ライフサイエンスコーパス: be stimulated with

1 EC) grown on laminar-flow perfusion channels were stimulated with 1 mug/mL lipopolysaccharide for 6 h

2 Human periodontal ligament (PDL) cells were stimulated with: 1) 10 ng/mL BMP2; 2) 1 mug/mL doxy

3 When macrophages were stimulated with 10 isolates of each RST1, RST2, or

4 r chondrocytes isolated from ankle cartilage were stimulated with 10 ng/ml of interleukin-1beta (IL-1

5 d when unstimulated; however, when the cells were stimulated with 10 nm alpha-thrombin, we were able

6 ed CD69 expression of gammadeltaT cells that were stimulated with 100 ng/mL lipopolysaccharide.

7 Isolated peripheral blood neutrophils were stimulated with 19 periodontal bacteria.

8 nonuclear cells from 45 children with asthma were stimulated with 2 and 200 ng/ml lipopolysaccharide

9 When cnrN cells expressing myc-tagged CnrN are stimulated with a mixture of rAprA and rCfaD, levels

10 ing reminiscent of wakefulness when cultures are stimulated with a mixture of waking neurotransmitter

11 The retina was stimulated with a liquid crystal display (LCD) integ

12 Each eye was stimulated with a low (Lc) and a high (Hc) Michelson

13 When PBMCs from patients with Lyme arthritis were stimulated with a B burgdorferi RST1 strain, the 18

14 11 engagement, human RA synovial fibroblasts were stimulated with a chimeric construct consisting of

15 T cells that were stimulated with a high concentration of antigen upr

16 sing the protective HLA-DQB1*06 (DQ6) allele were stimulated with a mixture of streptococcal superant

17 Cells were stimulated with a monoclonal antibody against CD3,

18 CD4 T cells were stimulated with Ag presented by B7-negative APC and

19 Notably, when the iTreg were stimulated with Ag, treatment with IL-2/anti-IL-2 c

20 IFN-gamma when total human endometrial cells were stimulated with agonists to TLR2 or TLR3 (peptidogl

21 hmatic and non-atopic non-asthmatic subjects were stimulated with agonists to TLR3, TLR4 & TLRs7-9 an

22 Cells were stimulated with agonists, and secretion of Hsp90, u

23 m the All Babies In Southeast Sweden cohort, were stimulated with Ags (tetanus toxoid and beta-lactog

24 eosinophils were incubated with T cells that were stimulated with allogeneic leukocytes or CD3/CD28 c

25 s if, in parallel to antigen uptake, the DCs were stimulated with alpha-CD40.

26 ng slow waves was modified if the animal had been stimulated with an odor within the receptive field

27 AF was stimulated with an intra-esophageal burst pacing pro

28 lar neurons predicted which of four pathways were stimulated with an accuracy of 76% and performed si

29 PBMCs were stimulated with an anti-CD3 antibody and IL-4 or IL

30 Primary cultures of hfRPE were stimulated with an inflammatory cytokine mixture (I

31 PBMCs were stimulated with and without CpG and were subsequent

32 However, when ECs are stimulated with Ang1 and Ang2, Ang2 dose-dependently

33 Cardiomyocyte hypertrophy was stimulated with AngII or vasopressin, significantly

34 crovascular endothelial cells (MPMVECs) that were stimulated with angiotensin II; the interaction of

35 CD4+ T cells were stimulated with anti-CD3 and anti-CD28 mAb in the p

36 T cells were stimulated with anti-CD3 in the absence or presence

37 hy donor peripheral blood-derived Tregs that were stimulated with anti-CD3/CD28 monoclonal antibodies

38 Purified naive CD4+ T cells were stimulated with anti-CD3/CD28 under Th1, Th2, Th17,

39 Isolated B cells were stimulated with anti-cluster of differentiation (CD

40 Human peripheral blood-derived mast cells were stimulated with anti-IgE Ab in the presence of dexa

41 Human B cells were stimulated with anti-IgM antibody, and effects of I

42 M detected no ZAP70 recruitment when T cells were stimulated with antigen in the presence of the src-

43 moted disinhibited neurite growth when cells were stimulated with appropriate neurotrophic factors.

