Although cool-sensitive fibers are largely C-fibers, this lead us to suspect that the small number of P-mTOR positive A-fibers we detected are probably sensitive to cooling and contribute to the acetone sensitivity in nerve injury models of neuropathic pain.
Elasmobranchs, such as rays and sharks, have distinctive sense organs, called ampullae of Lorenzini, that are highly sensitive to cooling.
Microelectrode investigations suggest that just three receptor cells located in the third antennal segment and probably not more than one receptor cell in the maxillary palp are sensitive to cooling.
The results have shown that the α→γ transformation is sensitive to cooling rate and is accompanied by large discontinuous changes in resistivity and thermal arrest.
Furthermore, the graphene formation under PT-CVD is much less sensitive to cooling rate than that observed for T-CVD process.
It is found that the stabilizing mechanism of lattice distortions is the most sensitive to cooling rate, and that of oxygen vacancies is relatively insensitive while providing roughly four times more stability against m phase.
The morphology of the transformation products is shown to be sensitive to cooling rate and the results of the microstructural observations are used to construct a schematic continuous cooling transformation (CCT) diagram for these alloys.
While eggs and larvae (in open brood cells) can tolerate lower temperatures for some time, the pupae (in sealed brood cells) are very sensitive to cooling.
