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Laboratory technic for detecting and measuring a specific ADN sequence concentration.
qpcr
1
MMP-3 expression was determined by enzyme-linked immunosorbent assay and
quantitative
polymerase
chain
reaction
.
2
Differentially regulated transcripts were validated by reverse transcription-
quantitative
polymerase
chain
reaction
.
3
The amplification was further validated with real-time
quantitative
polymerase
chain
reaction
.
4
LTL was measured with a
quantitative
polymerase
chain
reaction
method.
5
Gpr35 messenger RNA expression in cardiovascular tissues was assessed using
quantitative
polymerase
chain
reaction
.
6
The lung tissue was characterized by histological and real-time
quantitative
polymerase
chain
reaction
analysis.
7
Preferential upregulation of these plasma membrane-linked genes was validated by
quantitative
polymerase
chain
reaction
.
8
Copy number analysis was measured by
quantitative
polymerase
chain
reaction
and fluorescence in situ hybridization.
9
Cytokine gene expression in the urinary sediment was studied by real-time
quantitative
polymerase
chain
reaction
.
10
These findings were verified by
quantitative
polymerase
chain
reaction
.
11
The genotype and viral load of HPV were determined by fluorescence
quantitative
polymerase
chain
reaction
.
12
Reverse transcription-
quantitative
polymerase
chain
reaction
was used to validate the different expression levels of selected lncRNAs.
13
Reverse transcription-
quantitative
polymerase
chain
reaction
was conducted to verify the candidate miRNAs discovered by microarray analysis.
14
Autophagy and apoptosis-related gene expression were assessed by real-time
quantitative
polymerase
chain
reaction
and Western blot.
15
The expression of UASR1 in tissues and cells were detected by reverse transcription-
quantitative
polymerase
chain
reaction
.
16
Real-time
quantitative
polymerase
chain
reaction
evaluated RHOF expression in lymphocyte subpopulations, and normal and malignant lymphoid tissue.