44 released from platelets whose NO production was stimulated with ATP (a nitric oxide synthase stimulu

45 PBMC were stimulated with autologous dendritic cells infected

46 CD4(+) T cells from allergic donors were stimulated with autologous monocyte-derived allerge

47 BAM from CD-1 mice were stimulated with B. dermatitidis without or with nor

48 ed from 14-week-old but not younger NOD mice were stimulated with both p217 and p290.

49 In total, 40 clones were stimulated with both PPD and PPD-modified HSA.

50 portion of transient fusions when astrocytes were stimulated with bradykinin, a stimulus otherwise re

51 Patients were stimulated with brush, noxious cold, and noxious he

52 Polymorphonuclear neutrophils were stimulated with buffer or 2 microM PAF (1 min), and

53 n peripheral blood mononuclear cells (PBMCs) were stimulated with C. burnetii Nine Mile and the Dutch

54 Normal esophageal keratinocytes were stimulated with calcium chloride to induce terminal

55 Peripheral blood mononuclear cells were stimulated with Candida albicans.

56 Fresh mouse and human eosinophils were stimulated with CCL11 and CCL24, and the secretion

57 In vitro, cultured HSCs were stimulated with cholangiocyte supernatants and alph

58 from 28 RA patients and 18 healthy controls were stimulated with citrullinated or noncitrullinated a

59 T-cell interferon gamma (IFNgamma) secretion was stimulated with CMV lysate.

60 after (POST) 30-minutes of cycling exercise were stimulated with CMV (pp65 and IE1) and EBV (LMP2A a

61 CFSE-labeled PBMCs were stimulated with CMV, tetanus toxoid (TT), and C alb

62 ation, as it proceeds even when the receptor is stimulated with collagenase-resistant collagen I (r/r

63 hesis, cultured respiratory epithelial cells were stimulated with combinations of purified siderophor

64 Normal human bronchial epithelials were stimulated with conditioned medium from monocytes i

65 Human lung fibroblasts grown in collagen were stimulated with conditioned medium from Mtb-infecte

66 Cultured hRPE and mRPE cells were stimulated with cytokines for various times or with

67 When LPS-primed glial cells were stimulated with DAMPs under acidic conditions (pH 6

68 ulosis-induced production of cytokines, PBMC were stimulated with DEP and M. tuberculosis or purified

69 RASFs were stimulated with different concentrations of visfati

70 s and genetically matched wild type controls were stimulated with diverse pro-inflammatory stimuli.

71 The model was stimulated with dopamine pulses mimicking those reco

72 Human PDL cells and primary osteoblasts were stimulated with doses of 1 to 200 ng/mL BMP2.

73 , peripheral blood mononuclear cells (PBMCs) were stimulated with each of the VLPs, and secretion of

74 lating proteasomal proteolysis in cells that are stimulated with EGF.

75 The cells were stimulated with EGF (10(-7) M) for 1 and 5 minutes

76 The cells were stimulated with EGF (10(-7) M) for 1 minute to 24 h

77 Rabbit corneal epithelial (RCE) cells were stimulated with EGF or LXA4 at different times.

78 d phosphorylation, only those receptors that were stimulated with EGF progressed to lysosomal degrada

79 on (20 s) to a complex moving pattern, while being stimulated with either sham or tRNS across differe

80 shwork (TM) cells and corneoscleral explants were stimulated with either dexamethasone (DEX) or trans

81 llular cAMP on HIV-infected podocytes, cells were stimulated with either forskolin or 8-bromo-cAMP.

