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Mutant mice display laterality defects and shorter cilia with irregularities in the axonemal structure but pronephroi were not studied (70).
Furthermore, Dkk3-deficient mice display hyperactivity.
Caveolin-1 knockout mice display BBB hyperpermeability46.
Conversely, DBA/2J mice display low rates of ethanol consumption.
Pax3 mutant mice display absence of muscular diaphragm.
Homozygous mice display erythrodontia, moderate photosensitivity, hepatosplenomegaly, and hemolytic anemia.
WNT7A mutant mice display several Müllerian duct derivative abnormalities.
Treated dy2J/dy2J mice display substantial improvement in muscle histopathology and function without signs of paralysis.
Heterozygous neuregulin 1 mice display greater baseline and Delta 9 -tetrahydrocannabinol-induced c-Fos expression.
Glucose intolerant NAS-drinking mice display normal insulin levels and tolerance.
Regan, C. P. et al. Erk5 null mice display multiple extraembryonic vascular and embryonic cardiovascular defects.
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