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1 bacterial species, Streptococcus mutans and Porphyromonas gingivalis.
2 clearance by opportunistic pathogens such as Porphyromonas gingivalis.
3 ontal disease, whose main infective agent is Porphyromonas gingivalis.
4 of F. alocis are enhanced in coculture with Porphyromonas gingivalis.
5 roded titanium surfaces on the attachment of Porphyromonas gingivalis.
6 etween HIV-1 and an invasive oral bacterium, Porphyromonas gingivalis.
7 obulin (TG), Escherichia coli LPS, or intact Porphyromonas gingivalis.
8 ood mononuclear cells (PBMCs) in response to Porphyromonas gingivalis.
9 rally infected with the periodontal pathogen Porphyromonas gingivalis.
10 m johnsoniae and the nonmotile oral pathogen Porphyromonas gingivalis.
11 isease that is triggered by bacteria such as Porphyromonas gingivalis.
12 . pylori as well as Streptococcus mutans and Porphyromonas gingivalis.
13 y Actinobacillus actinomycetemcomitans), and Porphyromonas gingivalis.
14 f LPS purified from the periodontal pathogen Porphyromonas gingivalis.
15 eriodontal disease is an anaerobic bacterium-Porphyromonas gingivalis.
17 er actinomycetemcomitans (MT4/MSP: 42%/36%), Porphyromonas gingivalis (78%/66%), Tannerella forsythia
21 erase Chain Reaction (qPCR) for detection of Porphyromonas gingivalis, a keystone pathogen and to ass
23 important role in eliciting inflammation to Porphyromonas gingivalis, a keystone pathogen in periodo
24 rted between RA and periodontal disease, and Porphyromonas gingivalis, a known driver of periodontiti
27 nalysed in mice after oral administration of Porphyromonas gingivalis, a representative periodontopat
28 n 9 times with 10(9) colony-forming units of Porphyromonas gingivalis A7436 through an oral gavage mo
29 he chronic periodontitis-associated pathogen Porphyromonas gingivalis activates a Toll-like receptor
30 operties against three periodontal bacteria: Porphyromonas gingivalis, Aggregatibacter actinomycetemc
33 contamination with >/=3 specific pathogens (Porphyromonas gingivalis, Aggregatibacter actinomycetemc
34 issue-degrading enzymes in the oral pathogen Porphyromonas gingivalis Although a number of subunits o
35 re Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis amounts in saliva and their ant
36 lipid A structures in the outer membrane of Porphyromonas gingivalis, an agent of human periodontal
38 eases are critical virulence determinants of Porphyromonas gingivalis, an emerging Alzheimer's diseas
40 killing of periodontal pathogens, including Porphyromonas gingivalis and Aggregatibacter actinomycet
42 he same biofilm plus the periodontopathogens Porphyromonas gingivalis and Aggregatibacter actinomycet
44 54, are produced by the periodontal pathogen Porphyromonas gingivalis and can be detected in lipid ex
47 ring inhibition of the periodontal pathogens Porphyromonas gingivalis and Fusobacterium nucleatum gro
48 odontitis was induced by oral inoculation of Porphyromonas gingivalis and Fusobacterium nucleatum in
49 ) on the virulence of a mixed infection with Porphyromonas gingivalis and Fusobacterium nucleatum in
52 ribosomal RNA analysis of keystone pathogen Porphyromonas gingivalis and its consortium members Fuso
53 se in 2 animal models through inoculation of Porphyromonas gingivalis and ligature around the murine
55 mDC microbiome by 16S rDNA sequencing showed Porphyromonas gingivalis and other species, including (c
57 d oral inoculations of periodontal pathogens Porphyromonas gingivalis and Prevotella nigrescens induc
58 The Orange-Red cluster score (that included Porphyromonas gingivalis and Prevotella spp.) was positi
59 d Treponema denticola, and the prevalence of Porphyromonas gingivalis and T. denticola associated sig
60 ted with periodontal pathology and number of Porphyromonas gingivalis and Tannerella forsythia (forme
61 tus), two red-complex periodontal pathogens (Porphyromonas gingivalis and Tannerella forsythia), and
62 es that gram-negative oral bacteria, such as Porphyromonas gingivalis and Tannerella forsythia, use d
65 modes of mucosal vaccination with whole-cell Porphyromonas gingivalis and to test the role of various
67 how galactose-inhibitable coaggregation with Porphyromonas gingivalis and were defective in cell bind
68 presence of specific bacterial species (i.e. Porphyromonas gingivalis) and their effects in immune re
69 the proteases of Pseudomonas aeruginosa and Porphyromonas gingivalis, and enables its antimicrobial
70 uced the numbers of Streptococcus anginosus, Porphyromonas gingivalis, and Fusobacterium nucleatum, a
71 iodontitis is initiated by bacteria, such as Porphyromonas gingivalis, and is caused largely by host
72 ously Actinobacillus actinomycetemcomitans), Porphyromonas gingivalis, and Prevotella intermedia.
