Sentence examples for serum relative from inspiring English sources
In blood serum, relative OD initially increased after drying-off, before a drop around calving was observed.
The percentage of NO released from the O2-methyl and O2-acetoxyethyl compounds was higher (18.0 37.8% of the theoretical maximal release of one molecule of NO/molecule of the parent compound) upon incubation in the presence of rat serum, relative to incubation with phosphate buffer saline (PBS) at pH 7.4 (3.8–11.6% range).
The percentage of NO released from these diazen-1-ium-1,2-diolates was significantly higher (59.6 74.6% of the theoretical maximal release of 2 molecules of NO/molecule of the parent hybrid ester prodrug) upon incubation in the presence of rat serum, relative to incubation with phosphate buffer (PBS) at pH 7.4 (5.0 7.2% range).
The prodrugs were also remarkably stable in mouse, rat, and human serum (relative serum stability: human ∼ rat ≫ mouse) displaying a parabolic trend in the SAR with hydrolysis rates increasing with chain length up to eight carbons (t1/2 = 1.6 h for octanoyl prodrug 7 in mouse serum) and then decreasing again with higher chain lengths.
Amino acids increased in the PPARδ agonist treated mice serum relative to control were aspartate and isoleucine.
For each plate, the cut-off value was calculated as two times the percentage positivity of the negative control serum relative to the positive control serum [ 14, 17].
Furthermore the sputum from P2 showed markedly reduced virulence in G. mellonella, increased inflammatory properties, and enhanced serum susceptibilities relative to the blood isolates from the same patient, highlighting that Bcc also shows adaptive responses to the blood environment, even in the short term.
Finally, in patients with nutrition status determined (N = 6,923) there was no significant difference in serum Mg relative to nutrition status (ANOVA P-value < 0.001).
The distribution of 123I-labeled human serum albumin relative to target anatomy and catheter position was analyzed.Intracerebral CED infusions were well-tolerated and some resulted in a broad distribution of 123I-labeled human serum albumin, but target anatomy and catheter positioning had a significant influence on infusate distribution even within non-contrast-enhancing areas of brain.
However, a mouse model might not be readily translatable to human studies to estimate liver and kidney toxicities developing from catabolites due to differences in stability of radiolabelled conjugates in human serum and relative size of tissue compartments between mouse and human.
This unsuspected finding could not be explained by the observed modification of adhesion and growth factor associated signaling involving FAK, Paxillin, p130CAS, Src, AKT, GSK3β and ERK1/2 under suspension and serum withdrawal relative to adhesion conditions with serum.
