The inherent quantitative capacity of the reverse transcription-polymerase chain reaction.
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Changes in the expression of human cell division autoantigen-1 influence Toxoplasma gondii growth and developmentReal-time PCR in virologyThe 'permeome' of the malaria parasite: an overview of the membrane transport proteins of Plasmodium falciparum.A new experimental approach for studying bacterial genomic island evolution identifies island genes with bacterial host-specific expression patternsMolecular techniques for studying gene expression in carcinogenesis.Quantitation of TGF-beta1 mRNA in porcine mesangial cells by comparative kinetic RT/PCR: comparison with ribonuclease protection assay and in situ hybridization.An inexpensive gel electrophoresis-based polymerase chain reaction method for quantifying mRNA levels.Optimized viral dose and transient immunosuppression enable herpes simplex virus ICP0-null mutants To establish wild-type levels of latency in vivo.Alpha/Beta interferon and gamma interferon synergize to inhibit the replication of herpes simplex virus type 1.Colon cancer: prevalence, screening, gene expression and mutation, and risk factors and assessment.Re-evaluating natural resistance to herpes simplex virus type 1.Sample pretreatment and nucleic acid-based detection for fast diagnosis utilizing microfluidic systems.Evaluation of reverse transcription-PCR and a bacteriophage-based assay for rapid phenotypic detection of rifampin resistance in clinical isolates of Mycobacterium tuberculosis.Coordinated upregulation of a series of endogenous antioxidants and phase 2 enzymes as a novel strategy for protecting renal tubular cells from oxidative and electrophilic stress.Solid phase DNA amplification: a simple Monte Carlo Lattice model.Use of multiplex reverse transcription-PCR to study the expression of a laccase gene family in a basidiomycetous fungus.Effect of poly-L-lysine coating on macrophage activation by alginate-based microcapsules: assessment using a new in vitro method.Identifying and quantifying genotypes in polyclonal infections due to single species.Metabolic selection of glycosylation defects in human cells.Angiotensin II activates the GFAT promoter in mesangial cells.Defects in insulin receptor signaling in vivo in the polycystic ovary syndrome (PCOS).Antioxidants and phase 2 enzymes in macrophages: regulation by Nrf2 signaling and protection against oxidative and electrophilic stress.Use of reverse transcriptase-polymerase chain reaction-restriction fragment length polymorphism to examine the interaction between infectious bronchitis virus strains Massachusetts 41 and JMK in ovo.Expression of six expansin genes in relation to extension activity in developing strawberry fruit.Apple juice intervention modulates expression of ARE-dependent genes in rat colon and liver.
P2860
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P2860
The inherent quantitative capacity of the reverse transcription-polymerase chain reaction.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
The inherent quantitative capa ...... ion-polymerase chain reaction.
@ast
The inherent quantitative capa ...... ion-polymerase chain reaction.
@en
The inherent quantitative capa ...... ion-polymerase chain reaction.
@nl
type
label
The inherent quantitative capa ...... ion-polymerase chain reaction.
@ast
The inherent quantitative capa ...... ion-polymerase chain reaction.
@en
The inherent quantitative capa ...... ion-polymerase chain reaction.
@nl
prefLabel
The inherent quantitative capa ...... ion-polymerase chain reaction.
@ast
The inherent quantitative capa ...... ion-polymerase chain reaction.
@en
The inherent quantitative capa ...... ion-polymerase chain reaction.
@nl
P2093
P356
P1476
The inherent quantitative capa ...... ion-polymerase chain reaction.
@en
P2093
B M Gebhardt
W P Halford
P304
P356
10.1006/ABIO.1998.2913
P407
P577
1999-01-01T00:00:00Z