Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
about
Influence of long time storage in mineral water on RNA stability of Pseudomonas aeruginosa and Escherichia coli after heat inactivation.Stress- and growth rate-related differences between plate count and real-time PCR data during growth of Listeria monocytogenes.Use of ethidium monoazide and PCR in combination for quantification of viable and dead cells in complex samples.A sensitive nested reverse transcriptase PCR assay to detect viable cells of the fish pathogen Renibacterium salmoninarum in Atlantic salmon (Salmo salar L.).Optimization of reverse transcriptase PCR to detect viable Shiga-toxin-producing Escherichia coli.Development of reverse transcription (RT)-PCR and real-time RT-PCR assays for rapid detection and quantification of viable yeasts and molds contaminating yogurts and pasteurized food productsEvaluation of the use of PCR and reverse transcriptase PCR for detection of pathogenic bacteria in biosolids from anaerobic digestors and aerobic composters.Microbial quality and direct PCR identification of lactic acid bacteria and nonpathogenic Staphylococci from artisanal low-acid sausages.Development and validation of qualitative SYBR®Green real-time PCR for detection and discrimination of Listeria spp. and Listeria monocytogenes.Expression of Surface Protein LapB by a Wide Spectrum of Listeria monocytogenes Serotypes as Demonstrated with Anti-LapB Monoclonal AntibodiesThe ability to enter into an avirulent viable but non-culturable (VBNC) form is widespread among Listeria monocytogenes isolates from salmon, patients and environmentComparison of Culture, Conventional and Real-time PCR Methods for Listeria monocytogenes in Foods.RNA-Based Detection Does not Accurately Enumerate Living Escherichia coli O157:H7 Cells on Plants.Detection of viable Listeria monocytogenes with a 5' nuclease PCR assayQuantification of Clostridium botulinum toxin gene expression by competitive reverse transcription-PCR.mRNA detection by reverse transcription-PCR for monitoring viability over time in an Enterococcus faecalis viable but nonculturable population maintained in a laboratory microcosm.Physiological states of individual Salmonella typhimurium cells monitored by in situ reverse transcription-PCR.Detection of mRNA by reverse transcription-PCR as an indicator of viability in Escherichia coli cells.Application of Reverse Transcriptase -PCR (RT-PCR) for rapid detection of viable Escherichia coli in drinking water samples.Detection of cytotoxin-hemolysin mRNA in nonculturable populations of environmental and clinical Vibrio vulnificus strains in artificial seawater.Detection of Listeria monocytogenes from a model food by fluorescence resonance energy transfer-based PCR with an asymmetric fluorogenic probe set.Exploring specific primers targeted against different genes for a multiplex PCR for detection of Listeria monocytogenes.
P2860
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P2860
Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
description
1997 nî lūn-bûn
@nan
1997 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
@ast
Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
@en
type
label
Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
@ast
Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
@en
prefLabel
Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
@ast
Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
@en
P2860
P1476
Sensitive detection of viable Listeria monocytogenes by reverse transcription-PCR.
@en
P2093
P2860
P304
P407
P577
1997-11-01T00:00:00Z