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We hypothesised that TBF could affect tracer uptake: low perfused areas might show low tracer uptake due to perfusion-limited delivery of [18F]FLT.
However, it might be possible that perfusion affects tracer uptake: low perfused tumour lesions might show low tracer uptake due to limited supply of the tracer to the lesion.
One possible explanation is that HRV and RSFA might show low dependency in regions sensitive to susceptibility artefacts.
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Suppressed basal activity in the prefrontal cortex found in patients with orally localized somatoform pain disorder [ 2] raises the hypothesis that patients with unexplained occlusal discomfort might have some functional deficits in top-down control that usually ameliorates unpleasant somatosensory input and might therefore show low tolerance even to a slight modification of the occlusion.
Since the putative serum SEPs might show very low abundance and high dynamics, 11 WT mouse samples and four ob/ob mouse samples were chosen for the following MS detection, respectively (Fig. 3B, C).
However, other sites that we might have expected to show low D values did not, such as the IRES of DWV, which has been mapped to the 300 bp 5' of the polyprotein coding sequence [ 35].
This is an attractive hypothesis although the alternative explanation, that tumours with higher levels of genetic instability might be those which tend to show low level amplification (generating allelic imbalance and perhaps AEI) and high levels of expression of AURKB, cannot be discounted without further analysis.
Will the returns show low income?
Of particular interest is the comparison between older high performers and younger low performers: in fact, older high performers, unlike younger low performers, might show a similar neural response pattern as younger high performers reflecting an at least partly successful compensation of age-related behavioral working memory deficits [ 10, 51].
Also, genes with very low basal expression might show a two-fold increase in response to decitabine but still have biologically insignificant amounts of gene expression.
3) High-risk and low-risk patients might show different sensitivity to precipitating factors and interventions.
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