1 Stimulation of ECs with 1- or 10-microg/mL W6/32, L2, or
2 Stimulation of neutrophils with 1-1,000 ng/mL lipopolysa
3 Stimulation of PKC with 1-oleoyl 2-acetylglycerol (OAG),
4 Secondary
stimulation of PMNs with 1 muM N-formyl-methionyl-leucyl
5 Stimulation of Th17 cells with 1,25D3, in a concentratio
6 Stimulation of Rb cells with 10% FBS resulted in an incr
7 Stimulation of the cells with 100 pM ART activated RET a
8 se interactions enhanced significantly after
stimulation of cells with 5-HT and TG.
9 armacological and neural effects of possible
stimulation of these receptors with 6-fluoronorepinephri
10 TPRP induced the highest
stimulation of angiogenesis with a fourfold increase com
11 Following
stimulation of cells with a TLR3 or TLR4 ligand, we iden
12 p-regulated upon tumor necrosis factor alpha
stimulation of cells, consistent with a critical role in
13 Stimulation of chilling stress with a pre-treatment with
14 e membrane of adrenal chromaffin cells after
stimulation of exocytosis with a high K(+) solution.
15 hibited a markedly decreased carbamylcholine
stimulation of I(KAch) with a peak value of -181+/-31 pA
16 phosphorylation/activation of AMPK, whereas
stimulation of macrophages with a proinflammatory stimul
17 Stimulation of macrophages with a set of cytokines revea
18 contrast, negative lenses caused a transient
stimulation of ocular elongation with a fall-time of 0.4
19 Similarly,
stimulation of PBMCs with a TLR3 agonist indicated that
20 preferentially associated with PKC-delta on
stimulation of platelets with a GPVI agonist, but not wi
21 Stimulation of temporoammonic synapses with a physiologi
22 Stimulation of microglia with Abeta increased acetylatio
23 anslocated to the membrane within seconds of
stimulation of the cells with ACh.
24 Stimulation of H295R cells with ACTH (10(-6) M) was foll
25 but also proinflammatory responses following
stimulation of MDDCs with activators of RIG-I-like recep
26 Stimulation of PMd with adjusted (reduced) intensity to
27 Stimulation of these receptors with AG simultaneously wi
28 Furthermore,
stimulation of cells with agents that elevate cAMP incre
29 Taken together, these results suggest that
stimulation of BTLA with agonistic agents has therapeuti
30 Stimulation of HEL cells with agonists significantly inc
31 and GRK2 S-nitrosylation increases following
stimulation of multiple GPCRs with agonists.
32 cognitive function may be best preserved by
stimulation of NMDA receptors with agonists rather than
33 sulin resistance, pharmacologic secretagogue
stimulation of beta-cells with an incretin hormone gluca
34 d in mice lacking the PGE2 receptor EP3, and
stimulation of cultured DCs with an EP3 agonist increase
35 f age, mice with Ostm1 loss showed 3-10-fold
stimulation of reactive gliosis, with an increased astro
36 Electrical
stimulation of retinal neurons with an advanced retinal
37 Furthermore,
stimulation of ECs with Ang1 increased SMC migration tow
38 Stimulation of B cells with anti-CD40 mAb, LPS, CpG DNA,
39 Stimulation of B cells with anti-CD40 plus interleukin-4
40 Stimulation of CLL cells with anti-IgM or CXCL12 caused
41 ted a high level of Fas expression in BMSCs,
stimulation of Fas with anti-Fas antibody did not result
42 Stimulation of macrophages with anti-inflammatory cytoki
43 In addition, we reported previously that
stimulation of macrophages with anti-inflammatory cytoki
44 Stimulation of BDCA-2 with antibodies leads to an anti-i
45 into extracellular compartments during brief
stimulation of murine macrophages with ATP.
46 Stimulation of cells with atRA results in the dissociati
47 We show that
stimulation of human monocytes with B. burgdorferi lysat
48 all five NF-kappaB proteins before and after
stimulation of monocytic cells with bacterial lipopolysa
49 Primary
stimulation of T cells with Bet v 1 or Cor a 1 resulted
50 Stimulation of LQT2 cells with beta-adrenergic agonist i
51 Stimulations of 7 s with blue light result in an average
52 gamma production was measured after in vitro
stimulation of whole blood with C. burnetii antigens.
