ライフサイエンスコーパス: preincubate

1 reaction in which Tus and template have been preincubated.

2 Preincubated Abeta interacted with bilayer-reconstituted

3 ve T cells were coincubated with ganglioside-preincubated, Ag-exposed DCs, naive Th cell differentiat

4 eas this activity was retained when EftM was preincubated at 25 degrees C.

5 gnificantly reduced in ts13 nuclear extracts preincubated at 30 degrees C but not in similarly treate

6 jection of mutant G85R SOD1YFP that had been preincubated at 37 degrees C or of cross-linked dimers o

7 Virus preincubated at pH 4.9 and 30 degrees C in the absence o

8 nt with its inability to bind to Neisseriae, preincubating bacteria with native properdin followed by

9 substantially if the enzyme and peptide were preincubated before substrate was added.

10 NP-1 through HNP-3 in gingival tissue and in preincubated cell monolayers, immunohistochemical and im

11 ertussis toxin sensitive and desensitized by preincubating cells with G protein-coupled receptor agon

12 Preincubating cells with PI 3-kinase inhibitor LY294002

13 This increase in current was inhibited by preincubating clusters in sphinganine.

14 proximately 1 mol of CO was released from CO-preincubated CODH upon denaturation of the protein.

15 tion of spindle elongation can be rescued by preincubating concurrently with the fusion protein again

16 Finally, preincubating CPE with soluble recombinant Claudin-4, or

17 Even when pulsed with TT, these ganglioside-preincubated DC remained deficient in costimulatory mole

18 In contrast, systemic injection of APCs preincubated ex vivo with the encephalitogenic peptide o

19 hed cell membranes isolated from ganglioside-preincubated fibroblasts.

20 ponse by approximately 50% after 50 ms; when preincubated for 10 s, it decreased the peak initial res

21 When cells were preincubated for 15 h with excess copper (15 microM Cu(I

22 was inhibited 98% by CO and 65% by coumarin preincubated for 15 min with REM (Ki, 120 microM) but wa

23 3T3-L1 adipocytes were preincubated for 18 h in media +/- 0.6 nmol/l insulin co

24 ly times if the perforated synaptosomes were preincubated for 2 min with anti-NSF.

25 luence the observed effect of NO, cells were preincubated for 24 hours in L-cystine- and glutathione

26 Rat extensor digitorum longus muscles were preincubated for 4 h in Krebs-Henseleit solution contain

27 Cells preincubated for 4 h with a source of apoE3 or apoE4, fo

28 neralization with PyOM additions in the soil preincubated for 6 months.

29 ed using the oxygenase domain which has been preincubated for an extended length of time at 4 degrees

30 In a lysate from chloroplasts that had been preincubated for various lengths of time in an import re

31 nd western blot reactivity were abolished by preincubating HAM/TSP IgG with HTLV-I protein lysate but

32 Inhibition of cPLA(2alpha) involved preincubating HCE cells for 1 hour with cPLA(2alpha) inh

33 tor (EGFR) transactivation was suppressed by preincubating HCECs with capsazepine, matrix metalloprot

34 Moreover, preincubating host cells with GST-tagged forms of both A

35 G(D1a)-preincubated human dendritic cells (DC) were also affect

36 When human monocytes were preincubated in 50 micro M highly purified ganglioside G

37 nished by 60%, compared with that of muscles preincubated in a glucose-free medium; whereas activatio

38 lease of calcium was blocked when cells were preincubated in BAPTA, in the presence of ruthenium red,

39 act-induced chondrocyte death, explants were preincubated in culture medium containing various concen

40 with porcine aqueous humor (78% +/- 77% when preincubated in DMEM containing porcine aqueous humor ve

41 Avena coleoptile sections were preincubated in either fusicoccin (FC), cycloheximide, p

42 ified LPS-stimulated monocytes that had been preincubated in G(D1a) likewise showed inhibition of CD8

43 PMN preincubated in T/HS lymph showed significant elevations

44 t lipid efflux from these cells, apo A-1 was preincubated in the presence of unlabeled SMC or fibrobl

45 mbilical vein endothelial cells (HUVEC) were preincubated in the presence or absence of tumor necrosi

46 ; or 3) with rat macrophages or 4) platelets preincubated in vitro with LPS (200 microg/ml).

