ライフサイエンスコーパス: coincubation

1 alpha, and TGF-beta expression within 3 h of coincubation.

2 etry and confocal microscopy after 2-18 h of coincubation.

3 ssing pIL-1 beta, requiring at least 24 h of coincubation.

4 stimulated production of IL-8 within 8 h of coincubation.

5 iate ciliary binding capacity throughout the coincubation.

6 We show that coincubation a synthetic Cap-Pol fusion protein with lys

7 for 5 days before the SK-RC-45/T lymphocyte coincubation, a regimen that reduced tumor-associated ga

8 image acquisition pairs of AF-SHG (+/-eosin coincubation), AF-eosin, and SHG-eosin were captured.

9 s are formulated to readily enter cells upon coincubation and contain two cyanine-based fluorescent r

10 e acquisition pairs of AF-SHG (without eosin coincubation) and SHG-eosin.

11 peptide in both a preincubation assay and a coincubation assay.

12 Coincubation assays detected fusion of prelabeled OVS wi

13 5 as coreceptors, increasingly long times of coincubation at 23 degrees C reduced the efficacy of the

14 As the time of cell coincubation at 23 degrees C was prolonged, more cells q

15 Upon coincubation, CP-2 changes the aggregation pathway of Ab

16 During 24 h of coincubation, cultures challenged with untreated or UV l

17 pletely blocked bimatoprost's effects, while coincubation decreased its effects on average by 74%.

18 thelial permeability induced by IFN-gamma in coincubation experiments.

19 sion of pIL-1 beta by stromelysin-1 required coincubation for at least 1 h, and biologic activity fad

20 Coincubation in the presence of VER resulted in 4.5-fold

21 ing molecular mechanisms, we have found that coincubation in vitro of epinephrine-treated SS RBCs wit

22 istent for short (<1 h) and long (24 h) term coincubation indicating that mineral surface inhibition

23 ither spent culture exchange, transwell, nor coincubation internalization experiments supported a rol

24 n a few minutes at 42 degrees C, with longer coincubation leading to an increased population of stabl

25 In ex vivo coincubation models of IMA/PVAT, the activation of arter

26 oupling and uncoupling were monitored during coincubation of (S)-naproxen and CYP2C9 over a range of

27 Coincubation of 3dSB or 3dSB-PNBS with the caspase-9 inh

28 Coincubation of 9L tumor cells with DCs was found to ind

29 ory response were monitored with and without coincubation of a free-radical scavenger (trolox).

30 ase 6 pre-mRNA can be visualized directly by coincubation of a radiolabeled substrate RNA and a synth

31 sus 19+/-2% at 10(-8) mol/L) and restored by coincubation of AA (37+/-2%), tempol (33+/-2%), losartan

32 Coincubation of airway smooth muscle with peripheral blo

33 e standardized assay was rapid (single 2.5-h coincubation of all reagents), required no wash steps, a

34 Coincubation of astrocytes (or their conditioned medium)

35 In vitro coincubation of B cells with plasma from CML patients on

36 Coincubation of BKV but not mouse polyomavirus with clin

37 Importantly, coincubation of blood samples with antibiotics facilitat

38 Coincubation of BMDM with both fatty acids counteracted

39 Coincubation of CD4(+) T cells with human ASM cells puls

40 Coincubation of chymase-rich BR mastocytoma cells with A

41 mall intestinal loop assay, preincubation or coincubation of CPE with the claudin-4 ECL-2 peptide sig

42 Coincubation of cultured hepatocytes with 25-hydroxychol

43 Coincubation of DAPH and Abeta1-42 greatly reduces the b

44 Coincubation of DCs with parasite extracts along with kn

45 Coincubation of diabetogenic T cells with activated B ce

46 me fractions with ATP at 37 degrees C and by coincubation of endosomes at 22 degrees C before the ass

47 Coincubation of FMLP with zileuton, a selective inhibito

48 Finally, we show that coincubation of HeLa cells with epinephrine increases EH

49 Coincubation of hRPE cells with the mitogen-activated pr

50 Coincubation of human peripheral blood mononuclear cells

51 -I; and 3) whose regulation was abolished by coincubation of IGFBP-3 with IGF-I.