53 Stimulation of PMN with C5a led to upregulation of activ
54 Stimulation of M3R with carbachol significantly increase
55 Stimulation of B cells with CD40 ligand and interleukin-
56 In particular,
stimulation of CLL cells with CD40L results in substanti
57 Optogenetic
stimulation of RTN with channelrhodopsin-2, or inhibitio
58 These plasmanylinositols respond acutely to
stimulation of cells with chemoattractants, and their le
59 Stimulation of enteric neurons, with cholinergic and nit
60 sessed by phenotype analysis and by in vitro
stimulation of PBMCs with CICs as a source of Ags.
61 Stimulation of awake rats with citric acid and quinine r
62 The
stimulation of blood leukocytes with CMV lysate induced
63 atelet subpopulations are formed upon potent
stimulation of platelets with collagen and/or thrombin.
64 th off-the-shelf non-biological scaffold and
stimulation of regeneration with commercially available
65 y adenosine shortened ipRGC light responses,
stimulation of this pathway with compounds such as forsk
66 onses by conventional T cells: upon in vitro
stimulation of splenocytes with Con A or anti-CD3, type
67 likely to act early in T cell activation, as
stimulation of T cells with concanavalin A, but not phor
68 The effects of BDNF are partly mediated by
stimulation of local translation, with consequent altera
69 ith GPi DBS could be explained by retrograde
stimulation of striatopallidal axons with consequent act
70 Stimulation of B cells with CpG produced significantly l
71 Stimulation of follicular melanocytes with CRH and CRH p
72 However, repeated
stimulation of mast cells with CRH (1 muM) leads to down
73 Second,
stimulation of cells with Cristin/R-spondin was accompan
74 Stimulation of HTM cells with CTGF for 24 hours induced
75 In contrast, we show that in vivo-targeted
stimulation of B cells with CXCL13-coupled CpG oligonucl
76 g to flow cytometry and confocal microscopy,
stimulation of platelets with CXCL16 induced platelet de
77 The test involves
stimulation of whole blood with cytokine that induces NK
78 Stimulation of cells with cytokines and microbial pathog
79 A single
stimulation of cells with cytokines causes rapid ERK1/2
80 Stimulation of NK cells with cytokines and PNU-282987 de
81 Recent studies in mice have shown that
stimulation of NK cells with cytokines or in the context
82 on was rapidly and transiently diminished by
stimulation of cells with d-glucose.
83 +) CD4(+) CFSE(low) cells proliferating upon
stimulation of PBMC with Dau c 1 or Bet v 1.
84 Global
stimulation of Dictyostelium with different chemoattract
85 Stimulation of macrophages with dsRNA, viral RNA, or its
86 NT-3
stimulation of U2OS cells with ectopic TrkC expression t
87 Stimulation of BAEC with EGCG also resulted in dose- and
88 We show that
stimulation of epidermal keratinocytes with EGF, but not
89 Stimulation of cells with either PGE(2) or the selective
90 ell expressed and secreted (RANTES), whereas
stimulation of NK cells with either agent alone had mini
91 l synapse in C. elegans by combining optical
stimulation of targeted neurons with electrophysiologica
92 Thus, in situ
stimulation of resident hCSCs with ephrin A1 or their ex
93 Stimulation of cells with epidermal growth factor (EGF)
94 Here, we describe that
stimulation of epithelial cells with epidermal growth fa
95 Stimulation of motility with epidermal growth factor ind
96 d that MTA1 is a target of inflammation, and
stimulation of macrophages with Escherichia coli lipopol
97 Stimulation of dendritic cells with F. tularensis result
98 Stimulation of Vav(-/-) microglia with fAbeta failed to
99 Stimulation of angiogenesis with FGF-2 at the time of ca
100 We show that
stimulation of microglia with FL-MCP1 or K104Stop-MCP1 t
101 CR conformation-sensitive FRET we found that
stimulation of endothelial cells with fluid shear stress
102 Stimulation of monocytes with fMLP resulted in activatio
