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burn model
Ignition and detonation of solid explosives: a micromechanical burn model
      
pyogenes wound colonization on bacterial translocation in a burn model
      
In earlier experiments, it was shown in a burn model that BT exceeded the role of wound dissemination when burn wounds were colonized with Pseudomonas aeruginosa.
      
In this study, the authors investigated the relationship between peroxynitrite-mediated tissue nitration and tissue damage with thermal injury using an experimental burn model.
      
With an experimental burn model in mice, we were able to demonstrate the identity of a specific burn toxin isolated from skin burntin vitro and producedin vivo under identical thermal injuries.
      
Murine skin was thermally injured under controlled conditions in a standard high temperature burn model.
      
We also propose a new explosive burn model which incorporates a partial release of the heat of detonation in a fast reaction zone, followed by a diffusion-limited release of the remaining energy.
      
Hydrodynamic applications of the new burn model to LX-17 show that computed expansion and compression results both agree closely with experimental data.
      
Second, the behavior of burning cracks is addressed by coupling those differential equations to a burn model to show that burning cracks can exhibit either mild or violently unstable behavior.
      
The heating stage involves thermal expansion and decomposition according to an Arrhenius kinetics model while a pressure-dependent burn model is employed during the explosive phase.
      
As shown in Table 3, PA14 r was significantly less pathogenic than wild-type PA14 in a mouse burn model.
      
Contrary to other studies, we did not observe an increase in 02 consumption for enterally administered MCTs in this burn model.
      
Development of an acute burn model in adult mice for studies of cardiac function and cardiomyocyte cellular function.
      
For the Arrhenius burn model, the only irregularities currently capable of being modelled are the gas pores.
      
However, scientific evidence on the optimal duration of cooling in a consistent burn model is lacking.
      
It has been designed to operate either with the existing pore collapse hot spot model or with a particle burn model.
      
Sex hormones modulate distant organ injury in both a trauma hemorrhagic shock model and a burn model.
      
This is interesting in light of the decreased virulence of PA14 r in the mouse burn model.
      
The main disadvantage of the above burn model is that it is not possible to visualize dynamic events that occur after a burn injury.
      
The total strain value T is divided by the current burn model time-step to get a strain rate for the shell.
      
 

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