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1 licles on the face, neck, chest, and back by Propionibacterium acnes.
2 e immune response to the commensal bacterium Propionibacterium acnes.
3 antimicrobial activity against S. aureus and Propionibacterium acnes.
4 es, is caused by multiple factors, including Propionibacterium acnes.
5 ion of 2.0 micrograms per milliliter against Propionibacterium acnes.
6 against Escherichia coli., and 12 mm against Propionibacterium acnes.
7 46% vs 80%; 3) the most frequent isolate was Propionibacterium acnes (11/26) vs coagulase-negative St
8 iome at the strain level and genome level of Propionibacterium acnes, a dominant skin commensal, betw
9 mechanism by which S. aureus may commandeer Propionibacterium acnes, a key member of the human skin
10 In this issue, Kistowska et al. confirm that Propionibacterium acnes activates inflammasomes leading
12 asts, 6 nonfermenters, and 1 isolate each of Propionibacterium acnes and coagulase-negative staphyloc
13 olleagues present strain-based resolution of Propionibacterium acnes and its association with the com
14 the presence of the Gram-positive bacterium Propionibacterium acnes and its potential association wi
17 s associated with formation of resistance in Propionibacterium acnes and other bacteria, with clinica
18 ndependent growth, requiring helpers such as Propionibacterium acnes and Prevotella intermedia for st
19 on in common skin commensal bacteria such as Propionibacterium acnes and Staphylococcus epidermitis.
22 ites from the abundant skin-resident microbe Propionibacterium acnes can influence cytokine expressio
25 Bradyrhizobium, Anaerococcus, Peptoniphilus, Propionibacterium acnes, Dorea, and Ruminococcus and red
26 rial pathogens including Bacillus anthracis, Propionibacterium acnes, Enterococcus faecalis, and both
28 resulting from the immune response targeting Propionibacterium acnes has a significant role in its pa
31 e primed 12 days in advance with heat-killed Propionibacterium acnes, IL-18BP-Fc prevents LPS-induced
32 ase-negative staphylococci in 6.0% (27/448), Propionibacterium acnes in 4.7% (21/448), and Pseudomona
33 ica charantia Linn. var. abbreviata Ser.) on Propionibacterium acnes-induced inflammation and to iden
34 us studies showed that TLR9 and TLR2 mediate Propionibacterium acnes-induced sensitization to lipopol
52 1), Propionibacterium species (n = 15), and Propionibacterium acnes (n = 19) isolates; all of these
53 stigated the in vitro susceptibilities of 23 Propionibacterium acnes ophthalmic isolates to ertapenem
55 S (20 microg/mouse) 7 days after heat-killed Propionibacterium acnes (P. acnes) injection into wild-t
56 monstrate that fermentation of glycerol with Propionibacterium acnes (P. acnes), a skin commensal bac
57 ne treatment as a natural antibiotic against Propionibacterium acnes (P. acnes), which promotes folli
58 e investigated the roles of TLR2 and TLR4 in Propionibacterium acnes (P. acnes)-primed, LPS-induced l
62 overed, including Escherichia coli phage T3, Propionibacterium acnes phage PA6, and Streptococcus mit
63 on of early childhood acne, the emergence of Propionibacterium acnes resistance, and the rare but ser
64 teen of the species or phylotypes, including Propionibacterium acnes, Staphylococcus spp., and the op
65 observed the decline of an early-colonizing Propionibacterium acnes strain similar to SK137 and the
66 ny countries reporting that more than 50% of Propionibacterium acnes strains are resistant to topical
67 es of the human skin microbiome suggest that Propionibacterium acnes strains may contribute different
70 and four different Cutibacterium (previously Propionibacterium) acnes strains, and compare outcomes w
71 s-wide comparative analysis of 90 genomes of Propionibacterium acnes that represent the known diversi
72 rect antimicrobial activity in vitro against Propionibacterium acnes, the bacterium linked to the pat
79 ct to sequence multiple clinical isolates of Propionibacterium acnes, we have produced a draft genome
80 teria such as Staphylococcus epidermidis and Propionibacterium acnes, were identified in bacteriologi
81 ulture showed antimicrobial activity against Propionibacterium acnes, whereas the enhanced antimicrob
83 t contributes to the pathogenesis of acne is Propionibacterium acnes; yet, the molecular mechanism by