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Tibial baseplates of a fixed bearing and a mobile bearing design were fatigue-tested in vitro to study their fatigue resistance.
These experiments demonstrate how flow cytometry can be used to measure cytotoxicity by earthworm coelomocytes cultured and exposed to DMBA in vitro to study the immunosuppressive effects of DMBA on NK-like effector cells of E. fetida.
Finally, the new configuration proposed here could be advantageously used in vitro to study the activity-dependent dynamics and plasticity of neural networks, and could also be adapted in vivo for the development of neural prostheses.
There have been many reports showing that hNPCs can be used in vitro to study the mechanisms of neurogenesis and also transplanted into the developing or adult rodent brain [8] [12].
In the present study we exposed F3 and F3.Akt1 hNSCs to hydrogen peroxide injury in vitro to study the neuroprotectiion provided by Akt1 under the conditions of oxidative stress, and the results indicate that F3.Akt1 cells showed a higher survival rate following H2O2 -induced injury as compared to the F3 controls (Figs. 2A C).
Many investigators use chondrocytes in vitro to study physiological and pathophysiological events while mimicking in vivo biological conditions.
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Plasmonic nanostructures are also employed in in vitro studies to study biological processes by using plasmon resonance energy transfer (PRET) [33].
Micro- and macro-flow systems have been used as in vitro platforms to study bacterial adhesion under physiological conditions.
Against this background, hESC-derived neurons could be an alternative in vitro model to study tau physiology and pathology.
Hence the vSMC-EC co-culture system represents a novel in vitro model to study vascular basement membrane assembly.
We developed an in vitro model to study whether MCP-1 interacts with MMP-1at the biological level.
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