73 tory responses to a keystone oral bacterium, Porphyromonas gingivalis, and restrains periodontal infl
74 or more overtly pathogenic organisms such as Porphyromonas gingivalis, and the two species assemble i
76 , FimA and Mfa1, of the periodontal pathogen Porphyromonas gingivalis are responsible for adherence t
77 rial manipulation of neutrophil responses by Porphyromonas gingivalis as a mechanism that contributes
78 early and late colonizer pathogens, such as Porphyromonas gingivalis, as the biofilm ages and period
79 gnaling in alveolar bone resorption, using a Porphyromonas gingivalis-associated ligature-induced per
80 , in particular, Fusobacterium nucleatum and Porphyromonas gingivalis, based on results from epidemio
81 gens (Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Campylobacter rectus, and Tann
83 en" where low-abundance microbial pathogens (Porphyromonas gingivalis) can orchestrate inflammatory d
84 the periodontitis-associated oral bacterium Porphyromonas gingivalis, can subvert host immunity to r
85 rated that antibodies raised in mice against Porphyromonas gingivalis caused fetal loss in a mouse pr
87 in substrates of a novel secretion system of Porphyromonas gingivalis contain a conserved C-terminal
91 echanism by which the opportunistic pathogen Porphyromonas gingivalis dampens innate immune responses
92 ved exaggerated proinflammatory responses to Porphyromonas gingivalis-derived lipopolysaccharide in c
93 ignificantly increased in the RA group, only Porphyromonas gingivalis displayed significant correlati
94 human gingival epithelial (HGEp) cells with Porphyromonas gingivalis disrupts barrier function by in
96 complex), produced by the keystone pathogen Porphyromonas gingivalis, dramatically increased their a
97 0068, Fusobacterium nucleatum ATCC10953, and Porphyromonas gingivalis DSM20709) were placed in a seri
98 periodontitis caused by oral infection with Porphyromonas gingivalis enhances articular bone loss.
99 that infection with the periodontal pathogen Porphyromonas gingivalis enhances the activity of Janus
101 ., Peptoniphilaceae [G-1] bacterium HMT 113, Porphyromonas gingivalis, Fretibacterium fastidiosum, Fi
102 taxa implicated in periodontitis, including Porphyromonas gingivalis, Fretibacterium fastidiosum, Fi
103 latter consisted of five microbial species (Porphyromonas gingivalis, Fusobacterium nucleatum, Actin
104 ntal pathogens such as Streptococcus mutans, Porphyromonas gingivalis, Fusobacterium nucleatum, and P
106 , traditional periodontal pathogens, such as Porphyromonas gingivalis, Fusobacterium nucleatum, and T
107 Additionally, we compare a nearly complete Porphyromonas gingivalis genome to previously published
111 virulence factor of the periodontal pathogen Porphyromonas gingivalis, has been shown to induce prote
113 of Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis have been shown to induce diffe
115 dy, we hypothesized that histatin 5 binds to Porphyromonas gingivalis hemagglutinin B (HagB) and atte
118 the mechanism of action of ROS stimulated by Porphyromonas gingivalis in gingival epithelial cells.
119 ion, immunoglobulin (Ig)G subclasses against Porphyromonas gingivalis in individuals with pre-RA and
120 ly Actinobacillus actinomycetemcomitans) and Porphyromonas gingivalis in patients with chronic period
122 tory stimulus (lipopolysaccharide [LPS] from Porphyromonas gingivalis) in a manner consistent with th
124 acid (FA) levels on alveolar bone loss in a Porphyromonas gingivalis-induced model of periodontal di
125 wild-type (WT) controls in a murine model of Porphyromonas gingivalis-induced periodontitis and repor
126 s demonstrated in distinct models, including Porphyromonas gingivalis-induced periodontitis, ligature
128 etiological agent of chronic periodontitis, Porphyromonas gingivalis, infect blood myeloid dendritic
