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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
43      Oral injections of LPS derived from the periodontal pathogen A. actinomycetemcomitans can induce
44                                          The periodontal pathogen A. actinomycetemcomitans has been k
45                                 All targeted periodontal pathogens (A. actinomycetemcomitans, P. ging
46 bone loss in rats using LPS derived from the periodontal pathogen Actinobacillus actinomycetemcomitan
47               Fresh clinical isolates of the periodontal pathogen Actinobacillus actinomycetemcomitan
48 fresh clinical isolates of the gram-negative periodontal pathogen Actinobacillus actinomycetemcomitan
49                                          The periodontal pathogen Actinobacillus actinomycetemcomitan
50  Some clinical isolates of the gram-negative periodontal pathogen Actinobacillus actinomycetemcomitan
51                            The Gram-negative periodontal pathogen Actinobacillus actinomycetemcomitan
52                     Here, we report that the periodontal pathogen Actinobacillus actinomycetemcomitan
53 cts associated with a virulence locus of the periodontal pathogen Actinobacillus actinomycetemcomitan
54                               Strains 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
58                               Among putative periodontal pathogens, Actinobacillus actinomycetemcomit
59 ne whether Prevotella intermedia, a putative periodontal pathogen, activates populations of specific
60                                          The periodontal pathogen Aggregatibacter (Actinobacillus) ac
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
65                     Biofilm formation by the periodontal pathogen Aggregatibacter actinomycetemcomita
66 e major clonal lineages of the Gram-negative periodontal pathogen Aggregatibacter actinomycetemcomita
67                                          The periodontal pathogen Aggregatibacter actinomycetemcomita
68                                          The periodontal pathogen Aggregatibacter actinomycetemcomita
69                                          The 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
73       Porphyromonas gingivalis is a keystone periodontal pathogen and its lipopolysaccharide (PgLPS)
74 hat patterns of high and low levels of eight periodontal pathogens and antibody levels against those
75      After the 2-week study period, putative periodontal pathogens and cariogenic bacteria were overa
76 maxillas and spleens from mice infected with periodontal pathogens and compared to those in the maxil
77 his may suggest possible association between periodontal pathogens and DG.
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
80              Clarithromycin inhibits several periodontal pathogens and is concentrated inside gingiva
81                               High levels of periodontal pathogens and low maternal IgG antibody resp
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,
84              It increases the acquisition of periodontal pathogens and periodontal disease, colonizat
85  for the presence of familial aggregation of periodontal pathogens and periodontitis and have alluded
86 ciated with the subgingival presence of some periodontal pathogens and periodontitis.
87 hol consumption on the levels of subgingival periodontal pathogens and proinflammatory cytokines (int
88                        In addition, putative periodontal pathogens and resistance of subgingival bact
89         MC-2 was correlated with traditional periodontal pathogens and several newly identified putat
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
94 king, age, IgG levels against other selected periodontal pathogens, and race.
95 of host cells by a limited number of 'model' periodontal pathogens, and therefore may not adequately
96                The wide variability found in periodontal pathogen antibiotic-resistance patterns shou
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
99                                              Periodontal pathogens are detrimental to periodontal hea
100                   While traditional putative periodontal pathogens are implicated, research involving
101                                              Periodontal pathogens are present in atherosclerotic pla
102 e by impairing the innate immune response to periodontal pathogens as well as by increasing free radi
103            Furthermore, in response to these periodontal pathogens (as mono- and polymicrobial heat-k
104            Persistence of putative and novel periodontal pathogens, as well as low prevalence of bene
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
109                                              Periodontal pathogens belonging to the genera Fusobacter
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
113                                              Periodontal pathogens/byproducts may reach the placenta
114 tainment proofs 1 to 6 provides support that periodontal pathogens can contribute to atherosclerosis.
115                  Porphyromonas gingivalis, a periodontal pathogen, can efficiently invade human gingi
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
119 ce on host genetic risk loci associated with periodontal pathogen colonization.
120                                              Periodontal pathogens colonized implants symptomatic thr
121                                              Periodontal pathogens commonly associated with chronic a
122                    Exposures consisted of 19 periodontal pathogens, constructed factors and clusters,
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
125       The study aim was to determine whether periodontal pathogens could be enriched from pooled sali
126 ew findings provide mechanistic support that periodontal pathogens create a unique microenvironment i
127                 Risk for harboring 2 or more periodontal pathogens decreased with the years the paren
128                       Rats infected with the periodontal pathogens displayed a five-fold increase in
129                          Increased levels of periodontal pathogens disrupt the homeostasis between th
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
132                             It is known that periodontal pathogens elicit host-derived immune respons
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
135 culated that periodontal probes can transmit periodontal pathogens from site to site.
