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(D) Body weights of mice were assessed.
The mice were assessed for systemic side effects of therapy, and tumour sizes were measured daily.
Additional mice were assessed for histological changes in lung and heart.
In vivo [18F]FTC-146 uptand and pharmacokinetics in WT and S1R-KO mice were assessed by dynamic PET/CT imaging.
The effects of mechanical loading on bone mass and architecture in adult mice were assessed using micro-computed tomography and in vivo structural stiffness measures.
Bilateral hippocampal-lesioned mice were assessed in the standard, hand-run, discrete-trial rewarded alternation paradigm and in the automated paradigm, according to a cross-over design.
The mice were assessed for home cage activity.
Mosquitoes raised in the same containers as the mosquitoes used to bite mice were assessed.
Levels of ATRX protein in chondrocytes from ribs of newborn mice were assessed by immunoblotting.
The session after attaining extinction criterion, mice were assessed for reinstatement of instrumental responding.
Orally intoxicated mice were assessed similarly using this antibody neutralization assay.
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