As autophagy seemed to be differentially activated under normoxia and hypoxia, mTOR activity was studied to investigate the upstream signaling responsible for autophagy activation.
The periodicity of genome-wide transcriptional activity was studied to provide a global view of gene expression profiling [ 4, 6, 31, 32].
Two cell line models of tamoxifen-resistant ER-positive breast cancer, MCF7/HER2 and BT474, showing increased AP-1 and NFκB DNA-binding and transcriptional activities, were studied to compare tamoxifen effects on NFκB and AP-1 regulated reporter genes relative to tamoxifen-sensitive MCF7 cells.
Their microstructure, nanohardness, tribological properties and photocatalytic activity were studied and compared to conventional atmospheric plasma sprayed (APS) and HVOF-sprayed TiO2 coatings manufactured using commercially available feedstock.
The effect of PM on XRE reporter activity was studied in order to test if PM from dairies would activate the AhR signaling pathway.
The effect of temperature on α-amylase activity was studied from 20 to 90°C.
In addition, DPP4 activity was studied in relation to platelet adhesion in human umbilical vein endothelial cells (HUVECs).
Therefore, autophagy activity was studied in MMV compared to HMV.
In addition, to evaluate the efficiency of the conjugates as photosensitizers, their photophysical properties and in vitro biological activities were studied in comparison to those of CMP-OH.
To evaluate the efficiency of the conjugates as photosensitizers, their photophysical properties and in vitro photodynamic activities were studied in comparison to those of TPP-OH.
Other stronger cold-shock promoters and enzymes with higher lytic activity could be studied to increase the effectiveness of the autolytic system.
