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The diagnosis efficacy of each marker we studied to detect renal dysfunction is shown in Tables 4 and 5.
By contrast, using flow cytometry and a highly-specific PGC marker, we studied both early and late allantoic bud stage embryos [53].
To further characterize the performance of WT1 expression as an MRD marker, we studied the association of WT1 expression levels in PB and bone marrow (BM) specimens.
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To investigate the effect of the low-dosed etonogestrel-releasing contraceptive implant Implanon on new cardiovascular risk markers, we studied the effect of this implant on adiponectin and its metabolically important isomer high-molecular-weight adiponectin (HMW).
Curiously, expression of BCL6 protein was related to absence of the unfavorable markers we studied in plasma.
Of the markers we studied, NTx appears to exhibit the greatest discrimination between participants with and those without BMLs.
Our studies revealed that some xenograft cells express more than one of the five surface markers we studied and significant correlations between different markers emerged.
However, we argue that the Rhizophagus isolates under study might be heterokaryotic, at least for the putative single copy markers we studied.
Fourth, we showed that the stainings of all the immune markers we studied were significantly decreased in the centre of the tumour.
In summary, among all the 26 biochemical markers we studied, only the level of UA was no significant difference in seminal plasma and serum.
Of note, we found that the expression of the six proapoptotic markers we studied (Bax, Smac, Fas, FasL, caspase-3, and PARP) was higher in the SCS compared to the DS chorion.
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Justyna Jupowicz-Kozak
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