47 Preincubating infected mouse serum with anti-IFN-gamma m

48 Preincubating inhibitors or ATP with biotin-p38alpha and

49 Preincubating IPAs in physiological saline solution (PSS

50 over, the transfer reaction was inhibited by preincubating macrophages with anti-CR3 or anti-Fc gamma

51 reating DC organisms with Asp14 antiserum or preincubating mammalian host cells with glutathione S-tr

52 to 19% and reduced tumorigenesis by 50% when preincubated MCF-7 breast cancer cells were inoculated i

53 ma release by the GTP-washing from these NAD-preincubated membranes was also suppressed to approximat

54 ffer containing GTP, the PDE activity of NAD-preincubated membranes was increased by the GTP-washing

55 le for 8OHG immunoreactivity was analyzed by preincubating midbrain sections from PD patients with RN

56 The enhanced permissiveness of CytD-preincubated monocytes was found to be due to TNFalpha,

57 induced c-Jun kinase activity was reduced by preincubating myocytes during the hypoxia phase with the

58 12 supernatants with anti-sAPP antibodies or preincubating naive PC12 cells with IL-1 receptor antago

59 r the deletions in myeloid leukemias because preincubating nuclear extracts from leukemic cells with

60 ater permeability, which was abolished after preincubating oocytes with very low concentrations of th

61 Preincubating PHUECs in 0.3 M sucrose or monodansylcadav

62 d by fixing platelets with paraformaldehyde, preincubating platelets with a TGF-beta1-blocking antibo

63 Preincubating platelets with specific monoclonal antibod

64 atelet aggregation that was not inhibited by preincubating platelets with the prostaglandin E(1) or t

65 d protamine is monitored after addition of a preincubated reaction mixture containing the sample and

66 low- and high-affinity binding was to first preincubate receptor membranes with the fluorescent part

67 Shoots can be induced in tissue culture by preincubating root explants on an auxin-rich callus indu

68 targeted to the RyR1 cytoplasmic assembly by preincubating sarcoplasmic reticulum membranes with a fl

69 Dilution experiments of cinaciguat/Tween 20-preincubated sGC revealed the irreversible character of

70 the longer term, both the 6-month and 1-day preincubated soils experienced net approximately 10% dec

71 ddition of high concentrations of NH4Cl to a preincubated solution of Pdx1 and R5P.

72 Preincubating T cells with either EDCI-fixed APC or iono

73 idermis, both of which could be abolished by preincubating the anti-serum with the peptide used for i

74 B receptor, and the abolition of staining by preincubating the antiserum with the C-terminus peptide

75 Preincubating the bacteria with recombinant ICAM-1 reduc

76 The activation of MSK1/MSK2 was prevented by preincubating the cells with a combination of two drugs

77 ration in Sup-T1 cells that was abolished by preincubating the cells with pertussis toxin or PMA and

78 ference in Abeta production was abolished by preincubating the cells with the receptor-associated pro

79 cells (keratocytes), which was inhibited by preincubating the corneas with PAF antagonists.

80 Drug resistance could not be overcome by preincubating the drugs with IN, consistent with the bin

81 e protected from CPE-induced cytotoxicity by preincubating the enterotoxin with soluble full-length r

82 e inactivation curve could not be altered by preincubating the enzyme and inhibitor in the absence of

83 protection from inactivation is achieved by preincubating the enzyme with ATP or ATP and proline, bu

84 nce of substrates but could be linearized by preincubating the enzyme with inhibitor, aspartate, GTP

85 Preincubating the extracytosolic face of TRPML3 in Na+-f

86 sion and activity could be blocked by either preincubating the glutamate-treated PC12 supernatants wi

87 At least one such complex is eliminated by preincubating the nuclear extract with an antibody with

88 is splicing inhibition could be prevented by preincubating the peptides with the corresponding partne

89 ossible high plasma kininogenase activity by preincubating the samples with protease inhibitor.

