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The peripheral tissues in these mice displayed variable phase relationships with respect to the feeding time.
Consistent with these observations, peripheral tissues in our control mice displayed variable phases relative to the FR schedule when conducted in constant darkness.
F2 mice displayed variable susceptibility to each of these traits and were divided into susceptible and resistant groups based on whether they exhibited the trait or not.
Since F2 mice displayed variable susceptibility, they were divided into two groups, low F2s and high F2s, based on whether or not they exhibited functional motor deficits or CNS vascular permeability.
T47D breast cancer xenotransplants in mice displayed variable acidosis (pH 6.5 to 6.9) and tumor regions with elevated GLUT1 displayed resistance to exogenous prolactin despite unaltered levels of prolactin receptors and Stat5.
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Further assessment revealed that in all mice these cells displayed variable expression of CD14 and CD34.
For example, by mating the lox-eGFP-lox-DTA mice with the Pax3-Cre mice, the mutant line displayed variable perinatal lethality rates with a lower number of astrocytes in the dorsal spinal cord, but without an increase in their BBB permeability.
It is noted that, while livers from Plk4+/- mice were grossly normal, they displayed variable amounts of Plk4 transcripts with an average that is significantly lower than that found in Plk4+/+ mouse livers.
End-stage symptomatic hA30Pα-syn mice but not their healthy littermates also displayed variable severity of ubiquitin pathology (Figures 4C and 5B).
The second triple mutant γB S11R/S11R) α8(Kiα3/−) α3 mice, with one copy of the α8(Kiα3) allele and without endogenous wild-type α3 connexin, displayed variable lens phenotypes.
However, the cells from different animals displayed variable osteogenic potential.
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