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Moreover, only baseline markers were analyzed, while the effect of current markers may be crucial, for instance the raise levels of bilirubin during atazanavir-containing antiretroviral therapy [ 28].
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Associations between subcutaneous adipocyte size at baseline, with and without adjusting for baseline FM, and overfeeding-induced changes in metabolic parameters (fat depots, glucose infusion, circulating and tissue markers) were analyzed using linear regression models.
Distortions of the array of nanodots used as spot markers were analyzed near the triple junction.
Forty SSR markers described by Spiller et al.24 as bridge markers were analyzed on the five parental lines: J14-3, OB, RF, VS, and LC.
For each gene, at least one marker within the gene and/or two tightly linked flanking markers were analyzed.
Peripheral blood lymphocyte markers were analyzed simultaneously.
EMT markers were analyzed by western blot.
Moreover, apoptosis markers were analyzed by western blot.
Several stemness genes and epithelial-mesenchymal transition markers were analyzed.
EMT and putative CSC markers were analyzed using Western blotting.
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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