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1 aracterized Staphylococcus and the other for Streptococcus mitis.
2 luded strains of Selenomonas, Neisseria, and Streptococcus mitis.
3 re: Streptococcus gordonii Blackburn, 10558, Streptococcus mitis 10712, 903, Streptococcus oralis 105
7 melaninogenica) or increased growth (such as Streptococcus mitis and Corynebacterium matruchotii) acr
8 t species in the human supragingival plaque, Streptococcus mitis and Corynebacterium matruchotii, to
12 termination was particularly problematic for Streptococcus mitis and Streptococcus oralis isolates.
13 t closely related oral streptococcal species Streptococcus mitis and Streptococcus oralis on the basi
16 were Streptococcus pseudopneumoniae, 12 were Streptococcus mitis, and 1 were Streptococcus oralis.
17 ococcus aureus, Streptococcus parasanguinis, Streptococcus mitis, and Corynebacterium pseudogenitaliu
18 CL14 potently killed Pseudomonas aeruginosa, Streptococcus mitis, and Streptococcus pneumoniae in a d
19 rating to an incorrect identification (e.g., Streptococcus mitis), as did matrix-assisted laser desor
21 of expression of multiple transposases in a Streptococcus mitis biofilm when the periodontopathogen
22 reactive with the pioneer oral streptococci Streptococcus mitis biovar 1 and Streptococcus oralis, t
23 IgA1 proteases from Streptococcus oralis and Streptococcus mitis biovar 1 strains but were cleaved to
24 to a limited set of oral microbes, including Streptococcus mitis, Gemella haemolysans, and, most prom
28 am-positive species Streptococcus mutans and Streptococcus mitis, however, lactoferrin containing Lys
32 subunit of the cell wall polysaccharide from Streptococcus mitis J22 are correlated with individual g
33 n; mean age, 77.7 years) from an outbreak of Streptococcus mitis/oralis endophthalmitis after bevaciz
34 confirmed the presence of a common strain of Streptococcus mitis/oralis in vitreous specimens and 7 u
35 is after intravitreal bevacizumab injection, Streptococcus mitis/oralis was cultured from the majorit
37 (P = .64), Streptococcus viridans (P = .46), Streptococcus mitis (P = .83), and Enterococcus faecalis
39 spp. dominance were followed by a switch to Streptococcus mitis predominance after 3 months of age.
40 with a nonpathogenic oral bacterial species, Streptococcus mitis, resulted in well-controlled infecti
42 es that significantly decreased included the Streptococcus mitis-S. pneumoniae-S. infantis group, Cor
44 A soluble platelet aggregation factor from Streptococcus mitis (Sm-hPAF) was characterized and show
48 lA and PblB are prophage-encoded proteins of Streptococcus mitis strain SF100 that mediate binding to
50 iofilms had higher counts and proportions of Streptococcus mitis, Streptococcus oralis, and Streptoco
51 coccus parasanguinis, Abiotrophia defectiva, Streptococcus mitis, Streptococcus oralis, and Streptoco
52 ced only by some members of the mitis group (Streptococcus mitis, Streptococcus oralis, Streptococcus
53 titative polymerase chain reaction to detect Streptococcus mitis, Streptococcus sobrinus, Streptococc
54 identified 5/15 clinical blood cultures with Streptococcus mitis/Streptococcus oralis and 1/3 blood c
56 of purified HlpA (5 to 100 microg/ml), from Streptococcus mitis, to induce the production of proinfl
57 Actinomyces naeslundii, Lactobacillus casei, Streptococcus mitis, Veillonella parvula, and Fusobacter
58 components that mediate platelet binding by Streptococcus mitis, we screened a Tn916deltaE-derived m
60 amylase-binding oral streptococci including Streptococcus mitis (with the exception of 1 of 14 strai