103 Although
stimulation of adenylate cyclase with forskolin did not
104 Brief extracellular
stimulation of PKA with forskolin (FSK) alone or in comb
105 Stimulation of hPSCs with fractalkine led to a significa
106 agonize interleukin-8 accumulation following
stimulation of epithelial cells with Fusobacterium nucle
107 Stimulation of cells with G-CSF activates multiple signa
108 Stimulation of adipocytes with GIP alone has no effect o
109 In vitro
stimulation of nTregs with GITR ligand increased phospho
110 that RhoGDI-Cdc42 complexes dissociated upon
stimulation of beta cells with glucose for 3 min, correl
111 Importantly,
stimulation of islets with glucose, alpha-ketoisocaproat
112 Prosaptide
stimulation of cells transfected with GPR37 or GPR37L1 i
113 In contrast,
stimulation of neutrophils with granulocyte colony-stimu
114 Stimulation of HMC with heat-aggregated IgA1 purified fr
115 Stimulation of cells with heparanase enhanced their resi
116 IP-10 (P = 0.0045) secretion during in vitro
stimulation of BC PBMC with HERV-K antigen.
117 Upon
stimulation of glioma cells with HGF, we show that IQ-do
118 It is well reported that
stimulation of cells with high [5HT](ex) induces transam
119 g live-cell imaging that transient (1-4 min)
stimulation of mouse macrophages with high extracellular
120 bility, and inhibition of PDE2A reversed the
stimulation of permeability seen with higher doses of AN
121 Stimulation of endothelium with histamine, a secretagogu
122 Moreover,
stimulation of oval cells with HMGB1 promoted an ERK1/2-
123 Stimulation of T cells with holotoxin (PTx) or the B sub
124 Stimulation of NOTCH signaling with human recombinant DL
125 asable pool (RRP) of vesicles as measured by
stimulation of release with hypertonic sucrose, or alter
126 tion steady-state levels were decreased upon
stimulation of cells with IFN-beta or virus infection.
127 Stimulation of DC with IFN-gamma and CD40L resulted in r
128 defect that was more pronounced after prior
stimulation of macrophages with IFN-gamma or lipopolysac
129 Concurrent
stimulation of Macs with IFN-gamma and IL-4 results in a
130 On
stimulation of these cells with IgE and antigen, copreci
131 Stimulation of platelets with IGF-1 resulted in phosphor
132 Following
stimulation of cartilage explants with IL-1 plus retinoi
133 Brief
stimulation of CECs with IL-1beta activated PI 3-kinase
134 Stimulation of CECs with IL-1beta also activated ERK1/2
135 Brief
stimulation of CECs with IL-1beta upregulated expression
136 igase TNF receptor-associated factor 6 after
stimulation of cells with IL-1beta.
137 idues were observed to be rapidly induced by
stimulation of cells with IL-2 or other gammac cytokines
138 Stimulation of colonic leukocytes with IL-23 induced the
139 Interestingly, further
stimulation of CTLs with IL-12 impacts exosome size and
140 Stimulation of effector cells with IL-2 downregulated mR
141 In this study, we found that
stimulation of fibroblasts with IL-1beta results in the
142 -6R) alone had no effect on VEGF production,
stimulation of HPMCs with IL-6 in combination with sIL-6
143 Stimulation of human chondrocytes with IL-1beta activate
144 12 results in loss of antiviral activity and
stimulation of leukocytes with IL-12/IL-18 enhances thei
145 In vitro assays showed that
stimulation of muscle cells with IL-10 had no effect on
146 Stimulation of mast cells with immobilized polyvalent li
147 This arises from
stimulation of myocyte proliferation with increases in c
148 Stimulation of mouse macrophages with increasing amounts
149 We show in this study that, following
stimulation of DCs with inflammatory stimuli, not only d
150 ntial for physiological glucose homeostasis:
stimulation of adipocytes with insulin results in insert
151 Stimulation of cells with insulin and IGF-1 decreased cy
152 ently associate with these microdomains upon
stimulation of cells with insulin.
