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1 FimA, in Porphyromonas gingivalis, a primary periodontal pathogen.
2 luding Porphyromonas gingivalis, a potential periodontal pathogen.
3 hatase and reveal an invasin of an important periodontal pathogen.
4 volved in the production of fimbriae by this periodontal pathogen.
5 from Actinobacillus actinomycetemcomitans, a periodontal pathogen.
6 t not by that of Porphyromonas gingivalis, a periodontal pathogen.
7 valis is a peptide-fermenting asaccharolytic periodontal pathogen.
8 nce the inflammatory response induced by the periodontal pathogen.
9 tially a good choice for inhibiting invasive periodontal pathogens.
10 altered immune-inflammatory response against periodontal pathogens.
11 overall showed a stronger inhibition of the periodontal pathogens.
12 re- or PCR-positive results for the targeted periodontal pathogens.
13 de antibiotic that is active against several periodontal pathogens.
14 ogenicity and ability to interact with other periodontal pathogens.
15 e bacterial test (CST) for the most relevant periodontal pathogens.
16 y lower prevalence and abundance of putative periodontal pathogens.
17 wn to have anti-microbial properties against periodontal pathogens.
18 on may be related to an elevated exposure to periodontal pathogens.
19 ctiveness of clarithromycin against invasive periodontal pathogens.
20 cts who harbored two, or all three, of these periodontal pathogens.
21 plex interplay between the immune system and periodontal pathogens.
22 ntal therapy significantly reduced levels of periodontal pathogens.
23 performed to detect the presence of selected periodontal pathogens.
24 haps symptomatic of colonization by residual periodontal pathogens.
25 determined the occurrence of potential major periodontal pathogens.
26 outcomes in addition to previously reported periodontal pathogens.
27 lation of the innate immune host response to periodontal pathogens.
28 oss, and bone resorption that are induced by periodontal pathogens.
29 chment gain had a high prevalence of these 3 periodontal pathogens.
30 following interaction with several putative periodontal pathogens.
31 were positive for at least one of the target periodontal pathogens.
32 bgingival colonization and multiplication of periodontal pathogens.
33 y at high levels, is primarily restricted to periodontal pathogens.
34 allows more sensitive detection of all three periodontal pathogens.
35 ilable polymerase chain reaction test for 11 periodontal pathogens.
36 ely as a result of increased colonization of periodontal pathogens.
37 ated with peri-implantitis are recognized as periodontal pathogens.
38 nvironment and a distributional shift of key periodontal pathogens.
39 ymicrobial infection with well-characterized periodontal pathogens.
40 s been primarily focused on a small group of periodontal pathogens.
41 d by corrosion may enhance the attachment of periodontal pathogens.
42 to 71% increase), bacterial killing of these periodontal pathogens (22 to 38% reduction of bacterial
46 bone loss in rats using LPS derived from the periodontal pathogen Actinobacillus actinomycetemcomitan
48 fresh clinical isolates of the gram-negative periodontal pathogen Actinobacillus actinomycetemcomitan
50 Some clinical isolates of the gram-negative periodontal pathogen Actinobacillus actinomycetemcomitan
53 cts associated with a virulence locus of the periodontal pathogen Actinobacillus actinomycetemcomitan
55 late three catalase-deficient mutants of the periodontal pathogen Actinobacillus actinomycetemcomitan
56 zation and confocal microscopy to detect the periodontal pathogens Actinobacillus actinomycetemcomita
57 d with intracellular bacteria, including the periodontal pathogens Actinobacillus actinomycetemcomita
59 ne whether Prevotella intermedia, a putative periodontal pathogen, activates populations of specific
61 e cytolethal distending toxin (Cdt) from the periodontal pathogen Aggregatibacter actinomycetemcomita
62 cytolethal distending toxin (Cdt), from the periodontal pathogen Aggregatibacter actinomycetemcomita
63 crease in antibacterial activity against the periodontal pathogen Aggregatibacter actinomycetemcomita
64 hal distending toxin (Cdt), expressed by the periodontal pathogen Aggregatibacter actinomycetemcomita
66 e major clonal lineages of the Gram-negative periodontal pathogen Aggregatibacter actinomycetemcomita
70 sed a dual-species biofilm consisting of the periodontal pathogen Aggregatibacter actinomycetemcomita
71 The aim of this investigation is to quantify periodontal pathogens (Aggregatibacter actinomycetemcomi
72 sent investigation was to identify potential periodontal pathogens among these newly identified speci
74 hat patterns of high and low levels of eight periodontal pathogens and antibody levels against those
76 maxillas and spleens from mice infected with periodontal pathogens and compared to those in the maxil
78 antibacterial activity against most putative periodontal pathogens and has been shown to kill bacteri
79 rivative possessing antimicrobial effects on periodontal pathogens and inhibitory properties on matri
82 o 19 species, including established/putative periodontal pathogens and non-pathogenic bacteria, in 5,
