Barely Significant

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Given that naïve cells do not produce cytokines upon anti-CD3 and anti-CD28 stimulation, the analysis of total CD8 T cells showed highly significant differences between iR- positive versus iR-negative cells in the case of iRs that are inherently expressed at clearly distinct levels between naïve versus differentiated subsets.
Inhibitory Receptors Beyond T Cell Exhaustion.
Front Immunol · 2015 · PMC4481276
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We performed GO and KEGG enrichment analysis of FAM110A-related genes in LIHC and found highly significant enrichment of GO terms associated with immune function, including interferon-γ production, T cell activation, B cell activation, adaptive immune response, mast cell-mediated immunity, and positive regulation of cell activation.
There is a marginal trend for GMRs to be closer to 1 using the FLUCOP protocol. %GCVs show a similar result ( Figure 4B ), with slightly lower (but not statistically significant) %GCVs for FLUCOP testing with the B strains, but little or no difference for H1N1 and H3N2 testing. 3.2.6 Impact of using ether split antigen for B virus HAI testing Laboratories testing B viruses used a mixture of native antigen and ether split antigen in their assays.
For metabolites contained in each subgroup, phosphatidylcholine (PC), lysophosphatidylcholine (LPC), phosphatidyl-ethanolamine (PE), and lysophosphatidylethanolamine (LPE) were significantly reduced in dNK cells and phosphatidylinositol (PI), phosphatidylserine (PS), and phosphatidylglycerol (PG) showed a trend of reduction ( Figure 3C ), indicating downregulation of glycerophospholipid metabolism in dNK from pNK cells.
In our study, HLA-DRB1*09:01 , - DQA1*03:02 and - DQB1*03:03 , the susceptibility alleles for MPO-AAV in East Asian populations ( 12 – 16 ) showed a trend toward a higher risk of relapse of MPO-AAV in a Japanese population, possibly suggesting that the susceptibility alleles for AAV may also be associated with relapse in each ethnic group.
The activities of AKP were fluctuant within limits in both serum and hepatopancreas, except for the extremely significant up-regulation of vaccinated groups in the hepatopancreas at 0 dpi, but the regulation of vaccination was also inconsistent at various time points post infection, indicating that the variable effects of vaccination on inflammatory response upon infection.