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6 opathologic observations were verified using quantitative gene expression analyses examining gob5 gen
7 ic cell culture and fluorescence microscopy, quantitative gene expression analysis and mathematical m
10 uorescence measurements, immunolabeling, and quantitative gene expression analysis point to S. oneide
13 acute phase and detoxification responses in quantitative gene expression and (phospho-)proteomics da
16 lity of seven microarray platforms and three quantitative gene expression assays in profiling the exp
17 ndorf and the National Cancer Institute, and quantitative gene expression assays included TaqMan Gene
19 esented here are various examples to present quantitative gene expression data using this method.
21 anging from qualitative trait information to quantitative gene expression data, which vary among inbr
24 or focused investigations of qualitative and quantitative gene expression differences between humans
25 amily-based sample of 14 human families, for quantitative gene expression dissection, and a sample of
30 y data set has been validated by alternative quantitative gene expression platforms thus supporting t
31 rom five different inbred lines of mice with quantitative gene expression profiling in normal brains
32 al analysis of six inbred mouse strains with quantitative gene expression profiling of several brain
38 ted the performance characteristics of three quantitative gene expression technologies and correlated
40 Here, we combine in vitro ligand binding, quantitative gene expression, protein-DNA interaction an
43 ltimate goal of delivering calibrated, truly quantitative gene-expression measurements on a genomic s
45 ve developed a new microarray technology for quantitative gene-expression profiling on the basis of r
47 ikely via PTB in order to accurately capture quantitative gene interaction dynamics and correctly pre
48 agent effects for each gene, ATARiS produces quantitative, gene-level phenotype values, which provide
49 ination is likely to be a general feature of quantitative gene regulation in a chromatin context.
50 Supporting the essential role of GluN2B, quantitative gene-tagging revealed a fourfold molar exce