90 ssembly in these clarified extracts requires preincubating the substrate sperm nuclei in an extract u

91 release from duodenal mucosa was assessed by preincubating the tissue with [(3)H] choline and measuri

92 than those lacking the 3' P2a sequence when preincubated under the standard low-Na+ conditions.

93 necessary for its interaction with HVEM, we preincubated virions with gD-specific monoclonal antibod

94 293 and Vero cells, and HFF was observed by preincubating virus with soluble alpha3beta1, alphaVbeta

95 SR asthma and 8 patients with SS asthma were preincubated with 1,25-dihydroxyvitamin D (1,25[OH]2D [V

96 t significantly different when myocytes were preincubated with 10 microM forskolin and 300 microM 3-i

97 In cells preincubated with 100 microM 8Br-cADPR, the [Ca2+]i resp

98 e largely abolished when the transporter was preincubated with 2164U90, suggesting that the binding o

99 IF RBCs were preincubated with 25 microM neomycin sulfate, an inhibit

100 ncubation; they were not observed in muscles preincubated with 25 mmol/l glucose + insulin for 5 min.

101 very rapidly (tau = 130 ms) when cells were preincubated with 300 nm 3alpha5alphaP before applicatio

102 Cells were preincubated with 4 microM estrogen for 2 h and then exp

103 monocytes levels, even when iNKT cells were preincubated with 4-1BB blocking Abs.

104 When normal SMC were preincubated with 4N1K or an anti-alpha2beta1 function-s

105 f Akt and ERK were abolished when cells were preincubated with 50 ng/ml PTX or with 1 microM L745,870

106 imal effect was obtained when the cells were preincubated with 80 mM of ethanol before PMA stimulatio

107 When the membranes were preincubated with [(3)H]NMS and then exposed to benzilyl

108 Photolysis of sea urchin egg homogenates preincubated with [(32)P-5N(3)]NAADP resulted in specifi

109 diographic examination of brainstem sections preincubated with [125I]p-iodoclonidine revealed no inte

110 f [3H]inositol phosphate production in cells preincubated with [3H]inositol provided a highly sensiti

111 ion, when purified caveolae preparations are preincubated with a myristoylated peptide derived from t

112 on was blocked completely when the toxin was preincubated with a peptide containing the toxin-binding

113 When PvuII methyltransferase was preincubated with a range of [3H-CH3]AdoMet concentratio

114 Some cells were preincubated with a slow releasing NO donor for 12 hours

115 5 minutes) was observed when the fibers were preincubated with acetoxymethyl ester of 1,2-bis (2-amin

116 and peripheral blood mononuclear cells were preincubated with acetylated low-density lipoprotein and

117 ated with normal sera, apoptotic cardiocytes preincubated with affinity-purified Abs to SSB/La, 52-kD

118 photoreceptor outer segment homogenates are preincubated with AMP-PNP (EC50 = 0.65 +/- 0.20 mM), GCA

119 Human platelets in suspension were preincubated with amrinone 2.5 to 15 microg/mL; stimulat

120 Murine RAW 264.7 macrophages were preincubated with an exogenous surfactant and exposed ov

121 Additional samples were preincubated with an IL-6-blocking antibody Fab fragment

122 Confluent ARPE-19 cells were preincubated with anthocyanin and nonanthocyanin phenoli

123 Allospecific cell lines were preincubated with anti-alpha(4)beta(1) or anti-alpha(L)b

124 (50% and 35%, respectively) when cells were preincubated with anti-annexin II IgG.

125 rence to Caco-2 cells and wild-type bacteria preincubated with anti-CD0873 antibodies showed signific

126 In blocking experiments, SF was preincubated with anti-CD14 antibody.

127 o in response to CD4 T cells and neutrophils preincubated with anti-CD277 mAb or HMBPP.

128 T cells preincubated with anti-CD44 or antiintegrin alpha4 were

129 ith those that specifically retained virions preincubated with anti-CP antibodies.

