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1 of F. alocis are enhanced in coculture with Porphyromonas gingivalis.
2 roded titanium surfaces on the attachment of Porphyromonas gingivalis.
3 etween HIV-1 and an invasive oral bacterium, Porphyromonas gingivalis.
4 obulin (TG), Escherichia coli LPS, or intact Porphyromonas gingivalis.
5 ood mononuclear cells (PBMCs) in response to Porphyromonas gingivalis.
6 rally infected with the periodontal pathogen Porphyromonas gingivalis.
7 m johnsoniae and the nonmotile oral pathogen Porphyromonas gingivalis.
8 isease that is triggered by bacteria such as Porphyromonas gingivalis.
9 . pylori as well as Streptococcus mutans and Porphyromonas gingivalis.
10 y Actinobacillus actinomycetemcomitans), and Porphyromonas gingivalis.
11 t virulence determinant of the oral anaerobe Porphyromonas gingivalis.
12 itates colonization of the dental biofilm by Porphyromonas gingivalis.
13 ly Actinobacillus actinomycetemcomitans) and Porphyromonas gingivalis.
14 m mice with DIO exposed to an oral pathogen, Porphyromonas gingivalis.
15 ly Actinobacillus actinomycetemcomitans) and Porphyromonas gingivalis.
16 ly Actinobacillus actinomycetemcomitans) and Porphyromonas gingivalis.
17 bacterial species, Streptococcus mutans and Porphyromonas gingivalis.
18 clearance by opportunistic pathogens such as Porphyromonas gingivalis.
19 ontal disease, whose main infective agent is Porphyromonas gingivalis.
21 er actinomycetemcomitans (MT4/MSP: 42%/36%), Porphyromonas gingivalis (78%/66%), Tannerella forsythia
22 were as follows: Tannerella forsythia, 81%; Porphyromonas gingivalis, 78%; and Aggregatibacter (form
25 sis of the genome-scale metabolic network of Porphyromonas gingivalis, a gram-negative anaerobe that
32 important role in eliciting inflammation to Porphyromonas gingivalis, a keystone pathogen in periodo
34 chronic inflammatory periodontal disease is Porphyromonas gingivalis, a non-motile, Gram-negative, r
35 bits production of a major adhesin, FimA, in Porphyromonas gingivalis, a primary periodontal pathogen
37 nalysed in mice after oral administration of Porphyromonas gingivalis, a representative periodontopat
38 n 9 times with 10(9) colony-forming units of Porphyromonas gingivalis A7436 through an oral gavage mo
39 he chronic periodontitis-associated pathogen Porphyromonas gingivalis activates a Toll-like receptor
40 esions, we injected the periodontal pathogen Porphyromonas gingivalis adjacent to calvarial bone with
42 contamination with >/=3 specific pathogens (Porphyromonas gingivalis, Aggregatibacter actinomycetemc
44 tes in diabetes showed a higher frequency of Porphyromonas gingivalis, Aggregatibacter actinomycetemc
45 operties against three periodontal bacteria: Porphyromonas gingivalis, Aggregatibacter actinomycetemc
47 issue-degrading enzymes in the oral pathogen Porphyromonas gingivalis Although a number of subunits o
48 re Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis amounts in saliva and their ant
49 lipid A structures in the outer membrane of Porphyromonas gingivalis, an agent of human periodontal
53 he same biofilm plus the periodontopathogens Porphyromonas gingivalis and Aggregatibacter actinomycet
54 killing of periodontal pathogens, including Porphyromonas gingivalis and Aggregatibacter actinomycet
57 derived from the common human oral bacterium Porphyromonas gingivalis and from bacteria commonly foun
58 ) on the virulence of a mixed infection with Porphyromonas gingivalis and Fusobacterium nucleatum in
59 odontitis was induced by oral inoculation of Porphyromonas gingivalis and Fusobacterium nucleatum in
62 that aPDT treatment can simultaneously kill Porphyromonas gingivalis and inactivate its virulence-as
64 mDC microbiome by 16S rDNA sequencing showed Porphyromonas gingivalis and other species, including (c
65 d oral inoculations of periodontal pathogens Porphyromonas gingivalis and Prevotella nigrescens induc
66 The Orange-Red cluster score (that included Porphyromonas gingivalis and Prevotella spp.) was positi
68 d Treponema denticola, and the prevalence of Porphyromonas gingivalis and T. denticola associated sig
69 ted with periodontal pathology and number of Porphyromonas gingivalis and Tannerella forsythia (forme
70 tus), two red-complex periodontal pathogens (Porphyromonas gingivalis and Tannerella forsythia), and
71 es that gram-negative oral bacteria, such as Porphyromonas gingivalis and Tannerella forsythia, use d
74 modes of mucosal vaccination with whole-cell Porphyromonas gingivalis and to test the role of various
75 how galactose-inhibitable coaggregation with Porphyromonas gingivalis and were defective in cell bind
76 presence of specific bacterial species (i.e. Porphyromonas gingivalis) and their effects in immune re
77 the proteases of Pseudomonas aeruginosa and Porphyromonas gingivalis, and enables its antimicrobial
78 uced the numbers of Streptococcus anginosus, Porphyromonas gingivalis, and Fusobacterium nucleatum, a
79 iodontitis is initiated by bacteria, such as Porphyromonas gingivalis, and is caused largely by host
80 nitiated by anaerobic oral pathogens such as Porphyromonas gingivalis, and it is characterized by hos
81 ously Actinobacillus actinomycetemcomitans), Porphyromonas gingivalis, and Prevotella intermedia.
