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We identify interferons (IFN), which have been detected in the periphery of individuals infected with HIV-1, as inducers of Sn expression in cultured monocytes.
They remained, however, confined to the gut epithelium as very few sdc1+ DN T cells were detected in the periphery of wt mice.
Interestingly, high level of VEGF-C was detected in the periphery of the regenerating area that is constituted by the pluripotent blastema cells and only weak VEGF-C expression was detected in the vessels.
In the absence of functional Fas pathway, sdc1-expressing B220+ DN T cells were simultaneously detected in the periphery and gut epithelium of gld mice (Fig. 3C and D).
Bone marrow samples were collected at week 4 and 5 after reconstitution, at which time mature T cells were not detected in the periphery and there were no signs of immunopathology in the crt−/− FLC.
Interestingly 30nm fibers are only detected in the periphery of the HC whereas the central part appears uniform and does not show any periodic signal at 1/30nm−1.
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This design meant that stimulus onsets could still be detected in the retinal periphery.
Rdx was detected in the nuclear periphery region in an immunostaining experiment using Triton X-100-treated clone-8 cells (Figure 5A, lower).
Co-localization of HAMLET and 20S proteasomes was detected in the cell periphery (65% co-localization) and throughout the cytoplasm of adherent cells (64% co-localization, Figure 2D).
Furthermore, multiple stable caveolae were detected in the cell periphery.
An elevated yellow mass with exudation was detected in the temporal inferior periphery.
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