130 whitefly vectors failed to transmit virions preincubated with anti-CPm antibodies but transmitted vi

131 f insects that specifically retained virions preincubated with anti-CPm antibodies were significantly

132 Similarly, bone marrow M phi preincubated with anti-CSF-1 receptor Ab or anti-CSF-1 n

133 of adhesion of rat basophilic leukemia cells preincubated with anti-dinitrophenyl IgE clones SPE-7 or

134 uld antagonized, in part, when PLT-Ecto were preincubated with anti-TGF-beta1 Ab.

135 n peripheral blood mononuclear cells (PBMCs) preincubated with anti-TLR10 antibody and HEK-293 cells

136 ed blood obtained from normal volunteers was preincubated with antibodies c7E3 Fab (anti-GPIIb/IIIa a

137 anti-CPm antibodies but transmitted virions preincubated with antibodies recognizing the major coat

138 ome experiments, endothelial monolayers were preincubated with antibody directed against adhesion mol

139 ke of Abeta by SY5Y cells was amplified when preincubated with ApoE and was mediated through lipoprot

140 redimerize, but had no effect on iNOS dimer preincubated with Arg and H4B.

141 me in experiments in which gamma complex was preincubated with ATP before adding beta or added direct

142 reveal that upon binding to LrPduO that was preincubated with ATP, both Co (2+)corrinoids undergo a

143 In contrast, when gamma complex is preincubated with ATP, DNA binding is faster than when g

144 ed-flow mixing of actin with labeled myosin, preincubated with ATP.

145 but not PAECs of other porcine origins, were preincubated with autologous human APCs before addition

146 occurred when the HUVEC-amnion cultures were preincubated with B. burgdorferi for 24 h and T lymphocy

147 rane proteins was largely prevented in cells preincubated with BAPN.

148 ginal challenge of macaques with SIV(mac251) preincubated with BCD prevented mucosal transmission, as

149 ages in the assembly process, the cells were preincubated with BFA (to reversibly inhibit the assembl

150 s strongest when the dibromide or epoxide is preincubated with both enzyme and substrate, indicating

151 alone, and the effect was blunted in vessels preincubated with both fibronectin and vitronectin.

152 When HL-60/Bcl-2 cells were preincubated with bryostatin 1 (10 nM; 24 hr) or coincub

153 ition of IgE dependent mediator release when preincubated with C(60) fullerenes.

154 Cleavage was markedly inhibited when C3b was preincubated with C1-INH.

155 derived from a G14D-CCV-immunized fish were preincubated with CC41 mAb, killing of G14D-CCV targets

156 was examined in cortical membranes that were preincubated with CCK-8S and CCK receptor agonist and an

157 in also appeared to undergo aggregation when preincubated with cholesterol, as determined by SDS-poly

158 from erythrocytes was observed when Act was preincubated with cholesterol, but not with myristylated

159 Staphylococcus aureus superantigen and, when preincubated with CMV antigens, induce a recall CD4(+) T

160 d not inhibit NK-cell activation when it was preincubated with cobra venom factor (CVF) to deplete C3

161 HAH1/WDp interaction is metalospecific; HAH1 preincubated with Cu(2+) or Hg(+) but not with Zn(2+), C

162 red the ability of Galpha(s), which had been preincubated with Cu(2+) or Zn(2+), to stimulate AC; AlF

163 In control experiments, where streptavidin preincubated with d-biotin in solution is added to bioti

164 egral membrane enzyme or the purified enzyme preincubated with decylubiquinol, this mode appears at 1

165 (VI)-exposed human lung A549 cells that were preincubated with dehydroascorbic acid to create normal

166 When preincubated with DHA, RPLTT but not C25S was protected

167 d retinal pigment epithelial microsomes were preincubated with different amounts of all-trans-retinol

168 Furthermore the neuroretinal cells were preincubated with different and concentrations of 14-3-3

169 Slices preincubated with diisopropylflurophosphate (to permanen

170 orcine aqueous humor versus 13% +/- 15% when preincubated with DMEM alone, n = 6, P = 0.03).