52 This effect was completely inhibited by coincubation of IMAs with DPI (100 micromol/L), a nonspe

53 uced potentiation of the DAMGO response, but coincubation of insulin with either the MAP kinase inhib

54 proinsulin (PI) and TNF-alpha coexpression; coincubation of isolated DRG neurons with PI-BMDCs in hi

55 Furthermore, coincubation of isolated synaptosomes with alpha(2)AR an

56 In the presence of MAb 2H1, coincubation of J774.16 cells with C. neoformans reduced

57 In the absence of MAb 2H1 to GXM, coincubation of J774.16 cells with C. neoformans reduced

58 Coincubation of KB or TERT-2 epithelial cells with equal

59 However, coincubation of low density lipoprotein with zymosan-sti

60 Coincubation of LPC (1 micromol/L) with H(2)O(2) (0.5 mi

61 red by a MCP-1 chemoattractant gradient, and coincubation of LPG with neutralizing mAb abrogated the

62 buted to the activity of IL-1 and TNF, since coincubation of LPS-stimulated PBMC with IL-1R antagonis

63 Coincubation of macrophages with cells that expressed Dl

64 Coincubation of MC38-specific CTLs with MC38-IFNalpha or

65 Coincubation of membranes with iodinated antagonist and

66 However, the coincubation of mesangial cells with TNF-alpha and dbcAM

67 Coincubation of microglia with L-arginine or the superox

68 Coincubation of MIF from hyperglycemic dogs with an angi

69 Coincubation of monocyte/plasmacytoid dendritic cells, N

70 nd human NB cell lines, we demonstrated that coincubation of murine bone marrow progenitors or human

71 Coincubation of murine CTLs with target cells expressing

72 By coincubation of NK cells with monolayers of CRIP cells o

73 In contrast to Nrf2(+/+) DCs, coincubation of Nrf2(-/-) DCs with PM and the antioxidan

74 These effects were inhibited by coincubation of pericytes with Axl-ECD and recombinant G

75 ducts and demonstrated their formation after coincubation of PGH(2) with synthetic peptides and prote

76 Coincubation of properdin and factor H did not hamper HS

77 We have previously shown that coincubation of purified B cells with IL-2-propagated NK

78 Coincubation of RRVs with heat-treated RRVs or with lent

79 Thus, coincubation of SCCHN with Fas-sensitive lymphocytes can

80 Coincubation of SMC from the midregion with ET-1 plus TG

81 Here we show that coincubation of SMC with macrophages or oxidized low den

82 Northern blot analysis revealed that coincubation of synovial fibroblasts with IL-1 and IL-4

83 Coincubation of T. vaginalis isolates with acutely HIV-1

84 is; (b) measured the cytokine secretion upon coincubation of TALL-104 cells with brain tumor cells; (

85 In vitro coincubation of TALL-104 cells with human brain tumor ce

86 Moreover, coincubation of TGN1412-treated T cells with B cells exp

87 Coincubation of the Abeta1-42 peptide with DAPH produces

88 Coincubation of the cells with pargyline and 5-hydroxytr

89 (8.0% and 12.8%, respectively) compared with coincubation of the CTLs with MC38-WT (43.5%; p < 0.001)

90 Importantly, coincubation of the engineered bacteria with recombinant

91 and to a lesser extent PCMB, is inhibited by coincubation of the receptor with the hydrolysis-resista

92 itro cell-free enzymatic studies showed that coincubation of the recombinant H-PGDS with either MnTMP

93 Finally, coincubation of the specific tyrosine kinase inhibitor g

94 Coincubation of the spirochete with HUVEC or HEK293 cell

95 Coincubation of these regulatory T-cell epitopes or "Tre

96 old increase in total TF expression, whereas coincubation of TNF-alpha with wild-type VEGF- or KDR-se

97 Coincubation of transfected hepatocytes with 10(-8) M de

98 t varying temperatures was monitored during "coincubation" of rhIL-1ra with peptides mimicking specif

99 In agreement, amifostine and WR-1065 coincubation reduced uptake in BN-16 but not in CA20948

100 After prolonged coincubation, short fibrils were formed, suggesting an e

101 We used blood coincubation studies of targeted knockout strains to con

102 Furthermore, coincubation studies revealed a significant increase in

103 Proteasome/synthetic peptide coincubation studies support a role for enhanced epitope

104 The coincubation study allowed estimation of oxidation rates

105 After 24 hours of coincubation, the majority of CD34+ cells remained nonad

106 ly functional in cell-cell fusion at shorter coincubation times and at lower temperatures than those

107 After 20 hours coincubation TNF-alpha inhibited neutrophil apoptosis; h

108 host cell Ca(2+) transients within 2 min of coincubation, whereas coincubation with an avirulent str

109 tested by blocking D(2/3)R with raclopride (coincubation with 10 muM in vitro, administration of 1.0

110 beta 1-42 for 24 h reduced viabilty to 36%; coincubation with 10(-7) M IL-1 further reduced viabilit

