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This study was conducted to identify and characterize dental follicle stem cells (DFSCs) by analyzing expression of embryonic, mesenchymal and neural stem cells surface markers.
An optimal spacer arm length of the RGD peptides was also necessary for minimizing cellular stress responses as determined by analyzing expression of heat shock proteins and Bcl-2 in cultured cells.
We began by analyzing expression of the miR-290, miR-302, and miR-17∼92 miR-17∼92in staged embryos.
Although the chromaffin tumor phenotype in neuroblastoma is easily revealed by analyzing expression of NESP55 and IGF2, the corresponding morphological features are relatively inconspicuous.
This could be done by analyzing expression of the rsmZ-GFP reporter in response to B. thai (as in Figure 4C) in a gacA or gacS mutant background.
To confirm this conclusion, we also tested whether knocking down hESC TAFs would induce differentiation by analyzing expression of a diverse set of differentiation markers: AFP (endoderm), CGB7 (trophoectoderm), IGF2 (mesoderm), NES (ectoderm) and SOX1 (neuroectoderm).
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We investigated the origin of the cells by analyzing expressions of STRO-1 and two intermediate filaments, cytokeratin-18 and vimentin.
We therefore decided to search for novel blood and vascular related genes downstream of etsrp by analyzing expression profiles of zebrafish embryos overexpressing etsrp.
Furthermore, we demonstrated the specificity of the amplified RNA pool by analyzing expression levels of different positive and negative gene markers using microarray hybridization and qRT-PCR.
By analyzing expression profiles of MAPKKK genes in grapevine microarray databases, we highlighted the modulation of different MAPKKKs in different organs and distinct developmental stages.
Microarray data were confirmed by analyzing expression levels of 17 representative genes using reverse transcription quantitative polymerase chain reaction (RT-qPCR).
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