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In [21], a closed-form expression on the capacity of partial relay selection under outdated CSI was studied, with non-adaptive fixed-rate transmission being considered.
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However, the aforementioned work [16] focused on the achievement of the closed-expression of the capacity performance and the performance analysis for the SER performance was not involved.
We compared of the effect of p85α, Δp85β and p85β expression on the invasive capacity of NIH3T3 cells; p85β-expressing cells exhibited an invasive capacity markedly higher than control, p85α- or Δp85β-expressing cells (supplementary material Fig. S3C).
We investigated the influence of varying Agt gene expression on the ovulatory capacity and early embryonic development in mice.
To assess the effect of ectopic miR-9 expression on the invasive capacity the BMMCs, a Matrigel invasion assay was again performed.
The effects of reduced PRDX6 expression on the invasion capacity of breast cancer cells were determined by in vitro invasion assay, as described previously.
Next to test the effect of HDAC7 expression on the lymphomagenic capacity of the Namalwa cell line, 1.5 × 10 cells were injected orthotopically into the spleen of 19 athymic mice and they were randomly allocated into two treatment groups.
Since both Gli3 and Her9 showed the ability to repress rx2 expression in vivo, we next addressed the impact of ectopic gli3/ hexpressionsion on the proliferative capacity of RSCs in the CMZ.
We first determined the effect of RAR β2 expression on the proliferative capacity of neuroblastoma cells in the presence and absence of 10 μ M all- trans-retinoic acid (aRA).
We suggest that the impact of baseline p53 expression on the apoptosis inducing capacity of single agents and drug combinations should be studied in detail due to the major impact on extrinsic and intrinsic apoptosis sensitivity detected here.
However, such analysis is labor-intensive and does not reveal more subtle changes that can be caused by random insertion of the vector DNA, such as small deletions or downstream effects on gene expression, or the capacity for tandem integrations of DNA leading to potential gene dosage problems with reporter gene constructs.
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