171 was able to promote DNA strand exchange when preincubated with double-stranded DNA.

172 and viral infection at 37 degrees C only if preincubated with E/T cells at the suboptimal temperatur

173 en cells were exposed to TTP plasma that was preincubated with EDTA or heat-inactivated, or to contro

174 t with 40 S ribosomal subunits that had been preincubated with eIF3, the 40 S preinitiation complex f

175 f the instrument whenever coenzyme B(12) was preincubated with enzyme prior to mixing with substrate.

176 oichiometric concentrations of inhibitor are preincubated with enzyme.

177 , addition of oxygenated buffer to premat-GO preincubated with excess Cu(II) generated the Y272 radic

178 were significantly enhanced when beads were preincubated with exogenous alpha2 laminins.

179 C activity is rescued when the 3i peptide is preincubated with exogenous beta-arrestin.

180 In contrast, in skin preincubated with FGF-2, FR1-AP binds avidly to FGF-2 im

181 Mice intranasally infected with D39 preincubated with FH had increased bacteremia and lung i

182 s fimA mutant DPG3 or when P. gingivalis was preincubated with fimbrillin peptide antisera prior to t

183 ificantly affected in stationary-phase cells preincubated with formate or succinate.

184 when carbachol was added to cells that were preincubated with forskolin, an agent that directly acti

185 After differentiation, cells were separately preincubated with free fatty acids (FFAs) and ceramide C

186 es to both sides of planar DC18:1PC bilayers preincubated with gA, which reduced channel activity up

187 nced when either T. cruzi or CASM cells were preincubated with galectin-3.

188 This was blocked when platelets were preincubated with Ginkgolide B.

189 oxygen consumption by stationary-phase cells preincubated with glucose, pyruvate or malate and caused

190 s that human peripheral blood monocytes when preincubated with gp120 either purified from laboratory-

191 Monocytes preincubated with gp41 of the MN strain showed markedly

192 Purified T cells were preincubated with GST-tagged HrHRF, followed by stimulat

193 erferon-gamma, unless the skin sections were preincubated with HA-1/HA-2 synthetic peptides.

194 ylation was strongly inhibited after PKR was preincubated with HCV E2.

195 ly, bone marrow-derived dendritic cells were preincubated with HDEs, and then LPS-induced IL-6 respon

196 r vx-LDL) was significantly reduced in cells preincubated with heparin or NaClO3, suggesting a role f

197 BT20 cells were rescued from apoptosis when preincubated with HER4 small interfering RNA, thereby co

198 nd that MDA-MB-453 human breast cancer cells preincubated with HGF/SF and then exposed to Adriamycin

199 However, when DCs were first preincubated with highly purified G(D1a) ganglioside, up

200 otella intermedia ATCC25611 on keratinocytes preincubated with HNP-1 were determined with a standard

201 We show that only bacteria preincubated with holoBPI are ingested by neutrophils an

202 In cardiac cells preincubated with hormones and/or drugs for 8 h, metabol

203 s treated with E. chaffeensis which had been preincubated with human anti-E. chaffeensis serum for 2

204 T6 and was not evident unless the cells were preincubated with IFN for at least 1 hr before IL-4 stim

205 nocytes and monocyte-derived dendritic cells preincubated with IFN-gamma before stimulation by LPS, s

206 rs of T(84) and HT29/cl.19A colonocytes were preincubated with IFN-gamma prior to stimulation with EG

207 with aluminum fluoride unless the cells were preincubated with IFN-gamma.

208 r than those observed in cells that had been preincubated with IgE alone; and 4) batches of human mas

209 ealthy cardiocytes and apoptotic cardiocytes preincubated with IgG from a healthy donor, respectively

210 ealthy cardiocytes and apoptotic cardiocytes preincubated with IgG from a healthy donor.