136 support the hypothesis of a translocation of periodontal pathogens from subgingival microbiota to the
137 patients with and without DM, and 2) isolate periodontal pathogens from these patients' blood.
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
141                                              Periodontal pathogens have been detected from atheromato
142                                  Since a few periodontal pathogens have been reported to invade oral
143                                However, some periodontal pathogens have developed strategies to evade
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
146                Porphyromonas gingivalis is a periodontal pathogen implicated in a range of pregnancy
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
151                                 Detection of periodontal pathogens in early periodontitis suggests an
152 ot an adequate method for identifying DNA of periodontal pathogens in low quantities because of the h
153 biotic resistance among selected subgingival periodontal pathogens in patients with CP.
154 a key role in the innate immune responses to periodontal pathogens in periodontal disease.
155 tion of S. dentisani supernatant against the periodontal pathogens in pure culture.
156 ere used to determine the IgG titres against periodontal pathogens in serum samples.
157  nested multiplex PCR method to detect three periodontal pathogens in subgingival plaque collected be
158 and their association with the levels of key periodontal pathogens in subgingival plaque.
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
166       Porphyromonas gingivalis, an important periodontal pathogen, infects primary gingival epithelia
167              However the mechanisms by which periodontal pathogens influence the development of predi
168                  One of the features of this periodontal pathogen is its ability to attach to a varie
169          The simultaneous detection of three periodontal pathogens is an advantage of this technique
170                 The inflammatory response to periodontal pathogens is dynamically controlled by the c
171 ibroblasts that occurs during infection with periodontal pathogens is, in part, mediated by TNF.
172       Porphyromonas gingivalis, an important periodontal pathogen, is an effective colonizer of oral
173              Porphyromonas gingivalis, a key periodontal pathogen, is capable of invading a variety o
174                       Treponema denticola, a periodontal pathogen, is relatively resistant to human b
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
178                    This study indicates that periodontal pathogens may play important roles in the sh
179  in the field and addressed the link between periodontal pathogens measured with the benzoyl-DL-argin
180                   The major fimbriae of this periodontal pathogen mediate binding to host gingival ep
181       In the surgical specimens positive for periodontal pathogens, more than 1 species was most ofte
182       Thus, in order to colonize, successful periodontal pathogens must devise means to interfere wit
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
186                                    Likewise, periodontal pathogens, opportunistic pathogens, or norma
187                  Baseline levels of selected periodontal pathogens or changes in these bacteria resul
188 lis (P gingivalis) (10(7) CFU), an important periodontal pathogen, or vehicle once per week for 14 or
189                              The presence of periodontal pathogens P.g., P.i., C.r., and B.f. in subg
190 serum levels of IgG antibody to the panel of periodontal pathogens (P = 0.0018), to P. gingivalis (P
191                      Thus, S. mutans and the periodontal pathogens, P. gingivalis and B. forsythus, w
192                                          The periodontal pathogens Pg, Pi, Tf, and Fn are associated
193 te genome representing a novel strain of the periodontal pathogen Porphyromonas gingivalis (P. gingiv
194                       The interaction of the periodontal pathogen Porphyromonas gingivalis (Pg) with
195 tide (VIP) modulates immune responses to the periodontal pathogen Porphyromonas gingivalis (Pg).
196                                          The periodontal pathogen Porphyromonas gingivalis adheres to
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
200                                          The periodontal pathogen Porphyromonas gingivalis and the en
201 Two types of fimbriae, FimA and Mfa1, of the periodontal pathogen Porphyromonas gingivalis are respon
202                                 However, the periodontal pathogen Porphyromonas gingivalis can contro
203                                          The periodontal pathogen Porphyromonas gingivalis employs a
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
208                                          The periodontal pathogen Porphyromonas gingivalis is implica
209                   One of the features of the periodontal pathogen Porphyromonas gingivalis is the pre
210 work suggests that brain colonization by the periodontal pathogen Porphyromonas gingivalis may link t
211                                 Although the periodontal pathogen Porphyromonas gingivalis must withs
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
215                Finally, the abundance of the periodontal pathogen Porphyromonas gingivalis trended wi
216 lutinin B (rHagB), a virulence factor of the periodontal pathogen Porphyromonas gingivalis, has been
217                                       In the periodontal pathogen Porphyromonas gingivalis, the CTD i
218 eated diabetic mice, infected with the human periodontal pathogen Porphyromonas gingivalis, with solu