111 Coincubation with 3-aminobenzamide, an inhibitor of poly

112 [3H]Ro48-8071 was competitively displaced by coincubation with a 1000-fold molar excess of 18-thia-2,

113 lls, and this internalization was blocked by coincubation with a cyclic RGD peptide (cyclo[RGDfV], f

114 activation could be completely inhibited by coincubation with a humanized monoclonal antibody direct

115 Coincubation with a miR-34a inhibitor diminished the eff

116 This was reversed by coincubation with a protein kinase C (PKC) inhibitor or

117 Likewise, coincubation with a specific IL-18Ralpha-blocking antibo

118 Coincubation with a specific p-ERK1/2 inhibitor reversed

119 hich lack PSMA, and binding was abolished by coincubation with a structurally unrelated NAALADase inh

120 at STAT down-regulation could be reversed by coincubation with A(2A)AR-selective inverse agonist 4-(2

121 Coincubation with actinomycin D inhibited the rapid disa

122 Interestingly, coincubation with adenosine deaminase reverses the antip

123 Preincubation or coincubation with AGN 211334 significantly blunted bimat

124 Furthermore, hepatocyte coincubation with alloantibody and macrophages resulted

125 This inhibition was reversed by coincubation with an anti-CD11b antibody that blocks the

126 sients within 2 min of coincubation, whereas coincubation with an avirulent strain (RB57) resulted in

127 Coincubation with an FAAH inhibitor, URB-597, competitiv

128 ntagonist, but germination was restored upon coincubation with an iGLR agonist or the putative ligand

129 GLR antagonist treatments and decreased with coincubation with an iGLR agonist, suggesting that germi

130 II-induced activation of calcineurin, as did coincubation with an inhibitor of PLC activity and with

131 Due to its low intrinsic activity, coincubation with anandamide effectively attenuated the

132 f fAbeta phagocytosis can be relieved by the coincubation with anti-inflammatory cytokines, cyclooxyg

133 yofibroblasts, an effect that was blocked by coincubation with anti-TGFbeta antibody.

134 Coincubation with antibodies to either Apoe or Abeta, or

135 mice greatly increased IL-12 expression upon coincubation with apoptotic thymocytes compared with wil

136 Coincubation with arachidonic acid (AA) was conducted to

137 , and this effect was completely restored by coincubation with ascorbic acid, Tempol, or apocynin.

138 proliferative response that is abolished by coincubation with basic FGF.

139 usively through beta(2)ARs, as determined by coincubation with betaAR subtype-selective antagonists.

140 both catabolism and anabolism were probed by coincubation with BODIPY-FL labeled LacCer (LacCer-BODIP

141 Coincubation with both TNF-alpha and anti-TNF-alpha neut

142 colony stimulating factor upon TALL-104 cell coincubation with brain tumor cells variably occurred wi

143 Coincubation with C1q tails prevented the induction of t

144 oduct on the basis of protection afforded by coincubation with catalase.

145 te affinity Fcgamma receptor IIB (CD32B), or coincubation with CD32B(+) transfectants, resulted in ro

146 tion to the cytotoxic potentiation caused by coincubation with Cu(2+), Zn(2+) rescued primary cortica

147 n SIPS within 24 hours that was prevented by coincubation with E3174 or catalase.

148 n external Ca2+, with marked reduction after coincubation with EGTA, Co2+, or high doses of verapamil

149 NMDA-induced oxidative injury was blocked by coincubation with either superoxide dismutase or the ani

150 TGF-beta-induced motility was blocked by coincubation with either the phosphatidylinositol 3-kina

151 This activity was restored by coincubation with equimolar amounts of the NH(2)-termina

152 In contrast, coincubation with ET(A) (BQ-123) or ET(B) (BQ-788) recep

153 Uptake of A beta was reduced by coincubation with excess acetyl-low density lipoprotein

154 nt manner, which was partially reversible by coincubation with excess monosaccharides, or pretreatmen

155 ts were treated with aspirin but returned by coincubation with exogenous 15(S)-HETE.

156 ath caused by erlotinib was not prevented by coincubation with FAS and TRAIL antagonists, ZB-4 monocl

157 FR tyrosine kinase was abrogated in vitro by coincubation with glycan having multiple GlcNAc termini

158 sistance to shear stress is also enhanced by coincubation with granulosa cells.

159 icantly decreased PGD(2) production, whereas coincubation with H(2)O(2) significantly increased PGD(2

160 Coincubation with hirudin does not alter the APC effect.

161 nt with proteinase K or polymyxin B prior to coincubation with IECs.

