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Increased GDF11 levels in aged mice also improved muscle structural and functional features and increased strength and endurance exercise capacity.
Vitamin E and vitamin C administration in fipronil exposed mice also improved histological architecture of the kidney and brain when compared with fipronil alone treated groups.
Mbnl1−/− mice also improved with time, acquiring the task whether measured as latency (Figure 4Ci) or pathlength to find the platform (Figure 4Ci inset).
Moreover, the transfer of T cells from Bcl-2 overexpressing mice into wild type septic mice also improved survival [ 124].
Augmented EPOR signaling in cEPOR TG mice also improved social memory, which is partly dependent on hippocampal functions [ 32].
Daumone in aged mice also improved hepatic insulin signaling and systemic insulin sensitivity and attenuated hepatic inflammation and macrophage infiltration, possibly through the suppression of NF-κB signaling.
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As the information content of the additional data source improves, variance estimates from D2 mice calculated with increasing sample sizes, the ability of the common variance to describe the observed gene variances, calculated from four replicates of B6 mice, also improves.
The general condition of the mice was also improved: the OVA-fed mice gained weight, while the control groups lost weight.
hPSC-derived EPs successfully formed functional capillary vessel networks with anastomoses to host vessels in vivo after engraftment into immunocompromised mice, and also improved heart function in mice after myocardial infarction (MI).
Intradermal administration of zinc oxide nanoparticles was found to significantly reduce the skin infection and inflammation in mice and also improved infected skin architecture.
Intradermal administration of ZnO-NPs significantly reduced the skin infection, bacterial load and inflammation in mice, and also improved infected skin architecture.
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