DNA amplification to enhance detection of genetically engineered bacteria in environmental samples.
about
Bacterial gene transfer by natural genetic transformation in the environmentInhibition and facilitation of nucleic acid amplificationMethods for microbial DNA extraction from soil for PCR amplification.How to Show the Real Microbial Biodiversity? A Comparison of Seven DNA Extraction Methods for Bacterial Population Analyses in Matrices Containing Highly Charged Natural NanoparticlesA Review of Membrane-Based Biosensors for Pathogen DetectionEstablishment of new genetic traits in a microbial biofilm community.In situ detection of the Clostridium botulinum type C1 toxin gene in wetland sediments with a nested PCR assayUse of bioluminescence for detection of genetically engineered microorganisms released into the environment.Luminescence-based nonextractive technique for in situ detection of Escherichia coli in soilA simple, efficient method for the separation of humic substances and DNA from environmental samples.Detection of methanotrophic bacteria in environmental samples with the PCR.Detection of ammonium-oxidizing bacteria of the beta-subclass of the class Proteobacteria in aquatic samples with the PCRAmplification of the amoA gene from diverse species of ammonium-oxidizing bacteria and from an indigenous bacterial population from seawater.Direct detection of recombinant gene expression by two genetically engineered yeasts in soil on the transcriptional and translational levels.DNA recovery from soils of diverse composition.Molecular mechanisms of genetic adaptation to xenobiotic compounds.Use of Polymerase Chain Reaction To Detect the Take-All Fungus, Gaeumannomyces graminis, in Infected Wheat Plants.Fate of DNA encoding hygromycin resistance after meiosis in transformed strains of Gibberella fujikuroi (Fusarium moniliforme).Detection and enumeration of bacteria in soil by direct DNA extraction and polymerase chain reaction.Detection of Aeromonas salmonicida from fish by using polymerase chain reaction amplification of the virulence surface array protein geneGene probe analysis of soil microbial populations selected by amendment with 2,4-dichlorophenoxyacetic acid.Detection of coliform bacteria in water by polymerase chain reaction and gene probes.Successful approach for detection of low numbers of enterotoxigenic Escherichia coli in minced meat by using the polymerase chain reactionRapid method for processing soil samples for polymerase chain reaction amplification of specific gene sequencesAmplification, cloning, and sequencing of a nifH segment from aquatic microorganisms and natural communities.Reverse sample genome probing, a new technique for identification of bacteria in environmental samples by DNA hybridization, and its application to the identification of sulfate-reducing bacteria in oil field samples.Amplification of the rbcL gene from dissolved and particulate DNA from aquatic environments.Gene escape model: transfer of heavy metal resistance genes from Escherichia coli to Alcaligenes eutrophus on agar plates and in soil samples.Polymerase chain reaction and gene probe detection of the 2,4-dichlorophenoxyacetic acid degradation plasmid, pJP4.Isolation and screening of plasmids from the epilithon which mobilize recombinant plasmid pD10.Evidence that some Frankia sp. strains are able to cross boundaries between Alnus and Elaeagnus host specificity groups.Detection of polychlorinated biphenyl degradation genes in polluted sediments by direct DNA extraction and polymerase chain reactionKinetics of the persistence of chromosomal DNA from genetically engineered Escherichia coli introduced into soil.Detection and identification of phytopathogenic Xanthomonas strains by amplification of DNA sequences related to the hrp genes of Xanthomonas campestris pv. vesicatoria.Survival of lux-lac-marked biosurfactant-producing Pseudomonas aeruginosa UG2L in soil monitored by nonselective plating and PCR.Detection of Escherichia coli in sewage and sludge by polymerase chain reactionPolymerase chain reaction amplification of naphthalene-catabolic and 16S rRNA gene sequences from indigenous sediment bacteria.Use of polymerase chain reaction and electroporation of Escherichia coli to monitor the persistence of extracellular plasmid DNA introduced into natural soils.Microbial degradation of hydrocarbons in the environment.Detection of the Lyme disease bacterium, Borrelia burgdorferi, by using the polymerase chain reaction and a nonradioisotopic gene probe
P2860
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P2860
DNA amplification to enhance detection of genetically engineered bacteria in environmental samples.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年学术文章
@wuu
1988年学术文章
@zh-cn
1988年学术文章
@zh-hans
1988年学术文章
@zh-my
1988年学术文章
@zh-sg
1988年學術文章
@yue
1988年學術文章
@zh
1988年學術文章
@zh-hant
name
DNA amplification to enhance d ...... eria in environmental samples.
@en
DNA amplification to enhance d ...... eria in environmental samples.
@nl
type
label
DNA amplification to enhance d ...... eria in environmental samples.
@en
DNA amplification to enhance d ...... eria in environmental samples.
@nl
prefLabel
DNA amplification to enhance d ...... eria in environmental samples.
@en
DNA amplification to enhance d ...... eria in environmental samples.
@nl
P2860
P1476
DNA amplification to enhance d ...... teria in environmental samples
@en
P2093
P2860
P304
P407
P577
1988-09-01T00:00:00Z