83 reduced the relative abundance of classical periodontal pathogens and of Fretibacterium fastidiosum,
85 for the presence of familial aggregation of periodontal pathogens and periodontitis and have alluded
87 hol consumption on the levels of subgingival periodontal pathogens and proinflammatory cytokines (int
90 ediates of microbial burden (levels of eight periodontal pathogens) and local inflammatory response (
91 e we report that Porphyromonas gingivalis, a periodontal pathogen, and Escherichia coli LPS induce os
92 anaerobe, Porphyromonas gingivalis, is a key periodontal pathogen, and several lines of evidence link
93 ship of gingivitis with salivary biomarkers, periodontal pathogens, and interleukin (IL)-1 polymorphi
95 of host cells by a limited number of 'model' periodontal pathogens, and therefore may not adequately
97 the hypothesis that oral bacteria other than periodontal pathogens are also associated with pregnancy
98 ntal disease, high levels of colonization of periodontal pathogens are associated with an increased r
102 e by impairing the innate immune response to periodontal pathogens as well as by increasing free radi
105 The oral spirochete Treponema denticola, a periodontal pathogen associated with human periodontitis
106 f this study was to test the hypothesis that periodontal pathogens associated with aggressive periodo
107 nema denticola, and Tannerella forsythia are periodontal pathogens associated with the etiology of ad
108 ophaga spp. have been implicated as putative periodontal pathogens associated with various periodonta
110 iodontal parameters and serum IgG levels for periodontal pathogens between PLBW and healthy delivery
111 ission is not limited to the well-recognized periodontal pathogens, but instead may also involve the
112 ached to gingival cells in vitro, inhibiting periodontal pathogens by competition, adherence, and dis
114 tainment proofs 1 to 6 provides support that periodontal pathogens can contribute to atherosclerosis.
116 sent an overreaction of the host response to periodontal pathogens caused by excessive production of
117 We used GWAS data of CP (n = 4,504) and periodontal pathogen colonization (n = 1,020) from a coh
118 6); AP3B2, p = 2.2 x 10(-6)) and 2 with high periodontal pathogen colonization (red complex-KCNK1, p
123 est positive for antiCl, likely because some periodontal pathogens contain antigens homologous to the
124 periodontitis patients contain aCl, and some periodontal pathogens contain antigens with peptide sequ
126 ew findings provide mechanistic support that periodontal pathogens create a unique microenvironment i
130 ne the role of saliva-derived biomarkers and periodontal pathogens during periodontal disease progres
131 ues, we tested the ability of three putative periodontal pathogens-Eikenella corrodens, Porphyromonas
133 hogens and several newly identified putative periodontal pathogens: Fretibacterium fastidiosum, Freti
134 d with increased odds of detection of common periodontal pathogens from individuals with aggressive p
136 support the hypothesis of a translocation of periodontal pathogens from subgingival microbiota to the
138 A defining characteristic of the suspected periodontal pathogen Fusobacterium nucleatum is its abil
139 s among the presence of three orange-complex periodontal pathogens (Fusobacterium nucleatum, Prevotel
140 that growth of the PFOR-containing anaerobic periodontal pathogens, grown in both monospecies as well
144 ampylobacter rectus has been implicated as a periodontal pathogen; however, association with periodon
145 Filifactor alocis is a recently recognized periodontal pathogen; however, little is known regarding
147 ent reports focusing on virulence factors of periodontal pathogens implicated proteinases as major de
148 ion was conducted to confirm the presence of periodontal pathogens in bone particles harvested intrao
149 gingivalis is recognized as one of the major periodontal pathogens in chronic periodontitis, a common
150 Importantly, the levels of IL-17 induced by periodontal pathogens in CII-specific T cells directly c
152 ot an adequate method for identifying DNA of periodontal pathogens in low quantities because of the h
157 nested multiplex PCR method to detect three periodontal pathogens in subgingival plaque collected be
159 his study is to detect and quantify the main periodontal pathogens in the oral microbiota of postmeno
160 ion is to compare the presence and number of periodontal pathogens in the subgingival microbiota of s
161 ted with decreased levels of IgG antibody to periodontal pathogens in women with periodontitis when a
162 logical testing showed the presence of known periodontal pathogens including Actinobacillus actinomyc
163 y 40% compared to that of HC, and killing of periodontal pathogens, including Porphyromonas gingivali
164 loading time increased, but colonization by periodontal pathogens, including red complex species, wa
165 their precise roles are not well understood, periodontal pathogens, including Treponema denticola, ar
171 ibroblasts that occurs during infection with periodontal pathogens is, in part, mediated by TNF.
