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The comparison of the AUC indicated that the total cell death marker is significantly different from the apoptotic marker (total cell death marker AUROC versus apoptotic marker AUROC: P = 0.0006; total cell death marker AUROC versus necrotic marker AUROC: P = 0.73; apoptotic marker AUROC versus necrotic marker AUROC: P = 0.0505).
For EXPLoRA a marker is significantly identified if the posterior probability assigned to the marker is larger than 0.95.
This marker is significantly associated with frost tolerance with both 'Intro' and 'Tokak' possessing the more tolerant allele.
A marker is significantly linked with the phenotype if its p-value passes correction for multiple testing at a 0.05 significance level [ 7, 20].
For MULTIPOOL a marker is significantly linked if its LOD (log10 likelihood ratio) score falls within a 90% confidence interval [ 16].
If a marker is significantly associated with outcome when the effects of other possible confounding factors are controlled, then the marker is considered to be prognostic.
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Moreover, collagen type I, a fibrocartilage/bone marker was significantly higher only in stiff scaffolds without plasma clot.
The number of subjects who had more than one marker was significantly larger in the SN+ subgroup than in the non-hyperechogenic group (9.2% vs. 2.1%).
No marker was significantly associated with HRY in all the six environments.
Consistent with these results was the observation that CD326 antigen, an epithelial marker, was significantly downregulated in 10A-TG2 cells.
The 12669C>A marker was significantly associated with IMCL (P = 0.0369 for the GLM analysis and P = 0.0055 for the QTDT test, respectively).
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