82 ously Actinobacillus actinomycetemcomitans), Porphyromonas gingivalis, and Tannerella forsythia (prev
83 eptide showed 82% homology with enolase from Porphyromonas gingivalis, and the levels of antibodies t
84 or more overtly pathogenic organisms such as Porphyromonas gingivalis, and the two species assemble i
86 hemistry, we have identified the presence of Porphyromonas gingivalis antigens in placental tissues.
87 ibular second premolars, followed by topical Porphyromonas gingivalis application (10(9) colony formi
88 riae proteins produced by the human pathogen Porphyromonas gingivalis are required for invasion of hu
89 , FimA and Mfa1, of the periodontal pathogen Porphyromonas gingivalis are responsible for adherence t
90 rial manipulation of neutrophil responses by Porphyromonas gingivalis as a mechanism that contributes
91 early and late colonizer pathogens, such as Porphyromonas gingivalis, as the biofilm ages and period
93 gnaling in alveolar bone resorption, using a Porphyromonas gingivalis-associated ligature-induced per
94 gens (Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Campylobacter rectus, and Tann
96 en" where low-abundance microbial pathogens (Porphyromonas gingivalis) can orchestrate inflammatory d
97 the periodontitis-associated oral bacterium Porphyromonas gingivalis, can subvert host immunity to r
100 in substrates of a novel secretion system of Porphyromonas gingivalis contain a conserved C-terminal
103 zation (red complex-KCNK1, p = 3.4 x 10(-7); Porphyromonas gingivalis-DAB2IP, p = 1.0 x 10(-6)).
104 echanism by which the opportunistic pathogen Porphyromonas gingivalis dampens innate immune responses
105 eomic responses to the periodontal pathogen, Porphyromonas gingivalis, donor-matched human blood mono
107 complex), produced by the keystone pathogen Porphyromonas gingivalis, dramatically increased their a
108 0068, Fusobacterium nucleatum ATCC10953, and Porphyromonas gingivalis DSM20709) were placed in a seri
109 periodontitis caused by oral infection with Porphyromonas gingivalis enhances articular bone loss.
110 s infection with the anaerobic oral pathogen Porphyromonas gingivalis exerts a regulatory effect on a
113 occus mutans and an unencapsulated strain of Porphyromonas gingivalis following as few as 100 pulses
117 virulence factor of the periodontal pathogen Porphyromonas gingivalis, has been shown to induce prote
119 of Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis have been shown to induce diffe
121 dy, we hypothesized that histatin 5 binds to Porphyromonas gingivalis hemagglutinin B (HagB) and atte
124 onin, and immunoglobulin G (IgG) antibody to Porphyromonas gingivalis in control patients or patients
125 the mechanism of action of ROS stimulated by Porphyromonas gingivalis in gingival epithelial cells.
126 ion, immunoglobulin (Ig)G subclasses against Porphyromonas gingivalis in individuals with pre-RA and
127 ly Actinobacillus actinomycetemcomitans) and Porphyromonas gingivalis in patients with chronic period
130 tory stimulus (lipopolysaccharide [LPS] from Porphyromonas gingivalis) in a manner consistent with th
132 s, Veillonella sp., and the middle colonizer Porphyromonas gingivalis, indicating specificity among t
133 acid (FA) levels on alveolar bone loss in a Porphyromonas gingivalis-induced model of periodontal di
134 wild-type (WT) controls in a murine model of Porphyromonas gingivalis-induced periodontitis and repor
135 the regeneration of alveolar bone following Porphyromonas gingivalis-induced periodontitis in rats.
