In a 16S rRNA gene-directed multiplex PCR, Prevotella intermedia- and Bacteroides forsythus-specific reverse primers were combined with a single conserved forward primer. A 660-bp fragment and an 840-bp fragment that were specific for both species could be amplified simultaneously. A total of 152 clinical samples, subgingival plaque and swabs of three different oral mucosae, from 38 periodontitis patients were used for the evaluation.link_to_subscribed_fulltex
OBJECTIVE: The aim of this study was to detect the prevalence of selected bacterial species in intra...
The purpose of this study was to detect the presence of Porphyromonas endodontalis, P. gingivalis, P...
Background: Microbial agents in root canal systems can induce periodontal inflammation. The aims of ...
A PCR assay was developed that could specifically amplify DNA from the periodontal pathogen Prevotel...
Oligonucleotide DNA probes complementary to the hypervariable region of the 16S rRNA of Bacteroides ...
Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis are strongly associated with perio...
Species-specific DNA probes were used to determine the presence of Actinobacillus actinomycetemcomit...
The aim of our research was to identify by bacterial genomicDNA analysis the prevalence of five diff...
Objective: The aim of the present study was to evaluate the reproducibility of a commercial kit for ...
Background: The aims of this study were to determine the genotypic diversity of Prevotella intermedi...
Background and Aim: For the analysis of subgingival plaque, anaerobic bacterial culture has been the...
this study was undertaken to develop PCR primers for the simultaneous detection of Fusobacterium nuc...
Introduction: Molecular ecological analysis based on 16S rRNA gene sequence analysis is well establ...
In the present study, detection patterns of subgingival Porphyromonas gingivalis (Pg), Prevotella in...
Whole genomic and randomly-cloned DNA probes for two fastidious periodontal pathogens, Porphyromonas...
OBJECTIVE: The aim of this study was to detect the prevalence of selected bacterial species in intra...
The purpose of this study was to detect the presence of Porphyromonas endodontalis, P. gingivalis, P...
Background: Microbial agents in root canal systems can induce periodontal inflammation. The aims of ...
A PCR assay was developed that could specifically amplify DNA from the periodontal pathogen Prevotel...
Oligonucleotide DNA probes complementary to the hypervariable region of the 16S rRNA of Bacteroides ...
Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis are strongly associated with perio...
Species-specific DNA probes were used to determine the presence of Actinobacillus actinomycetemcomit...
The aim of our research was to identify by bacterial genomicDNA analysis the prevalence of five diff...
Objective: The aim of the present study was to evaluate the reproducibility of a commercial kit for ...
Background: The aims of this study were to determine the genotypic diversity of Prevotella intermedi...
Background and Aim: For the analysis of subgingival plaque, anaerobic bacterial culture has been the...
this study was undertaken to develop PCR primers for the simultaneous detection of Fusobacterium nuc...
Introduction: Molecular ecological analysis based on 16S rRNA gene sequence analysis is well establ...
In the present study, detection patterns of subgingival Porphyromonas gingivalis (Pg), Prevotella in...
Whole genomic and randomly-cloned DNA probes for two fastidious periodontal pathogens, Porphyromonas...
OBJECTIVE: The aim of this study was to detect the prevalence of selected bacterial species in intra...
The purpose of this study was to detect the presence of Porphyromonas endodontalis, P. gingivalis, P...
Background: Microbial agents in root canal systems can induce periodontal inflammation. The aims of ...