ライフサイエンスコーパス: cells were cultured in

1 When MDA-MB 468 breast cancer cells were cultured in 1% O(2), uPAR expression increased, as

2 culture; larger increases in these parameters occurred when cells were cultured in 3% serum.

3 CD27+ and CD27- B cells were cultured in a 3-step system: (1) days 0 to 4: CpG,

4 Here, retinal precursor cells were cultured in a microfluidic chip with multiple arra

5 ed before performing the DBPCFC, and peripheral mononuclear cells were cultured in an 18-h ELISpot assay with casein, alp

6 seemed to be ligand-dependent because it was abrogated when cells were cultured in an androgen-depleted medium, but was r

7 Here, we used a 3D epithelial morphogenesis model in which cells were cultured in biochemically and mechanically defined

8 ary for the expansion of stress BFU-E, but only when spleen cells were cultured in BMP4 + SCF at low-oxygen concentration

9 The cells were cultured in chemical for 2 days and then, were fix

10 opulation of neurons and astrocytes, when neural progenitor cells were cultured in differentiation medium.

11 Rabbit and human corneal epithelial cells were cultured in DMEM/F12 medium containing 10% FBS and

12 Human corneal epithelial (HCE) cells were cultured in DMEM/F12 medium containing 10% FBS in

13 ARPE-19 cells were cultured in Dulbecco modified Eagle medium contain

14 INS-1 (832/13) cells were cultured in either a physiological (4 mm) or high

15 When neural progenitor cells were cultured in growth medium containing bFGF (20 ng/m

16 When human coronary smooth muscle cells were cultured in HG, similar findings were observed for

17 hen Kaposi's sarcoma-associated herpesvirus (KSHV) infected cells were cultured in high glucose medium.

18 For in vitro studies, hTCEpi cells were cultured in KGM-2 serum-free culture media contain

19 response to altered exogenous glucose concentration, MCF-7 cells were cultured in low (1 nM), physiological (5 mM), or h

20 his regimen is active against quiescent G(0)/G(1) MM cells, cells were cultured in low-serum medium to enrich the G(0)/G(

21 Bone marrow cells and, alternatively, fetal liver cells were cultured in media containing M-CSF for 7-10 d, res

22 To examine phosphorylation mediated by P2Y2, cells were cultured in media containing stable isotope-labele

23 Isolated epithelial cells were cultured in media with or without serum and/or 3T3

24 Human and murine antigen-presenting cells were cultured in medium containing 5% (2)H(2)O; class I

25 Retinal Muller cells were cultured in normal (5 mM) or high (25 mM) glucose

26 To examine this issue, A549 and Calu-6 lung cancer cells were cultured in normal media with or without tobacco s

27 Similar findings were observed when cells were cultured in reduced glucose concentrations.

28 phosphorylation in all cell lines examined, even when these cells were cultured in serum-free media.

29 Transformed RGC-5 cells were cultured in serum-free medium and were treated wit

30 Human CB-derived CD34+ cells were cultured in serum-free medium together with SCF, T

31 To induce differentiation, PLA cells were cultured in smooth muscle differentiation medium.

32 ly described process observed when mammary gland epithelial cells were cultured in suspension.

33 To understand the mechanisms of this effect, LTLT-Ca cells were cultured in the absence of letrozole for 16 weeks.

34 Spheroids of HT-29 human carcinoma cells were cultured in the microsystem for four weeks.

35 Pancreatic cancer MIA PaCa cells were cultured in the presence and absence of (15)N amin

36 ividing poorly differentiated human hepatoma-derived (Huh7) cells were cultured in the presence of 1% DMSO, cells became

37 Pre-activated CD4(+) T cells were cultured in the presence of either autologous EOS

38 also induced in the human intestinal Caco-2 cells when the cells were cultured in the presence of glucose.

39 In vitro, primary human monocytes and T cells were cultured in the presence of GW3965 or T1317, and t

40 One day postinjury, PP mixed cells were cultured in the presence of plate-bound anti-CD3/s

41 sed virus led to productive infection of cells, except when cells were cultured in the presence of the anti-gp120 mAb IgG

42 S10 in microfibril biogenesis, fetal bovine nuchal ligament cells were cultured in the presence or absence of ADAMTS10.

43 hRVE cells were cultured in the presence or absence of DHA(22:6,n3

44 ARPE-19 and primary mouse RPE cells were cultured in the presence or absence of varying con

45 AND MATERIAL: Immortalized human meibomian gland epithelial cells were cultured in the presence or the absence of IGF-1,

46 Ishikawa cells were cultured in vitro, and a range of AEA concentratio

47 When tumor cells were cultured in vitro, TAg transcription increased nea

48 er healthy controls, which however, gradually declined when cells were cultured in vitro.

49 derived P815 tumors was stable and permanent when the tumor cells were cultured in vitro.

50 mine the mechanism(s) underlying this phenomenon, Swiss 3T3 cells were cultured in zinc-deficient (D, 0.5 microM zinc), z