The level of both enzymes was significantly lower in the cerebral cortex than other brain regions tested.
It uses natural language processing so it understands when a paper is discussing its own results or those of another experiment, and from there can extract critical details like methods, materials, animal types or brain regions tested, etc.
Robust specific binding was observed in all four brain regions tested with cortex showing the highest specific binding with a specific/non-specific binding ratio of ~18.
Results demonstrated a significant, but relatively low anisotropic behavior, yet there were no conclusive mechanical differences between the two regions tested.
SNCA CpG-2 methylation levels differed among subjects and regions tested (Figure 4).
The finding was consistent in all nasal anatomic regions tested (i.e., superior nasal septum, middle turbinate and inferior turbinate).
Thus, none of the in total 7 regions tested was found to loose interaction when transcription was blocked.
Among the 17 cpDNA regions tested, two spacers (trnS-trnG and psbK-trnS) showed the highest levels of variation.
Each program had substantial false positive and false negative rates in at least one of the three CNV regions tested.
Sanger sequencing of the amplicons confirmed the predicted haplotypes of the three regions tested (see Materials and Methods).
By this quantitative method, RT-PCR, both FMR1 and FMR4 were shown to display robust expression levels in all three brain regions tested (Figure 2B).
