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In addition, the level of MRP8/14 concentrations analyzed with the two assays varied substantially.
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Primary outcomes, such as 24-hour UUN levels, nitrogen balance, serum albumin concentrations, and prealbumin concentrations were analyzed with a generalized linear model for repeated measures using dummy variables.
In 2007, plasma glucose concentrations were analyzed with a clinical chemistry analyzer (AU400; Olympus), and serum insulin concentrations were measured by microparticle enzyme immunoassay kit (Abbott Laboratories Diagnostic Division, Dainabot).
DC cultured from WT or Siglece −/− bone marrow were stimulated with indicated concentrations of LPS (A ), or poly(I C) (B ) for 16 hr, and supernatant cytokine concentrations were analyzed with cytokine bead array.
In the preterm labor group procalcitonin concentrations were analyzed with reference to laboratory indices suggestive of infection.
Seven equally spaced concentrations were analyzed with eight replicates at each level.
Knee synovial fluid biomarker concentrations were analyzed with a custom human SearchLight Proteome Multiplex Protein Array.
The hemoglobin, cholesterol, and triglyceride concentrations were analyzed with standard laboratory assays.
Supernatants were harvested 48 h after infection and the mCCL21 concentrations were analyzed with an ELISA kit (Boster, Wuhan, China).
For calculation, relative values of serum concentrations were analyzed with the first value (2 min) being set to 100%.
The correlation between measured and predicted tacrolimus blood concentrations was analyzed with a Spearman rank correlation coefficient.
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