175 the rate of preterm delivery, a decrease in periodontal pathogen load, and a decrease in both GCF IL
176 tween Helicobacter pylori (Hp) and groups of periodontal pathogens may alter the onset of Alzheimer's
177 tudy was devised to test the hypothesis that periodontal pathogens may be present and affect human pl
179 in the field and addressed the link between periodontal pathogens measured with the benzoyl-DL-argin
183 t group also demonstrated significantly less periodontal pathogens of red and orange complexes and a
184 g effects of co-eradication of Hp and select periodontal pathogens on neurodegenerative disease.
185 th Porphyromonas gingivalis (Pg), a putative periodontal pathogen, on the progression of atherosclero
188 lis (P gingivalis) (10(7) CFU), an important periodontal pathogen, or vehicle once per week for 14 or
190 serum levels of IgG antibody to the panel of periodontal pathogens (P = 0.0018), to P. gingivalis (P
193 te genome representing a novel strain of the periodontal pathogen Porphyromonas gingivalis (P. gingiv
195 tide (VIP) modulates immune responses to the periodontal pathogen Porphyromonas gingivalis (Pg).
197 ibute to osteolytic lesions, we injected the periodontal pathogen Porphyromonas gingivalis adjacent t
198 mine the antibacterial effects of EMD on the periodontal pathogen Porphyromonas gingivalis and 2) to
199 lipid 430 and lipid 654, are produced by the periodontal pathogen Porphyromonas gingivalis and can be
201 Two types of fimbriae, FimA and Mfa1, of the periodontal pathogen Porphyromonas gingivalis are respon
204 Here, we demonstrate that infection with the periodontal pathogen Porphyromonas gingivalis enhances t
205 Lipopolysaccharide (LPS) derived from the periodontal pathogen Porphyromonas gingivalis has been r
206 The capsular polysaccharide (CPS) of the periodontal pathogen Porphyromonas gingivalis is an impo
207 Previously, we have established that the periodontal pathogen Porphyromonas gingivalis is capable
210 work suggests that brain colonization by the periodontal pathogen Porphyromonas gingivalis may link t
212 f lipopolysaccharide (LPS) purified from the periodontal pathogen Porphyromonas gingivalis on human m
213 re, we investigate the direct effects of the periodontal pathogen Porphyromonas gingivalis on osteocl
214 el to study the effect of infection with the periodontal pathogen Porphyromonas gingivalis on pregnan
216 lutinin B (rHagB), a virulence factor of the periodontal pathogen Porphyromonas gingivalis, has been
218 eated diabetic mice, infected with the human periodontal pathogen Porphyromonas gingivalis, with solu
222 activity of major virulence factors from the periodontal pathogens Porphyromonas gingivalis and Actin
223 his probiotic by measuring inhibition of the periodontal pathogens Porphyromonas gingivalis and Fusob
227 , and Campylobacter rectus), two red-complex periodontal pathogens (Porphyromonas gingivalis and Tann
229 ously reported that oral administration of a periodontal pathogen, Porphyromonas gingivalis (Pg) to W
231 colonization with a well-characterized human periodontal pathogen, Porphyromonas gingivalis We found
232 es and subsequent proteomic responses to the periodontal pathogen, Porphyromonas gingivalis, donor-ma
233 ar premolars followed by an application of a periodontal pathogen, Porphyromonas gingivalis, to induc
234 the present study, LPS derived from the oral periodontal pathogen, Porphyromonas gingivalis, was comp
236 o characterize host responses of interest to periodontal pathogens, Porphyromonas gingivalis was intr
237 antibacterial activity against two anaerobic periodontal pathogens: Porphyromonas gingivalis and Acti
241 as well as a cysteine proteinase of another periodontal pathogen, Prevotella intermedia, resulted in
