Sentence examples for marker genes using from inspiring English sources

MGFM is a useful tool to predict tissue/cell type marker genes using microarray gene expression data.

The formation of the osteoblast phenotype was evaluated by quantification of osteoblast-related marker genes using real-time polymerase chain reaction (RT-PCR).

Cultures of a fibroblast cell line grown on urea-extracted collagen showed a higher motility and reduced stress levels than those grown on acetic acid-extracted collagen as determined by morphological studies and transcriptional analysis of selected marker genes using real time-PCR.

The result of the selection process shows a clear performance improvement when finding gender marker genes using post-globin reduction samples instead of pre-globin reduction samples.

Freshly sorted TN or TNreg CD4+ cells were activated with anti-CD3/CD28 beads at a bead: cell ratio of 1∶4, and transduced with a multiplicity of infection of 3. Cells were expanded in IL-2 containing media for 2 weeks and sorted for their GFP or RFP marker genes using BD FACS Aria before reactivation.

It has been shown previously, by the detection of a few marker genes using Q-PCR, that repression of Oct3/4 leads to the differentiation of ES cells into the trophoblast lineage, and that overexpression of Oct3/4 leads to primitive endoderm and mesoderm differentiation [19], [44].

The resulting observed significance calls were quite stable for pairs of same tissue type irrespective of the number of the marker genes used (Figure S1).

IHAT was used to identify isofunctional homologs of three polyphosphate metabolism genes (ppk1, ppk2, ppx), the high-affinity phosphate transporter, pstS, the alkaline phosphatase genes phoA and phoX, and the 35 single-copy marker genes used by Raes and colleagues for calculation of effective genome size [44], across 38 GOS samples [27].

Similarly, M. arosiense, despite having extremely limited divergence with MIP on comparison of its marker genes used in this study, is a pathogenic scotochromogen that grows optimally at 42°C and takes more than 14 days for visible colonies to appear on 7H11 agar, that too with a heavy inoculum [12].

Of the six marker genes used previously to further characterize the effects of VPA, only two (Pax6 and Nanog) are in the new set of consensus genes.

These were used to calculate weights for each of the tumour marker genes used in the CTC assay and to set the threshold of CTC positivity.