153 Stimulation of cardiac fibroblasts with interferon-gamma
154 Stimulation of keratinocytes with interferon-gamma resul
155 Third, mechanical
stimulation of skeletal muscle with intermittent passive
156 Stimulation of B cells with intracellular TLR3, TLR7 and
157 Stimulation of VSM cells with ionomycin, a calcium ionop
158 Furthermore, maximal
stimulation of cardiomyocytes with isoproterenol or prot
159 0 in cancer, we established a system for the
stimulation of CD30 with its physiological ligand.
160 In contrast,
stimulation of EPHA2 with its ligand ephrin-A5 eradicate
161 acellular pathways involved in IFN-beta upon
stimulation of dendritic cells with L. acidophilus and r
162 Here, we show that artificial
stimulation of ab1c neurons with light (normally attract
163 of proinflammatory cytokines in response to
stimulation of primary macrophages with lipopolysacchari
164 Stimulation of mice with lipopolysaccharide strongly ind
165 Here, we connect these facts by showing that
stimulation of mouse macrophages with lipopolysaccharide
166 erebral microglia in vitro demonstrated that
stimulation of TLR4 with lipopolysaccharide, widely used
167 phology, which is rescued by pharmacological
stimulation of Wnt signaling with lithium chloride (LiCl
168 iling to identify genes that were induced by
stimulation of cells with live spirochetes and that were
169 aximally expressed in THP-1 cells after 24-h
stimulation of these cells with live B. burgdorferi.
170 Stimulation of ABCA1 expression with liver X receptor ag
171 Golgi cells responded to
stimulation of peripheral afferents with longer latency
172 In stark contrast,
stimulation of the alpha1aAR with low dose phenylephrine
173 Stimulation of BMDM with LPS, IFN-beta, or IFN-gamma ind
174 Stimulation of BMDMs with LPS triggered the phosphorylat
175 iNOS and the production of NO in response to
stimulation of cells with LPS/IFNgamma or TNF/IFNgamma,
176 In this report, we demonstrate that in vitro
stimulation of mouse MCs with LPS and IFN-gamma induces
177 Ex vivo
stimulation of peritoneal macrophages with LPS elicited
178 Ex vivo
stimulation of PerMphi with LPS produced a similar 3-fol
179 Stimulation of mBMMCs with LTB4 induced transient, dose-
180 constitutively active mutant of G protein or
stimulation of cells with lysophosphatidic acid or endot
181 Stimulation of chromaffin cells with lysophosphatidic ac
182 Stimulation of hematopoietic progenitors with macrophage
183 Interestingly,
stimulation of PMNs with MALP-2 resulted in an increase
184 Compatible with this hypothesis,
stimulation of monocytes with MCP-1 significantly increa
185 Stimulation of CD74 with MIF leads to c-Met activation,
186 SEB
stimulation of primary cells with mimetic affected newly
187 t enhance cytokine secretion in dNK, whereas
stimulation of dNK with mitogens or classical natural ki
188 In this study we test the hypothesis that
stimulation of endothelial cells with MMP-1 increases th
189 In vitro
stimulation of isolated neutrophils with MMP-9 decreased
190 assembly in normal glucose was increased by
stimulation of integrin activity with Mn(2+).
191 NA isolated from a CTL generated by in vitro
stimulation of PBMC with modified NY-ESO-1-specific pept
192 icrofluidic platform for culturing and focal
stimulation of cells with molecules of interest.
193 This effect can be partially mimicked by
stimulation of Hmox1(+/+) SCs with monocyte chemoattract
194 In fact,
stimulation of the cells with morphine resulted in a tra
195 Stimulation of macrophages with muramyl dipeptide, the N
196 ates edema and nerve sensitization following
stimulation of peripheral nerves with mustard oil, demon
197 Stimulation of podocytes with NaHS resulted in both shor
198 IFN-gamma promoter at rapid times after TCR
stimulation of memory compared with naive CD4 T cells.
