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(2015, May 1)
Likewise, the expression of the G2/M reporters CYCB1;2 , CYCA2;2 and CYCA2;3 remained unchanged, though a significant downregulation in CYCB1;2 was recorded in qPCR assay, which could again be explained as a delayed effect of MTX treatment
suggested that KPV may enter epithelial and immune cell cultures through the PepT1 transporter, where it appeared to slow IB- degradation and shorten NF-B activation windows while reducing ERK1/2, JNK, and p38 phosphorylation and lowering IL-8 output in these experimental settings
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