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Rat strains differ in sensitivity to the disruptive effects of dopamine agonists on sensorimotor gating, measured by prepulse inhibition (PPI) of startle.
Previously, we showed that rat strains differ in their free exploration of novel areas, i.e. the surroundings of their familiar home cage when the lid was removed.
Rat strains differ in their susceptibilities to mammary carcinogenesis.
Various outbred and inbred rat strains differ in their relative susceptibility to AA (Table 1).
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Artificial selective breeding, starting with a founder population of 186 genetically heterogeneous rats (N NIH stock), was used to produce rat strains differing in inherent aerobic capacity.
The relative proportion of CD45RChigh and CD45RClow T cell subsets varies between rat strains that differ in their susceptibility to develop immune mediated diseases [22], [23], [25].
To investigate the relationship between microRNA expression and type 2 diabetes, we compared global microRNA expression in insulin target tissues from three inbred rat strains that differ in diabetes susceptibility.
The two mouse strains differed markedly in basal anxiety level.
The overall time-budgets of the two strains differed significantly.
The E-Pae strains differed at 0-6×10−7 0-6×10−7tionsubstitutions
However, strains differed quantitatively.
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