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1 ide and possibly the secretion of the mature autoinducing peptide.
2 and AgrB and AgrD are required to produce an autoinducing peptide.
3 ay whose activating ligand is an agr-encoded autoinducing peptide.
5 st agr were noncompetitive inhibitors of the autoinducing peptide (AIP) activated AgrC receptor, by a
6 via agr-dependent quorum sensing in which an autoinducing peptide (AIP) activates AgrC, a histidine p
7 transduction module that is activated by an autoinducing peptide (AIP) encoded within the agr locus
8 e AgrC receptor histidine kinase detects its autoinducing peptide (AIP) ligand and generates an intra
10 coccus aureus, AgrD is the propeptide for an autoinducing peptide (AIP) pheromone that triggers the A
11 ce factors via the production and sensing of autoinducing peptide (AIP) signal molecules by the agr l
13 S. epidermidis strains, but only one of the autoinducing peptide (AIP) signals has been identified (
14 reus is a major human pathogen that utilizes autoinducing peptide (AIP) signals to mediate QS and the
15 due thiolactone-containing peptide called an autoinducing peptide (AIP) that is biosynthesized from t
16 e, is initiated by the binding of a specific autoinducing peptide (AIP) to the extracellular domain o
17 agr, activated upon binding of a self-coded autoinducing peptide (AIP) to the receptor-histidine kin
18 bitory activity suggested that the S. caprae autoinducing peptide (AIP) was responsible, and mass spe
19 rference: each agr type synthesizes a cyclic autoinducing peptide (AIP) with a distinct sequence that
20 n RNAIII-activating protein (RAP) and by the autoinducing peptide (AIP), and is inhibited by RNAIII-i
21 a polytopic receptor, AgrC, activated by an autoinducing peptide (AIP), to coordinate quorum sensing
24 we recently developed analogues of a native autoinducing peptide (AIP-III) signal that can inhibit A
25 sensing system, staphylococci secrete unique autoinducing peptides (AIPs) and detect their concentrat
27 aureus virulence is regulated when secreted autoinducing peptides (AIPs) are recognized by a membran
29 charomyces cerevisiae and the elucidation of autoinducing peptides (AIPs) from supernatants of pathog
30 " which involves generation and secretion of autoinducing peptides (AIPs) into the surrounding enviro
31 f 10 truncated analogues based on the parent autoinducing peptides (AIPs) of Staphylococcus lugdunens
32 regulated by macrocyclic peptide signals (or autoinducing peptides (AIPs)) and their cognate transmem
34 Thus, oxidant-mediated inactivation of an autoinducing peptide from S. aureus is a critical innate
35 d the regulation of a virulence factor by an autoinducing peptide in pneumococci has been demonstrate
36 addition to the quorum sensing effect of the autoinducing peptide of agr, the sarT-sarU pathway may r
37 s to detect delta-hemolysin activity and agr autoinducing peptide production indicated that 15 ( appr
38 ntation of the culture medium with synthetic autoinducing peptide (sAIP) significantly increased Agr
39 N-terminal region, is the propeptide for an autoinducing peptide that is the ligand for AgrC; and Ag
40 enes are essential for the production of the autoinducing peptide, which functions as a signal for th
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