82 HLA-B8(+) HLA-B44(-) EBV-seropositive PBMCs were stimulated with either HLA-B*44:02(+) or HLA-B*44:0

83 g age-matched male control subjects (n = 16) were stimulated with either lipopolysaccharide or phytoh

84 Vascular smooth muscle cells were stimulated with either SAA or CRP (1 to 100 mg/L) a

85 enic T cells isolated from Mus musculus that were stimulated with either T-cell receptor (TCR) cross-

86 r during the pollen season or out of season, were stimulated with either TG extract or a pool of prev

87 When cells were stimulated with EL-4 gag or D5 (but not MCA304 tumo

88 ain surgery, specific areas in the brain can be stimulated with electrical impulses to reversibly cha

89 Nerves were stimulated with electrical field stimulation (0.1-2

90 ro model, primary smooth muscle cells (SMCs) were stimulated with elevated transforming growth factor

91 eration was significantly elevated when PMNs were stimulated with EMD (200 mug/mL) (P <0.01).

92 of runx2 and desmin, and the cocultures that were stimulated with EMD and BMP-2 achieved significantl

93 Human PDL cells were stimulated with EMD.

94 NRVMs with PLCepsilon depletion were stimulated with endothelin (ET-1), norepinephrine,

95 hin non-gas-permeable microchannels, as they are stimulated with endotoxin.

96 elial cells and glomerular endothelial cells were stimulated with endotoxins, cytokines, and human le

97 red primary oligodendroglial precursor cells were stimulated with ENV protein to determine the effect

98 Human mast cells were stimulated with epithelial cell-derived supernatant

99 Cells were stimulated with equimolar amounts of rFlaA, rBet v

100 Whole blood was stimulated with Escherichia coli derived lipopolysac

101 nts expressing wild-type or polymorphic TLR4 were stimulated with Escherichia coli (predominantly hex

102 er RNAs is enriched when breast cancer cells are stimulated with estrogen.

103 tive to normal cells, even when normal cells are stimulated with exogenous epidermal growth factor.

104 e cooperativity, and its autoproteolysis can be stimulated with exogenous substrates or peptides that

105 eosinophils cocultured with epithelial cells were stimulated with FMLP/cytochalasin B (FMLP/B) and/or

106 Antennae were stimulated with forces approximating those of natur

107 response was detected when Gr64 mutant flies were stimulated with fructose.

108 Moreover, TEC were stimulated with genomic double-stranded (ds)DNA or

109 MIN6 beta cells and mouse islets were stimulated with globular (2.5 mug/ml) or full-lengt

110 This DC subset was stimulated with granulocyte-macrophage colony-stimul

111 (API)-2, a specific Akt inhibitor, and then were stimulated with H2O2 at different doses for various

112 2) or variant TLR2 genes (HEK293-TLR2-R753Q) were stimulated with HCV core and NS3 proteins.

113 ells (PBMC) from 20 HDM-allergic individuals were stimulated with HDM extracts and assayed with a set

114 ells (PBMC) from 20 HDM-allergic individuals were stimulated with HDM extracts and assayed with a set

115 HDM allergic and 10 non-allergic individuals were stimulated with HDM extracts and assayed with a set

116 Macrophages and PMNs of BHS and DS were stimulated with heat-killed M. haemolytica or LPS.

117 Human corneal epithelial (HCE) cells were stimulated with HGF with or without bpV(phen).

118 signaling in a coordinated manner when cells are stimulated with high levels of TGF-beta.

119 plasma levels, PBMCs from uninfected donors were stimulated with HIV-1 infectious virions, HIV-1 ssR

120 rimary human aortic endothelial cells (HAEC) were stimulated with HLA class I antibodies in the prese

121 16HBE cells were stimulated with house dust mite (HDM) extracts.

122 This animal was stimulated with human GM-CSF, and an increase in hum

123 Caco-2 monolayers were stimulated with human IgE-antigen (Ag) complexes.

124 First, "donor"-derived CD8 T cells were stimulated with human leukocyte antigen-unmatched "

125 uccinimidyl ester-labeled human CD4+ T cells were stimulated with human or pig PBMC.

126 Active adenosine release was stimulated with hypoxia and trains of electrical sti

127 Bone marrow-derived myeloid DCs were stimulated with ICs composed of IgG autoantibody an

128 ription factor STAT2 only in cells that have been stimulated with IFN-I.