219 LR4(-/-)) mice were orally infected with the periodontal pathogen Porphyromonas gingivalis.
220 presence or absence of LPS purified from the periodontal pathogen Porphyromonas gingivalis.
221                              The presence of periodontal pathogens Porphyromonas gingivalis (P.g.), P
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
224                Repeated oral inoculations of periodontal pathogens Porphyromonas gingivalis and Prevo
225                             For example, the periodontal pathogens Porphyromonas gingivalis and Tanne
226                     Growth inhibition of the periodontal pathogens Porphyromonas gingivalis, Prevotel
227 , and Campylobacter rectus), two red-complex periodontal pathogens (Porphyromonas gingivalis and Tann
228                              The presence of periodontal pathogens (Porphyromonas gingivalis, Aggrega
229 ously reported that oral administration of a periodontal pathogen, Porphyromonas gingivalis (Pg) to W
230                       We postulated that the periodontal pathogen, Porphyromonas gingivalis may suppr
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
235              Deoxyribonucleic acids (DNA) of periodontal pathogens, Porphyromonas gingivalis (Pg) and
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
238                     Thirteen (59%) of the 22 periodontal pathogen-positive surgical specimens were po
239        Recent evidence suggests that certain periodontal pathogens preferentially stimulate T cells e
240           This study evaluated the levels of periodontal pathogens Prevotella intermedia, Porphyromon
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
249        Porphyromonas gingivalis, an invasive periodontal pathogen, secretes the HAD family phosphoser
250 pants assembled into three clusters based on periodontal pathogens, serum and salivary biomarkers.
251       In response to endotoxins derived from periodontal pathogens, several osteoclast-related mediat
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
254 onizing the colonization and accumulation of periodontal pathogens such as P. gingivalis.
255                                              Periodontal pathogens such as Porphyromonas gingivalis a
256                               Known putative periodontal pathogens such as Porphyromonas gingivalis,
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
261                       Virulence factors from periodontal pathogens, such as Porphyromonas gingivalis
262                             The virulence of periodontal pathogens, such as Porphyromonas gingivalis,
263 crobial co-occurrence analysis revealed that periodontal pathogens, such as Porphyromonas gingivalis,
264                        Moreover, traditional 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
268                                 We found the periodontal pathogen Tannerella forsythia to be associat
269 e genes, (iv) a genome reconstruction of the periodontal pathogen Tannerella forsythia, (v) 239 bacte
270                    Antepartum, the levels of periodontal pathogens tended to be higher in the preterm
271 tis have higher levels of GCF biomarkers and periodontal pathogens than clinically healthy sites from
272                Porphyromonas gingivalis is a periodontal pathogen that also localizes to atherosclero
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
275           Treponema denticola is a consensus periodontal pathogen that has recently been associated w
276 d to RA through the production of enzymes by periodontal pathogens that citrullinate proteins.
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
281                                     Selected periodontal pathogen titers, factors, and clusters inter
282  parameters and the salivary presence of six periodontal pathogens to age-related macular degeneratio
283                                          The periodontal pathogen Treponema denticola produces dentil
284         The metabolism of glutathione by the periodontal pathogen Treponema denticola produces hydrog
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
288 d" DNA-DNA hybridization quantification of 8 periodontal pathogens was performed.
289                           Detection of known periodontal pathogens was rare.
290  minutes after membrane placement, suspected periodontal pathogens were detected in several ePTFE mem
291 cocci, was measured in 78.2% of thrombi, and periodontal pathogens were measured in 34.7%.
292 , whereas the carriage rates of the examined periodontal pathogens were not.
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
296                Porphyromonas gingivalis is a periodontal pathogen whose primary niche is the anaerobi
297 y worsen oral health, favoring the growth of periodontal pathogens, whose detection could improve the
298                    Campylobacter rectus is a periodontal pathogen with a 150-kDa protein on its cell
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

 
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