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1 -management practices (e.g., row spacing and seeding density).
2 anagement treatments (two row spacing, three seeding densities).
3 ell extravasation by having a suitable tumor seeding density.
4 ification reached approximately 20 times the seeding density.
5 the limiting structure can be independent of seeding density.
6 redict the most appropriate environments and seeding densities.
7 from only a small number of cells and at low seeding densities.
8 size of neuronal spheres with different cell seeding densities.
9 of cellular proliferation is rescued by high seeding densities.
10 or the optimisation of electrostatic diamond seeding densities.
11 es with the response plateauing only at high seeding densities.
12 rds earlier times and plateau only at higher seeding densities.
13 bFGF, TFP, FBS) and self-assembled construct seeding density (2, 3, 4 million cells/5 mm dia. constru
14 y analyze AP morphology from iPSC-CMs at two seeding densities: 60,000 cells/well (confluent monolaye
15 efore important to quantitatively assess how seeding density affects clonality loss so that experimen
16 ons and parameters, such as the initial cell seeding densities and cell proliferation rates, is shown
17                In this study, the effects of seeding density and a change in YAP signaling on 3D card
18 ture parameters, such as pH, oxygen tension, seeding density and feeding schedules, significantly aff
19 mber of cells per microwell for a given cell seeding density and microwell geometry.
20  the shape can also be tuned to increase the seeding density and orientation of dropicles within a we
21 ed the peak in proliferation at intermediate seeding densities, and that the proliferation arrest at
22 requency of media replacement, reducing cell seeding density, and adjusting the serum concentration a
23 alysis of donor variability, passage number, seeding density, and cost.
24 uded fibronectin concentration, temperature, seeding density, and immobilization time.
25 s work demonstrates that at low and moderate seeding densities AR-BP sidedness significantly impacts
26                         High epithelial cell-seeding densities are required in regenerative medicine,
27 0.85/day, and is extracted from initial cell seeding densities as low as 10(5) cells/mL.
28 ing the growth of hESC colonies from a given seeding density based on stochastic exponential growth.
29   We assessed the total cell number for cell seeding density (cells per unit volume) across four valu
30 e conditions are customized in terms of cell seeding density, composition of culture medium, and feed
31 uent pancreatic development, three different seeding density cultures were analyzed.
32                      The spheroids with high seeding density exhibited more alpha-actinin(+) cells an
33 otential trend, higher MSC/CD34 + HSPCs cell seeding densities generally tended to increase levels of
34                          At low and moderate seeding densities hAEC proliferation was significantly i
35                                  At moderate seeding densities, hAEC production of human laminin was
36            Data suggest that increasing cell seeding density has the potential to enhance bladder tis
37  Clonal homogeneity can be obtained with low seeding densities; however, this leads to low yield and
38 y culturing these nonmetastatic cells at low seeding density in ECM-derived gels in vitro, in which t
39 ted epithelial cell line, we found that high seeding density induced these characteristics, whereas l
40                                 Because hESC seeding density influences the subsequent pancreatic dev
41 of differentiation such as cell shape and/or seeding density inform this transcriptional program rema
42 only occurs as a consequence of varying cell-seeding densities, it can also be observed within a smal
43 P morphology, and when observed in different seeding densities may encompass any shape including thos
44 + precursors can be improved by manipulating seeding density, monitoring metabolic secretion and alte
45 ly, cloning efficiencies were highest at low seeding densities of 10(2) or 10(3) PBMC per well.
46 rous cells with normal cells, increasing the seeding density of either normal or precancerous cells a
47 lts demonstrate the pivotal role of the cell seeding density of normal and precancerous cells in modu
48 e observed that progressively decreasing the seeding density of normal rat kidney-52E (NRK-52E) or MC
49                               Increasing the seeding density of transformed cells shifts the kinetics
50 rticular, we found that cells either at high seeding density or with the CCR-7 receptor inhibited mig
51 ed by varying the serum concentration or the seeding density, or by addition of suramin, transforming
52 of the medium and the ability to grow at low seeding densities, precedes polyploidization of these cu
53              Changing the starting bacterial seeding density produces three variations in the sequenc
54 ndrogenesis in vitro also requires high cell seeding density, reminiscent of the cellular condensatio
55 mploy this random walk model to estimate the seeding density required to minimise the occurrence of h
56 ocytes in isolation, this was optimal at low seeding densities, required endothelial cell contact, an
57          Unexpectedly, a further decrease in seeding density so that cells were isolated from neighbo
58 egnated with 50,000 keratinocytes per cm2, a seeding density that produces a confluent epidermis with
59  of percent muscle ( 45% muscle) with higher seeding densities was observed for F/POC S- [CD34-50/MSC
60 erin engagement specifically at intermediate seeding densities, was required for the cadherin-stimula
61                  Treatment duration and cell seeding density were both found to be significant factor