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Pain interference was assessed on a 0 (does not interfere) to 10 (completely interferes) rating scale.
The degree of interference was assessed through comparison of the chromatograms of blank plasma with the chromatograms of plasma spiked with lesinurad and IS.
Interference was assessed by salmon DNA sample processing control (SPC) and internal amplification control (IAC) assay analysis results and pre-established acceptance criteria of <3.0 and <1.5 cycle threshold (Ct) offsets from control samples, respectively.
The efficiency of RNA interference was assessed by qRT-PCR and immunofluorescence analysis (IF).
On the same chip, RF interference was assessed and false positive results caused by RF were eliminated.
For utility with anthrax therapeutics, AIG interference was assessed by spiking AIG at an equivalent of 200 μg/mL anti-PA IgG into all 15 standards, plasma blank, and QC samples over the entire range from 24.3 to 0.0024 ng/mL.
Similar(53)
Depression, coping, pain intensity and interference were assessed.
The specificity of the different RNA interference (RNAi) platforms was assessed by DNA microarray analysis.
The severity and interference of pain was assessed via the self-reported numeric rating scales (range, 0 10) of the m-BPI-sf [ 15].
The degree of interference by endogenous substances was assessed by inspection of chromatograms derived from processed blank plasma samples.
Furthermore, possible drug interference with adrenal steroidogenesis was assessed by measuring 17-hydroxycorticosteroid (17-OHCS) urinary levels.
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