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Results from both methods demonstrated a virtual invariance in chain conformation as a function of degradation.
Both methods demonstrated a significant 20 30% decrease in the number of motor neurons in 7-month-old MCK-UCP1 mice, as compared to 3-month-old MCK-UCP1 or wild-type animals.
The results derived by using the ATP and DNA methods demonstrated a significant linear relationship (r = 0.95) and IC50 values obtained from the ATP and DNA assays were similar: 55 µM of EGCG for LNCaP and 35 µM EGCG for MCF-7 cells at 72 h.
The values obtained with both approaches different methods demonstrated a high correlation.
The remaining three methods demonstrated a considerably higher false-positive rate.
Both typing methods demonstrated a high degree of similarity between the strains of human and porcine origin.
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Our methods are found to be efficient and fast, and our methods demonstrate a significant reduction in computational time and feasibility.
Compared with one of the top performing methods in the 2004 Face Verification Competition (FVC2004), our methods demonstrate a clear advantage over existing methods in accuracy, computation efficiency, and memory cost.
These methods demonstrate a higher predictive validity and are transparent and replicable [ 43, 44, 46].
Importantly, in our study PrP3F4 expression caused a reduction in the number of release-ready vesicles with simultaneously enhanced pvr as determined by independent methods demonstrating a synaptic role of PrPC.
This method demonstrated a complete penetration of one cell into another (Fig. 1f,h).
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