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In this study, we evaluated the functions of ovarian cells by measuring the change in androgen concentrations.
We next evaluated the functions of the hyperoxia-induced, epithelial cell-derived EVs, using alveolar macrophages as the target cells.
To understand better the regulatory specificity of an individual FC identity HD, we evaluated the functions of atypical binding sites that are preferentially bound by Slou relative to other HDs within muscle enhancers that are either activated or repressed by this TF.
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We further evaluated the function of H3mm7 in isogenic C2C12 cells, which express H3mm7 prior to differentiation stimuli and are used as a differentiation model of myogenesis24.
Following TD exposure, we evaluated the function of specific mitochondrial electron transport chain complexes.
In this study, we evaluated the function of nestin in zebrafish embryogenesis by injecting nestin morpholino (MO) into fertilized eggs.
We presently evaluated the function of the AP-1 subunit JunB in cytokine-mediated β-cell dysfunction and death.
We next evaluated the function of ICAM-2 WT and variants in an in vivo model of metastatic neuroblastoma.
Then, we evaluated the function of the PI3K/Akt and ERK pathways in VEGF-induced VEGFR1 expression in HDMEC.
We then evaluated the function of TGF- β and IL-10 in MSC-DC-mediated Treg differentiation.
Thus, we evaluated the function of the putative NES and NLS signals, exploring their ability to direct the subcellular localization of EGFP, used as a reporter.
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