Sentence examples for microarray to define from inspiring English sources

We used high density oligonucleotide microarray to define the transcriptional profile induced by Dbl in the lenses of 2 days, 2 weeks, and 6 weeks old transgenic mice.

Mintz et al. and Ochi et al. used expression analysis by microarray to define classifiers of a poor response to chemotherapy [ 30, 31].

The workflow involves (i) using a combinatorial PTM histone peptide microarray to define reader specificity and suitability for MARCC and (ii) utilization of MARCC to enrich, identify and quantify unique chromatin states.

To examine molecular events associated with aging and its retardation by caloric restriction (CR), we have employed high-density oligonucleotide microarrays to define transcriptional patterns in mouse tissues, including skeletal muscle, brain, heart, and adipose.

The previous section mentioned several studies that used gene-expression microarrays to define lists of genes responding to ethanol or otherwise relevant to AUDs.

Next, we used protein-binding microarrays to define the sequences that are bound by Slou, Msh and other HD TFs that have mesodermal expression.

We then used protein-binding microarrays to define the specific sequences that are bound by Msh, Slou and other mesodermal HD TFs.

To better understand the genome-wide response to mitochondrial dysfunction, we have employed Affymetrix 3′ gene expression microarrays to define the transcriptional changes in Drosophila S2 cells knocked down for CoVa as a follow-up of our initial mechanistic studies.

We used high-resolution aCGH and DNA microarrays to define the genome and gene expression profiles of BCs with 17q12-q21-amplification. Results concerning cell lines are given for information to the scientific community.

To better characterize this particular group of BCs, we used high-resolution array-comparative genomic hybridization (aCGH) and whole-genome DNA microarrays to define the genome and gene expression profiles of 54 BCs with ERBB2 amplification.

The goal of this current study was to extend the work of Blanco et al. [ 14] by using microarrays to define gene expression profiles of piglets identified in that study as exhibiting low ('Fully Resistant') or high ('Susceptible') susceptibility to Glässer's disease at early (24 hours) and late (72 hours) stages of the challenge experiment.