Examples of using Microarray analysis in English and their translations into Portuguese
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More recently, microarray analysis revealed the deregulation of microRNAs(miRNAs) in PTC samples.
A submicroscopic chromosomal deletion is detected by FISH,MLPA or chromosomal microarray analysis.
The gene expression was evaluated by microarray analysis and validated by rtqpcr polymerase chain reaction real-time.
Rody et al. observed the greatest loss of this receptor gene expression after neoadjuvant chemotherapy in microarray analysis 63.
Chromosomal microarray analysis is an important tool for the detection and microdeletion and microduplications in the genomes.
To determine which genes in a sample are being expressed,the following steps of DNA microarray analysis are undertaken.
Table 3 shows the comparison between tissue microarray analysis and the standard method for lymph node analysis in terms of advantages and cost.
The aim of this study was to identify genes orchromosomal regions related to oavs using mlpa and chromosome microarray analysis.
Using the combination of tissue microarray analysis and immunohistochemistry, pathologists are now able to perform unprecedented large-scale analyses. .
We described five patients with phenotypic variability that carries deletions or reciprocal duplications at 22q11.2detected by chromosomal microarray analysis.
It is worthwhile noting that microarray analysis(in endothelial cells) pointed the involvement of PDGFR(platelet-derived growth factor receptor) in Losac-induced cell survival.
Lu et al. reported the frequency of genomic imbalances identified in 638 neonates with various birth defects referred for chromosomal microarray analysis.
A total of 44 WD genes(37.60%) through microarray analysis revealed modulated during the process of differentiation and peptides were identified for 9 WD proteins, reinforcing the functional importance of this family.
Due to the fact that the selected genes have in general showed a similar responsein different tresses studied, a specific microarray analysis was performed to select genes that are expressed significantly different among the stresses.
Chromosomal microarray analysis(cma) allowed extending the range and sensitivity in detection of submicroscopic deletions or duplications.
Currently, application of new molecular cytogenetics technologies,as multiplex ligation-dependent probe amplification(mlpa) and chromosomal microarray analysis(cma), has increasingly allowed the identification of microdeletions and microduplications as di causes idiopathic.
Mechanism of action: using whole-genome microarray analysis, functional genetics(siRNA and miRNA) and small molecules targeting known signaling pathways we will explore the mechanism of action of the candidate drugs.
The following variables were analyzed: cellular viability MTT assay cellular density hoeschst 33258 staining and apoptosis TUNEL assay, before and 1, 2 and4 days after the procedure."cDNA microarray" analysis of the SV sections was used to determine the precociously changed molecular targets in the veins cultivated under arterial conditions.
The ability of chromosome microarray analysis(cma) to detect submicroscopic genetic abnormalities has revolutionized the clinical diagnostic approaches to individuals with intellectual disability, neurobehavioral phenotypes and congenital malformations.
Genomic microarrays have been extensively used in the studying the genetic causes of intellectual disability, and the chromosomal microarray analysis is recommended as the first-tier cytogenetic diagnostic test for patients with intellectual disability/global developmental delay, autism spectrum disorders and/or multiple congenital anomalies.
Through microarray analysis and cell sorting, we have shown that igf2 and cd105 expression levels contribute to these osteopontential cell differences, that is, higher igf2 expression levels and lower cd105 expression levels were associated with the increased osteogenic potential of shed as com.
We postulate that an alternative method,combining tissue microarray analysis and immunohistochemistry, can reduce costs and be effective in detecting micrometastases in lymph nodes that have previously tested negative for NSCLC by routine hematoxylin-eosin staining.
Microarray analysis of the k562 cell line derived from a chronic myeloid leukemia patient in blast crisis and its derivative cells carrying the multidrug resistance(mdr) phenotype, lucena 1 and feps selected by vincristine and daunorubicin, respectively, showed differential gene expression of the notch signaling pathway.
Microarray analyses were applied to assess the gene expression profiles.
After the treatment, the animais were anesthetized and the collected ovaries were immediately placed in liquid nitrogen andthen frozen at -80°c for further cdna microarray analyses.
Whole blood cells were collected and used to profile gene expression analysis by microarray.
Statistical methods for cDNA microarray data analysis in an integrated computational….
Fluorescence is measured with a laser scanner andresults are evaluated using Phadia Microarray Image Analysis(MIA) software.