Evaluation of the Propidium Monoazide-quantitative Polymerase Chain Reaction Method for the Detection of Viable Enterococcus faecalis.

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Journal of Endodontics

• Publication date

  2016-07-01

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1016/j.joen.2016.04.003PMID 27179593
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• RNA-based Assay Demonstrated Enterococcus faecalis Metabolic Activity after Chemomechanical Procedures.

  2015cited by this paper
• A propidium monoazide–quantitative PCR method for the detection and quantification of viable Enterococcus faecalis in large-volume samples of marine waters

  2014cited by this paper
• Quantitative real-time PCR combined with propidium monoazide for the selective quantification of viable periodontal pathogens in an in vitro subgingival biofilm model.

  2014cited by this paper
• In vivo quantitative evaluation of live and dead bacteria in root canal infection by using propidium monoazide with real-time PCR.

  2013cited by this paper
• DNA binding to hydroxyapatite: a potential mechanism for preservation of microbial DNA.

  2013cited by this paper
• Method to quantify live and dead cells in multi-species oral biofilm by real-time PCR with propidium monoazide

  2013cited by this paper
• Analysis of viable vs. dead Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis using selective quantitative real-time PCR with propidium monoazide.

  2013cited by this paper
• Progress in understanding preferential detection of live cells using viability dyes in combination with DNA amplification.

  2012cited by this paper
• Enumeration of viable Enterococcus faecalis, a predominant apical periodontitis pathogen, using propidium monoazide and quantitative real‐time polymerase chain reaction

  2011cited by this paper
• Live/dead real-time polymerase chain reaction to assess new therapies against dental plaque-related pathologies.

  2011cited by this paper
• Propidium monoazide combined with real-time quantitative PCR underestimates heat-killed Listeria innocua.

  2011cited by this paper
• Novel approaches toward preferential detection of viable cells using nucleic acid amplification techniques.

  2009cited by this paper
• Diversity of Endodontic Microbiota Revisited

  2009cited by this paper
• Quantitative real-time PCR analysis of total and propidium monoazide-resistant fecal indicator bacteria in wastewater.

  2009cited by this paper
• Clinical implications and microbiology of bacterial persistence after treatment procedures.

  2008cited by this paper
• Microbial analysis of canals of root-filled teeth with periapical lesions using polymerase chain reaction.

  2008cited by this paper
• Use of Propidium Monoazide for Live/Dead Distinction in Microbial Ecology

  2007cited by this paper
• Detection and quantitation of E. faecalis by real-time PCR (qPCR), reverse transcription-PCR (RT-PCR), and cultivation during endodontic treatment.

  2006cited by this paper
• Comparison of propidium monoazide with ethidium monoazide for differentiation of live vs. dead bacteria by selective removal of DNA from dead cells.

  2006cited by this paper
• Enterococcus faecalis in dental root canals detected by culture and by polymerase chain reaction analysis.

  2006cited by this paper
• Polymerase chain reaction-based analysis of microorganisms associated with failed endodontic treatment.

  2004cited by this paper
• Microorganisms from canals of root-filled teeth with periapical lesions.

  2003cited by this paper

• Microbial viability assessment with PMA-qPCR: challenges, opportunities, and future directions

  2025cites this paper
• Establishment of a Protocol for Viability qPCR in Dental Hard Tissues

  2024influential citation
• DNA and RNA Stability of Marine Microalgae in Cold-Stored Sediments and Its Implications in Metabarcoding Analyses

  2024cites this paper
• Detection of Viable Streptococcus equi equi Using Propidium Monoazide Polymerase Chain Reaction.

  2023cites this paper
• Regenerative endodontic procedures in immature permanent teeth with pulp necrosis: the impact of microbiology on clinical and radiographic outcome

  2023cites this paper
• Rapid and multiplex detection of nosocomial pathogens on a phage‐based magnetoresistive lab‐on‐chip platform

  2021cites this paper
• Clinical and Molecular Microbiological Evaluation of Regenerative Endodontic Procedures in Immature Permanent Teeth.

  2020cites this paper
• Quantitative PCR Assays Developed for Diaporthe helianthi and Diaporthe gulyae for Phomopsis Stem Canker Diagnosis and Germplasm Screening in Sunflower (Helianthus annuus).

  2020cites this paper
• Comparison of rRNA-based reverse transcription PCR and rDNA-based PCR for the detection of streptococci in root canal infections

  2019cites this paper
• Real-Time PCR for Diagnosing and Quantifying Co-infection by Two Globally Distributed Fungal Pathogens of Wheat

  2018cites this paper
• Evaluating the newly developed dye, DyeTox13 Green C-2 Azide, and comparing it with existing EMA and PMA for the differentiation of viable and nonviable bacteria.

  2018cites this paper
• Oral hygiene in intensive care unit patients with photodynamic therapy: study protocol for randomised controlled trial

  2017cites this paper
• Relic DNA is abundant in soil and obscures estimates of soil microbial diversity

  2016cites this paper