Przykłady mice

• Nobody else is here but us little mices.

• I suspect that for a lot of the more basic research, it will be mice and rats and rabbits that will be used.

• On the one hand, clear biobehavioral differences exist between strains of mice and rats on dimensions such as behavioral and adrenocor tical reactivity to stressors.

• Neonatal endotoxin exposure alters the development of social behavior and the hypothalamic - pituitary - adrenal axis in selectively bred mice.

• Prenatal nicotine exposure modifies behavior of mice through early development.

• When investigating new pathways or genetic defects, mice may die before prostate cancer actually develops, if indeed it does develop.

• As discussed above, both of these proteins have been localised to cilia in mice.

• Homozygous -thalassaemia is embryonic lethal in mice, since the globin switch occurs in utero.

• Mtmr2-null mice also have defects in spermatogenesis, which become apparent from 3 to 4 weeks of age.

• Modelling coxsackie-virus infection in pregnant mice in long-term experiment.

• More than half of them, however, used mice.

• However, it is now clear from classical experiments in mice and from examples of human genetic disease that this is not the case.

• Furthermore, no disease could be transmitted from these mice to either transgenic or non-transgenic mice.

• In addition, these mice display poor survival and a markedly reduced capacity for experimental clot lysis.

• The availability of gene-disrupted (knockout) mice has allowed an intensive investigation of specific immunological parameters that are associated with disease in the murine models.