129 IOBA-NHC and Jurkat cells were stimulated with IFNgamma, TNFalpha, alphaFas, or PM

130 Both cell types were stimulated with IgE-ICs consisting of 4-hydroxy-3-i

131 MCF-7 cells were stimulated with IGF-I for 3 or 24 hours and were pr

132 Supernatants derived from NK cells that had been stimulated with IL-21 and mAb-coated breast cancer

133 Primary KCs were stimulated with IL-17 or TNF-alpha alone, or in com

134 Primary bronchial epithelial cells were stimulated with IL-17A and/or IL-22, with and witho

135 with no evidence of translation unless cells were stimulated with IL-1alpha.

136 Therefore, normal tendon explants were stimulated with IL-1beta and prostaglandin E2, and

137 Astrocytes were stimulated with IL-1beta or TNF-alpha, and CCL2 and

138 pression was detected only when tendon cells were stimulated with IL-1beta, and CTGF and significantl

139 L-5 and IL-13 expression by human ILC2s that were stimulated with IL-2 and IL-33.

140 al cells from healthy and asthmatic subjects were stimulated with IL-22, IFN-gamma, or the combinatio

141 o the generation of IgE, naive human B-cells were stimulated with IL-4 and anti-CD40.

142 When intestinal organoids were stimulated with IL-4, tuft cells and IL-25 were ind

143 , and IL-22 were blocked when naive Th cells were stimulated with IL-6 and IL-23.

144 However, it did not do so when ILC2s were stimulated with IL-7 and thymic stromal lymphopoiet

145 no contest when adoptively transferred cells are stimulated with immunization and IL-2.

146 Fetal cardiovascular function was stimulated with increasing bolus doses of phenylephr

147 he human HSC line LX2 and primary human HSCs were stimulated with increasing doses of IL-17A and comp

148 DCs were stimulated with influenza-J-LEAPS peptides (influen

149 sing the human insulin receptor and rat IRS1 were stimulated with insulin in the absence or presence

150 When cells were stimulated with insulin-like growth factor-1 (IGF-1

151 er27 became phosphorylated when HEK293 cells were stimulated with insulin-like growth factor-1 (IGF-1

152 lower than those observed when CD14(+) cells were stimulated with interferon.

153 eron (IFN-gamma)-producing NK cells that had been stimulated with interleukin-12 (IL-12)/IL-15.

154 expression in vitro, normal tendon explants were stimulated with interleukin-1 beta and prostaglandi

155 Chondrocytes were stimulated with interleukin-1beta (IL-1beta) in vit

156 rt hairpin RNA to suppress FSTL1 expression, were stimulated with interleukin-1beta (IL-1beta), tumor

157 (PBMC), CD4+ T cells, or CD4+ CD25- T cells were stimulated with irradiated human or wild type (WT)

158 hydrochloride (ISO; 30 minutes) pretreatment were stimulated with ISO (10 minutes).

159 circumvallate taste buds and the taste buds were stimulated with KCl (50 mm) or a mixture of taste c

160 nd primary human bronchial epithelial cells, were stimulated with LIGHT and LTalphabeta, and expressi

161 Cord blood was stimulated with lipid A, peptidoglycan (Ppg), or PHA

162 nt macrophages when the cells had previously been stimulated with lipopolysaccharide (LPS) or E. coli

163 Bone marrow-derived macrophages (BMMs) were stimulated with lipopolysaccharide (LPS) and were e

164 ures of mononuclear cells from patients that were stimulated with lipopolysaccharide, with or without

165 Cells were stimulated with live or sonicated B. burgdorferi or

166 When monocytes were stimulated with live P. acnes, caspase-1 and caspas

167 Human corneal epithelial cells (HCECs) were stimulated with LL-37.

168 Aortic EC were stimulated with low-dose TNFalpha (0.3 ng/ml) in a

169 sa infection when the animals had previously been stimulated with LPS.

170 cells were treated with TE 90 minutes before being stimulated with LPS (TE90 DCs).

171 y, decidual DCs remained immobile even after being stimulated with LPS and exhibiting responsiveness

172 acrophages were treated with collinin before being stimulated with LPS.

