For relocations, P- and S-wave readings were used, and the magnitudes were always calculated by applying the duration-dependent formula, which is widely used for local earthquakes at KOERI.
However, whether a relocated gene has male-biased expression is not independent of whether it is the result of →A or →X relocation (P < 0.05, F.E.T).
In all models the annual relocation probability (p) was kept constant as initial data exploration indicated that there was no a priori year-specific bias on the relocation probability.
The effect derives from an increased solubility of H2 and O2 which increases the reaction rate, but also determines a relocation of Pd particles which migrate inside the mesopore channels of SBA-15.
Additionally, there is an excess of X→ relocated genes relative to A→ relocations (Gadj = 21.7, P < 3.2 × 10−6), and there is a deficiency of →X relocated genes (Gadj = 4.54, P < 0.05).
For the hypocenter relocation, we used the manually picked P and S arrival times, with P and S arrival time differences for 27,440 and 38,883 pairs, respectively.
Starting at COI the first observed rearrangement is the relocation of tRNA-P within C. nemoralis.
This was significantly higher than the mortality of patients who were NRBC-negative on the relocation day (8.6%, 28/325; p < 0.01).
The difference between pre- and postoperative GSA values in the relocation group was statistically significant (p = 0.005).
Following relocation, transport-related walking declined overall (p < 0.001) and recreational walking increased (p < 0.001): access to transport- and recreational destinations changed in similar directions.