242 ormerly Bacteroides forsythus) is one of the periodontal pathogens recently implicated in the develop
243 is report was to compare the distribution of periodontal pathogens recovered from failing implants an
244 hat activation of the acquired immunity by a periodontal pathogen reduces the coupling of bone format
245 United States frequently yielded subgingival periodontal pathogens resistant in vitro to therapeutic
246 of the patients with CP revealed subgingival periodontal pathogens resistant to at least one of the t
247 een percent of patients harbored subgingival periodontal pathogens resistant to both amoxicillin and
248 parental and feoB1-deficient strains of the periodontal pathogen revealed that the feoB1-deficient m
250 pants assembled into three clusters based on periodontal pathogens, serum and salivary biomarkers.
252 selected controls from the above cohort, the periodontal pathogen-specific maternal serum IgG levels
253 provide mechanistic support that SCFAs from periodontal pathogens stimulate KSHV replication and inf
257 al has strong antibacterial activity against periodontal pathogens such as Streptococcus mutans, Porp
258 tegerin) combined with red-complex anaerobic periodontal pathogens (such as Porphyromonas gingivalis
259 cells of the periodontium to encounter known periodontal pathogens, such as Actinobacillus actinomyce
260 was associated with elevated levels of known periodontal pathogens, such as P. nigrescens, T. forsyth
263 crobial co-occurrence analysis revealed that periodontal pathogens, such as Porphyromonas gingivalis,
265 ssociation of miR-146a expression with these periodontal pathogens, suggesting that miR-146a may dire
266 Aggregatibacter actinomycetemcomitans, a periodontal pathogen, synthesizes leukotoxin (LtxA), a p
267 athogens by reconstructing the genome of the periodontal pathogen Tannerella forsythia and also ident
269 e genes, (iv) a genome reconstruction of the periodontal pathogen Tannerella forsythia, (v) 239 bacte
271 tis have higher levels of GCF biomarkers and periodontal pathogens than clinically healthy sites from
273 Porphyromonas gingivalis (Pg) is a major periodontal pathogen that contains immunostimulatory com
274 Porphyromonas gingivalis is a consensus periodontal pathogen that has been implicated in adult f
277 obacillus actinomycetemcomitans are putative periodontal pathogens that may be harbored in subgingiva
278 addition, in comparison with other anaerobic periodontal pathogens, the removal of 8-oxoG was unique
279 gingival epithelium forms a barrier against periodontal pathogens, this study was undertaken to dete
280 response to systemic inflammation induced by periodontal pathogens through mechanisms involving downr
282 parameters and the salivary presence of six periodontal pathogens to age-related macular degeneratio
285 ue samples were assessed for the presence of periodontal pathogens using indirect immunofluorescence.
286 nd assessed their response to infection with periodontal pathogens using microarray analysis, quantit
287 ontal pockets and the prevalence of selected periodontal pathogens was assessed in 10 patients with a
290 minutes after membrane placement, suspected periodontal pathogens were detected in several ePTFE mem
293 Microbiologic assessments of eight putative periodontal pathogens were performed using the checkerbo
294 The samples were cultured, and selected periodontal pathogens were tested in vitro for susceptib
295 ar lipids of Porphyromas gingivalis, a known periodontal pathogen, were previously shown to promote d
297 y worsen oral health, favoring the growth of periodontal pathogens, whose detection could improve the
299 newly developed CST can detect five typical periodontal pathogens with a somewhat lower sensitivity
300 ence intervals (CIs) for the associations of periodontal pathogens with total cancer and site-specifi