Barely Significant
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an interesting trend

1,038 sentences · 1,038 papers · 2,459 search hits before verification · confirmed specimen

Sighted at

p=0.1

Listed by Hankins (2013) · Otte et al. (2022)

In the literature

We observed an interesting trend wherein glucosinolate concentration in the margin of GTR ‐edited lines having in‐frame mutations in at least one BjuGTR1 homologue (L18‐16, L34‐3, and L34‐4; hereafter referred to as Category‐I (Ct‐I) lines) ranged from 190.22 to 226.54 μmoles/g DW, which was somewhat higher than the lines having mutations in all the four BjuGTR1 homologues (L4‐11, L4‐15, L15‐19, L30‐13, and L40‐9; referred to as Ct‐II lines) with glucosinolates ranging from 160.10 to 190.95 μmoles/g DW (Figure 5a ).
The N/P = 14 and 21 formulations of pMAT- b -AEMA-2 and N/P = 7 formulation of pMAT- b -AEMA-3 were found to be statistically similar to the positive control jetPEI. While none of the pMAT- b -AEMA-2 formulations nor any of the positive controls differed statistically from each other when compared to the cells-only control, an interesting trend appeared in the other samples: both the shortest and longest MAT polymers showed decreased uptake values with an increase in N/P ratio with U87 cells.
Although this difference was not statistically significant, it represents an interesting trend because this cell loss was much more profound in the DR case, in which approximately 60% of both interneuron types were lost compared with that in control eyes (PV plus cells: 3.63 ± 1.07 vs. 1.36 ± 0.84; PKCα plus cells: 4.75 ± 1.39 vs. 1.97 ± 1.09; P < 0.0001 for both) ( Fig. 6 D and F ).
Optimal identification of cytoplasmic membrane proteins requires a combined computational and laboratory approach Examining the detailed PSORTb results for the proteins reviewed in the present analysis, we observed an interesting trend in the output of the HMMTOP module, which predicts the number of transmembrane alpha-helices in a query protein.
Importantly, time-lag estimation with both dSTE and cross-correlation of amplitude envelopes revealed an interesting trend in wrong trials compared to correct: right PO (rPO α2 ) brain region (i.e., channels P6, P8, PO8, PO4, and O2) showed zero time-lag with bilateral F brain regions (bF θ ) across the five CWLs ( Figure 7 ).