ライフサイエンスコーパス: culture dish

1 monolayer epithelium attached to the tissue culture dish.

2 when cells are prevented from adherence to a culture dish.

3 human lung fibroblast cells when coated on a culture dish.

4 ells rounded up and detached from the tissue culture dish.

5 same collagen matrix that is attached to the culture dish.

6 xplants by scraping nongoblet cells from the culture dish.

7 nt cytoplasm that died and detached from the culture dish.

8 recapitulating the in vivo situation in the culture dish.

9 in viable cells before they detach from the culture dish.

10 in the controlled environment of the tissue culture dish.

11 entering contractile cells of the heart in a culture dish.

12 a collagen bed (-astrocyte) within the same culture dish.

13 s of motor neurons in the spinal cord and in culture dishes.

14 t cells grown on standard, very stiff tissue culture dishes.

15 n carried out using cells on the surfaces of culture dishes.

16 s determined by measuring DNA content of the culture dishes.

17 ot occur until the 5th day after seeding the culture dishes.

18 enin bound most abundantly to gelatin-coated culture dishes.

19 ant fibronectin fragments coated onto tissue culture dishes.

20 s of the test molecules were placed in 35 mm culture dishes.

21 rom P. includens to spread on the surface of culture dishes.

22 d methods were used to prepare IVF or embryo culture dishes.

23 hat were differentiated in vitro on uncoated culture dishes (2D) or encapsulated in self-assembling,

24 ne corneal endothelial cells attached to the culture dish and grew to fill the flask.

25 y, chick lens capsular bags were pinned to a culture dish and grown in the presence or absence of the

26 l recapitulated the disease phenotype in the culture dish and provided important mechanistic insights

27 dispersion of the cells by removal from the culture dish and replating had substantial positive effe

28 res approximately 2 h for preparation of the culture dishes and a further 3-4 h for isolation and pla

29 pressing cells displayed reduced adhesion to culture dishes and were found to secrete an extracellula

30 were grown to confluence on 35 x 10 mm cell culture dishes and were used from passages 10-14.

31 to communicate over many millimeters in cell culture dishes and, thereby, form a spatially extended,

32 fiber hydrogel, 3 D GelMA hydrogel, and 2 D culture dish) and chemical factors (serum, ascorbic acid

33 ave prominent nucleoli, attach poorly to the culture dish, and are sensitive to apoptosis but have in

34 al genes expression after cell detached from culture dish, and this finding highlights the importance

35 Compared with traditional culture dish approaches, this pipeline enhances experime

36 atest increases seen at the periphery of the culture dish, at the point of the greatest deformation.

37 ose pretreated with RANKL in vitro in tissue culture dishes, bone slices, and a co-culture system con

38 all tumor cell lines examined that attach to culture dishes but not in cell lines that grow in suspen

39 pithelial cells (Caco-2) were grown on 35-mm culture dishes, chamber slides, or in a bicameral cultur

40 1 and tested under static conditions in cell culture dishes coated with cerebral microvasculature cel

41 NSCs were induced to differentiate in culture dishes coated with poly-l-lysine and mouse lamin

42 al endothelial cells were plated onto tissue culture dishes coated with purified fibronectin or a mat

43 acrophages, but not those attached to tissue culture dishes, contained approximately 10-15% of ACAT o

44 HTM cells were plated in culture dishes containing a polymerized deformable silic

45 These explants were transferred to new culture dishes every week for 9 weeks.

46 bodies immobilized on the surface of plastic culture dishes failed to induce resistance and resulted

47 t the gas/liquid interface in standard organ culture dishes, fed with DMEM/F12 plus 2% B-27 supplemen

48 ial clusters that form within a 22 cm square culture dish filled with soft agar over two days.

49 hat exhibited spontaneous contraction in the culture dish for up to 21 d.

50 MT has also proven to be a fertile culture dish--full of direction- and disparity-selective

51 a spindled morphology, are less adherent to culture dishes, grow to a higher saturation density, and

52 fly in culture, and fibroblasts overgrow the culture dish in 1 or 2 weeks.

53 Herein, a novel transwell insert culture dish method is used to show that X-irradiation i

54 ates (DNA and protein synthesis), and tissue culture dishes (migration).

55 expressed in proliferating HMEC adherent to culture dishes mostly excluded exon 17B, whereas 4.1 tra

56 ing a cooled-CCD camera either directly from culture dishes or by implanting them into mice.

57 radiolabeled cells were washed, seeded into culture dishes or glass slides, covered with photographi

58 wing RPE cell removal after day 21 on tissue culture dishes or on BM.

59 own in the presence of bacteria or on tissue culture dishes rather than in suspension culture.

60 y high level lost their ability to adhere to culture dishes, suggesting a role for Porimin in cell ad

61 >1,000 times more infectious virus per cell culture dish than the much more labor-intensive organoty

62 ays of asymmetric adhesive islands on tissue culture dishes that rectify the random movement of cells

63 Matrix gel islands are spotted on a cell culture dish to act as support for receiving and culturi

64 MSCs cultivated on temperature-responsive culture dishes to a confluent 2D monolayer were harveste

65 glets (n = 4) were seeded on matrigel coated culture dishes to stimulate migration of muscle-derived

66 2 disease phenotype and drug response in the culture dish, to provide novel insights into disease and

67 crocolonies were harvested directly from the culture dishes under a fluorescence microscope, and tota

68 of c-Myc-transformed fibroblasts adherent to culture dishes under normoxic conditions, the growth of

69 ollowed by counting of cells attached to the culture dish using image analysis.

70 The previously occupied culture dish was stained for lacZ to detect transduced e

71 When tissue culture dishes were coated with fibronectin, the cells a

72 xial stretching was then applied to silicone culture dishes with a 4% or 8% stretch at a stretching f

73 tion of elastically supportive surface (ESS) culture dishes with defined stiffnesses and single-cell

74 m on polylysine by growing neurons on tissue culture dishes with different net surface charges.

75 e subcultured by transferring spheres to new culture dishes without employing enzymatic dissociation.

76 s of dish preparation, especially for embryo culture dishes, without significantly altering medium os