Cell
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CELL. A small room in a prison. See Dungeon.
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References in periodicals archive
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Thus, which protein regulates the global GTP level during the cell cycle remains an important unanswered question because there are large quantities of cytosolic GTPase protein-based machineries, such as the ribosome complex and mitotic spindles, in the cytosol, both of which are regulated during cell cycle progression.
Casticin induces apoptosis and G0/G1 cell cycle arrest in gallbladder cancer cells.
A main mechanism by which PLK1 inhibits antitumor immunity lies in that the PLK1 upregulation activates the cell cycle which may decrease tumor immunogenicity (Figure 8(a)).
Once the cells have entered a state of senescence, numerous genetic changes take place including cyclins, CDKs and the cyclin - dependent -kinase inhibitors 12 the cell cycle check points are controlled by p53 and pRB proteins; the tumour suppressor genes and disruption in this pathway due to DNA damage responses or other factors leads to replicative lifespan and crises.13 A lot of work has been done on fibroblasts and keratinocytes and their attachment to FN.
While, compared with control siRNA, silencing FOXO3A had no significant effect on the cell cycle (Figure 2(d)), expression of the FOXO3A downstream targets CDKN1A and CDKN1B was decreased, with the effect on CDKN1A being particularly striking (Figure 2(e)).
Sevoflurane Decreased Cell Cycle Exit and Increased S-Phase Duration of Neural Progenitors in the Fetal PFC.
The effect of TNA nanosurface on cell cycle progression for a 7-day incubation period was studied on epithelial HT29 cells, compared to control surfaces, namely, plastic, glass, and TiP.
In this study, we presented the evidence that ethanol extract of root of Prunus persica can inhibit the growth of HepG2 cells in vitro by impairing cell cycle and migration.
FGF21 Showed Similar Expression Pattern to Myogenic Marker Genes and Cell Cycle Exit Genes during Myogenic Differentiation.
The functional activity of these proteins are well deliberated as the hypophosphorylated pRB has the ability to restrict cell cycle progression at the G1/S transition of the cell cycle by binding E2F transcription factors, which is thought to be essential for its tumor suppression function.
In parallel, honokiol induced activations of caspase-8, -9, and -3, apoptosis, and G1 cell cycle arrest.
Mitosis is a part of the cell cycle process by which chromosomes in a cell nucleus are separated into two identical sets of chromosomes, each in its own nucleus.
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