211 reduction in invasion was observed in PHUECs preincubated with increasing concentrations of NaOH-deac

212 Acini were preincubated with inhibitors for 20 minutes before addit

213 Cartilage explants were preincubated with inhibitors of ERK1/2 and p38 activatio

214 bserved that the enzyme was inactivated when preincubated with iodoacetamide, and protected from inac

215 mozoin-laden monocytes/macrophages that were preincubated with iRBCs also stimulated HIV production.

216 n superoxide yields is observed when nNOS is preincubated with L-arginine.

217 Neutrophils preincubated with LAM 1-116 displayed similar behavior t

218 UVECs and HMVECs that was inhibited in cells preincubated with LAU8080 or with a VEGF-blocking antibo

219 ated in endosomes/lysosomes in variant cells preincubated with LDL cholesterol but targeted to the Go

220 to MOLT-4 cells was not enhanced when it was preincubated with lipid-free apoprotein B, which suggest

221 ngly suppressed in L6 myotubes or HeLa cells preincubated with LOA.

222 n IBa was abolished in oocytes that had been preincubated with losartan (an AT1A receptor antagonist)

223 reated keratinocytes, neither irradiated nor preincubated with melatonin.

224 ylated RGS16 or RGS4 WT but not C98A or C95A preincubated with membranes expressing 5-HT1a/G alpha o1

225 simultaneously with agonist and when it was preincubated with membranes.

226 was reduced greatly if the enzyme was first preincubated with metal ions.

227 Antibodies against metaxin, when preincubated with mitochondria, partially inhibited the

228 drial fractions prepared from rat brain were preincubated with MnCl2 in vitro, followed by the enzyme

229 Capture slides preincubated with mouse immunoglobulins were used for pr

230 ng the t-SNAREs syntaxin-1A and SNAP-25 were preincubated with Munc18 for 30 min.

231 CM preincubated with neutralizing alpha-TNF or alpha-IFN-ga

232 CM from CD3 mAb-stimulated T-lymphocytes was preincubated with neutralizing anti-(alpha)-tumor necros

233 d by injecting splenic T cells that had been preincubated with noradrenaline or splenocytes harvested

234 ntains the HD recognition site, unless it is preincubated with nuclear extracts precleared by anti-Pa

235 ge-clamped oocytes expressing receptors were preincubated with one of the lipophilic probes and were

236 Isolated rat hepatocytes were preincubated with or without a microtubule stabilizing a

237 When rod membranes were preincubated with or without NAD and washed with a buffe

238 When LJ001 was preincubated with our model virus, infectious hematopoie

239 Corneas were stimulated with 120 nM PAF or preincubated with PAF antagonists, cyclohexamide (CHX) o

240 cells was blocked when the VP2 virions were preincubated with partially purified ABP.

241 Chymase I reduces pore formation when preincubated with perforin at 37 degrees C.

242 Increasing cAMP in hepatocytes preincubated with pertussis toxin completely inhibited t

243 ensitization by LPA was lost when cells were preincubated with pertussis toxin or C3 exotransferase.

244 The NE effect was abolished in cells preincubated with pertussis toxin, indicating coupling t

245 e to convert 5-HETE into 5-oxo-ETE even when preincubated with phorbol ester or with other lipid hydr

246 When A. phagocytophilum was preincubated with plasma from the infected horse and the

247 incubated in DMEM, but only if myocilin was preincubated with porcine aqueous humor (78% +/- 77% whe

248 ibitor p27Kip1 are increased when cells were preincubated with pravastatin for 1 h and then exposed t

249 rotective response if endothelial cells were preincubated with protein C.

250 When preincubated with protein S, antibodies raised against P

251 While the wild-type strains preincubated with purified salivary amylase grew well in

252 asmin was significantly delayed when Plm was preincubated with purified, soluble alpha(M)beta(2).

253 However, when one set of vesicles was preincubated with Rab5 D136N plus XTP and the second set

254 s nuclear export in cells that have not been preincubated with RanQ69L.

