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Moreover, to examine the effect of CatL-inh administration on T cell activation, CD44 expression, an activation marker, was analyzed using PLN T cells.
Each marker was analyzed separately.
Each marker was analyzed for each group separately.
After compiling alignments of orthologous sequences, each molecular marker was analyzed independently and in a concatenated supermatrix.
aEach serum marker was analyzed separately in the model, adjusting for age, sex, smoking status, clinical stage, and treatment.
1 Sequence of the two or three selective nucleotides at the 3' end of the AFLP primer Each polymorphic marker was analyzed by Chi-square tests.
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The PCR products produced by the GS5-indel1 marker and the SCM2-indel1 marker were analyzed by Fragment Analyzer.
Selected nutrients and acid-insoluble ash (used as an internal flow marker) were analyzed in the starter and feces to estimate digestibility.
The expression levels of different surface antigen markers as well as an intracellular proliferating marker were analyzed from GFP positive EBV infected cells.
The non-injected cells were scraped off and the injected cells (identified by the co-injected fluorescent marker) were analyzed by EM.
Changes from baseline to week 48 of each marker were analyzed for association with change from baseline to week 48 in CD4+ cell count using Pearson's correlation.
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