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1             Neither altered secretion to the basal medium.
2 M-treated cultures as compared with those in basal medium.
3 n injury; control animals were injected with basal medium.
4 essed in response to IL-1beta, IFN-gamma, or basal medium.
5 f insulin, which was not protective alone in basal medium, along with dipyridamole significantly enha
6 ethylformamide, an average of 7 ns in Bold's basal medium, and 8 ns in Chlorella cells.
7 cells underwent spontaneous wound healing in basal medium, and exogenously added HB-EGF and HGF signi
8 re period in a chemically defined serum-free basal medium (BM), with or without recombinant CDMPs 1 a
9                      Neurons died rapidly in basal medium but were rescued in large measure by 10 mic
10 se of soluble 170-kD EGF into the apical and basal medium by 7 and 60%, respectively, and caused a co
11 reased if pituitary extract was added to the basal medium chamber or retina-conditioned medium was ad
12 red on filters that separated the apical and basal medium compartments.
13 ere incubated for 24-48 h in basal medium or basal medium conditioned by activated microglial cells (
14 ted for 24, 48, or 72 h with basal medium or basal medium conditioned by retina-derived Muller cells
15 nCysP1 x BnCysP1Si when germinated on the MS basal medium containing PPT (5 mg/l) and hygromycin (70
16 arge increases in cell density in a limiting basal medium, demonstrating that these reactions are tie
17 tured on decellularized renal scaffolds with basal medium, differentiated into proximal and distal tu
18 ventional Dulbecco's modification of Eagle's basal medium (DME) produce no transformed foci when grow
19 lls were maintained for 2 to 3 months in the basal medium (DMEM containing 2% fetal bovine serum) wit
20              About 25% of cells treated with basal medium for 72 h were positive for bromodeoxyuridin
21                          After incubation in basal medium for more than 2 months, hRPE cells were lar
22 onstrated, with culture on Gresshoff and Doy basal medium in the presence of 4-amino-3,5,6,trichloro-
23                                    The N2B27 basal medium in which mouse gastruloids are cultured can
24 cis RAL release into the apical, but not the basal, medium in the presence of apo IRBP suggests that
25 embryonic CNS neurons cultured in serum-free basal medium lacking trophic factors or other additives.
26  vivo experiments, animals were treated with basal medium (MI: n=6), a fibrin patch (Patch: n=6), a p
27 ccus mutans bacteria were grown for 3 d in a basal medium mucin solution.
28 d short circuit current (Isc) dependent upon basal medium Na+ and Cl-/HCO3- but independent of the pr
29     661w Cells were incubated for 24-48 h in basal medium or basal medium conditioned by activated mi
30  cells were treated for 24, 48, or 72 h with basal medium or basal medium conditioned by retina-deriv
31 mber from 24 to 72 h following incubation in basal medium or MCCM, but not in MGCM, where the cells r
32 ompared with 19-20% of cells grown in either basal medium or MCCM.
33 ition of apotransferrin or iron chelators to basal medium or use of iron-free medium also afforded pr
34 cultured for 0 or 20 hours or 4 or 7 days in basal medium or with added FGF2.
35   Apo IRBP was added to either the apical or basal medium, or was absent from the incubation entirely
36        When apo IRBP was present only in the basal medium, or was absent from the incubation entirely
37  and minimizing antibiotic concentrations in basal medium reduced this carry-over effect.
38 ium consisting of just three components: the basal medium RPMI 1640, L-ascorbic acid 2-phosphate and
39                 The improvement in BrainPhys basal medium to support neurophysiological activity is a
40 ormed DNA ladders in MGCM-treated but not in basal medium-treated samples.
41 , approximately 1 x 10(6) cells suspended in basal medium were injected into the vitreous of normal r
42 teine provided comparable neuroprotection in basal medium, whereas an array of compounds that mimic o
43 y the standard method (MacConkey agar and OF basal medium with agar, polymyxin, bacitracin, and lacto
44 e intramyocardial injections of 70 microL of basal medium without cells (group 1) or containing 3x10(
45 grouped (n=12/group) to receive 80 microL of basal medium without rSkMs (group 1) or containing 1.5 x
46 ics to the optimization of a proprietary CHO basal medium yielded valuable insight regarding the nutr