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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
12               We added radiolabeled scHGF to serum-free cultures and confirmed that tcHGF was being g
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
15 optic nerve and stimulated to proliferate in serum-free culture by PDGF.
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
18            Supplementing defined stroma- and serum-free culture conditions with recombinant DPT prote
19              Remarkably, under hematopoietic serum-free culture conditions, hematopoietic outgrowth o
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
22 ach to cultivate primary human ECs (hECs) in serum-free culture conditions.
23 pendently increased viable cell number under serum-free culture conditions.
24 uripotent stem (iPS) cells that uses defined serum-free culture conditions.
25 tress, dependent on the transfection time in serum-free culture conditions.
26                                            A serum-free culture containing SCF, TPO, FGF-1, angiopoie
27 blood precursors with immobilized Delta-1 in serum-free cultures containing fibronectin and hematopoi
28                                              Serum-free culture filtrates of six Candida species and
29 he long-term survival of most of the SMNs in serum-free culture for 3 weeks.
30  interleukin-1alpha (IL-1alpha), and IL-3 in serum-free cultures for as few as 48 hours, the number o
31                                           In serum-free cultures, however, LIF is insufficient to blo
32                In this study, we report that serum-free cultured human monocyte-derived DCs after TLR
33  optic nerve can proliferate indefinitely in serum-free culture if prevented from differentiating; va
34 gic and phenotypic features were observed in serum-free cultures in the presence of FN/PMA.
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.
37 antities of the recombinant NC1 protein from serum-free culture media.
38      Factor VIII expression was performed in serum-free culture medium and in the absence of exogenou
39 medium containing 15% newborn calf serum, in serum-free culture medium containing either activated TG
40                         IL-9 was detected in serum-free culture medium harvested from ALK+ ALCL-cell
41 n a defined, essential-fatty-acid-deficient, serum-free culture medium without a feeder layer, that c
42 ature bovine articular cartilage explants in serum-free culture medium.
43 ll development by in vitro colony assay in a serum-free culture medium.
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
46                                 Treatment of serum-free cultures of osteoblast clones derived from IG
47 gh cloning frequencies in stromal cell-free, serum-free cultures, permitting this analysis of direct
48                                              Serum-free cultured rabbit corneal keratocytes and TGFbe
49          Studies using micromanipulation and serum-free culture showed that the effects of sTPOR and
50                                           In serum-free culture, supplementation of the medium with I
51                             In this study, a serum-free culture system and a transplantation assay fo
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
54                         Adapting a line to a serum-free culture system resulted in additional epigene
55                                    We used a serum-free culture system to study the effect of RA on c
56 ratinocytes cultured in a chemically defined serum-free culture system, devoid of animal-derived feed
57                          In an SCF-dependent serum-free culture system, LPA (2.5-10 microM) increased
58                                In a minimal, serum-free culture system, the synthetic GC dexamethason
59                                      Using a serum-free culture system, we discovered that IGF2 can s
60 SF), and exhibit autonomous proliferation in serum-free cultures that is inhibited by anti-IL-3 and a
61                                Compared with serum-free cultures, the use of serum resulted in an ave
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
68         TKT loss was induced by treatment of serum-free cultures with the serum cytokines platelet-de
69                                       TPO in serum-free cultures without any other exogenously added

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