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1 by the addition of conditioned medium from a high-density culture.
2 te outgrowth of SCG neurons significantly at high density cultures.
3 egree of spatial interactions even in planar high-density cultures.
4 beta-catenin is targeted for degradation in high-density cultures.
5 lexes is obligatory for the proliferation of high-density cultures.
6 hotobioreactors (PBRs) capable of supporting high-density cultures.
8 However, the protein becomes detectable in high-density cultures and is required for in-vivo tumor
10 lease occurred after 3 or 4 days in vitro in high-density cultures but was absent in low-density cult
11 L induced robust but transient competence in high-density cultures, but mutation of the ComRS locus a
13 rons, astrocytes, and oligodendrocytes under high-density culture condition, differentiated almost ex
16 ling is sufficient to induce neurogenesis in high-density cultures even in the absence of retinoic ac
18 contrast, RA does not induce neurogenesis in high-density cultures in the absence of beta-catenin sig
19 ed more SM alpha-actin mRNA and protein than high-density cultures, indicating that the low-density c
24 t of bone morphogenetic protein-2 (BMP-2) in high density cultures of the mouse multipotent mesenchym
25 stance to dauer formation has also arisen in high-density cultures of a different nematode species, C
28 forming growth factor-beta, other cytokines, high-density culture or serum withdrawal in p57KIP2 prom
29 certain extrinsic (low atmospheric oxygen or high density culture) or intrinsic (defects in oxygen-se
30 upflow bioreactors containing D. mccartyi as high-density culture production tools or as a high-rate,
31 hesis that neurite outgrowth was enhanced in high-density cultures, thereby increasing the probabilit
32 adaptive immunity when they need it most: in high-density cultures, when bacteriophage infections can
33 ell death, rescues the neurogenic ability of high density cultures, without any apparent effect on no
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