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1 ce of human serum, which was not observed in serum-free culture.
2 ar cells and HBEGF promote their survival in serum-free culture.
3 stimulated for varying times up to 72 hr in serum-free culture.
4 or cell proliferation and differentiation in serum-free culture.
5 human brains and to maintain these cells in serum-free cultures.
6 le sca-1(+)/c-kit(+)/Gr-1(-) marrow cells in serum-free cultures.
7 ny formation in serum-containing, but not in serum-free, cultures.
8 nd retinal ciliary bodies were maintained in serum-free culture and genetically modified by electropo
9 m albumin secretion was increased by 350% in serum-free cultures and by 166% in serum-containing cult
10 -term urea secretion was increased by 79% in serum-free cultures and by 76% in serum-containing cultu
11 me P450IA1 activity was increased by 140% in serum-free cultures and by 820% in serum-containing cult
13 donors, were treated with a 110-kDa FN-f in serum-free culture, and expression of various cytokine g
14 ied astrocytes, purified APCs rapidly die in serum-free culture but can be saved by basic fibroblast
16 n that it uses entirely defined, feeder- and serum-free culture conditions and produces very consiste
17 ue macrophage populations, we have optimized serum-free culture conditions to permit robust survival
20 od after high-salt intake can potentiate, in serum-free culture conditions, the differentiation of fr
21 NAs was assessed, after ET-1 treatment under serum-free culture conditions, with both a formazan assa
27 blood precursors with immobilized Delta-1 in serum-free cultures containing fibronectin and hematopoi
30 interleukin-1alpha (IL-1alpha), and IL-3 in serum-free cultures for as few as 48 hours, the number o
33 optic nerve can proliferate indefinitely in serum-free culture if prevented from differentiating; va
35 onor corneas of various ages and grown under serum-free (cultured keratocytes) or serum-added (cornea
36 studies, hTCEpi cells were cultured in KGM-2 serum-free culture media containing 0.15 mM calcium.
39 medium containing 15% newborn calf serum, in serum-free culture medium containing either activated TG
41 n a defined, essential-fatty-acid-deficient, serum-free culture medium without a feeder layer, that c
44 ntiation occurred in a clinically applicable serum-free culture model and was not accompanied by apop
45 rized hypertrophic responses in low-density, serum-free cultures of neonatal mouse cardiac myocytes a
47 gh cloning frequencies in stromal cell-free, serum-free cultures, permitting this analysis of direct
52 self-renewal of mouse SSCs and established a serum-free culture system for their proliferation in vit
53 ll (DC) differentiation, we have developed a serum-free culture system in which human CD14+ periphera
56 ratinocytes cultured in a chemically defined serum-free culture system, devoid of animal-derived feed
60 SF), and exhibit autonomous proliferation in serum-free cultures that is inhibited by anti-IL-3 and a
62 urified populations of CFU-MK were tested in serum-free cultures, these results suggest that SDF-1 di
63 uring marrow CD34+ cells for 7 to 10 days in serum-free cultures was able to expand CFU-Meg approxima
64 8.5 p.c.-ectoplacental cone (EPC) explant in serum-free culture, we have found parathyroid hormone-re
65 m mouse ciliary epithelium and maintained in serum-free culture were genetically modified by electrop
66 ail, we treated neonatal cardiac myocytes in serum-free culture with a combination of the macrophage-
67 er, TKT loss was not induced by treatment of serum-free cultures with a third serum cytokine, transfo
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