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EGF-R acquisition recruited quiescent SVZ cells to proliferate and it increased their rate of proliferation (Alagappan et al., 2009).
The increased rate of proliferation of the hindbrain progenitors was also confirmed using BrdU labeling of the proliferating progenitors.
These progenitors have a limited rate of proliferation and their maintenance is crucial for completion of the anterior-posterior axis.
However, their low rate of proliferation limits obtainable space-time yields due to inefficient biomass accumulation.
Their effectiveness was initially thought to be due to the high rate of proliferation of cancer cells.
However, there is no correlation between cell size or rate of proliferation on the size of the mutant territory.
The rate of proliferation of neural stem cells decreased with increase in the modulus of the hydrogels.
High rate of proliferation, active migration, and invasiveness into non-neoplastic tissues are specific properties of neoplastic transformation.
Osteoblastic cells had a high rate of proliferation on all examined films and expressed alkaline phosphatase activity, an early-stage differentiation marker.
The rate of proliferation and survival was measured by radio-labelled thymidine incorporation method.
NP-Pt activated apoptosis as well as decreased the rate of proliferation of the brain cells.
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rate of diffusion
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rate of distribution
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rate of redeployment
frequency of proliferation
percentages of proliferation
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