ライフサイエンスコーパス: logarithmic phase

1 ne (0-3 d.p.i) as corresponding to the early logarithmic phase.

2 ptation time increased nearly twofold during logarithmic phase.

3 on of these fusions in cells at early to mid-logarithmic phase.

4 se but was reduced following entry into late logarithmic phase.

5 ed peak of gntT expression very early in the logarithmic phase, a pattern of expression similar to th

6 ain the different levels of RpoS observed in logarithmic phase, ammonia starvation, and glucose starv

7 c Trypanosoma brucei cells in early and late logarithmic phases and found that approximately 200 mRNA

8 identified as being QS regulated at the mid-logarithmic phase, and 450 genes were identified as bein

9 centrations of gluconate, for entry into the logarithmic phase, and for cometabolism of gluconate and

10 BL41 cells exhibited similar growth rates in logarithmic phase, BL41-3 cells remained largely viable

11 is process is regulated: RpoS is degraded in logarithmic phase but becomes stable upon carbon starvat

12 RNA was not detected in these strains at mid-logarithmic phase but was abundant in the parental strai

13 ga expression and Mga protein levels in late-logarithmic-phase cell growth.

14 al results were obtained in actively growing logarithmic phase cells and growth-arrested confluent ce

15 The role of RpoS regulation in these logarithmic phase cells was suggested by the functions o

16 TTP than antibiotic-free controls and early-logarithmic phase cells, respectively.

17 tarved cells is intermediate between that in logarithmic-phase cells and glucose-starved cells.

18 transcriptome analysis was performed on mid-logarithmic-phase cells grown in rich medium.

19 to 14 kDa contained isoaspartate, whereas in logarithmic-phase cells, nearly all of the detectable is

20 phase cells and, upon exposure to phenol, in logarithmic-phase cells.

21 Logarithmic phase cultures were exposed to pH 3.5 for va

22 mRNA increased > 15-fold when anaerobic, mid-logarithmic-phase cultures were exposed to O2, O2 with p

23 time when Vbeta3+ cell expansion was in the logarithmic phase (day 3 after transplantation).

24 i-analytic methods based on direct or double logarithmic phase expansions, steepest descent approache

25 exotoxin (referred to as leukotoxin) during logarithmic-phase growth that is a potent leukocyte-modu

26 eruginosa PAO1 versus its algR mutant in mid-logarithmic phase, (ii) P. aeruginosa PAO1 versus its al

27 ulated strains of S. pneumoniae grown to mid-logarithmic phase in suspension culture adhered to cultu

28 , we measured the adhesion of metacyclic and logarithmic-phase L. major promastigotes to complement r

29 y of tPMP-1 versus protoplasts prepared from logarithmic-phase (LOG) or stationary-phase (STAT) cells

30 Logarithmic-phase MCF-7 cells were not affected by < or

31 PSA was secreted into the medium during the logarithmic phase of cell growth at >9 microg/ml and was

32 lation of activity in the nucleus during the logarithmic phase of cell growth.

33 s more selective when the spirochetes are in logarithmic phase of growth compared to organisms obtain

34 B from a promoter expressed during the early logarithmic phase of growth could complement a ropB dele

35 f yqkI exhibited an abrupt arrest in the mid-logarithmic phase of growth on malate when low concentra

36 tion of promastigotes from the noninfectious logarithmic phase of growth to the infectious metacyclic

37 vels (quantity of sodF mRNA in cells in late logarithmic phase of growth) over approximately 24 h.

38 r alteration in parasite division during the logarithmic phase of growth, an accelerated cell death d

39 p levels were consistently lowest during the logarithmic phase of growth, but overall, there was not

40 in, cap8 mRNA was undetectable until the mid-logarithmic phase of growth, whereas CP8 production was

41 ss when in stationary phase than when in the logarithmic phase of growth.

42 the procyclic promastigotes collected at the logarithmic phase of the culture displayed a striking ab

43 protein-bound and free NADH at the early and logarithmic phase of the growth curve and a statisticall

44 he rate of p24 antigen production during the logarithmic phase of viral replication.

45 occurred during the mid-logarithmic and late-logarithmic phases of bacterial growth.

46 Cultures were grown to the mid-logarithmic phase on acidified glucose minimal medium, c

47 expression patterns of cells growing in late logarithmic phase on minimal glucose medium and on Luria

48 nds of laboratory experiments performed with logarithmic phase P. gingivalis Furthermore, this work h

49 trifugation of bacterial extracts during mid-logarithmic phase, peaked at the transition to stationar

50 tolerance of biofilms versus stationary- and logarithmic-phase planktonic cells with four different a

51 by bactericidal antimicrobials, compared to logarithmic-phase planktonic cells, and therefore exhibi

52 mRNA level in stationary phase compared with logarithmic phase promastigotes.

53 fected with serovar Typhimurium grown in the logarithmic phase quickly underwent cell death.

54 er corneas were injected intrastromally with logarithmic-phase S. aureus or purified alpha- or beta-t

55 In the logarithmic phase, the bacteria were found to be classic

56 nia chagasi promastigotes grow in vitro from logarithmic phase to stationary phase.

57 ng growth of the spirochetes in culture from logarithmic phase to stationary phase.

58 el gradually decreased in cells grown in the logarithmic phase to the stationary phase in culture.

59 genes are induced at the transition from the logarithmic phase to the stationary phase, and some gene

60 and zwf transcription were maximal in early logarithmic phase when inducing substrates such as glyce