Albeck et al. (Albeck et al., 2008) using single-cell analysis approaches demonstrated that upon defined metabolic conditions, cells induced to extrinsic apoptosis can recover.
The consistency observed between solution and nanosuspension IV formulations supported our modeling and demonstrated that upon injection, the DCU nanoparticles dissolved instantaneously and completely in the blood.
It is demonstrated that upon reduction to a one-dimensional case, the method is transformed to the known Ford and Fulkerson algorithm.
Although all scaffolds supported pre-osteoblast cell viability, alkaline phosphatase (ALP) staining demonstrated that upon induction, differentiation was pronounced in case of scaffolds with 10% HMPC scaffolds.
We developed a three-step engineering strategy to construct an optogenetic PKA (optoPKA) and demonstrated that, upon illumination, optoPKA migrates to specified intracellular sites.
We have developed a vital method that allows fluorescence-activated cell sorting of cells at different stages of the apoptotic pathway and demonstrated that upon pharmacological inhibition of Apaf1, cells recover from doxorubicin- or hypoxia-induced early apoptosis to normal healthy cell.
Wei et al. demonstrated that, upon osteogenic induction of MSCs, the levels of proteins involved in mitochondrial biogenesis are increased, including PGC-1α, mtTFA, DNA polymerase γ, enzymes of the TCA cycle, and protein subunits of respiratory enzymes (Hsu et al., 2016).
These results demonstrated that upon Y-27632 treatment the increased colony-forming activity is from the LSC basal cells.
Our results demonstrated that upon arrival in cytoplasm, miRNA activities can be modulated locally by the 3'UTR.
Our study also demonstrated that upon PL injection, the formed tumors by inoculating DU145 or PC3 cells into nude mice underwent a regression, by triggering an apoptotic processes.
In our study we demonstrated that upon nucleolin or ligand stimulation the DNLS mutant of ErbB1 does not undergo phosphorylation (Figure 4A).
