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We determined the contribution of gp150 by comparing sera from mice 2 months after infection with either wild-type or gp150-deficient viruses (Fig. 4A).

We analysed the serum phosphoproteins that comprised cancer cellular signal pathways by comparing sera from PaCa patients and benign controls including healthy volunteers (HVs) and pancreatitis patients.

We tested further the gH/gL dependence of gBΔ2 30 virus neutralization by comparing sera from mice infected with gL+ and gL− MuHV-4.

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To evaluate the specificity of the test we compared sera from 26 normal women with sera from 26 normal men matched for age.

In one study we compared sera and SF from 15 RA patients and 15 healthy control sera.

By comparing the binding of sera from humans infected with WNV or other flaviviruses to the wild type and the mutant E proteins, we analyzed the potential of this technology to specifically detect WNV antibodies.

Sera from women had significantly higher levels of antibodies against NP561 compared to sera from men of the same area in Ghana (p = 0.04).

VRP-TRP2 immune sera delayed tumor growth when compared with sera from mice immunized with VRP expressing other antigens (Figure 6A).

ANXA2 is significantly increased in the sera of HCC compared with the sera from healthy, benign tumor, hepatitis, and cirrhosis controls and other malignant tumors.

Rapid and strong stiffening of primary neutrophils and monocytes was induced within 30 minutes (mean ET >50 seconds) by sera from the ARDS group compared with both the healthy subjects and the ACPE groups (mean ET <1 second) (p < 0.05).

To analyse the influence of clinical parameters of disease activity on the inhibitory activity exhibited by the sera from patients with RA, sera from 20 patients with non-active disease were compared with sera from patients with high disease activity (for definition of active and non-active RA see the Patients and methods section).

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