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The tongue sample was obtained with a Stimudent®.
For the tongue sample, as seen in Fig. 3, we determine four values for ρ.
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Brain, pharynx-esophagus, larynx, lung, heart and tongue samples were collected from dead bats [26].
Heart and tongue samples were kept at + 4°C for 1-3 days until serological results were known.
SIRT3 staining intensity was significantly higher in OSCC tongue samples compared with normal tongue tissue samples (P ≤.04) (Fig. 1C, bottom; Table 1).
Furthermore, because the tongue accounts for 30% of oral malignancies, 1 we specifically examined tongue samples separately.
Furthermore, CS1 staining intensity was significantly higher for the tongue samples from OSCCs compared to the normal tissues (p < 0.05).
No difference between N+ and N0 carcinomas was detected for these genes, except for MFAP2 in tongue samples.
Pooled-analysis was performed on previous existing microarray datasets to determine the SOD2 mRNA levels in TSCC (n = 53) and normal tongue samples (n = 22).
The CEL files from all datasets (53 TSCCs and 22 normal tongue samples) were imported into the statistical software R 2.4.1 [ 12] using Bioconductor [ 13].
Concerning the chromosomal arms showing statistical significant segmental gains (p < 0.05) in the Tongue OPMLs with respect to all the other oral mucosa sites, we found the 7p e 20q (present in 5 out of 8 Tongue samples), 1p, 16p e 16q (present in 4 out of 8 Tongue samples).
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