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A rapid transient decrease in p400 binding was seen after 5-min treatment of MEFs with PMA (Fig 3D, left panel).
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On all cell types, the greatest binding was seen at the earliest time point (30 minutes) after injection, the amounts decreasing similarly thereafter irrespective of cell type.
Clear MAD1 kinetochore binding could be seen 10 15 min after addition of rapamycin to metaphase cells, as evidenced by accumulation of YFP signals to MIS12-tagRFP-positive kinetochores (Fig. 3a).
The SERS method was used to confirm the hypothesis that substances bind to DNA and to confirm which main bases are modified after this binding to DNA (see Supplementary Material).
No suppression was seen after cotransfection with a negative control vector expressing miR-9 [31], which has no predicted binding site in hPGRN mRNA (Fig. 2C).
However, mild paravalvular leakage was seen after TAV implantation.
No difference in lesion volume was seen after permanent MCAO.
Binding was seen to increase at higher percentages, perhaps due to non-specific binding after denaturation.
That 2002 non-binding declaration on the South China Sea was seen as a first step towards forging a binding agreement.
Wound infection was seen significantly more often after radiotherapy.
Results: After muromonab-CD3 infusion, an increase in the binding of MoAb anti-factor V/Va to platelets was seen, which was only statistically significant (2.2% vs. 12.8%, P=.04) after 15 min of the second dose.
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