173 Venous blood from human volunteers was stimulated with LPS, MPLA or vehicle.

174 Subsequently, the cells were stimulated with LPS (1-10 mug/mL) for 24 hours.

175 ed with decreased NO production by PECs that were stimulated with LPS and gamma interferon in the pre

176 When rat macrophages were stimulated with LPS and IFN-gamma separately, SP-A

177 Monocytes and T lymphocytes were stimulated with LPS and PHA, respectively.

178 hages (Mphi) and PMN from BALB/c and B6 mice were stimulated with LPS and treated with rVIP.

179 type 2 cytokine gene expression, macrophages were stimulated with LPS, and the expression of IL-4 and

180 Primary mouse macrophages were stimulated with LPS/IFNgamma or IL4 with or without

181 This pattern was preserved after the cells were stimulated with LTB4 or fMLP.

182 ted with staurosporine and SKW6.4 cells that were stimulated with LzCD95L.

183 Respiratory afferents have been stimulated with mechanical loads applied to breathi

184 Cultured FLS were stimulated with medium or IL-1beta, and immunoblott

185 rom peripheral blood and intestinal biopsies were stimulated with microbial phosphoantigen (1-hydroxy

186 te and shed active matriptase when the cells are stimulated with mildly acidic buffer or the hypoxia-

187 Human leukocytes were stimulated with mitogens on board the International

188 uman oligodendrocytes precursor cells (OPCs) were stimulated with moderate intensity SMF (0.3 T) for

189 s with TB or defective IFN-gamma receptor 1* were stimulated with Mtb antigen and SLPI, and IFN-gamma

190 Murine or human macrophages were stimulated with native fibrinogen (nFb), cFb, or in

191 DCs were stimulated with nCup a 1 and tested for their biolo

192 CD34(+) cells and HRECs were stimulated with NGF (1 to 4 pM) for 24, 48, and 72

193 RAW 264.7 macrophages or Kupffer cells were stimulated with oleate or palmitate, and levels of

194 Hsp90 release was stimulated with optimal doses of estradiol, IL-1, an

195 Human primary T cells were stimulated with or without anti-CD3 plus anti-CD28

196 The fibroblasts were stimulated with or without transforming growth fact

197 eatment in period 2; and hepatic lipogenesis was stimulated with oral fructose administration.

198 hatase positive colony size in cultures that were stimulated with osteoblast differentiation media.

199 also prevented activation of ERK1/2 when ECs were stimulated with other pro-angiogenic growth factors

200 PBMCs from 80 peanut-allergic patients were stimulated with overlapping 20-mer Ara h 2 peptides

201 ls from HIV-1-seropositive (HIV(+)) subjects were stimulated with overlapping RT peptide pools.

202 itope mapping, Mal d 1-specific T-cell lines were stimulated with overlapping synthetic 12-mer peptid

203 Human CAECs were stimulated with oxLDL.

204 Peripheral blood mononuclear cells were stimulated with P. falciparum antigen, and interfer

205 and TLR4, HGF and HPDLF from the same donors were stimulated with P. gingivalis LPS or with two synth

206 rom 3-day-old NZO and control C57BL/6J mice, were stimulated with P. gingivalis.

207 endritic cells (mdDC) from allergic patients were stimulated with Pam3CSK4 (TLR1/2 ligand), FSL-1 (TL

208 nsiveness was characterized, BAL macrophages were stimulated with pathogenic versus commensal microor

209 transgenic SHIP(-/-) and SHIP(+/+) mice that were stimulated with peptidoglycan (PGN) to examine the

210 THP-1 cells were stimulated with Pg-DNA (100 ng/muL), Fn-DNA (100 ng

211 man mandibular osteoblast-like cells (HMOBs) were stimulated with PGE2.

