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The strong correlations found between the proangiogenic factors revealed that mice showing high expression of angiogenic growth factors VEGF-A and VEGF-B, also showed high expression of their receptors, especially VEGFR-2.
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Formalin-inactivated RSV immune mice showed high levels of pulmonary inflammatory cytokines, macrophages, IL-4-producing T cells, and extensive histopathology.
In fact, individually housed mice showed high behavioral arousal, as well as altered immuno-endocrine parameters, when challenged with mild psychological novelty-stress.
In vivo microPET and optical imaging of U87MG tumor-bearing mice showed high uptake of the 64Cu-DOTA- AF SAv/biotin-PEG-RGD2 in the liver, spleen, and tumor (Fig. 5a).
As shown in Figure 1A, BMDCs originated from control mice showed high levels of Jak2 expression, while Jak2 was undetectable in BMDCs of tamoxifen induced mice.
TXNIP knock-out mice show high levels of accumulated inactive PTEN with higher levels of activated AKT resulting in more glycolytic oxidation in their skeletal muscle [94].
VLP vaccinated mice showed high levels of lung IgG antibodies specific to the homologous virus, and their levels were similar before and after challenge (Fig. 6A).
Vaccinated mice showed high antibody levels in sera at day 4 post challenge, which is consistent with the generation of antibody secreting cells in spleen and bone marrow.
In contrast, DRESSA24 mice showed high levels of basal SEAP activity.
GFP+ Schwann cells purified from GFP mice show high susceptibility to ML infection.
Some mice, however, had normal levels of ALT and AST whereas some other mice showed high transaminase levels.
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