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1 M-treated cultures as compared with those in basal medium.
2 essed in response to IL-1beta, IFN-gamma, or basal medium.
3 Neither altered secretion to the basal medium.
4 f insulin, which was not protective alone in basal medium, along with dipyridamole significantly enha
6 cells underwent spontaneous wound healing in basal medium, and exogenously added HB-EGF and HGF signi
7 re period in a chemically defined serum-free basal medium (BM), with or without recombinant CDMPs 1 a
9 se of soluble 170-kD EGF into the apical and basal medium by 7 and 60%, respectively, and caused a co
10 reased if pituitary extract was added to the basal medium chamber or retina-conditioned medium was ad
12 ere incubated for 24-48 h in basal medium or basal medium conditioned by activated microglial cells (
13 ted for 24, 48, or 72 h with basal medium or basal medium conditioned by retina-derived Muller cells
14 nCysP1 x BnCysP1Si when germinated on the MS basal medium containing PPT (5 mg/l) and hygromycin (70
15 arge increases in cell density in a limiting basal medium, demonstrating that these reactions are tie
16 tured on decellularized renal scaffolds with basal medium, differentiated into proximal and distal tu
17 ventional Dulbecco's modification of Eagle's basal medium (DME) produce no transformed foci when grow
18 lls were maintained for 2 to 3 months in the basal medium (DMEM containing 2% fetal bovine serum) wit
21 onstrated, with culture on Gresshoff and Doy basal medium in the presence of 4-amino-3,5,6,trichloro-
22 cis RAL release into the apical, but not the basal, medium in the presence of apo IRBP suggests that
23 embryonic CNS neurons cultured in serum-free basal medium lacking trophic factors or other additives.
24 vivo experiments, animals were treated with basal medium (MI: n=6), a fibrin patch (Patch: n=6), a p
25 d short circuit current (Isc) dependent upon basal medium Na+ and Cl-/HCO3- but independent of the pr
26 661w Cells were incubated for 24-48 h in basal medium or basal medium conditioned by activated mi
27 cells were treated for 24, 48, or 72 h with basal medium or basal medium conditioned by retina-deriv
28 mber from 24 to 72 h following incubation in basal medium or MCCM, but not in MGCM, where the cells r
30 ition of apotransferrin or iron chelators to basal medium or use of iron-free medium also afforded pr
32 Apo IRBP was added to either the apical or basal medium, or was absent from the incubation entirely
34 ium consisting of just three components: the basal medium RPMI 1640, L-ascorbic acid 2-phosphate and
37 , approximately 1 x 10(6) cells suspended in basal medium were injected into the vitreous of normal r
38 teine provided comparable neuroprotection in basal medium, whereas an array of compounds that mimic o
39 y the standard method (MacConkey agar and OF basal medium with agar, polymyxin, bacitracin, and lacto
40 e intramyocardial injections of 70 microL of basal medium without cells (group 1) or containing 3x10(
41 grouped (n=12/group) to receive 80 microL of basal medium without rSkMs (group 1) or containing 1.5 x
42 ics to the optimization of a proprietary CHO basal medium yielded valuable insight regarding the nutr
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