212 gation and puncture, thoracic aorta segments were stimulated with phenylephrine in the presence or ab

213 Cells were stimulated with phorbol ester and ionomycin in the

214 After cells were stimulated with phorbol myristate acetate, the amou

215 When human aortic endothelial cells were stimulated with physiologic concentrations of fruct

216 inhibited motility of MCF-10A cells that had been stimulated with PKC activator diacylglycerol lacton

217 and platelets removed from control subjects were stimulated with plasma and serum from 21 patients i

218 ed human HSC line hTERT and primary rat HSCs were stimulated with platelet-derived growth factor (PDG

219 When NIH 3T3 cells were stimulated with platelet-derived growth factor to g

220 Monocyte-derived dendritic cells (DCs) were stimulated with pneumococcal peptidoglycan (PGN) in

221 d peripheral blood mononuclear cells (PBMCs) were stimulated with poliovirus vaccine, and memory T ce

222 Fibroblast-like synoviocytes were stimulated with polyinosinic-polycytidylic acid (po

223 ed silencing of MyD88 or TRAM, HGF and HPDLF were stimulated with Porphyromonas gingivalis (Pg) lipop

224 atients, but not tolerant/naive individuals, were stimulated with PPD and PPD-modified HSA.

225 retreatment with single triterpenoids, cells were stimulated with pro-inflammatory cytokines (TNF-alp

226 BBE, HT29-Cl.19A, and human T cells (Jurkat) were stimulated with pro-inflammatory cytokines in the p

227 Fibroblasts were stimulated with proinflammatory cytokines (tumor ne

228 The cells were stimulated with PTH or PGE2 to induce MMP-13 mRNA e

229 HCAECs were stimulated with purified Aa serotype b lipopolysacc

230 When bone marrow cells derived from Xid mice were stimulated with receptor activator of NF-kappaB lig

231 m injured explants, rested explants that had been stimulated with recombinant FGF-2 or FGF-18, or who

232 BALB/c mice (peritoneal/bone marrow derived) were stimulated with recombinant a2NTD in both ex vivo a

233 Purified eosinophils were stimulated with recombinant human TSLP.

234 ultures of human gingival fibroblasts (HGFs) were stimulated with recombinant TGF-beta1 and TNF-alpha

235 Primary endothelial cells were stimulated with recombinant VEGF and exposed to hyp

236 Parallel samples were stimulated with related nonsteroidal anti-inflammat

237 d mononuclear cells (PBMC) from these groups were stimulated with relevant antigen for 48 h and flow

238 Isolated human CD3+T cells were stimulated with RNase 7 and screened for possible e

239 nterfering RNA-induced downregulation of MD2 were stimulated with RWPE, other pollen allergic extract

240 In addition, when ECs were stimulated with s-FKN, greater adhesion of human ne

241 of school-age children, whole-blood cultures were stimulated with S. mansoni soluble egg antigen (SEA

242 type and TLR2, TLR4, and MyD88 knockout mice were stimulated with Salmonella vector BRD509, the SBR-e

243 When DCs were stimulated with serotype b of A. actinomycetemcomit

244 tivating p21 expression when quiescent cells are stimulated with serum to reenter the cell cycle.

245 ON and OFF ganglion cells were stimulated with similar efficacy.

246 Peripheral blood mononuclear cells (PBMC) were stimulated with SLA to determine the frequencies of

247 lenocytes from wild-type or LAIR-1(-/-) mice were stimulated with soluble anti-CD3 Ab in the presence

248 n PBMC and purified naive and memory B cells were stimulated with specific ligands for TLR2, TLR3, TL

249 Bovine articular chondrocytes were stimulated with sphingomyelinase (SMase) to increas

250 Endothelial cells were stimulated with sphingosine 1-phosphate receptor 1

251 e TOFs, specific regions of the rod OS could be stimulated with spots of light highly confined in spa

252 treated with lysates from Jurkat cells that were stimulated with staurosporine and SKW6.4 cells that

253 human cord blood-derived cultured mast cells were stimulated with substance P (SP) or IgE/anti-IgE wi

254 type, trypsinogen 7, or cathepsin B-deleted) were stimulated with supramaximal cerulein, and the cyto

255 In vivo-primed T cells were stimulated with syngeneic APCs, with or without the

256 s the major promoter used when human T cells were stimulated with TGF-beta1 and fibroblast growth fac

257 l interference RNA (siRNA)-transfected NHLFs were stimulated with TGF-beta1.

