Barely Significant
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“a clear trend”

19,461 sentences · 19,461 papers · 31,348 search hits before verification · confirmed specimen

Sighted at

p<0.09

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

In the literature

While it has been shown that adsorption induced octahedral tilting can enhance hybridization of antibonding states near the VBM, we did not identify a clear trend of heterocycles causing tilting based on final adsorption geometries. 75 We believe that the stabilization of the Pb 6s – I 5p* antibonding states through hybridization with heteroatom orbitals was responsible for a downshift in the VBM and band gap, in accordance with previous work by Tao and co-workers. 76 We observed that with increasing electronegativity of the heteroatoms, the valence orbital energy of Pb was reduced, which in turn increased the band gap.
did not reach statistical significanceP = .0841.7× alphaplainly factual
Although the difference in relapse rates between the 2 groups did not reach statistical significance (χ 2 = 3.00, P = .084), the RTX group exhibited a clear trend toward a lower relapse incidence.
This variability in clinically healthy, uninfected animals, as well as limited sample size and the uncertainties inherent in the estimation method used to determine WBC, meant that despite a clear trend of increasing WBC, the changes over the course of the study were not found to be significant when comparing the sampling days.
As shown in Figure S2 , cryogels obtained at −20 °C appeared not homogenous, and the pore morphology did not show a clear trend among samples with different concentrations possibly because the cryogelation at −20 °C might be not sufficient to support fast phase separation and radical polymerization simultaneously.
Consistent with this notion, the survivin siRNA approach was used throughout the history of survivin studies [ 114 – 118 ]; the survivin siRNA studies in recent years show a clear trend of developing and using various new delivery technologies of survivin siRNA with or without combination of a cancer drug for therapeutics in vitro [ 119 – 123 ] and in vivo [ 124 – 131 ].