199 Finally,
stimulation of DCs with nCup a 1 resulted in ST2 upregul
200 Strikingly,
stimulation of the cells with NE or ectopic expression o
201 Subretinal
stimulation of the retina with neurotransmitters, the no
202 In vitro
stimulation of ILC2s with NMU induced rapid cell activat
203 Stimulation of epithelial cells with Nod1 stimulatory mo
204 Stimulation of GPR120 with omega-3 FAs or a chemical ago
205 The results thus show that conjunctive
stimulation of climbing fibres with other inputs to Golg
206 In vitro,
stimulation of alveolar macrophages with P. carinii indu
207 on Y1020, a marker for its activation, upon
stimulation of human platelets with PAR agonists SFLLRN
208 Stimulation of cells with PAR2-AP alone failed to enhanc
209 Stimulation of alpha1A-AR with phenylephrine or direct a
210 Herein, we demonstrated that
stimulation of cardiomyocytes with phenylephrine (PE), a
211 Stimulation of myocytes with phenylephrine or angiotensi
212 ransient activation of the gene, we used the
stimulation of MLP29 cells with phorbol esters and the i
213 The
stimulation of tissue with phorbol-12-myristate-13-aceta
214 Stimulation of cells with physiological concentrations o
215 Stimulation of cells with physiological concentrations o
216 3) The magnitude of serum
stimulation of NHE3 correlates with PI(4,5)P(2) and PI(3
217 Stimulation of pAEC with pIFN-gamma increased SLA II exp
218 Stimulation of KCs with pilocarpine significantly (p < 0
219 Stimulation of the cortex with pinprick or KCl granule w
220 Stimulation of Nrf2(-/-) DCs with PM augmented oxidative
221 Ex vivo
stimulation of lung leukocytes with poly(I:C), ssRNA40,
222 neurons, combining presynaptic thermogenetic
stimulation of dopaminergic neurons with postsynaptic fu
223 ic elastography using non-contact mechanical
stimulation of soft media with precise spatial and tempo
224 In vitro
stimulation of monocytes with products of the complement
225 s NTR1 and its expression is increased after
stimulation of preadipocytes with proinflammatory cytoki
226 ally occurring disease, we hypothesized that
stimulation of tendon explants with proinflammatory medi
227 stant to pericellular degradation, even upon
stimulation of the cells with proinflammatory cytokines.
228 Stimulation of the endothelium with proinflammatory cyto
229 Transient cAMP increases were observed upon
stimulation of HEK293 cells with prostaglandin E1.
230 Furthermore,
stimulation of hPTH1R with PTH analogues, [Trp1]PTHrp-(1
231 Stimulation of platelets with purified histones was suff
232 d gene regulation similar to that induced by
stimulation of TLR7 with R848.
233 Stimulation of murine splenocytes with recombinant prote
234 In addition, in vitro
stimulation of PMN with recombinant HMGB1 caused TLR4-de
235 ing either aggregation of suspended cells or
stimulation of cell monolayers with retinoic acid.
236 -Src through its PDZ binding motif following
stimulation of melanoma cells with rFVIIa and FX.
237 Stimulation of peritoneal macrophages with rHagB resulte
238 ion but also proinflammatory responses after
stimulation of MDDCs with RIG-I activators.
