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The tumor microenvironment influences these cell fate decisions in a metabolic manner.
Nsph-CM also regulates cell fate decisions [4] [5].
Within this approach cell fate decisions are basically reversible.
Such fate decisions are regulated in part by transcription factors [12].
The concentration of the morphogen is critical for fate decisions in the responding cells.
They might even be involved in the control of cell fate decisions [29], [30].
Wnt/β-catenin signalling is important for cell fate decisions during many developmental programs.
NOTCH proteins are single-pass trans-membrane receptors that regulate cell fate decisions during development.
We investigated whether Sox2 is involved in controlling cell fate decisions at an earlier stage.
Both manipulations influence fate decisions.
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Cell-fate decisions remain poorly understood at the chromatin level.
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