136 s demonstrated in distinct models, including Porphyromonas gingivalis-induced periodontitis, ligature
138 Specifically, the oral/systemic pathogen Porphyromonas gingivalis induces cross-talk between CXCR
139 etiological agent of chronic periodontitis, Porphyromonas gingivalis, infect blood myeloid dendritic
140 ression was higher in periodontal tissues of Porphyromonas gingivalis-infected mice as compared with
159 hereas the phylogenetically related pathogen Porphyromonas gingivalis is associated with the chronic
165 rthermore, the mechanism of TLR induction by Porphyromonas gingivalis is investigated in human gingiv
171 of the features of the periodontal pathogen Porphyromonas gingivalis is the presence of complex iron
172 st response to lipopolysaccharide (LPS) from Porphyromonas gingivalis is unusual inasmuch as differen
173 virulence of periodontal pathogens, such as Porphyromonas gingivalis, is expressed in the context of
174 umerous chronic infectious agents, including Porphyromonas gingivalis, is shown to drive-differentiat
179 olated from C57BL/6J mice were cultured with Porphyromonas gingivalis lipopolysaccharide (LPS) and cy
180 with three consecutive palatal injections of Porphyromonas gingivalis lipopolysaccharide (LPS) at 48-
181 roducts (AGE) in the presence and absence of Porphyromonas gingivalis lipopolysaccharide (LPS) on IL-
182 man monocytic cell line, we demonstrate that Porphyromonas gingivalis lipopolysaccharide (LPS), which
183 ived IFN-gamma in constitutively released or Porphyromonas gingivalis lipopolysaccharide (PgLPS)-stim
184 was induced via silk ligature placement with Porphyromonas gingivalis lipopolysaccharide injection in
185 e biopsies and in a preclinical rat model of Porphyromonas gingivalis lipopolysaccharide-induced expe
186 ls upon stimulation by heat-killed wild-type Porphyromonas gingivalis, live P. gingivalis protease-de
187 a [TNF-alpha]), bacterial virulence factors (Porphyromonas gingivalis LPS) or a combination in a biom
189 y be caused by periodontal bacteria, such as Porphyromonas gingivalis Mast cells are sentinels at muc
190 We postulated that the periodontal pathogen, Porphyromonas gingivalis may suppress the inflammasome a
193 Gram-negative, anaerobic periodontopathogen Porphyromonas gingivalis must withstand nitrosative stre
194 he present study is to analyze the effect of Porphyromonas gingivalis on differentiation of primary o
196 e direct effects of the periodontal pathogen Porphyromonas gingivalis on osteoclast differentiation a
197 esponsiveness of whole blood stimulated with Porphyromonas gingivalis or Escherichia coli LPS were mo
198 experimental periodontitis induced by either Porphyromonas gingivalis or ligature, gamma-proteobacter
199 lex anaerobic periodontal pathogens (such as Porphyromonas gingivalis or Treponema denticola) provide
200 g a novel strain of the periodontal pathogen Porphyromonas gingivalis (P. gingivalis JCVI SC001) usin
201 nts with chronic periodontitis and intraoral Porphyromonas gingivalis (P. gingivalis) and Tannerella
203 dontal health by investigating its effect on Porphyromonas gingivalis (P. gingivalis), lipopolysaccha
205 tudy is to determine whether the presence of Porphyromonas gingivalis peptidylarginine deiminase (PPA
206 ucleic acids (DNA) of periodontal pathogens, Porphyromonas gingivalis (Pg) and Tannerella forsythia,
207 nis (Ss) and Sg/Fusobacterium nucleatum (Fn)/Porphyromonas gingivalis (Pg) biofilms elicited signific
209 LM group also presented greater reduction of Porphyromonas gingivalis (Pg) DNA counts at 6 months (P
213 or TRAM, HGF and HPDLF were stimulated with Porphyromonas gingivalis (Pg) lipopolysaccharide (LPS) o
214 n vitro study examines the effect of EGCG on Porphyromonas gingivalis (Pg) lipopolysaccharide (LPS)-e
215 6 cells were used to determine the effect of Porphyromonas gingivalis (Pg) LPS on insulin secretion.
