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1 emonstrate the induction of apoptosis in the parent cell line.
2 1/10 as much N-acetylneuraminic acid as its parent cell line.
3 luding genes that are normally silent in the parent cell line.
4 e same in vivo growth characteristics as the parent cell line.
5 ) to high levels compared with the wild-type parent cell lines.
6 otein compared with the paclitaxel-sensitive parent cell lines.
8 altered cell morphology in comparison to the parent cell line and both had slower growth rates in vit
9 gic receptors, the cAMP assay itself, or the parent cell line; and (iii) increased the potency of PGE
10 rate as the parent cell line, but unlike the parent cell line, AW cells are factor independent and tu
11 ntains a similar in vitro growth rate as the parent cell line, but unlike the parent cell line, AW ce
13 on of CYP1A1 transcription compared with the parent cell line Huh7, whereas protein levels and enzyme
15 r enzyme activity profiles compared with the parent cell line, including the dramatic posttranscripti
16 toxicity in these cell lines relative to the parent cell line is indicative of compounds that are sub
19 cell line model composed of an MGMT-positive parent cell line, RPMI 8226/S, and its MGMT-negative var
20 ne expression pattern similar to that of the parent cell line, shows a significant reduction in RNase
21 3(0.03TR), and SKOV-3(0.3TR), as well as the parent cell line SKOV-3, was analyzed by cDNA array to e
23 duced HCT116-C19 cells and the hNIS-negative parent cell line were evaluated in vitro in the presence
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