130 ression was higher in periodontal tissues of Porphyromonas gingivalis-infected mice as compared with
134 vity by the Gram-negative bacterial pathogen Porphyromonas gingivalis is a key event in the initiatio
150 hereas the phylogenetically related pathogen Porphyromonas gingivalis is associated with the chronic
154 rthermore, the mechanism of TLR induction by Porphyromonas gingivalis is investigated in human gingiv
159 st response to lipopolysaccharide (LPS) from Porphyromonas gingivalis is unusual inasmuch as differen
161 virulence of periodontal pathogens, such as Porphyromonas gingivalis, is expressed in the context of
162 umerous chronic infectious agents, including Porphyromonas gingivalis, is shown to drive-differentiat
166 olated from C57BL/6J mice were cultured with Porphyromonas gingivalis lipopolysaccharide (LPS) and cy
167 ation and inflammatory gene expression using Porphyromonas gingivalis lipopolysaccharide (LPS) as a p
168 with three consecutive palatal injections of Porphyromonas gingivalis lipopolysaccharide (LPS) at 48-
169 roducts (AGE) in the presence and absence of Porphyromonas gingivalis lipopolysaccharide (LPS) on IL-
170 erichia coli lipopolysaccharide (Ec-LPS) and Porphyromonas gingivalis lipopolysaccharide (Pg-LPS) sti
171 resence and absence of ultrapure or standard Porphyromonas gingivalis lipopolysaccharide (PgLPS), Pam
172 ived IFN-gamma in constitutively released or Porphyromonas gingivalis lipopolysaccharide (PgLPS)-stim
173 was induced via silk ligature placement with Porphyromonas gingivalis lipopolysaccharide injection in
174 ls upon stimulation by heat-killed wild-type Porphyromonas gingivalis, live P. gingivalis protease-de
175 a [TNF-alpha]), bacterial virulence factors (Porphyromonas gingivalis LPS) or a combination in a biom
177 y be caused by periodontal bacteria, such as Porphyromonas gingivalis Mast cells are sentinels at muc
178 ain colonization by the periodontal pathogen Porphyromonas gingivalis may link these two inflammatory
179 We postulated that the periodontal pathogen, Porphyromonas gingivalis may suppress the inflammasome a
182 Gram-negative, anaerobic periodontopathogen Porphyromonas gingivalis must withstand nitrosative stre
183 he present study is to analyze the effect of Porphyromonas gingivalis on differentiation of primary o
185 e direct effects of the periodontal pathogen Porphyromonas gingivalis on osteoclast differentiation a
187 esponsiveness of whole blood stimulated with Porphyromonas gingivalis or Escherichia coli LPS were mo
188 experimental periodontitis induced by either Porphyromonas gingivalis or ligature, gamma-proteobacter
189 g a novel strain of the periodontal pathogen Porphyromonas gingivalis (P. gingivalis JCVI SC001) usin
190 nts with chronic periodontitis and intraoral Porphyromonas gingivalis (P. gingivalis) and Tannerella
191 analogs was synthesized and their effects on Porphyromonas gingivalis (P. gingivalis) elicited inflam
192 dontal health by investigating its effect on Porphyromonas gingivalis (P. gingivalis), lipopolysaccha
193 Tannerella forsythia (T.f.), 2.5 x 10(4) for Porphyromonas gingivalis (P.g.), 5.3 x 10(3) for Prevote
195 tudy is to determine whether the presence of Porphyromonas gingivalis peptidylarginine deiminase (PPA
197 ucleic acids (DNA) of periodontal pathogens, Porphyromonas gingivalis (Pg) and Tannerella forsythia,
198 nis (Ss) and Sg/Fusobacterium nucleatum (Fn)/Porphyromonas gingivalis (Pg) biofilms elicited signific
200 LM group also presented greater reduction of Porphyromonas gingivalis (Pg) DNA counts at 6 months (P
204 or TRAM, HGF and HPDLF were stimulated with Porphyromonas gingivalis (Pg) lipopolysaccharide (LPS) o
205 n vitro study examines the effect of EGCG on Porphyromonas gingivalis (Pg) lipopolysaccharide (LPS)-e
206 6 cells were used to determine the effect of Porphyromonas gingivalis (Pg) LPS on insulin secretion.
