Microsatellite markers are recognized as versatile molecular tools for inferring genetic structure and gene flow.
The evaluation of biological markers is recognized as necessary to the future of toxicology, epidemiology, and quantitative risk assessment.
Increasing evidence shows that H3K27me3 markers are recognized by polycomb protein and generally correlate with gene silencing and transcriptional repression [ 26, 37, 38].
SNP markers are recognized as 'markers of choice' due to their abundance and distribution in the genomes and the ability to screen populations at relatively low cost.
The power of combining multiple sepsis markers is recognized, but earlier studies used informal and suboptimal quantitative approaches to identify the optimal combination.
These markers are recognized by an equally large variety of receptors on phagocytes, including CD14, CD68, CD91 (LRP), SR-A, ATP-binding cassette transporter 1 (ABC-1), complement receptors, integrin αv β5 and αv β3/CD36/thrombospondin complexes.
Once an appropriate marker is recognized, a virtual model is then registered to the position of the marker.
This marker was recognized on equine MSC derived from peripheral blood but it was absent in MSC derived from adipose tissue [ 82, 83].
The aggresomes were recognized by the marker protein p62 (red).
Finally, specific decay markers have been recognized, by a comparison of the results obtained from the detached samples with those deriving from artificially aged models, to be used for a correct future monitoring and maintenance of the wall paintings.
