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1 monolayer epithelium attached to the tissue culture dish.
2 when cells are prevented from adherence to a culture dish.
3 recapitulating the in vivo situation in the culture dish.
4 human lung fibroblast cells when coated on a culture dish.
5 ells rounded up and detached from the tissue culture dish.
6 same collagen matrix that is attached to the culture dish.
7 xplants by scraping nongoblet cells from the culture dish.
8 a collagen bed (-astrocyte) within the same culture dish.
9 nt cytoplasm that died and detached from the culture dish.
10 in viable cells before they detach from the culture dish.
11 enin bound most abundantly to gelatin-coated culture dishes.
12 t cells grown on standard, very stiff tissue culture dishes.
13 n carried out using cells on the surfaces of culture dishes.
14 s determined by measuring DNA content of the culture dishes.
15 ot occur until the 5th day after seeding the culture dishes.
16 ant fibronectin fragments coated onto tissue culture dishes.
17 s of the test molecules were placed in 35 mm culture dishes.
18 rom P. includens to spread on the surface of culture dishes.
19 s of motor neurons in the spinal cord and in culture dishes.
20 hat were differentiated in vitro on uncoated culture dishes (2D) or encapsulated in self-assembling,
22 y, chick lens capsular bags were pinned to a culture dish and grown in the presence or absence of the
23 dispersion of the cells by removal from the culture dish and replating had substantial positive effe
24 res approximately 2 h for preparation of the culture dishes and a further 3-4 h for isolation and pla
25 pressing cells displayed reduced adhesion to culture dishes and were found to secrete an extracellula
27 ave prominent nucleoli, attach poorly to the culture dish, and are sensitive to apoptosis but have in
28 al genes expression after cell detached from culture dish, and this finding highlights the importance
30 atest increases seen at the periphery of the culture dish, at the point of the greatest deformation.
31 ose pretreated with RANKL in vitro in tissue culture dishes, bone slices, and a co-culture system con
32 all tumor cell lines examined that attach to culture dishes but not in cell lines that grow in suspen
33 pithelial cells (Caco-2) were grown on 35-mm culture dishes, chamber slides, or in a bicameral cultur
35 al endothelial cells were plated onto tissue culture dishes coated with purified fibronectin or a mat
36 acrophages, but not those attached to tissue culture dishes, contained approximately 10-15% of ACAT o
39 bodies immobilized on the surface of plastic culture dishes failed to induce resistance and resulted
40 t the gas/liquid interface in standard organ culture dishes, fed with DMEM/F12 plus 2% B-27 supplemen
42 a spindled morphology, are less adherent to culture dishes, grow to a higher saturation density, and
46 expressed in proliferating HMEC adherent to culture dishes mostly excluded exon 17B, whereas 4.1 tra
48 radiolabeled cells were washed, seeded into culture dishes or glass slides, covered with photographi
51 y high level lost their ability to adhere to culture dishes, suggesting a role for Porimin in cell ad
52 >1,000 times more infectious virus per cell culture dish than the much more labor-intensive organoty
53 ays of asymmetric adhesive islands on tissue culture dishes that rectify the random movement of cells
54 2 disease phenotype and drug response in the culture dish, to provide novel insights into disease and
55 crocolonies were harvested directly from the culture dishes under a fluorescence microscope, and tota
56 of c-Myc-transformed fibroblasts adherent to culture dishes under normoxic conditions, the growth of
60 xial stretching was then applied to silicone culture dishes with a 4% or 8% stretch at a stretching f
62 e subcultured by transferring spheres to new culture dishes without employing enzymatic dissociation.
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