207 al administration of a periodontal pathogen, Porphyromonas gingivalis (Pg) to WT mice results in insu
208 The interaction of the periodontal pathogen Porphyromonas gingivalis (Pg) with commensal streptococc
209 Quantification of Tannerella forsythia (Tf), Porphyromonas gingivalis (Pg), Aggregatibacter actinomyc
211 Aggregatibacter actinomycetemcomitans (Aa), Porphyromonas gingivalis (Pg), Campylobacter rectus (Cr)
212 ates biofilms, consisting of species such as Porphyromonas gingivalis (Pg), in the etiology of peri-i
213 were used for analysis of bacterial DNA for Porphyromonas gingivalis (Pg), Prevotella intermedia (Pi
214 y associated with the submucosal presence of Porphyromonas gingivalis (Pg), Prevotella intermedia (Pi
215 factors from periodontal pathogens, such as Porphyromonas gingivalis (Pg), stimulate the respiratory
217 on of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis (Pg), Tannerella forsythia (Tf)
218 study investigated the role of GRHL2 in the Porphyromonas gingivalis (Pg)-induced impairment of epit
221 by ligature; 3) group G-Pg: oral gavage with Porphyromonas gingivalis (Pg); 4) group G-PgFn: oral gav
223 AW264.7 and human monocyte THP-1 to LPS from Porphyromonas gingivalis (PgLPS), an oral microbe implic
224 of periodontitis and the anaerobic bacterium Porphyromonas gingivalis plays a key role in driving chr
228 owth inhibition of the periodontal pathogens Porphyromonas gingivalis, Prevotella intermedia, Fusobac
229 are anaerobic and include organisms such as Porphyromonas gingivalis, Prevotella intermedia, Fusobac
230 his adipokine and the presence and levels of Porphyromonas gingivalis, Prevotella intermedia, Prevote
231 is of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, Tannere
232 cteroidetes sp., Porphyromonas endodontalis, Porphyromonas gingivalis, Prevotella spp., Tannerella fo
233 c periodontitis, the Gram-negative bacterium Porphyromonas gingivalis, produces a vast arsenal of vir
236 show that intraoral inoculation of mice with Porphyromonas gingivalis resulted in infection, alveolar
240 enotype was also observed following LPS from Porphyromonas gingivalis stimulation during osteogenic d
242 sms of oral species Fusobacterium nucleatum, Porphyromonas gingivalis, Streptococcus mutans, and Camp
244 of pathogens related to periodontal disease (Porphyromonas gingivalis, Tannerella forsythensis, Trepo
245 alysis identified twenty-one OTUs, including Porphyromonas gingivalis, Tannerella forsythia and Filif
247 ding on probing and levels of microorganisms Porphyromonas gingivalis, Tannerella forsythia, and Camp
248 es were collected to determine the levels of Porphyromonas gingivalis, Tannerella forsythia, and Fuso
249 ls of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, and Fuso
250 ase) in GCF and subgingival plaque levels of Porphyromonas gingivalis, Tannerella forsythia, and Fuso
251 revealed that periodontal pathogens, such as Porphyromonas gingivalis, Tannerella forsythia, and Prev
252 lifactor alocis, Fretibacterium fastidiosum, Porphyromonas gingivalis, Tannerella forsythia, and Sele
253 on of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, and Trep
254 d for Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, and Trep
255 using immunofluorescence for the presence of Porphyromonas gingivalis, Tannerella forsythia, Fusobact
256 n for Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Fusobact
257 of bacterial DNA from Streptococcus mutans, Porphyromonas gingivalis, Tannerella forsythia, Prevotel
258 eria (Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Prevotel
260 rial, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponem
261 ts of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponem
262 eria (Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponem
263 Eikenella corrodens, Campylobacter concisus, Porphyromonas gingivalis, Tannerella forsythia, Treponem
264 ctus, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponem
266 ce factor secreted by the periodontopathogen Porphyromonas gingivalis that attacks host vasculature a
267 which activity was induced by infection with Porphyromonas gingivalis The expression of several miRNA
270 biosis and preponderance of bacteria such as Porphyromonas gingivalis, the main etiological agent of
271 have evaluated the periopathogenic roles of Porphyromonas gingivalis, the oral microbiome, and mecha
272 ntly reported that the oral mucosal pathogen Porphyromonas gingivalis, through its 67-kDa Mfa1 (minor
273 gainst invader pathobiotic bacteria, such as Porphyromonas gingivalis, through small danger molecule
274 ptococcus gordonii SspB (AgI/II) is bound by Porphyromonas gingivalis, thus promoting oral colonizati
276 biofilm formation promoted the tolerance of Porphyromonas gingivalis to oxidative stress under micro
277 SCs were seeded for 24 h and challenged with Porphyromonas gingivalis total protein extract (PgPE) (0
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 moderate evidence supporting association of Porphyromonas gingivalis, Treponema denticola, and Tanne
281 ed with polybacterial inoculum consisting of Porphyromonas gingivalis, Treponema denticola, and Tanne
282 For Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Treponema denticola, and Tanne
284 drugs against red complex pathogens, namely, Porphyromonas gingivalis, Treponema denticola, and Tanne
285 ealing of abutments, rats were infected with Porphyromonas gingivalis, Treponema denticola, and Tanne
286 uding Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Treponema denticola, Tannerell
287 the ability of a polymicrobial consortium of Porphyromonas gingivalis, Treponema denticola, Tannerell
289 periodontal pathogens Prevotella intermedia, Porphyromonas gingivalis, Treponema denticola, Tannerell
290 r 30 seconds and 1 minute, reducing, mainly, Porphyromonas gingivalis viability, with 2.78 and 1.7 lo
293 Mice were infected with the oral pathogen Porphyromonas gingivalis W50 (P. gingivalis) in the maxi
295 f F. alocis and its ability to interact with Porphyromonas gingivalis W83, several clinical isolates
297 nd the growth of Streptococcus sanguinis and Porphyromonas gingivalis was significantly reduced in th
298 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