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As seen in Figure 3A and Table 1, no significant transfer was detectable for any of the proteins that reside in intracellular compartments such as the nucleus, cytosol, or intracellular organites.
Taken together, these results indicate that the expressed K1 5 mediated by Ad/K1 5 gene transfer was detectable and displayed antiangiogenic activity in vitro and in vivo.
Similar(58)
Accordingly, a blocking effect of ALP on the firm leukocyte adhesion induced by anti-CII mAb transfer in vivo was detectable.
DNA amplification was detectable within 25 min.
No evidence of Luvisol development was detectable.
With the YES, no EEQ was detectable.
No clear co-localization was detectable.
Impaired LYVS transfer had a slow onset, requiring approx. 3 5 days exposure to 15 or 25 mmol/l glucose before a statistically significant decrement was detectable.
Whereas T cells were demonstrable in lymph nodes for at least 12 days after transfer, very few were detectable in the joint.
Due to the slow accumulation in the embryo, effects on the first hours of development (e.g. early teratogenic properties) will not be detectable without enhanced transfer.
Lifting, though, is detectable.
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