The survival of mice was evaluated by the log-rank (Mantel-Cox) test.
Collagen-induced arthritis (CIA) in DBA/1J Nampt+/− mice was evaluated by ELISA, micro-CT, and RNA-sequencing (RNA-seq).
One day after the Y maze test, the long-term memory of mice was evaluated by a passive avoidance test.
The in vivo skin analgesic effect in mice was evaluated using the von Frey tests.
The pharmacokinetics of gene drugs after intravenous injection into mice was evaluated based on clearance concepts.
Survival of the mice was evaluated from the first day of treatment until death or became moribund, at which time points the mice were euthanized by cervical dislocation.
(c) Cardiac function of the mice was evaluated by echocardiography before, 3rd and 5th day of TAM treatment, and at the indicated time point.
The degradation of NPG by MICE was evaluated through UV visible, fluorescence and Fourier Transform-Infra Red spectroscopy.
In vivo antimalarial efficacy in Plasmodium berghei infected mice was evaluated for four compounds, all of which showed good activity following oral administration.
To explain this phenomenon, the effect of genistein in spleen and liver of malaria-infected mice was evaluated by histological examination.
The bone architecture of F508del Cftrtm1Eur and wild-type (WT) littermate mice was evaluated by bone densitometry, microcomputed tomography, and analysis of the dynamic parameters of bone formation.
