ライフサイエンスコーパス: G0 phase

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1 e present at very low levels in cells at the G0 phase.

2 f normal HBE cells, which accumulated in the G0 phase.

3 cess, required for both cell-cycle arrest in G0 phase and high-level expression of late muscle-differ

4 However, fermenting cells arrest in G1/G0 phase and suffer massive vacuolization and eventual c

5 eated with 1.0 microM tamoxifen underwent G1-G0-phase arrest but did not undergo apoptosis.

6 populating cells were predominant within the G0 phase, because transplantation of CD34(+) cells resid

7 r investigations revealed an increase in the G0 phase cell population depicting that majority of cell

8 study, the effect of caffeine in quiescent (G0 phase) cells was investigated.

9 able to leave the division cycle and enter a G0 phase; cells past this point are unaffected by a shor

10 A replication in S phase cytosol, but not in G0 phase cytosol.

11 ed an incomplete arrest in the cell cycle at G0 phase, increased phagocytic ability, and enhanced exp

12 nparenchymal cells from the normal quiescent G0 phase into the cell cycle during liver regeneration a

13 Bone marrow (BM) CD34+ cells residing in the G0 phase of cell cycle may be the most suited candidates

14 ngle human marrow CD34+CD38-/lo cells in the G0 phase of cell cycle were cultured under 7 different c

15 les, whereas the fraction of cells in the G1/G0 phase of the CDC increases monotonically from 90 to 9

16 show that Bcl11b induces cells to enter the G0 phase of the cell cycle and become quiescent.

17 Human dermal fibroblasts in G0 phase of the cell cycle and Chinese hamster ovary cel

18 each instance, most of the HSCs were in the G0 phase of the cell cycle and exhibited reduced oxidati

19 Cells arrest in the G1 or G0 phase of the cell cycle in response to a variety of n

20 t-RA) arrests the growth of HBE cells in the G0 phase of the cell cycle through activation of retinoi

21 ntiation to cells that have entered into the G0 phase of the cell cycle under mitogen withdrawal.

22 RNAi) as a major requirement for quiescence (G0 phase of the cell cycle) in Schizosaccharomyces pombe

23 They are in the G0 phase of the cell cycle, and their transcriptome is t

24 ppropriate co-stimulation triggers exit from G0 phase of the cell cycle, increased size and metabolis

25 arge number of the Flt3low cells were in the G0 phase of the cell cycle, whereas Flt3high cells were

26 AT1, a gene known to regulate entry into the G0 phase of the cell cycle.

27 elial cells in culture to be arrested in the G0 phase of the cell cycle.

28 critical for cell cycle withdrawal in the G1/G0 phase of the cell cycle.

29 protein that controls progression out of the G0 phase of the cell cycle.

30 w cytometry revealed growth arrest in the G1/G0 phase of the cell cycle.

31 p21/WAF1 and arrested cell growth in the G1/G0 phase of the cell cycle.

32 f AML cells, but not of normal cells, in the G0 phase of the cell cycle.

33 ower in the G1 phase than those in the S and G0 phases of the cell cycle.

34 as indicated by accumulation of cells in the G0-phase of the cell cycle and growth recovery when cell

35 ling glial cells recruit quiescent cells (in G0 phase) onto the cell cycle, via a calcium signalling

36 ival factor, failing to advance B cells from G0 phase or stimulate thymidine incorporation.

37 Subconfluent cells were synchronized in the G0 phase (quiescence) by serum starvation for 24 hours.

38 In vivo cell cycle quiescent (G0 phase) stem cell keratinocytes in primary culture seq

39 o need to postulate a restriction point or a G0 phase to explain the serum starvation results.

40 sitively controls p27(Kip1) stability in the G0 phase via p27(Kip1) Ser(10) phosphorylation, which is

41 feration and induced cell cycle arrest at G1/G0 phase via PPARgamma signalling pathway.

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