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The 343 biomarker candidate genes for brain were analyzed with WebGestalt for tissue expression pattern and gene enrichment analyses.
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(A) One hundred μg of lysates prepared from NIH 3T3 cells and mouse brain were analyzed by Western blotting with the indicated antibodies.
Sections at all levels of the brain were analyzed.
To determine if the FE-Pro complexes were well-retained and encapsulated within NSCs after implantation into the mouse brain and subsequent tumor-tropic migration, the brain samples were analyzed with TEM and immunohistochemistry.
From each brain at least 10 cryosections (each showing 3 brain sections) were analyzed, with at least 70 μm between individual sections analyzed.
Blood monocytes and discrete brain regions were analyzed with respect to the MDCB populations.
Ordinal scaled response variable (Multi-Score) and nominal explanatory variable (brain area) were analyzed with a contingency analysis and subsequently tested using the likelihood-ratio test.
Blood and brain tissues were analyzed with regard to tumor and contralateral hemisphere using fluorescence-activated cell sorting analysis, histology, and enzyme-linked immunosorbent assay.
Per individual brain section-pairs were analyzed with at least 70 μm between them.
Local and distant brain failure (DF) rates were analyzed with competing risk analysis, with death as a competing risk.
The A β plaques in sections from the brains of mice studied were analyzed with an antibody against A β (4G8, 1 : 500; Signet Laboratories) detected with FITC-conjugated secondary antibodies (1 : 75; Vector Laboratories).
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