12104 and Streptococcus oralis ATCC 9811, grown on machine-etched
26 e species or together with initial colonizer Streptococcus oralis but showed mutualistic growth when
27 aggregation receptor polysaccharide (RPS) of Streptococcus oralis C104 have distinct ecological roles
28 yromonas pasteri, Prevotella nanceiensis and Streptococcus oralis decreased, while Veillonella specie
31 ombinant blocks identified originated from a Streptococcus oralis isolate, demonstrating for the firs
33 Streptococcus gordonii 38 and type 2G RPS of Streptococcus oralis J22 are composed of heptasaccharide
34 rides (RPS) of Streptococcus gordonii 38 and Streptococcus oralis J22 was eliminated by replacement o
36 treptococcal species Streptococcus mitis and Streptococcus oralis on the basis of three differentiati
40 ggregation receptor polysaccharides (RPS) of Streptococcus oralis strains C104 and SK144 mediate reco
41 ers of the mitis group (Streptococcus mitis, Streptococcus oralis, Streptococcus gordonii, Streptococ
42 ability of C. albicans to form biofilms with Streptococcus oralis, Streptococcus sanguinis, or Strept
43 results indicated that PC-bearing strains of Streptococcus oralis, Streptococcus sanguis, Haemophilus
45 olonizer and cause of infective endocarditis Streptococcus oralis subsp. dentisani displays a strikin
46 g the coaggregation of Actinomyces oris with Streptococcus oralis that helps to seed biofilm developm
47 a previously identified gene (i.e., wefM) of Streptococcus oralis that is associated with alpha1-1 tr
48 second set of genetic elements imported from Streptococcus oralis, the choline-independent streptococ
49 treptococci Streptococcus mitis biovar 1 and Streptococcus oralis, the late oral colonizer Streptococ
50 nas gingivalis, Fusobacterium nucleatum, and Streptococcus oralis were formed on titanium specimens f
51 nnerella forsythia, Treponema denticola, and Streptococcus oralis were measured with real-time polyme
53 one or mixed with Actinomyces naeslundii and Streptococcus oralis, were initially formed onto saliva-