217 Aggregatibacter actinomycetemcomitans (Aa), Porphyromonas gingivalis (Pg), Campylobacter rectus (Cr)
218 ates biofilms, consisting of species such as Porphyromonas gingivalis (Pg), in the etiology of peri-i
219 y associated with the submucosal presence of Porphyromonas gingivalis (Pg), Prevotella intermedia (Pi
220 were used for analysis of bacterial DNA for Porphyromonas gingivalis (Pg), Prevotella intermedia (Pi
221 factors from periodontal pathogens, such as Porphyromonas gingivalis (Pg), stimulate the respiratory
223 on of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis (Pg), Tannerella forsythia (Tf)
226 by ligature; 3) group G-Pg: oral gavage with Porphyromonas gingivalis (Pg); 4) group G-PgFn: oral gav
227 AW264.7 and human monocyte THP-1 to LPS from Porphyromonas gingivalis (PgLPS), an oral microbe implic
233 owth inhibition of the periodontal pathogens Porphyromonas gingivalis, Prevotella intermedia, Fusobac
234 are anaerobic and include organisms such as Porphyromonas gingivalis, Prevotella intermedia, Fusobac
235 his adipokine and the presence and levels of Porphyromonas gingivalis, Prevotella intermedia, Prevote
236 mpylobacter rectus, Fusobacterium nucleatum, Porphyromonas gingivalis, Prevotella intermedia, Tannere
237 cteroidetes sp., Porphyromonas endodontalis, Porphyromonas gingivalis, Prevotella spp., Tannerella fo
239 c periodontitis, the Gram-negative bacterium Porphyromonas gingivalis, produces a vast arsenal of vir
242 show that intraoral inoculation of mice with Porphyromonas gingivalis resulted in infection, alveolar
246 sms of oral species Fusobacterium nucleatum, Porphyromonas gingivalis, Streptococcus mutans, and Camp
248 of pathogens related to periodontal disease (Porphyromonas gingivalis, Tannerella forsythensis, Trepo
249 tinomycetemcomitans), Prevotella intermedia, Porphyromonas gingivalis, Tannerella forsythia (previous
251 alysis identified twenty-one OTUs, including Porphyromonas gingivalis, Tannerella forsythia and Filif
253 ding on probing and levels of microorganisms Porphyromonas gingivalis, Tannerella forsythia, and Camp
254 ase) in GCF and subgingival plaque levels of Porphyromonas gingivalis, Tannerella forsythia, and Fuso
255 revealed that periodontal pathogens, such as Porphyromonas gingivalis, Tannerella forsythia, and Prev
256 lifactor alocis, Fretibacterium fastidiosum, Porphyromonas gingivalis, Tannerella forsythia, and Sele
257 d for Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, and Trep
258 on of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, and Trep
259 using immunofluorescence for the presence of Porphyromonas gingivalis, Tannerella forsythia, Fusobact
260 n for Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Fusobact
261 of bacterial DNA from Streptococcus mutans, Porphyromonas gingivalis, Tannerella forsythia, Prevotel
263 Eikenella corrodens, Campylobacter concisus, Porphyromonas gingivalis, Tannerella forsythia, Treponem
264 ctus, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponem
265 rial, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponem
266 ts of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponem
268 ce factor secreted by the periodontopathogen Porphyromonas gingivalis that attacks host vasculature a
269 cell surface anionic polysaccharide (APS) in Porphyromonas gingivalis that is required for cell integ
270 which activity was induced by infection with Porphyromonas gingivalis The expression of several miRNA
273 biosis and preponderance of bacteria such as Porphyromonas gingivalis, the main etiological agent of
274 have evaluated the periopathogenic roles of Porphyromonas gingivalis, the oral microbiome, and mecha
275 ntly reported that the oral mucosal pathogen Porphyromonas gingivalis, through its 67-kDa Mfa1 (minor
276 ptococcus gordonii SspB (AgI/II) is bound by Porphyromonas gingivalis, thus promoting oral colonizati
278 y, the abundance of the periodontal pathogen Porphyromonas gingivalis trended with higher risk of ESC
279 IgG levels to several species, including Porphyromonas gingivalis, Treponema denticola, and Campy
280 ealing of abutments, rats were infected with Porphyromonas gingivalis, Treponema denticola, and Tanne
282 moderate evidence supporting association of Porphyromonas gingivalis, Treponema denticola, and Tanne
283 ed with polybacterial inoculum consisting of Porphyromonas gingivalis, Treponema denticola, and Tanne
284 For Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Treponema denticola, and Tanne
285 ously Actinobacillus actinomycetemcomitans), Porphyromonas gingivalis, Treponema denticola, Tannerell
286 uding Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Treponema denticola, Tannerell
287 the ability of a polymicrobial consortium of Porphyromonas gingivalis, Treponema denticola, Tannerell
291 Mice were infected with the oral pathogen Porphyromonas gingivalis W50 (P. gingivalis) in the maxi
292 ranscriptome analysis for a microbial genome Porphyromonas gingivalis W83 can be viewed at http://bio
293 y been used to identify 115 genes induced in Porphyromonas gingivalis W83 during human infection.
294 f F. alocis and its ability to interact with Porphyromonas gingivalis W83, several clinical isolates
296 ll-characterized human periodontal pathogen, Porphyromonas gingivalis We found that oral mucosal LCs
299 virulence factors of the periodontopathogen Porphyromonas gingivalis, which causes chronic periodont
300 ns Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis with extended NO-release kineti
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