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Research of RNA viability markers was previously studied for many bacterial species.
A genetic linkage map of M. zebra consisting of 834 RAD-tag markers was previously constructed [ 34].
A preliminary linkage map with AFLP, RFLP and a small number of SSR markers was previously constructed for the tenera parent.
A similar anomaly between the degree of inhibition of IκB degradation and its effect on mRNA or protein expression level for several inflammation-related markers was previously reported by Liu and colleagues [ 35].
mRNA and protein expression of neural crest and stem cell markers was previously confirmed in a panel of hemangioma samples, revealing variable expression levels for Oct4, Myc, Sox2, and Nanog [ 10, 11].
Since expression of progenitor markers was previously detected in Defined medium and increased over time, we wanted to investigate if changes in culture media could enrich a certain cell phenotype.
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The markers were previously segmented using a threshold-based algorithm.
These vegetal markers were previously considered to have been deposited in the lacustrine system, in restricted isolation.
This allowed the development of a set of PCR-based markers for specific HMW glutenin genes encoding By-subunits for which no markers were previously available.
Primers for each of the 5 markers were previously described [12], [13].
Fifteen SNP markers were previously identified in An. funestus [ 18].
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