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Intriguingly, multiple means may exist to post-translationally control BiP activity to benefit cells under oxidative stress.
Previous studies have shown that reversible IS-induced mutations with precise excisions may benefit cells in fluctuating environments [ 35, 36].
Inactivation of ATPase activity for a pool of BiP upon oxidation may additionally benefit cells by limiting ATP turnover during oxidative stress.
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The results indicated that the highly porous and interconnected structure of scaffolds could benefit cell ingrowth.
Bioactive glass is known to benefit cell interactions of polymeric tissue engineering scaffolds.
This is a significant improvement in lifetime determination, which will benefit cell designers.
It suggested that stronger cell substrate interactions benefit cell adhesion, and better cell flexibility improve cell spreading.
The resulted HA scaffold with surface stripe pattern is proposed to benefit cell attachment and tissue ingrowth.
Moreover, MTT assessments suggested that the smaller pore size should benefit cell attachment and growth in the scaffold.
These results agree with finite element predictions and suggest that reduction of electrode thickness does not exclusively benefit cell performance.
The ability to access and manipulate larval stage cells would greatly benefit cell and tissue specific studies of post-embryonic developmental events.
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