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1 n synthase kinase-3 (GSK3) inhibitor, and in serum-free media.
2 ined, even when these cells were cultured in serum-free media.
3 fection using standard cell culture media or serum-free media.
4  WNT signaling, cell growth, and survival in serum-free media.
5 ter monolayer expansion, and after 1 week in serum-free media.
6 hneider insect (S2) cells, and purified from serum-free media.
7 and then TGF-beta2 was added for 24 hours in serum-free media.
8  and at 5 DPS media were replaced with fresh serum-free media.
9 olated rabbit keratocytes plated in defined, serum-free media.
10 ic phenotype and appearance when cultured in serum-free media.
11 tes also cleave IgG in both growth media and serum-free media.
12 roliferation and motility when maintained in serum-free media.
13 st model, cells were grown in low density on serum-free media.
14 ptosis and that apoptosis was potentiated in serum-free media.
15 and 100 micrograms/ml) for up to 48 hours in serum-free media.
16 m is 22 days) were incubated in hormone- and serum-free media.
17 ry explants were generated and maintained in serum-free media.
18 al cells results in sustained cell growth in serum-free media, a predisposition to develop hyperplasi
19 ectin (VN), or collagen (CL) in supplemented serum-free media alone or with TGF-beta1 or fibroblast g
20  proteoglycans synthesized by keratocytes in serum-free media also more closely resembled that of ker
21 d (G12V)Ha-ras or (Q61K)N-ras proliferate in serum-free media and have constitutive MAPK activity.
22 atal neurons grown in low density culture on serum-free media and in the absence of glia die within 3
23 -alpha) in fetal bovine serum-containing and serum-free media and were analyzed by Wright's stain for
24  sham-operated rats, cultured on Matrigel in serum-free media, and briefly exposed to rat cytomegalov
25 roliferation induced by nonconducting EAG in serum-free media, and EAG increased p38 MAP kinase activ
26 sal-like phenotype in vitro when cultured in serum-free media, and undergoes phenotypic changes consi
27      Furthermore, cultured RGC maintained in serum-free media are also C1q and C3 immunoreactive, dem
28 well tissue culture plates and maintained in serum-free media at 37 degrees C.
29 ly isolated chondrocytes died when plated in serum-free media at low density on poly-L-lysine, but sh
30 f complement on CD19 loss was examined using serum-free media, C3- and C5-deficient sera, and a C5-bl
31                                        Also, serum-free media conditioned by transiently compressed g
32                  CSp-EMVs were isolated from serum-free media conditioned for 3 days by cardiospheres
33 ult (12 weeks) rat ganglia and maintained in serum-free media containing glucose (10-100 mM) in the p
34 her concentrations of PLL (1.5 microg/mL) in serum-free media during initial FE-PLL complex formation
35 l as acutely isolated astrocytes cultured in serum-free media, failed to respond to 5-HT by changes i
36 cubated in either control, acid, or alkaline serum-free media for 12 h.
37              Confluent cells were exposed to serum-free media for 24 h, then incubated in either cont
38 SC were cultured as free-floating pellets in serum-free media for 3 weeks.
39 e agonists/antagonists to their receptors in serum-free media for 5-7 days.
40 uccessful use of an ITS+ Premix-supplemented serum-free media for prolonged islet culture and its com
41 ddition of TGF-beta1 to endothelial cells in serum-free media further potentiated the induction of ap
42  TRA-1-60(-)/SSEA4(-)/SOX1(+) cells grown in serum-free media give rise to multipotent NSCs with an e
43 ultured in gas-permeable bags containing 1-L serum-free media, granulocyte colony-stimulating factor,
44 rapidly increased after exposure of cells to serum-free media, heat shock, or staurosporine.
45 n as VEGFA) and dickkopf homolog 1 (DKK1) in serum-free media, human embryonic-stem-cell-derived embr
46 an pancreatic cells were proliferated with a serum-free media in monolayer cultures through multiple
47 ed marker shows spheroid colony formation in serum-free media in vitro, as well as tumorigenic abilit
48 neration lentiviral vector in FreeStyle 293 (serum-free media) in suspension.
49 NA levels in neuroblastoma cells cultured in serum-free media increased after 8 to 16 hours in BDNF.
50                                          The serum-free media-induced decrease in permeability was co
51 incubation of mouse embryonic fibroblasts in serum-free media induces caspase-3 activation, an effect
52 TGF-beta1 to vascular smooth muscle cells in serum-free media inhibited apoptosis.
53            Culturing human islets in Memphis serum-free media (M-SFM) is associated with excellent po
54                                  In defined, serum-free media, NHBEs undergo mucosecretory differenti
55                            Exposing cells to serum-free media on their basolateral side significantly
56   However, when cells were grown with either serum-free media or at high densities, CDK2 levels decli
57  and express five-fold fewer IGF-IRs, die in serum-free media or following exposure to metabolic stre
58                                           In serum-free media, p50E4F accelerated E1A-induced apoptos
59 ated dishes and cultured for up to 7 days in serum-free media, platelet derived growth factor BB (PDG
60                          However, culture in serum-free media, presence of nerve growth factor, or ad
61 o the apoptotic effect of PI3K inhibition in serum-free media, reflecting the heterogeneous nature of
62 ures of hepatocytes and endothelial cells in serum-free media seeded under 95% oxygen maintain functi
63 ent of cells with tyrphostin AG879 prevented serum-free media (SFM) induction of cell proliferation.
64 were cultured in parallel in (A) CMRL + ITS (serum-free media; SFM) or (B) CMRL +10% fetal bovine ser
65         Growth in either serum-containing or serum-free media supplemented with GM-CSF and IL-4 yield
66                           Here, we define in serum-free media the minimal factor requirement controll
67                  Pellet cultures of hCSSC in serum-free media upregulated the expression of keratocyt
68 This increased proportion of KS synthesis in serum-free media was caused by a moderate increase in KS
69 media and forms neurospheres in supplemented serum-free media was developed from retinal tumors isola
70  cells, NGF's ability to promote survival in serum-free media was reduced.
71 NTM5 and GTM3) human TM cells conditioned in serum-free media were incubated in the absence or presen
72 an as keratan sulfate (KS), whereas cells in serum-free media were quiescent, appeared dendritic, and
73 aT-AR) displayed autonomous proliferation in serum-free media when compared with controls (HaCaT-NIE)
74 ts before SCT, which were cultured 4 days in serum-free media with hematopoietic growth factors.
75 growth factor and hematopoietic cytokines in serum-free media, yielded a precursor population enriche

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