ライフサイエンスコーパス: cells were grown in

1 ARPE19 cells were grown in 24-well and 96-well plates.

2 lf-renewal capacity of hemangioblasts, single CD34(+)KDR(+) cells were grown in 3-month extended long-term culture (ELTC)

3 HCT-8 cells were grown in a reduced-gravity, low-shear, rotating-wa

4 Epithelial cells were grown in air-liquid interface culture, and ST2L an

5 However, when cells were grown in biofilms, the mutants became more acid re

6 also functions to mediate cochemotactic activity, U937-C5aR cells were grown in chlorate to inhibit CSPG sulfation or tre

7 Phenotypical reversions were noted for both mutants when cells were grown in continuous culture at a low pH, suggestin

8 Kidney cells were grown in culture and adapted to 250 mM NaCl and 25

9 Urothelial and muscle cells were grown in culture, and seeded on a biodegradable bl

10 sion led to autophagic cell death when SKOv3 ovarian cancer cells were grown in culture, it enabled the cells to remain d

11 challenge, and bronchoscopy, and their airway smooth muscle cells were grown in culture.

12 Cells derived from the explants and the acinar cells were grown in DMEM supplemented with 10% fetal bovine s

13 e cell line (RGC-5), human and bovine TM cells, and control cells were grown in Dulbecco's modified Eagle's medium contai

14 Adherent cells were grown in either 96- or 384-well plates.

15 When cells were grown in extracellular matrix gels (Matrigel), and

16 Conversely, when the cells were grown in H(2)(18)O, partial labeling was observed

17 Rat Muller cells were grown in high (25 mM)- or low (5 mM)-glucose mediu

18 ression in rat microvascular endothelial cells (RMECs), the cells were grown in high (30 mM) glucose medium for 7 days, o

19 were detected in the DeltarpoZ strain compared with CS when cells were grown in high CO2 but not in ambient air.

20 tes mellitus and healthy controls, and HL60 neutrophil-like cells were grown in hyperglycemic conditions.

21 Using a model in which human breast cancer cells were grown in immunocompromised mice, we found that onl

22 spC, DbpA, and VlsE were synthesized at greater levels when cells were grown in limiting oxygen, whereas VraA was reduced

23 s in the csrA mutant were approximately twofold higher when cells were grown in Luria broth (LB) and 5- to 10-fold higher

24 In contrast, glycine incorporation was undetectable when cells were grown in M2G medium lacking glycine.

25 ltC-dependent gltAB expression was drastically reduced when cells were grown in media containing arginine or ornithine or

26 eraccumulation of AdoMet was a robust phenomenon when these cells were grown in medium containing glycine and formate but

27 of a similar upregulation of GPEET- procyclin when parental cells were grown in medium depleted of glucose.

28 When the cells were grown in medium supplemented with copper, the intr

29 MIN6 cells were grown in medium with glucose concentration of norm

30 Polarized epithelial Caco2-bbe cells were grown in medium with or without vitamin D and chal

31 E. coli cells were grown in minimal medium with fixed final concentra

32 t 100- to 1000-fold lower concentrations of AG1478 when the cells were grown in response to v-ErbB:ER as opposed to IL-3.

33 MEK, ERK and Akt activation, and induced apoptosis when the cells were grown in response to v-ErbB:ER.

34 C. albicans yeast cells were grown in rich medium with 2% glucose.

35 When cells were grown in rich medium, PhaZ1 was sufficient to acco

36 Cultured rat goblet cells were grown in RPMI 1640.

37 The cells were grown in RPMI culture medium supplemented with 10%

38 Gal- YAH1 cells were grown in standard rich media (YPD and YPGal) under

39 eased significantly (3.7- and 17.4-fold, respectively) when cells were grown in standing liquid broth compared to their l

40 on INO1 expression, and this effect was only observed when cells were grown in the absence of inositol.

41 nce was significantly reduced when the c-Met down-regulated cells were grown in the orthotopic liver site.

42 When the cells were grown in the presence of (13)CO, the two CO-ligand

43 ates being weaker, approximately threefold, when the b.End3 cells were grown in the presence of C6 astroglial factors.

44 sion changed both qualitatively and quantitatively when the cells were grown in the presence of either or both interferon

45 MCF-7 Tet-Off-TAM67 cells were grown in the presence of increasing concentrations

46 ocytes or their precursors developed when embryonic retinal cells were grown in the presence of Noggin and/or inductive c

47 E. coli filamentation was observed by light microscopy when cells were grown in the presence of phenanthriplatin, cis-[Pt

48 Furthermore, when cells were grown in the presence of synthetic d-mannosamine a

49 n led to increased copper binding by human thioredoxin when cells were grown in the presence of this trace element.

50 In additional studies, buccal cells were grown in vitro and incubated with SB216763.