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Eight genes (Fkbp5, Irak1, Mobp, Dlk1, Plagl1, Ddc, Mllt2h, and Eya2) had significantly stronger expression in KO mice in all the tissues studied.
These results confirm that significantly stronger expression of NF-κB in both CT-2A tumor and cells compared to normal brain or mouse astrocytes.
The results for B cells (CD19+) in 33 patients and 27 controls (survey 1 and 2) and for B-cell activation markers (CD69+, CD95+) in 16 patients and 14 controls (survey 2) are presented in Table 2. Patients displayed significantly stronger expression of B-cell activation markers than did controls (P = 0.03 and 0.0001, respectively).
Five genes showed significantly stronger expression in exo (Table 4).
Inoculated R plants, however, showed significantly stronger expression of these genes relative to inoculated S plants.
We observed a significantly stronger expression of Calb1 in mutant subpallium when compared with control subpallium.
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In the present investigation, clear cell carcinoma showed significantly stronger TF expression than non-clear cell carcinoma (Table 2).
Tissues from clear cell carcinoma exhibited significantly stronger TF expression than tissues from non-clear cell carcinoma (P<0.05).
Similarly 58 out of 60 (96.7%) prostate carcinomas exhibited significantly stronger Tiam1 expression levels than the respective benign secretory epithelium (P<0.001).
We observed significantly stronger CD44 expression in resected endometrioid than in papillary serous cancer specimens, where the molecule was virtually absent.
In addition, clear cell carcinoma (n=11) showed a high frequency of VTE (five out of 11; 45%) and significantly stronger TF expression than non-clear cell carcinoma (P<0.05).
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