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Models studied here are cantilever beams with concentrated moments placed at belt truss locations.
For example, decreasing SNR due to reduced radiation exposure resulted in a "shell" of small additional thickness to the bone STL models studied here.
In the third-order neuronal models studied here, the rapid-spiking solutions - which exist for parameter values before the torus bifurcation values - deform continuously into bursting solutions as the parameter increases beyond the torus bifurcation point.
In the mouse models studied here, we found that the majority of bacilli were indeed intracellular within macrophages through most of the infection.
We find that the decaying response, on the other hand, is well fit by an exponentially decaying sinusoidal function for all models studied here.
Specifically, the existence of a hard threshold introduces an instantaneous component into the response onset of a leaky-integrate-and-fire model that is not present in other models studied here.
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The propofol model studied here is a prime example.
The model studied here presents results on firms' equilibria when competing against time.
The monolayer of MoS2 model studied here contains 24 atoms in total (8 Mo and 16 S atoms).
In the JWBG1 model studied here, for (c<1-alpha ) everything is entirely similar to what occurs in the JWBG2 model in Olaizola and Valenciano (2015a).
Interestingly, in the model studied here, LRTCs were observed when h = 1 / N but not for lower levels of external input.
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Justyna Jupowicz-Kozak
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