258 Human primary lung fibroblasts were stimulated with TGFbeta or IGFBP-3 in the presence

259 d peripheral blood mononuclear cells (PBMCs) were stimulated with TGFbeta, IL-13, poly(I-C), or TSLP.

260 d after overnight starvation, expanded cells are stimulated with the same peptides from the initial c

261 Whole blood was stimulated with the M. tuberculosis-specific antigen

262 When muscarinic receptors were stimulated with the agonist oxotremorine-M, several

263 Cells were stimulated with the aromatase substrate, androstene

264 the angiotensin II type 1A receptor (AT1aR) were stimulated with the beta-arrestin-biased ligand Sar

265 t of these signaling events when eosinophils were stimulated with the combination of TNF-alpha plus I

266 Acini were stimulated with the P2X(7) receptor agonist, (benzo

267 Acini were stimulated with the P2X7 receptor agonist, (benzoyl

268 Extracted monocytes were stimulated with the toll-like receptor (TLR)-4 liga

269 Bim(-/-) mice were stimulated with thioglycollate or LPS and examined

270 hRPE cells were stimulated with thrombin TNF-alpha, monocytes, and

271 When washed human platelets were stimulated with thrombin, cAMP-dependent phosphodie

272 ys, non-transfected MDCK-II and HEK293 cells were stimulated with thrombin.

273 e phosphorylated in kindlin-3 when platelets were stimulated with thrombin.

274 When HEL cells were stimulated with thrombopoietin or phorbol 12-myrist

275 ine production when Th2 central memory cells are stimulated with thymic stromal lymphopoietin (TSLP)-

276 Peripheral whole-blood samples were stimulated with TLR ligands and analyzed by means o

277 duals with T1D and diabetes-free individuals were stimulated with TLR ligands in the presence and/or

278 IECs were stimulated with TLR ligands, and expression of Fas

279 Fresh PBMCs or CD14(+) monocytes were stimulated with TLR4, TLR7/8-selective ligands, or

280 lpha/beta receptor 1 (IFNAR1)-deficient mice were stimulated with TLR9 or TLR2 ligands.

281 rmal human bronchial epithelial (NHBE) cells were stimulated with TNF, IL-4, IFN-gamma, IL-17A, and d

282 issues of patients with RA or osteoarthritis were stimulated with TNFalpha and assayed for gene expre

283 n was increased when myelin-specific T cells were stimulated with tolerogenic altered self-peptides.

284 (DEHP) and butyl benzyl phthalate (BBP), and were stimulated with Toll-like receptor (TLR)-9 agonist

285 ment epithelial cells (ARPE-19 and B6-RPE07) were stimulated with toll-like receptor ligands, and ene

286 However, when axons were stimulated with trains of pulses mimicking bursting

287 lood-and peripheral blood-derived mast cells were stimulated with TSLP in vitro to assess PGD2 genera

288 ry (PA) endothelial cells deficient in BMPR2 were stimulated with tumor necrosis factor (TNF), a twof

289 When cells were stimulated with tumor necrosis factor-alpha (or hig

290 When cells were stimulated with tumor promoters, such as epidermal

291 secutive responses when the olfactory neuron is stimulated with two brief pulses.

292 use macrophages and dendritic cells that had been stimulated with type A F. tularensis did not releas

293 man HEK 293 cells, and murine RAW264.7 cells were stimulated with U1 RNA and other known Toll-like re

294 Blood was stimulated with ultrapure LPS from Escherichia coli,

295 A mouse macrophage cell line (RAW 264.7) was stimulated with various concentrations of MAX and li

296 nocytes and monocyte-derived dendritic cells were stimulated with various activating ligands, includi

297 o obtain hepatocyte organoid cultures, which were stimulated with various growth factors (GFs) includ

298 om 43 persistent carriers and 49 noncarriers was stimulated with viable S. aureus T-helper type 1 (Th

299 y purified CD28(-) CD45RA(hi) CD8(+) T cells are stimulated with viral peptide presented by autologou

300 Cells were stimulated with voltage pulses; at 1 and 5 Hz frequ