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Using axonal and dendritic markers, we tested whether cytoskeletal changes could cause similar transformations, and found that actin depolymerization induced multiple axons in unpolarized neurons.
Of the eight plant DNA markers we tested (rbcLa, rpoC1, rpoB, matK, ycf5, trnL, psbA-trnH, ITS), matK and ITS had a low rate of sequencing success.
Considering the 10 selected genes as representative prognostic molecular markers, we tested whether expression of the genes or their subsets could predict the duration of survival in an independent cohort.
To look for candidate nuclear DNA markers, we tested 17 different nuclear loci.
For 16S rRNA markers, we tested only those with mean relative abundance >0.01% but for metagenome markers used all markers.
To assess the transferability of our EST-SSR markers, we tested their amplification in four individuals each of 7 further Silene species.
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Using seven nuclear microsatellite markers, we test the hypothesis that genetic diversity and the number of pollen donors are lower in remnant populations.
With these markers, we test whether populations are genetically structured by host species associations (peach and apple) or other factors such as geographic distance.
Using PD as a neurocognitive marker, we tested five predictions derived from the decoupling hypothesis of offline thought.
Utilizing the GFP marker, we tested the recombination efficiency by flow cytometry.
To validate methylation in NT5E as an independent prognostic marker, we tested a second novel epigenetically regulated gene, RasL12.
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