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Real-time PCR in virologyDetection and quantification of gene expression in environmental bacteriologyA new reverse transcription-polymerase chain reaction method for accurate quantificationExpression of cyclins A, E and topoisomerase II alpha correlates with centrosome amplification and genomic instability and influences the reliability of cytometric S-phase determinationMolecular methods of measurement of hepatitis B virus, hepatitis C virus, and human immunodeficiency virus infection: implications for occupational health practiceA new mathematical model for relative quantification in real-time RT-PCRAssaying estrogenicity by quantitating the expression levels of endogenous estrogen-regulated genesSimple, sensitive and accurate method for the quantification of prothrombin mRNA by using competitive PCRRelative expression software tool (REST©) for group-wise comparison and statistical analysis of relative expression results in real-time PCRTopographic and quantitative display of integrated human immunodeficiency virus-1 provirus DNA in human lymph nodes by real-time polymerase chain reaction.Rapid detection and identification of the bacterium Pantoea stewartii in maize by TaqMan real-time PCR assay targeting the cpsD gene.Reverse transcription-quantitative polymerase chain reaction: description of a RIN-based algorithm for accurate data normalization.Proteomic analysis of interactions between a deep-sea thermophilic bacteriophage and its host at high temperatureA model for transition of 5'-nuclease domain of DNA polymerase I from inert to active modesApplication of the 5'-nuclease PCR assay in evaluation and development of methods for quantitative detection of Campylobacter jejuniApplication of the 5' fluorogenic exonuclease assay (TaqMan) for quantitative ribosomal DNA and rRNA analysis in sediments.TaqMan PCR for detection of Vibrio cholerae O1, O139, non-O1, and non-O139 in pure cultures, raw oysters, and synthetic seawaterDetection and quantification of methyl tert-butyl ether-degrading strain PM1 by real-time TaqMan PCR.Multiplex fluorogenic real-time PCR for detection and quantification of Escherichia coli O157:H7 in dairy wastewater wetlandsReal-time quantitative PCR for detection of Helicobacter pyloriReal-time and quantitative PCR: applications to mechanism-based toxicology.Conditional expression of the mutant Ki-rasG12C allele results in formation of benign lung adenomas: development of a novel mouse lung tumor model.Diagnostic testing in Epstein-Barr virus infection.Methods for estimating gene frequencies and detecting selection in bacterial populations.A PALB2 mutation associated with high risk of breast cancer.Thermodynamic contributions of single internal rA·dA, rC·dC, rG·dG and rU·dT mismatches in RNA/DNA duplexes.Quantitative real-time PCR: a critique of method and practical considerations.Gene expression in peripheral arterial chemoreceptors.A high-throughput screening method to reengineer DNA polymerases for random mutagenesis.Analysis of the temporal expression of chemokines and chemokine receptors during experimental granulomatous inflammation: role and expression of MIP-1alpha and MCP-1.Planarian homolog of puromycin-sensitive aminopeptidase DjPsa is required for brain regeneration.The hepatic transcriptome in human liver diseaseReal-time PCR quantification using a variable reaction efficiency modelRapid detection of Ceratocystis platani inoculum by quantitative real-time PCR assay.An electrochemical RNA hybridization assay for detection of the fecal indicator bacterium Escherichia coli.Comparison of SYBR Green and TaqMan methods in quantitative real-time polymerase chain reaction analysis of four adenosine receptor subtypes.Development of a quantitative gene expression assay for Chlamydia trachomatis identified temporal expression of sigma factors.Reliable detection of human papillomavirus in recurrent laryngeal papillomatosis and associated carcinoma of archival tissue.Improved multiplex PCR using conserved and species-specific 16S rRNA gene primers for simultaneous detection of Actinobacillus actinomycetemcomitans, Bacteroides forsythus, and Porphyromonas gingivalis.PCR bias in ecological analysis: a case study for quantitative Taq nuclease assays in analyses of microbial communities.
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh
1998年學術文章
@zh-hant
name
Developments in quantitative PCR.
@en
type
label
Developments in quantitative PCR.
@en
prefLabel
Developments in quantitative PCR.
@en
P356
P1476
Developments in quantitative PCR
@en
P2093
P304
P356
10.1515/CCLM.1998.045
P577
1998-05-01T00:00:00Z