162 melanoma patients were activated in vitro by coincubation with infected dendritic cells and tested fo

163 effect of GA on phagocytosis was blocked by coincubation with inhibitors of transcription (actinomyc

164 nced during the differentiation process, and coincubation with its ligand GIP augmented the expressio

165 nhibited NO formation, which was reversed by coincubation with L-arginine (1 mM).

166 Furthermore, coincubation with LiCl during the 2 h exposure to insuli

167 okines/cytokines, Ccl2, Il1b, and Tnf, after coincubation with ligands that activate innate immunity.

168 Coincubation with local anesthetics but not tetrodotoxin

169 Thus, stimulation with opsonized zymosan or coincubation with low density lipoprotein was unassociat

170 nt at -107 to -99 that can be deprotected by coincubation with molar excess of a consensus Sp1 oligon

171 n (5.9-6.2 ng/ml), but this was abolished by coincubation with MSU crystals.

172 However, coincubation with MSU led to a significant suppression o

173 d observed a reduced abundance of SNO during coincubation with N. meningitidis, S. enterica, or E. co

174 Consistent with this, coincubation with neutrophils greatly enhanced the upreg

175 mouse and human iNKT cells was inhibited by coincubation with neutrophils.

176 part to shear-induced release of NO, because coincubation with nitro-L-arginine completely abolished

177 itrotyrosine antibody binding was blocked by coincubation with nitrotyrosine or nitrated bovine serum

178 germinate, but germination was restored upon coincubation with NO3-, but not NH4+.

179 significant in the hepatoma cells following coincubation with NS5A TCR-transduced T cells, which is

180 Moreover, coincubation with OmpA-pretreated macrophages enhances t

181 Coincubation with OPC cell lines with conditioned medium

182 Coincubation with OPG, the decoy receptor for RANKL, att

183 box P3(+) regulatory T cells after in vitro coincubation with OVA/IgG-containing AF.

184 4-deficient mice did not increase Ccl2 after coincubation with photoreceptor proteins.

185 phatase activity of SHPTP1 was attenuated by coincubation with PKCdelta in vitro.

186 activity and energy state were inhibited by coincubation with propranolol, suggesting involvement of

187 ID) animals, and this effect was enhanced by coincubation with rapamycin, demonstrating that mTOR reg

188 icity in vitro was not detectably altered by coincubation with recombinant MBNL1.

189 d growth inhibition was partially blocked by coincubation with rough LPS vesicles.

190 Coincubation with SB-505124, an inhibitor of TGFbetaRI/A

191 In contrast, coincubation with soluble DC-specific ICAM-3-grabbing no

192 Coincubation with soluble DCAL-1 enhanced the proliferat

193 Through coincubation with supplemental arginine and the arginine

194 Coincubation with T. vaginalis isolates induced disrupti

195 ate at levels equivalent to WT NK cells upon coincubation with target cells.

196 Coincubation with the AMPK activators AICAR and alpha-li

197 In human endothelial cells, coincubation with the antioxidant polyethylene glycol-co

198 nducing activities of CHX were suppressed by coincubation with the aryl hydrocarbon receptor (AhR) an

199 product DYRK1A inhibitor, was suppressed by coincubation with the calcineurin inhibitor FK506, sugge

200 The increase was blocked by coincubation with the CB(1) antagonist, SR141716A, and w

201 nducer 3-methylcholanthrene and decreased by coincubation with the CYP1A inhibitor alpha-naphthoflavo

202 Coincubation with the cytokines interleukin (IL)-1, IL-6

203 as orlistat-induced cell death is rescued by coincubation with the global translation inhibitor cyclo

204 Coincubation with the isomerase substrate blocked the la

205 Inhibition was abolished by coincubation with the phosphatidylinositol-3 kinase inhi

206 Coincubation with the sialic acid analog 2-deoxy-2,3-did

207 APC caused efficient PAR1 cleavage and upon coincubation with thrombin APC supported additional PAR1

208 o 16 + or - 6.3%) and completely restored by coincubation with tiron, tempol or apocynin.

209 Coincubation with TNF-alpha and MEK inhibitors caused pe

210 elial gate function that were potentiated by coincubation with TNF-alpha.

211 mited and could be improved significantly by coincubation with tPA.

212 nd this increase was completely abolished by coincubation with troglitazone.

213 ation with agonistic anti-Fas antibody or by coincubation with tumor necrosis factor-alpha (TNF-alpha

214 ates was initiated between 1 and 5 min after coincubation with tumor targets.

215 Coincubation with unlabeled chemokines decreased (125)I-

216 s showed lower DOX uptake than HL-60S cells; coincubation with VER (10 mmol/L) increased uptake 2.6-f

217 Coincubation with VER increased DOX retention in HL-60/D