239 Furthermore,
stimulation of monocytes with S100 proteins was found to
240 Stimulation of chondrocytes with S100A4 increased the ph
241 Moreover, the long-term
stimulation of keratinocytes with Sandalore positively a
242 Stimulation of cells with serotonin (5-hydroxytryptamine
243 corporate microfluidic cell culture, precise
stimulation of cells with signaling molecules or drugs,
244 Stimulation of macrophages with silica results in the ac
245 in sympathetic nerve activity in response to
stimulation of chemoreceptors with sodium cyanide was ma
246 Stimulation of hippocampal astrocytes with soluble ephri
247 Furthermore, new experiments involving
stimulation of the OB with specific temporal patterns al
248 ctivation of NK cells was observed following
stimulation of PBMC with ssRNA40, negligible activation
249 Stimulation of HUVECs with sublytic complement concentra
250 We propose that
stimulation of AT1 receptors with subsequent activation
251 A combination of electrical
stimulation of affected muscles with suggestion of immin
252 In previous studies, we have shown that
stimulation of cultured neurons with surrogate NCAM liga
253 This effect is specific for the co-
stimulation of IGFBP-3 with TGF-beta1 because a combinat
254 Stimulation of fibroblasts with TGFBI down-regulated MMP
255 Prolonged
stimulation of A1Rs with the agonist N(6)-cyclopentylade
256 mediated uptake and an enhancement of T cell
stimulation of Ags with the inherent ability to bind HSP
257 Consistently,
stimulation of CLL cells with the chemokine CXCL12 induc
258 Whereas
stimulation of control platelets with the BH3-mimetic AB
259 We show that
stimulation of interphase cells with the mitogens epider
260 We demonstrate that
stimulation of macrophages with the arginine- and lysine
261 Stimulation of melanoma cells with the MERTK ligand GAS6
262 Selective
stimulation of PKA with the agonist N(6)-benzoyl-cAMP (5
263 Stimulation of platelets with the PAR-1 agonist SFLLRN r
264 Stimulation of primary melanocytes with the OR51E2 ligan
265 by reward-related lateral hypothalamic brain
stimulation of rats injected with the neurotransmitter s
266 T cells in vivo after treatment with CpG and
stimulation of the TCR with the staphylococcal enterotox
267 Stimulation of UEC with the TLR3 agonist poly(I:C) induc
268 unosorbent assay (ELISA) following overnight
stimulation of whole blood with the peptide antigens, an
269 Stimulation of cells with thrombin resulted in an increa
270 interaction between eNOS and Cav-1 following
stimulation of endothelial cells with thrombin, vascular
271 Stimulation of MEG-01 with thrombin reduced levels of WD
272 Stimulation of murine platelets with thrombin plus the g
273 Flow cytometry revealed that
stimulation of platelets with thrombin/convulxin signifi
274 Stimulation of cells with TLR agonists such as LPS in th
275 Stimulation of macrophages with TLR agonists results in
276 Stimulation of murine DRGNs with TLR ligands induced exp
277 Stimulation of autophagy with TLR7 ligands was functiona
278 Transient
stimulation of cells with TNF-alpha for 15 min induced o
279 Stimulation of FLSs with TNF increased their capacity to
280 Stimulation of pulmonary macrophages with TNF-alpha and/
281 Stimulation of cells with TNFalpha leads to the formatio
282 ted PGC-1beta on inflammatory cytokines upon
stimulation of muscle cells with TNFalpha, Toll-like rec
283 Stimulation of RASFs with TNFalpha or IL-1beta led to in
284 In our prior work, we showed that
stimulation of innate immunity with Toll-like receptor 9
285 Stimulation of IPSCs with trains of impulses (10 at 20 H
286 Stimulation of dendritic cells with trophic forms, but n
287 Stimulation of cells with tumor necrosis factor (TNFalph
288 After
stimulation of ECs with tumor-necrosis factor-alpha (TNF
289 Stimulation of WT cells with tumor necrosis factor alpha
290 We discover that mechanical
stimulation of the skin with ultrasound can overturn hea
291 Furthermore,
stimulation of HSG cells with UTP induced phosphorylatio
292 Stimulation of cells with VEGF-A or -B also led to large
293 We found that
stimulation of lymphangiogenesis with VEGF-C156S, a muta
294 Neurons in S1 responded to
stimulation of POm with what has been termed Class 2 pro
295 were detected in all pigs analyzed following
stimulation of immune lymphocytes with whole virus.
296 ollowing infection with HSV-1 and found that
stimulation of DCs with wild-type HSV-1 required intact
297 Stimulation of human macrophages with WISP1 led to a pro
298 Stimulation of chondrocytes with Wnt-3a in vitro led to
299 Notably,
stimulation of cells with WT NRG1 induced co-precipitati
300 In this study we show that
stimulation of macrophages with zymosan, which contains