This effect may help explain experimental observation of different biofilm phenotypes under what are assumed to be similar or even replicate growth conditions.
These two processes may explain the experimental data.
The increase of friction and compression rate can lead to early appearance of tension stress in the deformation localisation zone, which may explain the experimental finding that crack tendency increases with higher compression rate and poorer lubrication.
The significant factor accumulation that can occur if the particles were to embed in the cell membrane may explain observed experimental data regarding enhanced T-cell activation and nanoparticle-mediated improvement in the drug delivery process to non-internalizing cellular targets.
This may explain our experimental observations, in which EBCall (in its default setting) failed to identify the majority of sSNVs despite the fact that the normal references we used were sequenced from the same Illumina platform as the tumors.
This conclusion may explain some recent experimental observations.
Furthermore, molecular determinants that may explain the observed experimental data were found by MD simulations analyzing the interaction of GR LBD-ligand complexes and a peptide corresponding to the TIF2 coactivator.
Our procedure, including the 32Dcl3 cell line we use, may explain why our experimental system to induce apoptosis is so fast and synchronized.
These data suggest that bruxism and central orofacial pain can coexist, but are two independent symptoms, which may explain why numerous experimental and clinical studies fail to reach unequivocal conclusions.