255 fter coculture with antigen-presenting cells preincubated with recombinant Escherichia coli expressin

256 Bone marrow-derived macrophages preincubated with recombinant RBP4 led to attenuation of

257 dependent manner when unfertilized eggs were preincubated with recombinant ZP3R/sp56 (74% drop at the

258 th LPS preincubated with whole blood vs. LPS preincubated with saline.

259 tive (SIV(+)) plasma but became sensitive if preincubated with sCD4.

260 ls from healthy CMV-seropositive donors were preincubated with serial dilutions of tacrolimus, mycoph

261 ium adenosinetriphosphatase of sheep kidney, preincubated with sodium and magnesium (E.Nae), reacts w

262 tion of the linker region, chondrocytes were preincubated with specific MAPK inhibitors (PD98059 for

263 When ssDNA was preincubated with SsbA, but not SsbB, DprA was able to a

264 activity of RecOR is seen only when RecOR is preincubated with ssDNA prior to the addition of SSB.

265 in a bc(1) complex inhibited at center P and preincubated with substoichiometric concentrations of an

266 ated neutrophils (FMLP) to endothelial cells preincubated with sulfasalazine was inhibited in a dose-

267 Four iterations of the motif, preincubated with TBP, inhibited its binding to high-den

268 al cell carcinoma (RCC) with dendritic cells preincubated with the autologous apoptotic renal tumor l

269 When preincubated with the CD4+ve MM6 macrophage cell line, w

270 n of purified recombinant CdtB to HeLa cells preincubated with the CdtA-CdtC complex resulted in the

271 ed in nearly quantitative yield when CobA is preincubated with the co-substrate ATP.

272 16 displayed similar behavior to neutrophils preincubated with the control anti-L-selectin mAb, LAM1-

273 vitro requires that both activators must be preincubated with the DNA prior to addition of RNA polym

274 hia coli enzyme, depending on whether it was preincubated with the enzyme or not.

275 ly inhibited unwinding reactions when it was preincubated with the helicase-nucleic acid complex.

276 More prominent in cells preincubated with the high dose, reduced basal IkappaBal

277 In cells preincubated with the high TNF dose, we observed blockad

278 otinic acetylcholine receptors (nAChRs) were preincubated with the hydrophobic probe 3-(trifluorometh

279 ng of [3H]WIN 35,428 in tissue that had been preincubated with the ligand and then thoroughly washed

280 ited at least 80% in merbarone-treated cells preincubated with the pan-caspase inhibitor z-VAD-fmk [Z

281 Cultured goblet cells were preincubated with the PKC inhibitor calphostin C (10(-10

282 Acini were preincubated with the PKC inhibitors calphostin C or Ro-

283 transcription/translation, cell extract was preincubated with the proteasomal inhibitor MG132 in the

284 secretion was observed only when cells were preincubated with these agents.

285 on, and moreover, addition of Oxo-M to cells preincubated with this agent elicited a further increase

286 th either infliximab or adalimumab, alone or preincubated with TNF-alpha.

287 When the CM was preincubated with uPAR-neutralizing antibody or when uPA

288 a time- and temperature-dependent manner if preincubated with vac5-1 cytosol and ATP, suggesting the

289 )-stimulated ERK phosphorylation in REC when preincubated with VEGF.

290 n vitro portion of the study, rat cells were preincubated with vehicle (saline and/or dimethyl sulfox

291 reater extent than did 80 mug/ml ReoPro when preincubated with Vero E6 cells.

292 from the spleens of young and old mice were preincubated with vitamin E or vehicle control.

293 When Cry6Aa1 was preincubated with Western corn rootworm (WCRW) midgut ju

294 ntly reduced in volunteers injected with LPS preincubated with whole blood vs. LPS preincubated with

295 Mast cells preincubated with wortmannin failed to develop the class

296 When the PARPzf peptide is preincubated with Zn(II) followed by incubation with inc

297 Activation of ERK was inhibited by preincubating with a DOP1 receptor antagonist.

298 Preincubating with the RCS, methylglyoxal (MGO) likewise

299 ly to approximately 50% of that of membranes preincubated without NAD.

300 also suppressed to approximately 50% of that preincubated without NAD.