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Here, our data indicate that the level of serum IL-7 in CTX-treated mice is less than that in Rag2KO mice (~30 pg/ml).
Hence the concentration of Aβ1 42 in acute slices from CRND8 mice is less than 150 pM.
One day after injection, the ratio of myogenin in cardiotoxin-treated to PBS injected muscle in α-KO mice is less than 25% that of control mice.
It is also interesting that the defect we observe in Egr-2f/f lck-Cre mice is less profound than the defect reported in the fetal liver chimeras from Egr-2-/ mice [11].
This may also explain why high TSLP levels in fetal or neonatal Notch mutant mice cause a B-LPD [13], while the effect on B cells in adult mice is less dramatic.
In contrast to cocaine, the l-DOPA administration for mice is less well-established.
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Some obesity researchers, though, say there may be other reasons that the mice were less fat.
When the histone modification was chemically blocked, the mice were less likely to become addicted.
KO mice were less physically active than WT in cages with or without running wheels.
Activated mice are less likely to interact with intruders, while lower activation causes mice to ignore pups in favor of interacting with other mice.
The genetically modified mice were less anxious than the normal mice and were more resilient in the face of social stress.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com