In support of this hypothesis, we found strong patterns of convergence within the set of promoters that underwent a GA-to-GC box conversion in eutherian mammals and those containing the same conversion in birds.
In support of this hypothesis, the learning and memory pattern observed in Dyrk1A+/− mice is similar to hippocampally-lesioned animals that also learn at a slower rate than sham-lesioned animals [41], [42], but show partially preserved memory.
Also in support of this hypothesis, we observed a consistent pattern of cis-regulatory conversions in genes involved in specific functional categories.
In support of this idea we observed that higher multivoxel pattern dissimilarity in the hippocampus selectively predicted more effective suppression of newly acquired memories, but higher pattern dissimilarity in the LPC predicted more effective suppression of consolidated memories.
In support of this assumption, statistical analysis of the expression pattern of 280 phylogenetically identified paralogous pairs in Arabidopsis revealed that 85% of the pairs showed differential expression levels depending on the organ investigated.
In support of this notion, we found that the APA pattern can be used to separate samples according to reprogramming state and cell type by hierarchical clustering (Figure 2D) and principal component analysis (Figure 2E).
In support of this idea, rats displayed a different movement pattern when tested with a trapped cagemate or stranger.
In support of this idea, ezrin and moesin show distinct patterns of movement and post-translational modification during T cell activation [12], [28], [29] and proteins such as L-selectin and CD95/Fas bind ezrin and moesin differentially [9], [18].
In support of the evenness pattern (Figure 5c), the strength of the relationship (expressed as the slope of the regression model) between rIinflow and vf-indDOC in individual flume models significantly (r2 = 0.71, P<0.05) decreased with increasing flow heterogeneity.
