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All samples displayed a straightforward behavior during stepwise demagnetization (Fig. 5a d), yielding reverse ChRM directions that show a directional similarity between samples treated by AFD and ThD.
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Phage samples treated by heat and UV were characterized by spectrophotometry and electron microscopy.
The XRD analysis indicated the enhancement of nanocrystallization for the samples treated by USRP and the formation of a nitride layer for the samples treated by USRP and PN.
Rp increased by factor 8 times for samples treated by zirconate dilute solution.
Asterisks denote statistically significant differences between samples treated with and without 1 mM NH4Cl (*, P < 0.05 by Student's t-test).
Asterisks denote statistically significant differences between samples treated without 1 mM NH4+ and each treated sample (*, P < 0.05 by Student's t-test).
Figure 11 SEM morphologies of sample (a) untreated (b) surface of sample treated by Primal SF (c) interior of sample treated by PrimalSF (d) surface of sample treated by hybrid material (e) interior of sample treated by hybrid material.
Gene set enrichment analysis was performed between the two groups of samples (treated and non-treated by abexinostat).
Asterisks denote statistically significant differences between the samples treated without nitrogen nutrients (-N) and each treated sample (*, P < 0.05 by Student's t-test).
Significance of differences between control and samples treated with various drugs was determined by one-way ANOVA followed by post hoc least significant difference (LSD) test.
∆∆Ct values were obtained by subtracting ∆Ct values of control samples from those of treated samples.
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