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T3 compared to controls modulated cell multiplication, up-regulated collagen synthesis time and dose dependently, and stimulated protein synthesis.
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It is presumed that the brakes on cell multiplication come off because of it, leading to uncontrolled proliferation of cells into a tumor.
This results from a balance between cell multiplication by division and cell loss from the SAM.
Accurate chromosome segregation during mitosis is an essential event for proper cell multiplication.
G2/M phase is important for cell multiplication.
Panobinostat modulated cell cycles and angiogenic genes.
► We show that T3 dose dependently regulates cell multiplication.
Moreover, GGPP alone significantly decreased cell multiplication as well.
Signals stimulate cell multiplication of both the plant cells and the bacteria.
Similarly, in CCL-51 cells GGPP could rescue ibandronate attenuated cell multiplication but, differentially, did only marginally influence cell multiplication (Fig. 7C).
Time course of cell multiplication was also measured by cell counting.
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